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Information on EC 4.2.1.92 - hydroperoxide dehydratase
for references in articles please use BRENDA:EC4.2.1.92
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IUBMB Comments
Acts on a number of unsaturated fatty-acid hydroperoxides, forming the corresponding allene oxides. The product of the above reaction is unstable and is acted upon by EC 5.3.99.6, allene-oxide cyclase, to form the cyclopentenone derivative (15Z)-12-oxophyto-10,15-dienoate (OPDA), which is the first cyclic and biologically active metabolite in the jasmonate biosynthesis pathway . The enzyme from many plants belongs to the CYP-74 family of P-450 monooxygenases .
The expected taxonomic range for this enzyme is: Bacteria, Eukaryota
- 4.2.1.92
- lipoxygenase
-
jasmonic
- oxylipins
-
linolenic
-
12-oxo-phytodienoic
- aroma
- hevea
-
divinyl
- epoxyalcohols
-
9-hydroperoxides
- lyases
-
cyclopentenone
-
alpha-linolenic
-
13-hpot
-
13-lipoxygenase
-
wound-induced
-
octadecanoids
-
laticifer
-
alpha-ketols
- aloxe3
- 12r-lox
-
13-hydroperoxy
- e-2-hexenal
-
hepoxilins
- homomalla
-
coronatine
-
homolytic
- hexenal
-
heterolytic
-
gaeumannomyces
-
antarafacial
- attenuata
-
plexaura
- food industry
- medicine
- synthesis
Reaction Schemes
showSynonyms
allene oxide synthase, hydroperoxide lyase, cyp74, hydroperoxide isomerase, elox3, rubber particle protein, osaos1, fatty acid hydroperoxide lyase, oshpl3, cyp74c, more
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SYNONYM 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
13-HPL
13-hydroperoxide lyase
13-hydroperoxide-lyase
9R-DOX-AOS
9S-DOX-AOS
allene oxide synthase
AOS
AOS1
AOS2
CmHPL
CYP74
CYP74A
CYP74c
cytochrome P450 74A
-
-
-
-
EC 5.3.99.1
-
-
formerly
-
eLOX3
-
-
-
-
fatty acid 9-hydroperoxide lyase
fatty acid hydroperoxide lyase
fatty acid hydroperoxide-metabolizing enzyme
Fg-cat
FG02216.1
FGSG_02217
FOXB_01332
HPI
-
-
-
-
HPL
HPL1
HPLS
hydroperoxide dehydrase
-
-
-
-
hydroperoxide isomerase
hydroperoxide lyase
hydroperoxidehydrase
-
-
-
-
isomerase, hydroperoxide
-
-
-
-
KC525886
linoleate hydroperoxide isomerase
-
-
-
-
linoleic acid hydroperoxide isomerase
-
-
-
-
LOX
RPP
-
-
-
-
rubber particle protein
-
-
-
-
hydroperoxide isomerase
-
-
-
-
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REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
mechanism
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
mechanism
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
mechanism
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
mechanism
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
acts on a number of unsaturated fatty-acid hydroperoxides, forming the corresponding allene oxides
-
-
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
reaction mechanisms of wild-type AOS and mutant F137L, QM/MM calculations, overview
-
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate = (9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
mechanism
-
-
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REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
C-O bond cleavage by elimination of water
-
-
-
-
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PATHWAY SOURCE
PATHWAYS
MetaCyc
9-lipoxygenase and 9-allene oxide synthase pathway, jasmonic acid biosynthesis
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SYSTEMATIC NAME
IUBMB Comments
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate 12,13-hydro-lyase [(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate-forming]
Acts on a number of unsaturated fatty-acid hydroperoxides, forming the corresponding allene oxides. The product of the above reaction is unstable and is acted upon by EC 5.3.99.6, allene-oxide cyclase, to form the cyclopentenone derivative (15Z)-12-oxophyto-10,15-dienoate (OPDA), which is the first cyclic and biologically active metabolite in the jasmonate biosynthesis pathway [3]. The enzyme from many plants belongs to the CYP-74 family of P-450 monooxygenases [4].
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CAS REGISTRY NUMBER
COMMENTARY
118390-60-6
-
37318-50-6
-
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SUBSTRATE
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
LITERATURE
COMMENTARY
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
(12R)-hydroperoxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid
(8R)-hydroxy-(11R,12R)-epoxyeicosa-(5Z,9E,14Z)-trienoic acid + H2O
(12S)-hydroperoxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid
(10R)-hydroxy-(11S,12S)-epoxyeicosa-(5Z,8Z,14Z)-trienoic acid + (8R)-hydroxy-(11S,12S)-epoxyeicosa-(5Z,9E,14Z)-trienoic acid + H2O
-
Substrates: -
Products: the former being a isomer of hepoxilin A3, ration of products is 2:1
Products: the former being a isomer of hepoxilin A3, ration of products is 2:1
?
(13R)-hydroperoxylinolenic acid
13-ketolinolenic acid + threo-11-hydroxy-(12R,13R)-epoxy-(9Z,15Z)-octadecadienoic acid + erythro-11-hydroxy-(12R,13R)-epoxy-(9Z,15Z)-octadecadienoic acid
Substrates: the G316A mutant converts (13R)-hydroperoxylinolenic acid to 13-ketolinolenic acid (with an apparent Km of 0.01 mM) and to epoxyalcohols viz. erythro- and threo-11-hydroxy-(12R,13R)-epoxy-(9Z,15Z)-octadecadienoic acids and one of the corresponding cis-epoxides as major products
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(9Z)-12,13-epoxy-9,11-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E,15Z)-octadecatrienoic acid
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid + H2O
-
Substrates: -
Products: 12-oxo-13-hydroxy-(9Z,15Z)-octadecadienoic acid + 12-oxo-(10,15Z)-phytodienoic acid, formed by spontaneous chemical or enzyme-catalyzed cyclization
Products: 12-oxo-13-hydroxy-(9Z,15Z)-octadecadienoic acid + 12-oxo-(10,15Z)-phytodienoic acid, formed by spontaneous chemical or enzyme-catalyzed cyclization
?
(13S)-hydroperoxy-(9Z,11Z,15Z)-octadecatrienoic acid
(12,13S)-epoxy-(9Z,11Z,15Z)-octadecatrienoic acid + H2O
A9SNA2, A9S014
Substrates: by AOS1
Products: -
Products: -
?
(13S)-hydroperoxyoctadecadienoic acid
13-hydroxy-12-oxo-9(Z)-octadecenoic acid + 12-oxo-10-phytoenoic acid
-
Substrates: -
Products: 13-hydroxy-12-oxo-(9Z)-octadecenoic acid is the major product
Products: 13-hydroxy-12-oxo-(9Z)-octadecenoic acid is the major product
?
(13S)-hydroperoxyoctadecatrienoic acid
13-hydroxy-12-oxo-(9Z,15Z)-octadecadienoic acid + 12-oxo-(10Z,15Z)-phytodienoic acid
-
Substrates: -
Products: OsAOS1 produces a 1:1 racemic mixture of cis-(+)/cis-(-)-12-oxo-(10Z,15Z)-phytodienoic acid via non-enzymatic cyclization of 12,13-epoxy-9,11,15-octadecatrienoic acid, an unstable allene oxide
Products: OsAOS1 produces a 1:1 racemic mixture of cis-(+)/cis-(-)-12-oxo-(10Z,15Z)-phytodienoic acid via non-enzymatic cyclization of 12,13-epoxy-9,11,15-octadecatrienoic acid, an unstable allene oxide
?
(13S,9Z,11E,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
?
-
Substrates: is converted to an allene oxide
Products: -
Products: -
?
(15S)-hydroperoxyeicosatetraenoic acid
(15S)-hydroxy-11,12-epoxyeicosatrienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(5Z,8Z,11E,13Z,15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid
14,15-hepoxilin A3 + 14,15-hepoxilin B3 + H2O
(8E,10S,12Z)-10-hydroperoxyoctadeca-8,12-dienoic acid
(8E)-10-oxodecenoic acid + 1-octen-3-ol + (2Z)-octen-1-ol
Substrates: the catalase-related hemoprotein reacts rapidly and specifically with linoleate 10S-hydroperoxide with a hydroperoxide lyase activity specific for the 10S-hydroperoxy enantiomer
Products: in a 3:1 ratio, strict enzymatic control in formation of the 3R alcohol configuration with 99% enantiomeric excess
Products: in a 3:1 ratio, strict enzymatic control in formation of the 3R alcohol configuration with 99% enantiomeric excess
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
(8R)-hydroperoxylinoleic acid + H2O
(5S,8R)-dihydroxylinoleic acid
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroperoxylinoleic acid + H2O
(8R,11S)-dihydroxylinoleic acid
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroxyeicosatetraenoic acid
(8R)-hydroxy-(9R,10R)-trans-epoxy-eicosa-(5Z,11Z,14Z)-trienoic acid
-
Substrates: the native, unmodified enzyme shows no activity with (8R)-hydroxyeicosatetraenoic acid, but the oxidized enzyme epoxidizes the substrate analogue stereospecifically on the 9,10-double bond to form (8R)-hydroxy-(9R,10R)-trans-epoxy-eicosa-(5Z,11Z,14Z)-trienoic acid as the predominant product, via Compound I (FeV=O) intermediate
Products: erythro and threo diastereomers of (8R)-hydroxy-9,10-trans-epoxy-eicosa-5Z,11Z,14Z-trienoate
Products: erythro and threo diastereomers of (8R)-hydroxy-9,10-trans-epoxy-eicosa-5Z,11Z,14Z-trienoate
?
(9R)-hydroperoxy-(10E,12Z,15Z)-octadecatrienoic acid
9-hydroxy-10-oxo-(12Z,15Z)-octadecadienoic acid
-
Substrates: -
Products: -
Products: -
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(12Z)-9,10-epoxy-10,12-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
9-oxononanoic acid + (3Z)-nonenal
-
Substrates: -
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z,15Z)-octadecatrienoic acid
(9S,10)-epoxy-(10Z,12Z,15Z)-octadecatrienoic acid + H2O
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
threo-9,10-dihydroxy-12-octadecenoic acid + erythro-9,10-dihydroxy-12-octadecenoic acid
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
threo-9,10-dihydroxy-12,15-octadecadienoic acid + erythro-9,10-dihydroxy-12,15-octadecadienoic acid
(9Z,11E,13R)-13-hydroperoxyoctadeca-9,11-dienoic acid
11-hydroxy-12(13)-epoxy-octadecadienoic acid + 9-hydroxy-12(13)-epoxy-octadecadienoic acid + H2O
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
threo-12,13-dihydroxy-9-octadecenoic acid + erythro-12,13-dihydroxy-9-octadecenoic acid
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
13-hydroperoxy-(10E,12Z)-octadecadienoic acid
11-hydroxy-12(13)-epoxy-octadecadienoic acid + 9-hydroxy-12(13)-epoxy-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
13-hydroperoxy-9,11-octadecadienoic acid
(10E,12Z)-12-[(3S)-3-methyl-3-propyloxiran-2-ylidene]dodec-10-enoic acid + H2O
-
Substrates: wild-type AOS activity
Products: -
Products: -
?
13-hydroperoxy-9,11-octadecadienoic acid
(10E,12Z)-13-[(2-hydroxypentan-2-yl)oxy]trideca-10,12-dienoic acid + H2O
-
Substrates: activity of AOS mutant F137L
Products: -
Products: -
?
13-hydroperoxylinoleic acid
(Z)-3-hexanal + 12-oxododecenoic acid
-
Substrates: -
Products: -
Products: -
?
13-hydroperoxylinolenic acid
12-oxo-cis-10,15-phytodienoic acid + (12Z,15Z)-9-hydroxy-10-oxooctadeca-12,15-dienoic acid + H2O
-
Substrates: -
Products: the latter is a minor product of approximately 5%
Products: the latter is a minor product of approximately 5%
?
9-hydroperoxylinolenic acid
13-hydroxy-10-oxo-cis-15-trans-11-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
alpha-linolenic acid
(E,Z)-3,6-nonadienal + 9-oxononanoic acid
-
Substrates: cleavage of 9-hydroperoxy fatty acid
Products: -
Products: -
?
heptadecatrienoic acid
12-hydroperoxyheptadecatrienoic acid + (8Z,10S,11Z,14Z)-10-hydroperoxyheptadeca-8,11,14-trienoic acid
Substrates: the G316A mutant transforms 17:3n-3 to both 12-hydroperoxyheptadecatrienoic acid (about 93%) and 10-hydroperoxyheptadecatrienoic acid (7%)
Products: -
Products: -
?
linoleate hydroperoxide + H2O
9,12,13-trihydroxy-trans-10-octadecenoic acid + 9,10,13-trihydroxy-trans-11-octadecenoic acid
-
Substrates: -
Products: -
Products: -
?
linoleic acid
(Z)-3-nonenal + 9-oxononanoic acid
-
Substrates: cleavage of 9-hydroperoxy fatty acid
Products: -
Products: -
?
linoleic acid
?
Substrates: Mn-LO G316A metabolizeS 18:2n-6 to (11S)-hydroperoxyoctadecadienoic acid and (13R)-hydroperoxyoctadecadienoic acid in approximately the same relative amounts as the native enzyme, and (13R)-hydroperoxyoctadecadienoic acid accumulates as the end product
Products: -
Products: -
?
linolenic acid
(13R)-hydroperoxyoctadecatrienoic acid + (11S)-hydroperoxyoctadecatrienoic acid
Substrates: Mn-LO G316A metabolizes 18:3n-3 to (13R)-hydroperoxyoctadecatrienoic acid and (11S)-hydroperoxyoctadecatrienoic acid
Products: -
Products: -
?
linolic acid hydroperoxide + H2O
9,12,13-trihydroxy-trans-10-octadecenoic acid + 9,10,13-trihydroxy-trans-11-octadecenoic acid
-
Substrates: -
Products: -
Products: -
?
(12R)-hydroperoxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid
(8R)-hydroxy-(11R,12R)-epoxyeicosa-(5Z,9E,14Z)-trienoic acid + H2O
-
Substrates: intramolecular oxygenation with retention of the configuration of the carbon atom hydroxylated
Products: -
Products: -
?
(12R)-hydroperoxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid
(8R)-hydroxy-(11R,12R)-epoxyeicosa-(5Z,9E,14Z)-trienoic acid + H2O
-
Substrates: poor substrate
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: substrate listed without specification of steroisomer used
Products: products are 10,13-dihydroxyoctadec-11-enoic acid + 12,13-dihydroxyoctadec-9-enoic acid + trace amounts of 9,12-dihydroxyoctadec-10-enoic acid
Products: products are 10,13-dihydroxyoctadec-11-enoic acid + 12,13-dihydroxyoctadec-9-enoic acid + trace amounts of 9,12-dihydroxyoctadec-10-enoic acid
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: (S)-hydroperoxy-(9Z,11E)-octadecadienoic acid is a poor substrate
Products: products are: (11R,12R)-epoxy-(13S)-hydroxy-(9Z)-octadecenoic acid + (9S,10R)-epoxy-(13S)-hydroxy-(11E)-octadecenoic acid
Products: products are: (11R,12R)-epoxy-(13S)-hydroxy-(9Z)-octadecenoic acid + (9S,10R)-epoxy-(13S)-hydroxy-(11E)-octadecenoic acid
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: products are: 13-hydroxy-12-oxo-cis-9-octadecenoic acid + small amounts of the gamma ketol
Products: products are: 13-hydroxy-12-oxo-cis-9-octadecenoic acid + small amounts of the gamma ketol
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12S,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: spontaneous hydrolysis to 12-keto-13-hydroxy-(9Z)-octadecenoic acid (72% 13(R) and 28% 13(S))
Products: spontaneous hydrolysis to 12-keto-13-hydroxy-(9Z)-octadecenoic acid (72% 13(R) and 28% 13(S))
?
(5Z,8Z,11E,13Z,15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid
14,15-hepoxilin A3 + 14,15-hepoxilin B3 + H2O
-
Substrates: high stereoselectivity, not with 15(R)-substrate
Products: mixture of both products
Products: mixture of both products
?
(5Z,8Z,11E,13Z,15S)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid
14,15-hepoxilin A3 + 14,15-hepoxilin B3 + H2O
-
Substrates: poor substrate
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: stereospecific elimination of the pro-S hydrogen from C-7 and intramolecular suprafacial insertion of oxygen at C-7 with retention of the absolute configuration at C-7
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: stereospecific elimination of the pro-S hydrogen from C-7 and intramolecular suprafacial insertion of oxygen at C-7 with retention of the absolute configuration at C-7
Products: -
Products: -
?
(8R)-hydroperoxy-(9Z,12Z)-octadecadienoic acid
(7S,8S)-dihydroxy-(9Z,12Z)-octadecadienoic acid + H2O
-
Substrates: poor substrate
Products: -
Products: -
?
(8R)-hydroperoxyeicosatetraenoic acid
?
-
Substrates: the substrate is converted to an unstable allene oxide product via the FeIV-OH intermediate, Compound II, the native enzyme shows a strong preference for its natural substrate
Products: -
Products: -
?
(8R)-hydroperoxyeicosatetraenoic acid
?
-
Substrates: the substrate is converted to an unstable allene oxide product via the FeIV-OH intermediate, Compound II
Products: -
Products: -
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
Substrates: -
Products: an unstable allene oxide
Products: an unstable allene oxide
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
Substrates: -
Products: an unstable allene oxide
Products: an unstable allene oxide
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-10(E),12(Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (90S)-(10)-epoxy-10,12(Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-10(E),12(Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (90S)-(10)-epoxy-10,12(Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
-
Substrates: -
Products: 9-hydroxy-10-oxo,cis-12-octadecenoic acid and 13-hydroxy-10-oxo-trans-11-octadecenoic acid in the ratio 2:1
Products: 9-hydroxy-10-oxo,cis-12-octadecenoic acid and 13-hydroxy-10-oxo-trans-11-octadecenoic acid in the ratio 2:1
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
-
Substrates: (S)-hydroperoxy-(10E,12Z)-octadecadienoic acid is a poor substrate
Products: products: (10R,11R)-epoxy-(9S)-hydroxy-(12Z)-octadecenoic acid + (12R,13S)-epoxy-(9S)-hydroxy-(10E)-octadecenoic acid
Products: products: (10R,11R)-epoxy-(9S)-hydroxy-(12Z)-octadecenoic acid + (12R,13S)-epoxy-(9S)-hydroxy-(10E)-octadecenoic acid
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
-
Substrates: -
Products: in presence of linoleate the product is (9R)-linoleoyloxy-10-oxo-cis-12-octadecenoic acid
Products: in presence of linoleate the product is (9R)-linoleoyloxy-10-oxo-cis-12-octadecenoic acid
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
10-oxo-(9R)-hydroxy-cis-12-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z,15Z)-octadecatrienoic acid
(9S,10)-epoxy-(10Z,12Z,15Z)-octadecatrienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z,15Z)-octadecatrienoic acid
(9S,10)-epoxy-(10Z,12Z,15Z)-octadecatrienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
?
-
Substrates: the divinyl ether synthase enzyme mutant E292G shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol and 12-oxo-10,15-phytodienoic acid, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74B16
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
?
-
Substrates: the divinyl ether synthase enzyme mutant V379F shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74D3
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
threo-9,10-dihydroxy-12-octadecenoic acid + erythro-9,10-dihydroxy-12-octadecenoic acid
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
threo-9,10-dihydroxy-12-octadecenoic acid + erythro-9,10-dihydroxy-12-octadecenoic acid
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
threo-9,10-dihydroxy-12,15-octadecadienoic acid + erythro-9,10-dihydroxy-12,15-octadecadienoic acid
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
threo-9,10-dihydroxy-12,15-octadecadienoic acid + erythro-9,10-dihydroxy-12,15-octadecadienoic acid
-
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
threo-9,10-dihydroxy-12,15-octadecadienoic acid + erythro-9,10-dihydroxy-12,15-octadecadienoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13R)-13-hydroperoxyoctadeca-9,11-dienoic acid
11-hydroxy-12(13)-epoxy-octadecadienoic acid + 9-hydroxy-12(13)-epoxy-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,13R)-13-hydroperoxyoctadeca-9,11-dienoic acid
11-hydroxy-12(13)-epoxy-octadecadienoic acid + 9-hydroxy-12(13)-epoxy-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: 13-HPOD
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
threo-12,13-dihydroxy-9-octadecenoic acid + erythro-12,13-dihydroxy-9-octadecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
threo-12,13-dihydroxy-9-octadecenoic acid + erythro-12,13-dihydroxy-9-octadecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
?
-
Substrates: the divinyl ether synthase enzyme mutant E292G shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol and 12-oxo-10,15-phytodienoic acid, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74B16
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
?
-
Substrates: the divinyl ether synthase enzyme mutant V379F shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74D3
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
-
Substrates: -
Products: -
Products: -
?
additional information
?
-
Substrates: the enzyme catalyzes the first specific reaction in the formation of 12-oxophytodienoic acid, a signaling compound with multiple functions that is also the immediate precursor of jasmonic acid
Products: -
Products: -
?
additional information
?
-
-
Substrates: the enzyme catalyzes the first specific reaction in the formation of 12-oxophytodienoic acid, a signaling compound with multiple functions that is also the immediate precursor of jasmonic acid
Products: -
Products: -
?
additional information
?
-
Substrates: galactoplid bound hydroperoxides are substrates for CYP74 members
Products: -
Products: -
?
additional information
?
-
-
Substrates: two hydroperoxide isomerases in Aspergillus clavatus acting on hydroperoxylinoleic acid: the 5,8-linoleate diol synthase exhibiting 5,8-hydroperoxide isomerase activity, and the 8, 11-linoleate diol synthase exhibiting 8,11-hydroperoxide isomerase activity, overview
Products: -
Products: -
?
additional information
?
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Substrates: Asn964 may facilitate homolytic cleavage of the dioxygen bond of (9R)-hydroperoxy-10(E),12(Z)-octadecadienoic acid with formation of compound II. No activity with 18:2n-6
Products: -
Products: -
?
additional information
?
-
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Substrates: Asn964 may facilitate homolytic cleavage of the dioxygen bond of (9R)-hydroperoxy-10(E),12(Z)-octadecadienoic acid with formation of compound II. No activity with 18:2n-6
Products: -
Products: -
?
additional information
?
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Substrates: Asn964 may facilitate homolytic cleavage of the dioxygen bond of (9R)-hydroperoxy-10(E),12(Z)-octadecadienoic acid with formation of compound II. No activity with 18:2n-6
Products: -
Products: -
?
additional information
?
-
Substrates: the recombinant enzyme (encoded by gene CYP74B24) produces (Z)-3-hexenal from 13-HPOT with the optimal pH 6.0 in vitro
Products: -
Products: -
?
additional information
?
-
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Substrates: the recombinant enzyme (encoded by gene CYP74B24) produces (Z)-3-hexenal from 13-HPOT with the optimal pH 6.0 in vitro
Products: -
Products: -
?
additional information
?
-
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Substrates: cleavage of 9-hydroperoxy fatty acids or 13-hydroperoxy fatty acids by a hydroperoxide lyase results in formation of aldehydes (Z)-3-nonenal/(E,Z)-3,6-nonadienal or (Z)-3-hexanal, and omega-oxo fatty acid 9-oxo-nonanoic acid or 12-oxo-dodecenoic acid, respectively
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additional information
?
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
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additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview. No activity with (9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
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Products: -
?
additional information
?
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
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Products: -
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additional information
?
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
Products: -
Products: -
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additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
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additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
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Products: -
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additional information
?
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Substrates: mechanism of formation of fatty acid diepoxy ketone, overview. No reaction with 9R- and 9S-hydroperoxy-9,11-octadecadienoates. Peroxidase assay monitoring the oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulphonic acid (ABTS), enzyme Fg-cat exhibits robust activity (kcat 550 s/1) using the 13S-hydroperoxy-C18 fatty acids as the oxidizing co-substrate
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Products: -
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additional information
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Substrates: mechanism of formation of fatty acid diepoxy ketone, overview. No reaction with 9R- and 9S-hydroperoxy-9,11-octadecadienoates. Peroxidase assay monitoring the oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulphonic acid (ABTS), enzyme Fg-cat exhibits robust activity (kcat 550 s/1) using the 13S-hydroperoxy-C18 fatty acids as the oxidizing co-substrate
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Products: -
?
additional information
?
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Substrates: mechanism of formation of fatty acid diepoxy ketone, overview. No reaction with 9R- and 9S-hydroperoxy-9,11-octadecadienoates. Peroxidase assay monitoring the oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulphonic acid (ABTS), enzyme Fg-cat exhibits robust activity (kcat 550 s/1) using the 13S-hydroperoxy-C18 fatty acids as the oxidizing co-substrate
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Products: -
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additional information
?
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Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
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additional information
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Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
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Products: -
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additional information
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Substrates: (9S)-dioxygenase-allene oxide synthase converts 9S-hydroperoxyoctadecadienoic acid to alpha- and gamma-ketols, likely formed by hydrolysis of (9S,10)-(10)-epoxy-(10Z,12Z)-octadecadienoic acid, along with small amounts of epoxy alcohols. The (9R)-hydroperoxyoctadecadienoic acid preparation contains a few percent (9S)-hydroperoxyoctadecadienoic acid, and only the latter is apparently transformed to an alpha-ketol by (9S)-dioxygenase-allene oxide synthase. (13S)-hydroperoxyoctadecadienoic acid, (13S)-hydroxy-(10E,12Z,15Z)-octadecatrienoicacid, (13R)-hydroperoxyoctadecadienoic acid, and (13R)-hydroxy-(10E,12Z,15Z)-octadecatrienoicacid are not transformed to detectable amounts of allene oxides/alpha-ketols, but variable amounts of epoxy alcohols accumulate, mass spectrometric analysis of products, substrate specificity, overview
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Products: -
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additional information
?
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Substrates: (9S)-dioxygenase-allene oxide synthase converts 9S-hydroperoxyoctadecadienoic acid to alpha- and gamma-ketols, likely formed by hydrolysis of (9S,10)-(10)-epoxy-(10Z,12Z)-octadecadienoic acid, along with small amounts of epoxy alcohols. The (9R)-hydroperoxyoctadecadienoic acid preparation contains a few percent (9S)-hydroperoxyoctadecadienoic acid, and only the latter is apparently transformed to an alpha-ketol by (9S)-dioxygenase-allene oxide synthase. (13S)-hydroperoxyoctadecadienoic acid, (13S)-hydroxy-(10E,12Z,15Z)-octadecatrienoicacid, (13R)-hydroperoxyoctadecadienoic acid, and (13R)-hydroxy-(10E,12Z,15Z)-octadecatrienoicacid are not transformed to detectable amounts of allene oxides/alpha-ketols, but variable amounts of epoxy alcohols accumulate, mass spectrometric analysis of products, substrate specificity, overview
Products: -
Products: -
?
additional information
?
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Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
Products: -
Products: -
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additional information
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-
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Substrates: overview on substrates, configurations and mechanism
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additional information
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Substrates: catalytic properties of Mn-LO and the G316A mutant with heptadecatrienic acid, 18:2n-6, octadecatrienoic acid, and nonadecatrienoic acid as substrates: increasing the fatty acid chain length from C17 to C19 shifts the oxygenation by Mn-LO from the n-6 toward the n-8 carbon. The G316A mutant increases the oxygenation at the n-8 carbon of 17:3n-3 and at the n-10 carbon of the C17 and C18 fatty acids (from 12% to 711%). The most striking effect of the G316A mutant is a 2fold, 7fold, and 15fold increase in transformation of the n-6 hydroperoxides of 19:3n-3, 18:3n-3, and 17:3n-3, respectively, to keto fatty acids and epoxyalcohols. The n-3 double bond is essential. Both oxygen atoms are retained in the epoxyalcohols. (R)-Hydroperoxides at n-6 of C17:3, 18:3, and 19:3 are transformed 5times faster than (S)-stereoisomers
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additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
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Products: -
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additional information
?
-
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Substrates: overview on substrates, configurations and mechanism
Products: -
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additional information
?
-
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Substrates: 13-HPL and 9-HPL activities on oxylipins, traumatin derivatives, in different plant organs, overview
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additional information
?
-
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Substrates: CYP74 enzymes use their fatty acid hydroperoxide substrate to activate the enzyme and substrate in one and the same step
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Products: -
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additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
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additional information
?
-
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Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid
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additional information
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Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid. GC-MS product analysis
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additional information
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-
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Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid
Products: -
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additional information
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Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid. GC-MS product analysis
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additional information
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Substrates: the enzyme mainly acts as an oleate or linoleate dioxygenase, albeit with alpha-linolenic acid very competitive at low substrate concentrations, substrate specificity and kinetics, overview
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additional information
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Substrates: according to their specificity, HPLs can act on the 9- or 13-hydroperoxides of linoleic and linolenic acids (hydroperoxyoctadecadienoic acid (HPOD) and hydroperoxyoctadecatrienoic acid (HPOT)) and catalyze the cleavage of these hydroperoxides into C6- or C9-aldehydes and the C12- or C9-oxo-acids, respectively
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additional information
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Substrates: the recombinant 13-HPL enzyme is assayed as biocatalyst to produce C6-aldehydes. Bioconversion of 13-hydroperoxides of linoleic and linolenic acids by recombinant enzyme with or without chloroplast targeting signal sequence, reaction products are identified and quantified using gas chromatography and mass spectrometry. Recombinant HPL enzyme with targeting sequence allows production of 5.61 mM hexanal and 4.39 mM (Z)-3-hexenal, corresponding to high conversion yields of 93.5% and 73%, respectively. The HPL enzyme without targeting sequence fails to obtain greater quantities of hexanal or (Z)-3-hexenal. No undesirable products are formed, and no isomerization of (Z)-3-hexenal in (E)-2-hexenal occurs
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additional information
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Substrates: OsHPL3 possesses intrinsic hydroperoxide lyase activity hydrolyzing hydroperoxylinolenic acid to produce green leaf volatiles, it catabolizes 9/13-hydroperoxylinoleic acid to form (Z)-3-hexenal
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additional information
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Substrates: cleavage of 9-hydroperoxy fatty acids in vivo, AOS enzymes also convert hydroperoxy fatty acids to aldehydes via an HPL-like activity
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additional information
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Substrates: allene oxide synthase converts fatty acid hydroperoxides into unstable fatty acid epoxides (allene oxides). OsAOS1 exhibits dual positional substrate specificity and prefers 13-positional isomeric to 9-positional isomeric substrates in vitro. OsAOS1 converts (9S)-hydroperoxyoctadecadienoic acid or (9S)-hydroperoxyoctadecatrienoic acid into the corresponding unstable allene oxides, which are non-enzymatically transformed into a 9alpha-ketol as the major product, and 13gamma-ketols and cyclopentenone derivatives as minor products
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additional information
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Substrates: allene oxide synthase is a key cytochrome P450 enzyme in the oxylipin pathway leading to allene oxide synthase-derived jasmonates
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additional information
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Substrates: allene oxide synthase is a key cytochrome P450 enzyme in the oxylipin pathway leading to allene oxide synthase-derived jasmonates
Products: -
Products: -
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additional information
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Substrates: the native enzyme is completely unreactive with polyunsaturated fatty acids or their hydroxylated analogues. Mass spectrometric product analysis, overview
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additional information
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Substrates: in case of hydroperoxide lyases the homolytic isomerization of fatty acid hydroperoxides leads to a short-lived hemiacetal, which spontaneously disintegrates into (Z)-3-hexenal and (9Z)-12-oxo-9-dodecenoic acid
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additional information
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Substrates: overview on substrates, configurations and mechanism
Products: -
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additional information
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Substrates: analysis of hexanal, (Z)-3-hexenal, (E)-2-hexenal, and (Z)-3-hexen-1-ol levels by gas chromatography
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: no activity with (9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
Products: -
Products: -
?
additional information
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Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview. No activity with (9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
Products: -
Products: -
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NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
LITERATURE
COMMENTARY
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
(8R)-hydroperoxyeicosatetraenoic acid
?
-
Substrates: the substrate is converted to an unstable allene oxide product via the FeIV-OH intermediate, Compound II, the native enzyme shows a strong preference for its natural substrate
Products: -
Products: -
?
(8R)-hydroperoxylinoleic acid + H2O
(5S,8R)-dihydroxylinoleic acid
-
Substrates: -
Products: -
Products: -
?
(8R)-hydroperoxylinoleic acid + H2O
(8R,11S)-dihydroxylinoleic acid
-
Substrates: -
Products: -
Products: -
?
(9R)-hydroperoxy-(10E,12Z,15Z)-octadecatrienoic acid
9-hydroxy-10-oxo-(12Z,15Z)-octadecadienoic acid
-
Substrates: -
Products: -
Products: -
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
13-hydroperoxy-9,11-octadecadienoic acid
(10E,12Z)-12-[(3S)-3-methyl-3-propyloxiran-2-ylidene]dodec-10-enoic acid + H2O
-
Substrates: wild-type AOS activity
Products: -
Products: -
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13-hydroperoxy-9,11-octadecadienoic acid
(10E,12Z)-13-[(2-hydroxypentan-2-yl)oxy]trideca-10,12-dienoic acid + H2O
-
Substrates: activity of AOS mutant F137L
Products: -
Products: -
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13-hydroperoxylinoleic acid
(Z)-3-hexanal + 12-oxododecenoic acid
-
Substrates: -
Products: -
Products: -
?
alpha-linolenic acid
(E,Z)-3,6-nonadienal + 9-oxononanoic acid
-
Substrates: cleavage of 9-hydroperoxy fatty acid
Products: -
Products: -
?
linoleic acid
(Z)-3-nonenal + 9-oxononanoic acid
-
Substrates: cleavage of 9-hydroperoxy fatty acid
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(13S)-hydroperoxy-(9Z,11E)-octadecadienoic acid
(12,13S)-oxido-(9Z,11)-octadecadienoic acid + H2O
-
Substrates: -
Products: -
Products: -
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
Substrates: -
Products: an unstable allene oxide
Products: an unstable allene oxide
?
(9R,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9R,10)-10-epoxy-(10Z,12Z)-octadecadienoic acid
Substrates: -
Products: an unstable allene oxide
Products: an unstable allene oxide
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid
(9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid + H2O
Substrates: recombinant FOXB_01332 oxidizes 18:2n-6 to (9S)-hydroperoxy-(10E,12Z)-octadecadienoic acid by hydrogen abstraction and antarafacial insertion of molecular oxygen and sequentially to an allene oxide, (9S,10)-epoxy-(10Z,12Z)-octadecadienoic acid, which gives nonenzymatic hydrolysis products alpha- and gamma-ketols
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
(9S,10S,11S,12Z)-9,10-epoxy-11-hydroxy-12-octadecenoic acid + 9-hydroxy-10-oxo-12-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + H2O + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
9-hydroxynonanoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
11-hydroxy-12,13-epoxy-9-octadecenoic acid + 9-hydroxy-12,13-epoxy-10-octadecenoic acid + (9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
hexanal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(9Z)-12-hydroxy-9-dodecenoic acid + (10E)-12-hydroxy-10-dodecenoic acid + ?
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
Substrates: -
Products: -
Products: -
?
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
(Z)-3-hexenal + 12-oxo-9-dodecenoic acid
-
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
Substrates: -
Products: -
Products: -
?
(9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate
(9Z,15Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate + H2O
-
Substrates: -
Products: -
Products: -
?
additional information
?
-
Substrates: the enzyme catalyzes the first specific reaction in the formation of 12-oxophytodienoic acid, a signaling compound with multiple functions that is also the immediate precursor of jasmonic acid
Products: -
Products: -
?
additional information
?
-
-
Substrates: the enzyme catalyzes the first specific reaction in the formation of 12-oxophytodienoic acid, a signaling compound with multiple functions that is also the immediate precursor of jasmonic acid
Products: -
Products: -
?
additional information
?
-
Substrates: galactoplid bound hydroperoxides are substrates for CYP74 members
Products: -
Products: -
?
additional information
?
-
-
Substrates: two hydroperoxide isomerases in Aspergillus clavatus acting on hydroperoxylinoleic acid: the 5,8-linoleate diol synthase exhibiting 5,8-hydroperoxide isomerase activity, and the 8, 11-linoleate diol synthase exhibiting 8,11-hydroperoxide isomerase activity, overview
Products: -
Products: -
?
additional information
?
-
-
Substrates: cleavage of 9-hydroperoxy fatty acids or 13-hydroperoxy fatty acids by a hydroperoxide lyase results in formation of aldehydes (Z)-3-nonenal/(E,Z)-3,6-nonadienal or (Z)-3-hexanal, and omega-oxo fatty acid 9-oxo-nonanoic acid or 12-oxo-dodecenoic acid, respectively
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specificities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
additional information
?
-
Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
Products: -
Products: -
?
additional information
?
-
-
Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
Products: -
Products: -
?
additional information
?
-
Substrates: FOXB_01332 is a linoleate 9-dioxygenase with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
additional information
?
-
-
Substrates: 13-HPL and 9-HPL activities on oxylipins, traumatin derivatives, in different plant organs, overview
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
additional information
?
-
-
Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid
Products: -
Products: -
?
additional information
?
-
-
Substrates: the enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid
Products: -
Products: -
?
additional information
?
-
Substrates: according to their specificity, HPLs can act on the 9- or 13-hydroperoxides of linoleic and linolenic acids (hydroperoxyoctadecadienoic acid (HPOD) and hydroperoxyoctadecatrienoic acid (HPOT)) and catalyze the cleavage of these hydroperoxides into C6- or C9-aldehydes and the C12- or C9-oxo-acids, respectively
Products: -
Products: -
?
additional information
?
-
-
Substrates: OsHPL3 possesses intrinsic hydroperoxide lyase activity hydrolyzing hydroperoxylinolenic acid to produce green leaf volatiles, it catabolizes 9/13-hydroperoxylinoleic acid to form (Z)-3-hexenal
Products: -
Products: -
?
additional information
?
-
-
Substrates: cleavage of 9-hydroperoxy fatty acids in vivo, AOS enzymes also convert hydroperoxy fatty acids to aldehydes via an HPL-like activity
Products: -
Products: -
?
additional information
?
-
Substrates: allene oxide synthase is a key cytochrome P450 enzyme in the oxylipin pathway leading to allene oxide synthase-derived jasmonates
Products: -
Products: -
?
additional information
?
-
-
Substrates: allene oxide synthase is a key cytochrome P450 enzyme in the oxylipin pathway leading to allene oxide synthase-derived jasmonates
Products: -
Products: -
?
additional information
?
-
Substrates: reaction products are identified and quantified using HPLC chromatography and mass spectrometry, product specifities, overview
Products: -
Products: -
?
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COFACTOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
METALS and IONS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
Fe2+
heme
-
CYP74 heme is strongly hold in place than usual via ionic interactions with its proprionate groups
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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
(13S)-hydroperoxyoctadecadienoic acid
Fg-cat is inactivated in the course of the transformation of 13S-hydroperoxyoctadecadienoic acid and reaction is reinitiated by further addition of enzyme, product inhibition
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
-
irreversible substrate inhibition
hexanal
-
irreversible product inhibition, hexanal efficiently and specifically binds to the sulfhydryl groups in the active site of the enzyme through conjugate addition, hexanal seems to form a schiff base with the surface amino groups of the zymoprotein
imidazole
-
imidazole may coordinate to ferric heme iron, triggering a heme-iron transition from high spin state to low spin state
additional information
-
HPL may display a suicidal behavior, being irreversibly inhibited by its own substrate during the catalytic reaction. HPL activity is also irreversibly inhibited by its catalytic products
-
additional information
analysis of susceptibility of Arabidopsis thaliana plants with altered oxylipin profile to photoinhibition, kinetics, overview
-
additional information
-
analysis of susceptibility of Arabidopsis thaliana plants with altered oxylipin profile to photoinhibition, kinetics, overview
-
additional information
13-HPOD substrate is used and a mix of alkyl and alkoxyl radicals is identified which may cause inhibition of the enzymatic activity
-
additional information
-
mechanism based suicide inactivation is a common feature of hydroperoxide lyases and many other enzymes of the P450 family
-
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ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
cytochrome P450
-
AOS is a non-classical cytochrome P450, which, like other CYP74 enzymes, does not require molecular oxygen and NADPH-dependent P450 reductase
-
additional information
-
exhibits weak activity prior to activation (in vitro), can be massively activated with detergent
-
additional information
for enzyme stability glycine (2.5% w/v), NaCl (0.5 M), and Na2SO4 (0.25 M) provide the highest activation of HPL full-length activity, while the best matured HPL activity is obtained with Na2SO4 (0.25 M) and NaCl (1 M), while for enzyme activity and C6-aldehyde production, glycine, NaCl, and Na2SO4 are appropriate additives and NaCl appears to be the best additive, at least for hexanal production
-
additional information
mechanical wounding and methyl jasmonate treatment induce the accumulation of AOS transcripts
-
additional information
-
mechanical wounding and methyl jasmonate treatment induce the accumulation of AOS transcripts
-
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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Dehydration
Herbivore-induced allene oxide synthase transcripts and jasmonic acid in Nicotiana attenuata.
Dehydration
Specific adduction of plant lipid transfer protein by an allene oxide generated by 9-lipoxygenase and allene oxide synthase.
Hyperalgesia
Systematic analysis of rat 12/15-lipoxygenase enzymes reveals critical role for spinal eLOX3 hepoxilin synthase activity in inflammatory hyperalgesia.
Ichthyosis
Mutations associated with a congenital form of ichthyosis (NCIE) inactivate the epidermal lipoxygenases 12R-LOX and eLOX3.
Infections
?-Carrageenan Suppresses Tomato Chlorotic Dwarf Viroid (TCDVd) Replication and Symptom Expression in Tomatoes.
Infections
A novel plastidial lipoxygenase of maize (Zea mays) ZmLOX6 encodes for a fatty acid hydroperoxide lyase and is uniquely regulated by phytohormones and pathogen infection.
Infections
Changing green leaf volatile biosynthesis in plants: an approach for improving plant resistance against both herbivores and pathogens.
Infections
Differential expression of jasmonate biosynthesis genes in cacao genotypes contrasting for resistance against Moniliophthora perniciosa.
Infections
Gene Expression Analysis of Plum pox virus (Sharka) Susceptibility/Resistance in Apricot (Prunus armeniaca L.).
Infections
Molecular Identification and Functional Characterization of the Fatty Acid- and Retinoid-Binding Protein Gene Rs-far-1 in the Burrowing Nematode Radopholus similis (Tylenchida: Pratylenchidae).
Infections
Overexpression of hydroperoxide lyase, peroxygenase and epoxide hydrolase in tobacco for the biotechnological production of flavours and polymer precursors.
Infections
Revealing complexity and specificity in the activation of lipase-mediated oxylipin biosynthesis: a specific role of the Nicotiana attenuata GLA1 lipase in the activation of jasmonic acid biosynthesis in leaves and roots.
Infertility, Male
A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis.
Mycoses
Inducible overexpression of a rice allene oxide synthase gene increases the endogenous jasmonic acid level, PR gene expression, and host resistance to fungal infection.
Neoplasms
In-depth proteome analysis of the rubber particle of Hevea brasiliensis (para rubber tree).
Paratuberculosis
Coordination modes of tyrosinate-ligated catalase-type heme enzymes: magnetic circular dichroism studies of Plexaura homomalla allene oxide synthase, Mycobacterium avium ssp. paratuberculosis protein-2744c, and bovine liver catalase in their ferric and ferrous states.
Starvation
The potassium-dependent transcriptome of Arabidopsis reveals a prominent role of jasmonic acid in nutrient signaling.
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KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
0.0593
(13S)-hydroperoxy-(9Z,11Z,15Z)-octadecatrienoic acid
A9SNA2, A9S014
with 0.0001 mg purified AOS1, in 1 mL of buffer containing 50 mM sodium phosphate, pH 6.0
additional information
additional information
Michaelis-Menten kinetics
-
0.009
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 5.5, 20°C, recombinant His6-tagged enzyme
0.0431
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
0.04322
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
0.1528
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
0.1739
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
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TURNOVER NUMBER [1/s]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
228.6
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
455.3
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
571.4
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L97F/TCFNSF enzyme
676.4
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
732.4
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L93F/G283A enzyme
773.3
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
949.6
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L98F/A287G enzyme
1115.9
(9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
173.8
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
337.6
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
356.1
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L98F/A287G enzyme
375.4
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
550
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L97F/TCFNSF enzyme
600
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
619.8
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L93F/G283A enzyme
867.7
(9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
17.89
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
26.38
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
42
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant full-length enzyme, with 2.5% glycine w/v
46.9
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant truncated enzyme, with 2.5% glycine w/v
73.2
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant truncated enzyme, with 0.5 M NaCl
133.9
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant full-length enzyme, with 0.5 M NaCl
290
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
471.4
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L97F/TCFNSF enzyme
596.4
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
712.7
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L93F/G283A enzyme
752.4
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
913.3
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
1011.6
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
1587.5
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.0, 23°C, recombinant mutant L98F/A287G enzyme
187.1
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L97F/TCFNSF enzyme
377.2
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
402.62
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
530.9
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
564.95
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
579
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant full-length enzyme, with 0.5 M NaCl
587.4
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant full-length enzyme, with 2.5% glycine w/v
701.6
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant truncated enzyme, with 0.5 M NaCl
768.9
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant wild-type enzyme
829.1
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L93F/G283A enzyme
843.3
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant truncated enzyme, with 2.5% glycine w/v
997
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.0, 23°C, recombinant mutant L98F/A287G enzyme
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kcat/KM VALUE [1/mMs-1]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
413.9
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
612.1
(9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
2315.2
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant truncated enzyme
3697.3
(9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid
pH 7.5, 25°C, recombinant full-length enzyme
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SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
0.2
-
purified recombinant enzyme, pH and temperature not specified in the publication
2.32
-
purified recombinant His-tagged enzyme, solubilized with Triton X-100, pH 7.0, 22°C
5.44
-
purified recombinant His-tagged enzyme, solubilized with dodecyl maltoside, pH 7.0, 22°C
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pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
6.5
6.8
7.5
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pH RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
20
22
23
25
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TEMPERATURE RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pI VALUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
collected from a pollution-free agricultural product base in Wuxi, China
-
-
brenda
susceptible and resistant pearl millet cultivars to Sclerospora graminicola infection, IP18292, ICMP451-P6, ICMR-01004, IP18293, H77/833-2, 700651, P310-17, 7042S, 843B and 852B, gene PgAOS1
-
-
brenda
i.e. Botryodiplodia theobromae, no activity in strain CBS 122127
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-
brenda
i.e. Botryodiplodia theobromae, no activity in strain CBS 122127
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brenda
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
-
maximum enzyme abundance in vascular as well as in the epidermal regions
brenda
-
maximum enzyme abundance in vascular as well as in the epidermal regions
brenda
additional information
-
embryos, activity decreases during germination
brenda
black olives of the Leccino variety harvested at 20 weeks after flowering. Olive HPL is active in a range of pH between 6.0 and 8.0 with an optimal pH at 6.5 and an optimal production of C6 compounds performed at 20°C
brenda
constitutive expression of CYP74B24 gene in intact tea leaves
brenda
-
9-HPL and 13-HPL activity, increasing with leaf age, no AOS activity, overview
brenda
-
9-HPL and 13-HPL activity, increasing with age, no AOS activity, overview
brenda
additional information
-
enzyme is bound in a catalytically active state to the insoluble barley grist
brenda
additional information
-
quantitative PCR expression analysis of OsHPL3, overview
brenda
additional information
-
CYP74A2 is most abundant in rubber, accounting for about 50% of the protein content
brenda
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
rhomboid proteases AtRBL8 and AtRBL9 in the chloroplast envelope affect the level of allene oxide synthase in Arabidopsis thaliana
brenda
additional information
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equally distributed between the high speed supernatant and particulate fractions
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brenda
rhomboid proteases AtRBL8 and AtRBL9 in the chloroplast envelope affect the level of allene oxide synthase in Arabidopsis thaliana
brenda
the enzyme contains a chloroplast transit peptide in its N-terminal end for targeting and insertion to the chloroplast envelope
brenda
Highest Expressing Human Cell Lines
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GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
evolution
malfunction
metabolism
physiological function
additional information
evolution
-
phylogenetic analysis and sequence comparisons of 5,8-linoleate diol synthase, overview
evolution
FOXB_01332 is a linoleate 9-DOX with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein. The conserved Tyr-(His/Arg)-Trp-His motif contains a Phe instead of the catalytic Tyr residue, which is oxidized by the heme to a radical that performs the hydrogen abstraction of LDS and COX, the replacement of Phe 416 with Trp does not affect the product profile of FOXB_01332
evolution
-
phylogenetic relationship of pearl millet PgAOS1 and other known allene oxide synthases, overview
evolution
-
AOS is a non-classical cytochrome P450, which, like other CYP74 enzymes, does not require molecular oxygen and NADPH-dependent P450 reductase
evolution
the fungal allene oxide synthases belongs to the CYP74 family
evolution
-
allene oxide synthases, like hydroperoxide lyases and divinyl ether synthases belong to the CYP74 family of cytochrome P450 enzymes. These enzymes rearrange fatty acid hydroperoxides differently, sharing an epoxyallylic radical as a common intermediate
evolution
hydroxyperoxide lyases belong to the CYP74C subfamily of fatty acid hydroperoxide transforming enzymes, unrooted phylogenetic tree of CYP74 family with special emphasis to CYP74C subfamily, overview
evolution
hydroxyperoxide lyases belong to the CYP74C subfamily of fatty acid hydroperoxide transforming enzymes, unrooted phylogenetic tree of CYP74 family with special emphasis to CYP74C subfamily, overview
evolution
hydroxyperoxide lyases belong to the CYP74C subfamily of fatty acid hydroperoxide transforming enzymes, unrooted phylogenetic tree of CYP74 family with special emphasis to CYP74C subfamily, overview
evolution
hydroxyperoxide lyases belong to the CYP74C subfamily of fatty acid hydroperoxide transforming enzymes, unrooted phylogenetic tree of CYP74 family with special emphasis to CYP74C subfamily, overview
evolution
hydroperoxide lyases are classified in the cytochrome P450 family and more particularly in the two subfamilies CYP74B (13-HPL) and CYP74C (9-HPL and 9/13-HPL)
evolution
hydroxyperoxide lyases belong to the CYP74C subfamily of fatty acid hydroperoxide transforming enzymes, unrooted phylogenetic tree of CYP74 family with special emphasis to CYP74C subfamily, overview
evolution
-
FOXB_01332 is a linoleate 9-DOX with homology to animal heme peroxidases and a 9-dioxygenase-allene oxide synthase fusion protein. The conserved Tyr-(His/Arg)-Trp-His motif contains a Phe instead of the catalytic Tyr residue, which is oxidized by the heme to a radical that performs the hydrogen abstraction of LDS and COX, the replacement of Phe 416 with Trp does not affect the product profile of FOXB_01332
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evolution
-
the fungal allene oxide synthases belongs to the CYP74 family
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malfunction
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loss-of-function mutant hpl3-1 produces disease-resembling lesions spreading through the whole leaves. Mutant hpl3-1 plants exhibit enhanced induction of jasmonic acid, trypsin proteinase inhibitors and other volatiles, but decreased levels of green leaf volatiles including (Z)-3-hexen-1-ol. Mutant hpl3-1 plants are more attractive to a BPH egg parasitoid, Anagrus nilaparvatae, than the wild-type, most likely as a result of increased release of BPH-induced volatiles. Mutant hpl3-1 plants also show increased resistance to bacterial blight (Xanthomonas oryzae pv. oryzae)
malfunction
the mutant enzyme preferentially utilises 9-hydroperoxylinoleic acid
malfunction
the mutant enzyme preferentially utilises 9-hydroperoxylinoleic acid. Multiple mutations of the hydroperoxide-binding domain leading to the TCFNSF motif virtually do not alter the specificity of catalysis compared to the wild-type enzyme. Conversely, the L97F variant offers good allene oxide synthase (AOS) activity with 9-hydroperoxylinoleic acid (9-HPOD)
malfunction
silencing HPL in wild-type Solanum lycopersicum increases potato aphid (Macrosiphum euphorbiae) host preference and reproduction on 5-week-old plants but has no influence on 3-week-old plants. Silencing HPL in spr2 mutants does not compromise this aphid resistance. Moreover, a mutation in the FAD7 gene in Arabidopsis thaliana also confers resistance to the green peach aphid (Myzus persicae) in a genetic background that carries a null mutation in HPL
metabolism
A9SNA2, A9S014
AOS is involved in jasmonic acid biosynthesis. AOS1 operates acid biosynthesis predominantly
metabolism
-
role for Phe137 in catalysis, mutation to Leu switches the product outcome from AOS to hydroperoxide lyase
metabolism
-
the enzymes are involved in the biosynthesis of (8R,11S)-dihydroxylinoleic acid via isomerization of (8R)-hydroperoxylinoleic acid to (5S,8R)-dihydroxylinoleic acid and to (8R,11S)-dihydroxylinoleic acid by abstraction of the pro-S hydrogens at C-5 and C-11 of (8R)-hydroperoxylinoleic acid, respectively, followed by suprafacial oxygenation
metabolism
AOS is involved in the jasmonate biochemical pathway, detailed overview
metabolism
allene oxide synthase is involved in jasmonic acid biosynthesis
metabolism
-
allene oxide synthase is an intermediary enzyme in the octadecanoid pathway involved in conversion of (13S,9Z,11E,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid to allene oxid
metabolism
-
allene oxide synthase and its relationship to the catalytic cycle of cytochrome P450s, overview
metabolism
-
jasmonic acid is synthesized from linolenic acid (18:3n-3) by sequential action of 13-lipoxygenase, allene oxide synthase, and allene oxide cyclase
metabolism
-
allene oxide synthase (AOS) and 13-hydroperoxide lyase (HPL) pathways, are best recognized as producers of defense compounds against biotic challenges, role of these two oxylipin branches in plant tolerance to the abiotic stress, namely excessive light, overview. Allen oxide synthase (AOS) and hydroperoxide lyase (HPL), the two enzymes functional in parallel branches of oxylipin pathway, compete for the common substrate hydroperoxide of linolenic acid (i.e. 13-hydroperoxy-(9Z,11E,15Z)-octadecatrienoic acid)
metabolism
hydroperoxide lyase (HPL) is an enzyme found in higher plants that is involved in a lipid oxidation pathway, called the lipoxygenase pathway, which is activated in response to wounds or pathogen attacks
metabolism
enzyme HPL is important in the biochemical pathway for synthesis of C6 volatiles in Solanum lycopersicum, pathway overview
metabolism
enzyme HPL1 competes with allene oxide synthase (AOS) for lipid-bound hydroperoxide fatty acids. The last step in the synthesis of galactolipid-bound OPDA and dnOPDA from unstable allene oxides is exclusively enzyme-catalyzed and not the result of spontaneous cyclization. All steps in arabidopside biosynthesis are enzyme-dependent and apparently all reactions can take place with substrates being esterified to galactolipids
metabolism
allene oxide synthase (AOS) and 13-hydroperoxide lyase (HPL) pathways, are best recognized as producers of defense compounds against biotic challenges, role of these two oxylipin branches in plant tolerance to the abiotic stress, namely excessive light, overview. Allen oxide synthase (AOS) and hydroperoxide lyase (HPL), the two enzymes functional in parallel branches of oxylipin pathway, compete for the common substrate hydroperoxide of linolenic acid (i.e. (9Z,11E,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid)
metabolism
-
the enzyme plays a role as a key regulatory point in jasmonic acid biosynthesis
metabolism
-
allene oxide synthase (AOS) and 13-hydroperoxide lyase (HPL) pathways, are best recognized as producers of defense compounds against biotic challenges, role of these two oxylipin branches in plant tolerance to the abiotic stress, namely excessive light, overview. Allen oxide synthase (AOS) and hydroperoxide lyase (HPL), the two enzymes functional in parallel branches of oxylipin pathway, compete for the common substrate hydroperoxide of linolenic acid (i.e. (9Z,11E,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid)
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metabolism
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jasmonic acid is synthesized from linolenic acid (18:3n-3) by sequential action of 13-lipoxygenase, allene oxide synthase, and allene oxide cyclase
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metabolism
-
jasmonic acid is synthesized from linolenic acid (18:3n-3) by sequential action of 13-lipoxygenase, allene oxide synthase, and allene oxide cyclase
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metabolism
-
jasmonic acid is synthesized from linolenic acid (18:3n-3) by sequential action of 13-lipoxygenase, allene oxide synthase, and allene oxide cyclase
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physiological function
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is a potential rubber transferase, the enzyme polymerizes thousands of isoprenes into molecules of rubber. Plays no role in jasmonate biosynthesis
physiological function
the lipoxygenase-catalyzed addition of molecular oxygen to alpha-linolenic acid initiates jasmonate synthesis by providing a 13-hydroperoxide substrate for formation of an unstable allene oxide by allene oxide synthase. This allene oxide then undergoes enzyme-guided cyclization to produce 12-oxophytodienoic acid. Phe137 stabilizes the carbon-centered radical intermediate, which is essential for AOS activity
physiological function
-
role for the rice enzyme in mediating plant-specific defense responses. OsHPL3 possesses intrinsic hydroperoxide lyase activity hydrolyzing hydroperoxylinolenic acid to produce green leaf volatiles, that play diverse roles in plant defense responses against insect pests and pathogens. OsHPL3 positively modulates resistance to the rice brown planthopper, Nilaparvata lugens, but negatively modulates resistance to the rice striped stem borer, Chilo suppressalis (Walker)
physiological function
-
the enzyme plays an important role in regulation of allene oxide synthase level and activity in pearl millet upon Sclerospora graminicola infection
physiological function
-
the enzyme is involved in synthesis of green note substances from linoleic acid and alpha-linolenic acid in the plant
physiological function
-
role for the hydroperoxide lyase branch of the oxylipin biosynthesis pathway in protecting the photosynthetic apparatus under high light conditions potentially exerted through tight regulation of free linolenic acid and 13-hydroperoxy linolenic acid levels, as well as competition with production of metabolites by the allene oxide synthase (AOS)-branch of the oxylipin pathway
physiological function
fatty acid hydroperoxide lyase (HPO lyase) is an enzyme widely found in plants and vegetables. HPO lyase is involved in the biosynthesis of volatile aldehydes and alcohols. It catalyses the breakdown of fatty acid hydroperoxides to generate omega-oxo-acids and aldehydes (C6 or C9 aldehydes) which are used industrially to reconstitute the fresh green odor of fruits and vegetables lost during processing
physiological function
green leaf volatiles (GLVs) are the main contributors to the characteristic odor of plants known under the name of green note. GLVs are naturally produced through a metabolic pathway of the C18-polyunsaturated fatty acids named the lipoxygenase pathway. First, the lipoxygenase (LOX) catalyzes the oxygenation of linoleic and linolenic acids to form corresponding fatty acid hydroperoxides which are then cleaved by hydroperoxide lyase (HPL) to generate short-chain aldehydes and oxoacids. GLVs are widely used by various industries to improve food quality by restoring the fresh and fruity green odor or to add a touch of freshness to fragrances. The C6-aldehyde compounds are the main components (about 80 %) of the virgine olive oil flavor
physiological function
hydroperoxide lyase (HPL) is an enzyme found in higher plants that is involved in a lipid oxidation pathway, called the lipoxygenase pathway, which is activated in response to wounds or pathogen attacks. Volatile C6-aldehydes and C9-aldehydes produced by HPLs and their corresponding alcohols are known as green leaf volatiles (GLVs) and are responsible for the fresh green odor of many fruits and vegetables. GLVs such as hexanal, (Z)-3-hexenal, and (E)-2-hexenal are associated to the green note odor that is of major importance in the fragrance and flavor industries. They are also widely used in the food and beverage industry to restore the fresh green character lost during processing or to enhance food storage due to their antimicrobial activities
physiological function
the HPL pathway can influence direct defenses against insects, volatiles (E)-2-hexenal, hexanol, (E)-2-hexenol, and (Z)-3-hexenol reduce aphid fecundity. HPL contributes to certain forms of aphid resistance in tomato, but that the effects of fatty acid desaturase 7 (FAD7) on aphids in tomato and Arabidopsis are distinct from and independent of HPL. Disrupted function of FAD7, confers resistance to the potato aphid (Macrosiphum euphorbiae) and modifies the plant's C6 volatile profiles in Solanum lycopersicum. Moreover, a mutation in the FAD7 gene in Arabidopsis thaliana also confers resistance to the green peach aphid (Myzus persicae) in a genetic background that carries a null mutation in HPL
physiological function
-
hydroperoxide lyase (HPL) is the major enzyme in the biosynthesis of natural volatile aldehydes and alcohols in plants. The enzyme is important for defense against insects in tea plants
physiological function
the activity of hydroperoxide lyase 1 (HPL1) regulates the accumulation of galactolipids containing 12-oxo-phytodienoic acid in Arabidopsis thaliana. Galactolipids containing esters of 12-oxo-phytodienoic acid (OPDA) and dinor-12-oxo-phytodienoic acid (dnOPDA) are referred to as arabidopsides (chloroplast membrane lipids containing (dn)OPDA) and accumulate in response to abiotic and biotic stress. Expression analysis of enzyme HPL1 shows large differences in transcript abundance between accessions C24 and Col-0. Accession C24 is identified as a poor accumulator of arabidopsides whereas the commonly used accession Col-0 is found to accumulate comparably large amounts of arabidopsides in response to tissue damage
physiological function
green leaf volatiles (GLVs) are C6-aliphatic aldehydes/alcohols/acetates, and biosynthesized from the central precursor fatty acid 13-hydroperoxides by 13-hydroperoxide lyases (HPLs) in various plant species. While GLVs have been implicated as defense compounds in plants, GLVs give characteristic grassy note to a bouquet of aroma in green tea, which is manufactured from young leaves of Camellia sinensis. Gene CYP74B24 encodes tea HPL enzyme. Constitutive expression of CYP74B24 gene in intact tea leaves might account for low but substantial and constitutive formation of a subset of GLVs, some of which are stored as glycosides
physiological function
role for the hydroperoxide lyase branch of the oxylipin biosynthesis pathway in protecting the photosynthetic apparatus under high light conditions potentially exerted through tight regulation of free linolenic acid and 13-hydroperoxy linolenic acid levels, as well as competition with production of metabolites by the allene oxide synthase (AOS)-branch of the oxylipin pathway
physiological function
-
role for the hydroperoxide lyase branch of the oxylipin biosynthesis pathway in protecting the photosynthetic apparatus under high light conditions potentially exerted through tight regulation of free linolenic acid and 13-hydroperoxy linolenic acid levels, as well as competition with production of metabolites by the allene oxide synthase (AOS)-branch of the oxylipin pathway
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additional information
the acid-alcohol pair Glu946-Ser949 lacks catalytic importance for the allene oxide synthase activity
additional information
-
the acid-alcohol pair Glu946-Ser949 lacks catalytic importance for the allene oxide synthase activity
additional information
-
putative type II ligand-induced spin state transition in OsAOS1
additional information
the enzyme has the distal heme signature sequence of Thr-His
additional information
-
the enzyme has the distal heme signature sequence of Thr-His
additional information
-
exogenously applied oxylipins (free linolenic acid (LA) and linolenic acid hydroperoxide (13-HPOT), AOS branch metabolites: 12-OPDA and methyl derivative of jasmonic acid (Me-JA), and HPL-branch metabolites: trans-2-hexenal, cis-3-hexenol, cis-3-hexenyl acetate, and traumatic acid (TA)) alter photochemical activity of isolated thylakoid membranes, overview. Cis-3-hexenal is excluded from the analysis
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
transformation of Col-0 plants with the C24 HPL1 allele under transcriptional regulation of the 35S promoter reveals a strong negative correlation between HPL1 expression and arabidopside accumulation after tissue damage. A quantitative trait loci analysis of an F2 population created from a cross between C24 and Col-0 locates a region on chromosome four strongly linked to the capacity to form arabidopsides
additional information
exogenously applied oxylipins (free linolenic acid (LA) and linolenic acid hydroperoxide (13-HPOT), AOS branch metabolites: 12-OPDA and methyl derivative of jasmonic acid (Me-JA), and HPL-branch metabolites: trans-2-hexenal, cis-3-hexenol, cis-3-hexenyl acetate, and traumatic acid (TA)) alter photochemical activity of intact leaves of growing Arabidopsis plants, overview. Cis-3-hexenal is excluded from the analysis
additional information
-
exogenously applied oxylipins (free linolenic acid (LA) and linolenic acid hydroperoxide (13-HPOT), AOS branch metabolites: 12-OPDA and methyl derivative of jasmonic acid (Me-JA), and HPL-branch metabolites: trans-2-hexenal, cis-3-hexenol, cis-3-hexenyl acetate, and traumatic acid (TA)) alter photochemical activity of intact leaves of growing Arabidopsis plants, overview. Cis-3-hexenal is excluded from the analysis
additional information
-
exogenously applied oxylipins (free linolenic acid (LA) and linolenic acid hydroperoxide (13-HPOT), AOS branch metabolites: 12-OPDA and methyl derivative of jasmonic acid (Me-JA), and HPL-branch metabolites: trans-2-hexenal, cis-3-hexenol, cis-3-hexenyl acetate, and traumatic acid (TA)) alter photochemical activity of intact leaves of growing Arabidopsis plants, overview. Cis-3-hexenal is excluded from the analysis
-
additional information
-
the enzyme has the distal heme signature sequence of Thr-His
-
additional information
-
the acid-alcohol pair Glu946-Ser949 lacks catalytic importance for the allene oxide synthase activity
-
Show AA Sequence and Transmembrane Helices (331 entries)
Please use the AA Sequence and Transmembrane Helices Search for a specific query.
Please use the AA Sequence and Transmembrane Helices Search for a specific query.
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PDB
SCOP
CATH
UNIPROT
ORGANISM
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MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
220000
-
gel filtration, 2 bands of enzyme activity, MW 220000 and MW 40000-45000
40000 - 45000
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gel filtration, 2 bands of enzyme activity, MW 220000 and MW 40000-45000
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SUBUNIT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
additional information
?
x * 57000, recombinant His6-tagged enzyme, SDS-PAGE, x * 55000, native enzyme, SDS-PAGE
?
x * 50000, about, recombinant enzyme with or without transit peptide, SDS-PAGE
additional information
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secondary structure analysis by circular dichroism, the enzyme consists of 13.53% alpha-helix, 32.73% beta-sheet, 21.76% turn and 31.13% unordered, overview
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
additional information
three-dimensional modelling of CYP74s and structure comparisons
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POSTTRANSLATIONAL MODIFICATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
proteolytic modification
the matured enzyme lacks the chloroplast transit peptide, which is cleaved off for maturation
additional information
additional information
rhomboid proteases AtRBL8 and AtRBL9 in the chloroplast envelope affect the level of allene oxide synthase in Arabidopsis thaliana
additional information
-
rhomboid proteases AtRBL8 and AtRBL9 in the chloroplast envelope affect the level of allene oxide synthase in Arabidopsis thaliana
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CRYSTALLIZATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
AOS free or in complex with 12R,13S-vernolic acid, sitting drop vapour diffusion method, using 100 mM Tris-HCl, pH 7.5, 15-20% polyethylene glycol 3350, and 39 mM nonanoyl-N-hydroxyethylglucamide
is a typical P450, the loop forms a compact beta-turn and incorporates the most typical P450 consensus sequence, FXXG, followed by three residues (XRX) followed by CXG encompassing the cysteine. CYP74 heme is strongly hold in place than usual via ionic interactions with its proprionate groups
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PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
F137L
F137L/S155A
C1073S
site-directed mutagenesis, the substitution in the P450 domain abolishes allene oxide synthase activity
N964D
site-directed mutagenesis, the mutation markedly reduces allene oxide synthase activity
N964V
site-directed mutagenesis, the mutation markedly reduces allene oxide synthase activity
C1073S
-
site-directed mutagenesis, the substitution in the P450 domain abolishes allene oxide synthase activity
-
N964D
-
site-directed mutagenesis, the mutation markedly reduces allene oxide synthase activity
-
N964V
-
site-directed mutagenesis, the mutation markedly reduces allene oxide synthase activity
-
L93F/G283A
site-directed mutagenesis, the mutant shows altered substrate specificity and increased activity compared to the wild-type enzyme. The mutant form preferentially utilise (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
L98F/A287G
site-directed mutagenesis, the mutant shows altered substrate specificity and increased activity compared to the wild-type enzyme. The mutant form preferentially utilise (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
E946V
site-directed mutagenesis, mutant Glu946Val oxidized 18:2n-6 as the native enzyme with formation of the alpha-ketol as the main product after 30 min
F416W
site-directed mutagenesis, the catalytic residue mutant shows an unaltered product profile compared to the wild-type enzyme
N921V
site-directed mutagenesis, the mutant shows activity similar to the wild-type enzyme
S949A
site-directed mutagenesis, the mutant also forms alpha-ketol like the native enzyme
E946V
-
site-directed mutagenesis, mutant Glu946Val oxidized 18:2n-6 as the native enzyme with formation of the alpha-ketol as the main product after 30 min
-
F416W
-
site-directed mutagenesis, the catalytic residue mutant shows an unaltered product profile compared to the wild-type enzyme
-
N921V
-
site-directed mutagenesis, the mutant shows activity similar to the wild-type enzyme
-
S949A
-
site-directed mutagenesis, the mutant also forms alpha-ketol like the native enzyme
-
G316A
the G316A mutant increases the oxygenation at the n-8 carbon of 17:3n-3 and at the n-10 carbon of the C17 and C18 fatty acids (from 12% to 711%). The most striking effect of the G316A mutant is a 2-, 7-, and 15-fold increase in transformation of the n-6 hydroperoxides of 19:3n-3, 18:3n-3, and 17:3n-3, respectively, to keto fatty acids and epoxyalcohols. G316A mutant augments the hydroperoxide isomerase activity by positioning the hydroperoxy group at the n-6 carbon of n-3 fatty acids closer to the reduced catalytic metal
E292G
-
site-directed mutagenesis, the divinyl ether synthase enzyme mutant E292G shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol and 12-oxo-10,15-phytodienoic acid, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74B16
F155L
the mutant does not show any qualitative alterations of catalytic activity compared to the wild type protein
L97F
site-directed mutagenesis, L97F/TCFNSF, multiple mutations of the hydroperoxide-binding domain leading to the TCFNSF motif virtually do not alter the specificity of catalysis compared to the wild-type enzyme. Conversely, the L97F variant offers good allene oxide synthase (AOS) activity with (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid (9-HPOD). The mutant form preferentially utilise (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid
V379F
-
the divinyl ether synthase enzyme mutant V379F shows allene oxide synthase activity, producing the typical allene oxide synthase product alpha-ketol, and lacks divinyl ether synthase activity in contrast to the wild-type divinyl ether synthase CYP74D3
F93L
-
the mutant converts (9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid mainly into 9,10-epoxy-13-hydroxy-11,15-octadecadienoic acid (epoxyalcohol synthase activity)
F108L
L93F/G283A
site-directed mutagenesis, the mutant shows altered substrate specificity and increased activity compared to the wild-type enzyme
L97F
site-directed mutagenesis, the mutant shows altered substrate specificity and decreased activity compared to the wild-type enzyme
L98F/A287G
site-directed mutagenesis, the mutant shows altered substrate specificity and increased activity compared to the wild-type enzyme
F95L
the mutant possesses mixed allene oxide synthase/epoxyalcohol synthase activity, producing mainly threo/erythro isomers of 9,10-dihydroxy-12,15-octadecadienoic acid as well as threo/erythro isomers of 9,10-epoxy-13-hydroxy-11,15-octadecadienoic acid, and 9,10-epoxy-11-hydroxy-12,15-octadecadienoic acid from (9S,10E,12Z,15Z)-9-hydroperoxy-10,12,15-octadecatrienoic acid
additional information
F137L
the mutant is severely compromised in its ability to generate allene oxide and exhibits robust hydroperoxide lyase activity
F137L
site-directed mutagenesis, mutation of this residue to Leu results in the enzyme having hydroperoxide lyase activity
F137L/S155A
the double mutant exhibits strong hydroperoxide lyase activity
F108L
the mutation converts the enzyme into an epoxyalcohol synthase
F108L
the mutant possesses mixed allene oxide synthase/epoxyalcohol synthase activity, and epoxyalcohol synthase activity is the main when the mutant is incubating with (9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid. Hydroperoxide lyase activity of the mutant is the same with that of wild type enzyme. The mutant form possesses trace 9-hydroperoxide lyase (in the same amount as the wild type enzyme) and no 13-hydroperoxide lyase activities
additional information
-
enzyme immobilization for hexanal synthesis using partially purified enzyme and hydrogel particles from chitosan and kappa-carrageenan with glutaraldehyde-activated 1,6-hexamethylenediamine spacer arms (HMDA-CCH particles), the enzyme is bound with carbodiimide coupling, method optimization and evaluation, overview. Optimum reaction conditions include a (9Z,11E)-13-hydroperoxy-9,11-octadecadienoic acid (13-HPOD) concentration of 43.54 mM and a residence time of 60.99 min. The maximum hexanal concentration is 3.56 g/l when 16 U of immobilized HPL are used. The stability of immobilized HPL is significantly improved in the packed-bed reactor evidenced by the slowed enzyme inactivation and prolonged operation time. Productivity in the packed-bed reactor is 5.35 mg/U, highly increased activity compared to the batch stirred reactor
additional information
-
development of a yeast-based whole cell biocatalyst able to transform polyunsaturated fatty acids into green note aldehydes and alcohols, evaluation, overview
additional information
reaction products are identified and quantified using HPLC chromatography and mass spectrometry
additional information
reaction products are identified and quantified using HPLC chromatography and mass spectrometry
additional information
reaction products are identified and quantified using HPLC chromatography and mass spectrometry
additional information
the recombinant 13-HPL enzyme is assayed as biocatalyst to produce C6-aldehydes, optimization of the biotransformation conditions of (9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatrienoic acid and (9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid into hexanal and (Z)-3-hexenal, respectively, to achieve the highest yields. The wild-type full-length enzyme acts more effectively on (9Z,11E,15Z)-(13S)-hydroperoxyoctadeca-9,11,15-trienoate and (9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid than on the truncated enzyme lacking the chloroplast transit peptide
additional information
optimization of recombinant full-length and truncated enzymes stabilization by additives for production of C6-aldehydes, overview
additional information
-
gene 13-hpl is used for random mutagenesis via gene shuffling using template based recombination of restriction fragments and in vitro ligations (L-shuffling) with DNA sequences from melon, Nicotiana attenuata (GenBank accession No. AJ414400), Citrus sinensis (GenBank accession No. AY242385), and Malus domestica and a guava hpl gene containing the 5'DELTA93 bp deletion. Mutant sequence analysis, overview. The mutant variants show highly increased trunover as well as reduced mechanism based suicide inactivation compared to the wild-type
additional information
reaction products are identified and quantified using HPLC chromatography and mass spectrometry. All three mutant forms preferentially utilise (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid. Multiple mutations of the hydroperoxide-binding domain leading to the TCFNSF motif virtually did not alter the specificity of catalysis compared to the wild-type enzyme. Conversely, the L97F variant offers good allene oxide synthase (AOS) activity with (9S,10E,12Z)-9-hydroperoxy-10,12-octadecadienoic acid (9-HPOD)
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pH STABILITY
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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TEMPERATURE STABILITY
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
10 - 80
-
purified enzyme, thermal denaturation at 80°C, unfolding starts at about 40°C
20
-
pH 7: 10% loss of activity after 20 h, pH 5: 60% loss of activity after 20 h
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GENERAL STABILITY
ORGANISM
UNIPROT
LITERATURE
for enzyme stability glycine (2.5% w/v), NaCl (0.5 M), and Na2SO4 (0.25 M) provide the highest activation of HPL full-length activity, while the best matured HPL activity is obtained with Na2SO4 (0.25 M) and NaCl (1 M), while for enzyme activity and C6-aldehyde production, glycine, NaCl, and Na2SO4 are appropriate additives and NaCl appears to be the best additive, at least for hexanal production
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STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
-20°C--80°C, purified recombinant full-length and matured enzymes, 100% of the rHPL activities are maintained during 5 weeks of storage in the presence of 10% v/v glycerol (best), about 70% activity are remaining at 40% glycerol after 5 weeks. Freezing without a cryoprotectant inactivates both enzymes rapidly. The enzyme activity is greatly reduced within 3 weeks for HPL full-length and within 1 week for matured HPL since only about 20% of the enzyme activity remain when they are stored at -20°C or -80°C
4°C, purified recombinant full-length and matured enzymes, quite stable for 5 weeks
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PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
recombinant His-tagged enzyme from Escherichia coli membranes by solubilization with Triton X-100 or dodecyl maltoside, the latter results in higher enzyme activity, followed by nickel affinity chromatography
-
recombinant His-tagged enzyme from Escherichia coli strain BL21(DE3)pLysS by nickel affinity chromatography
recombinant His-tagged full-length and truncated enzymes from Escherichia coli strain M15 by cobalt affinity chromatography
recombinant His-tagged wild-type and mutant enzymes from Escherichia coli strain BL21(DE3)pLysS by nickel affinity chromatography
recombinant His-tagged wild-type and mutant enzymes from Escherichia coli strain Rosetta-gami(DE3)pLysS B by nickel affinity chromatography
recombinant His-tagged wild-type enzyme from Escherichia coli strain BL21(DE3)pLysS by nickel affinity chromatography
recombinant His-tagged wild-type enzyme from Escherichia coli strain Rosetta-gami(DE3)pLysS B by nickel affinity chromatography
recombinant His6-tagged enzyme from Yarrowia lipolytica strain JMY 861 by solubilization by Triton X-100, nickel affinity chromatography, and ultrafiltration
recombinant N- or C-terminal His6-tagged enzyme from Escherichia coli strain BL21(DE3) by nickel affinity chromatography and dialysis
solubilization of the enzyme from plant leaves by 1% Tween-20
recombinant His-tagged wild-type enzyme from Escherichia coli strain BL21(DE3)pLysS by nickel affinity chromatography
recombinant His-tagged wild-type enzyme from Escherichia coli strain BL21(DE3)pLysS by nickel affinity chromatography
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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
a cDNA encoding for olive HPL of Leccino variety is isolated from black olive fruits, cloned in pQE-30 expression vector, and expressed as His-tagged proteins in Escherichia coli strain M15. In order to improve the enzyme solubility, the chloroplast transit peptide is deleted
a unique cDNA fragment is isolated by suppressive subtractive hybridization (SSH) from a tea plant subjected to herbivory by tea geometrid Ectropis obliqua, a full-length cDNA is acquired by RACE, DNA and amino acid sequence determination and analysis, recombinant expression of His-tagged enzyme in Escherichia coli strain Rosetta (DE3), quantitative RT-PCR expression analysis
-
CYP74C13_MT gene, sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged enzyme in Escherichia coli strain Rosetta-gami(DE3)pLysS B
CYP74C13_MT gene, sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged wild-type and mutant enzymes in Escherichia coli strain BL21(DE3)pLysS
CYP74C13_MT gene, sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged wild-type and mutant enzymes in Escherichia coli strain Rosetta-gami(DE3)pLysS B
CYP74C1_CS gene, sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged wild-type enzyme in Escherichia coli strain BL21(DE3)pLysS
CYP74C4_ST gene, sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged wild-type enzyme in Escherichia coli strain BL21(DE3)pLysS
expressed in an Arabidopsis thaliana enzyme null mutant and Nicotiana benthamiana leaves
-
expressed in Escherichia coli BL21 (DE3)pLysS cells
functional recombinant expression of His6-tagged enzyme in Yarrowia lipolytica strain JMY 861, the enzyme appears after 24 h cultivation at the end of the exponential phase when the yeast is grown on a culture medium containing 10 g/l of olive oil as the sole carbon source, enzyme production method optimization, overview
gene 13-hpl, sequence comparisons, functional expression in Escherichia coli partly in inculsion bodies, fusion of the maltose binding protein malE to the 5'-truncated 13-hpl gene improves functional expression to some extent
-
gene ATEG_02036, sequence comparisons with other enzymes, cloning and functional expression of the enzyme with V5 epitope and His6-tag from plasmid pIZ/V5-His in Spodoptera frugiperda Sf9 cells and in Escherichia coli
gene CmHPL, expression in Nicotiana benthamiana leaves via infiltration method with a aviral vector, real-time PCR expression analysis over 10 days after infiltration with increase of C-9 aldehyde production, overview
-
gene CYP74B24, three HPL-related genes from Camellia sinensis are identified via RNA-sequencing in silico, gene CYP74B24 encodes a functional tea HPL enzyme, recombinant expression of CYP74B24 protein in Escherichia coli
gene FG02216.1, transient transfection in HeLa cells using VTF-7, a recombinant vaccinia virus containing the T7 RNA polymerase gene, recombinant expression of His-tagged enzyme in Escherichia coli strain BL21(DE3)
gene FOXB_01332, phylogenetic tree, expression of wild-type and mutant enzymes
gene HPLCl, overexpression in Saccharomyces cerevisiae strain BY4743 isogenic
-
gene Npun_R5468, expression of the enzyme with N- or C-terminal His6 tags in Escherichia coli strain BL21(DE3)
gene OsHPL3, DNA and amino acid sequence determination, analysis, and comparison
-
gene PgAOS1, phylogenetic analysis, quantitative enzyme expression analysis in different cultivars with and without infection by Sclerospora graminicola
-
genetic mapping and quantitative real-time PCR expression analysis of HPL1 in plants of diverse accessions, e.g. accessions C24 and Ler display large difference in HPL1 expression, overview. Transformation of accession Col-0 plants with the C24 HPL1 allele under transcriptional regulation of the 35S promoter revealing a strong negative correlation between HPL1 expression and arabidopside accumulation after tissue damage. A quantitative trait loci analysis of an F2 population created from a cross between C24 and Col-0 locates a region on chromosome four strongly linked to the capacity to form arabidopsides
recombinant expression of His-tagged full-length enzyme or matured enzyme with truncated chloroplast transit peptide in Escherichia coli strain M15
sequence comparisons and phylogenetic analysis, recombinant expression of His-tagged enzyme in Escherichia coli strain BL21(DE3)pLysS
whole ORF of AOS1 amplified and ligated into cloning vector pBluescript SK II(+), sequenced and ligated int vector pET23a and overexpressed in Escherichia coli BL21
A9SNA2, A9S014
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EXPRESSION
ORGANISM
UNIPROT
LITERATURE
after mechanical wounding, the enzyme activity and amounts of volatiles increase significantly. Formation of (Z)-3-hexenal is rapidly but transiently enhanced after wounding, and only a trace amount is detected after 10 min of wounding. 4-Oxo-(E)-2-hexenal, which was an oxidation product of (Z)-3-hexenal, is also formed quickly after wounding
CsHPL is strongly upregulated in tea plants after Ectropis obliqua pathogen attack
-
induction of allene oxide synthase activity in both susceptible and resistant pearl millet cultivars during Sclerospora graminicola infection with higher induction observed in the resistant cultivar
-
isoform AOS2 is specifically upregulated when exposed to Thrips hawaiiensis attack
low temperature and wounding upregulates the enzyme and increases HPL enzyme activity, at 15°C, a strong and transient increase in OeHPL gene expression level occurs in fruit mesocarp, mechanical damage increases the enzyme activity level
-
temperature, light, wounding and water regime regulate olive the 13-HPL gene at transcriptional level
-
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APPLICATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
food industry
-
the enzyme produces aldehydes that are used as flavours in foods and beverages
medicine
-
enzyme is involved in skin differentiation and etiology of ichthyosiform diseases
synthesis
synthesis
the recombinant 13-HPL enzyme is valuated as biocatalyst to produce C6-aldehydes
synthesis
the recombinant 13-HPL enzyme is useful biocatalyst to produce C6-aldehydes
synthesis
-
enzymatic synthesis of volatile C6 aldehydes (hexanal, 2(E)-hexenal and 3(Z)-hexenal) using lipoxygenase (LOX) and hydroperoxide lyase (HPL) as biocatalysts. C6 aldehydes are widely used in perfume and food industry, because they are important contributors to the distinctive scent of fresh fruits and vegetables
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TITLE
JOURNAL
VOL.
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YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
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Studies on linoleic acid 8R-dioxygenase and hydroperoxide isomerase of the fungus Gaeumannomyces graminis
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30
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Gaeumannomyces graminis
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Hamberg, M.; Zhang, L.Y.; Brodowsky, I.D.; Oliw, E.H.
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Formation of gamma-ketols from 13- and 9-hydroxyperoxides of linoleic acid by flaxseed hydroperoxide isomerase
Lipids
16
377-379
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Linum usitatissimum
-
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Gardner, H.W.
Stereospecificity of linoleic acid hydroperoxide isomerase from corn germ
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14
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68
950-955
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Hordeum vulgare
brenda
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Biosynthesis of vicinal dihydroxy fatty acids in the red alga Gracilariopsis menaneiformis: Identification of a sodium-dependent 12-lipoxygenase and a hydroperxide isomerase
Arch. Biochem. Biophys.
305
115-122
1993
Gracilariopsis lemaneiformis
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Hamberg, M.
Fatty acid hydroperoxide isomerase in Saprolegnia parasitica: Structural studies of epoxy alcohols formed from isomeric hydroperoxyoctadecadienoates
Lipids
24
249-255
1989
Saprolegnia parasitica
-
brenda
Grossman, S.; Bergman, M.; Sofer, Y.
Purification and partial characterization of eggplant linoleate hydroperoxide isomerase
Biochim. Biophys. Acta
752
65-72
1983
Zea mays, Solanum melongena
-
brenda
Yabuuchi, S.; Amaha, M.
Partial purification and characterization of the linoleate hydroperoxide isomerase from grains of Hordeum distichum
Phytochemistry
15
387-390
1976
Hordeum vulgare subsp. vulgare
-
brenda
Heimann, W.; Dresen, P.
Uber den enzymatischen Hydroperoxidabbau in Cerealien Enzymcharakterisierung and Reaktionsprodukte
Helv. Chim. Acta
56
463-469
1973
Avena sativa
-
brenda
Reynaud, D.; Ali, M.; Demin, P.; Pace-Asciak, C.R.
Formation of 14,15-hepoxilins of the A(3) and B(3) series through a 15-lipoxygenase and hydroperoxide isomerase present in garlic roots
J. Biol. Chem.
274
28213-28218
1999
Allium sativum
brenda
Yu, Z.; Schneider, C.; Boeglin, W.E.; Marnett, L.J.; Brash, A.R.
The lipoxygenase gene ALOXE3 implicated in skin differentiation encodes a hydroperoxide isomerase
Proc. Natl. Acad. Sci. USA
100
9162-9167
2003
Homo sapiens
brenda
Kupfer, R.; Liu, S.Y.; Allentoff, A.J.; Thompson, J.A.
Comparisons of hydroperoxide isomerase and monooxygenase activities of cytochrome P450 for conversions of allylic hydroperoxides and alcohols to epoxyalcohols and diols: probing substrate reorientation in the active site
Biochemistry
40
11490-11501
2001
Rattus norvegicus
brenda
Hamberg, M.
Hydroperoxide isomerases
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12
283-292
1995
Gaeumannomyces graminis, Gracilariopsis lemaneiformis, Saprolegnia parasitica
brenda
Cristea, M.; Oliw, E.H.
A G316A mutation of manganese lipoxygenase augments hydroperoxide isomerase activity: mechanism of biosynthesis of epoxyalcohols
J. Biol. Chem.
281
17612-17623
2006
Gaeumannomyces graminis (Q8X151)
brenda
Chawengsub, Y.; Aggarwal, N.T.; Nithipatikom, K.; Gauthier, K.M.; Anjaiah, S.; Hammock, B.D.; Falck, J.R.; Campbell, W.B.
Identification of 15-hydroxy-11,12-epoxyeicosatrienoic acid as a vasoactive 15-lipoxygenase metabolite in rabbit aorta
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294
H1348-H1356
2008
Oryctolagus cuniculus
brenda
Jiang, K.; Pi, Y.; Hou, R.; Zeng, H.; Huang, Z.; Zhang, Z.; Sun, X.; Tang, K.
Molecular cloning and expression profiling of the first specific jasmonate biosynthetic pathway gene allene oxide synthase from Lonicera japonica
Mol. Biol. Rep.
36
487-493
2009
Lonicera japonica (A1X873), Lonicera japonica
brenda
Lee, D.; Nioche, P.; Hamberg, M.; Raman, C.S.
Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes
Nature
455
363-368
2008
Arabidopsis thaliana (Q96242), Arabidopsis thaliana
brenda
Siqueira-Junior, C.L.; Jardim, B.C.; Urmenyi, T.P.; Vicente, A.C.; Hansen, E.; Otsuki, K.; da Cunha, M.; Madureira, H.C.; de Carvalho, D.R.; Jacinto, T.
Wound response in passion fruit (Passiflora f. edulis flavicarpa) plants: gene characterization of a novel chloroplast-targeted allene oxide synthase up-regulated by mechanical injury and methyl jasmonate
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27
387-397
2008
Passiflora edulis (A7XY79), Passiflora edulis
brenda
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Cloning and functional analysis of an allene oxide synthase in Physcomitrella patens
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73
2356-2359
2009
Physcomitrium patens (A9SNA2), Physcomitrium patens (A9S014), Physcomitrium patens
brenda
Brash, A.
Mechanistic aspects of CYP74 allene oxide synthases and related cytochrome P450 enzymes
Phytochemistry
70
1522-1531
2009
Linum usitatissimum, Acaryochloris marina, Arabidopsis thaliana, Parthenium argentatum, Zea mays, Solanum tuberosum, Solanum lycopersicum
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Cho, K.B.; Lai, W.; Hamberg, M.; Raman, C.S.; Shaik, S.
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507
14-25
2011
Arabidopsis thaliana
brenda
Jernern, F.; Garscha, U.; Hoffmann, I.; Hamberg, M.; Oliw, E.H.
Reaction mechanism of 5,8-linoleate diol synthase, 10R-dioxygenase, and 8,11-hydroperoxide isomerase of Aspergillus clavatus
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1801
503-507
2010
Aspergillus clavatus
brenda
Mukhtarova, L.S.; Mukhitova, F.K.; Gogolev, Y.V.; Grechkin, A.N.
Hydroperoxide lyase cascade in pea seedlings: Non-volatile oxylipins and their age and stress dependent alterations
Phytochemistry
72
356-364
2011
Lathyrus oleraceus
brenda
Gfeller, A.; Dubugnon, L.; Liechti, R.; Farmer, E.
Jasmonate biochemical pathway
Sci. Signal.
109
1-6
2010
Arabidopsis thaliana (Q96242), Arabidopsis thaliana
brenda
Jerneren, F.; Eng, F.; Hamberg, M.; Oliw, E.H.
Linolenate 9R-dioxygenase and allene oxide synthase activities of Lasiodiplodia theobromae
Lipids
47
65-73
2012
Lasiodiplodia theobromae, Lasiodiplodia theobromae 2334
brenda
Buchhaupt, M.; Guder, J.C.; Etschmann, M.M.; Schrader, J.
Synthesis of green note aroma compounds by biotransformation of fatty acids using yeast cells coexpressing lipoxygenase and hydroperoxide lyase
Appl. Microbiol. Biotechnol.
93
159-168
2012
Citrullus lanatus
brenda
Yoeun, S.; Rakwal, R.; Han, O.
Dual positional substrate specificity of rice allene oxide synthase-1: insight into mechanism of inhibition by type II ligand imidazole
BMB Rep.
46
151-156
2013
Oryza sativa
brenda
Toporkova, Y.Y.; Ermilova, V.S.; Gorina, S.S.; Mukhtarova, L.S.; Osipova, E.V.; Gogolev, Y.V.; Grechkin, A.N.
Structure-function relationship in the CYP74 family: conversion of divinyl ether synthases into allene oxide synthases by site-directed mutagenesis
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587
2552-2558
2013
Nicotiana tabacum, Linum usitatissimum
brenda
Boeglin, W.E.; Brash, A.R.
Cytochrome P450-type hydroxylation and epoxidation in a tyrosine-liganded hemoprotein, catalase-related allene oxide synthase
J. Biol. Chem.
287
24139-24147
2012
Plexaura homomalla
brenda
Hoffmann, I.; Jerneren, F.; Oliw, E.H.
Expression of fusion proteins of Aspergillus terreus reveals a novel allene oxide synthase
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288
11459-11469
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Aspergillus terreus (Q0CW98), Aspergillus terreus, Aspergillus terreus A1156 (Q0CW98)
brenda
Brash, A.R.; Niraula, N.P.; Boeglin, W.E.; Mashhadi, Z.
An ancient relative of cyclooxygenase in cyanobacteria is a linoleate 10S-dioxygenase that works in tandem with a catalase-related protein with specific 10S-hydroperoxide lyase activity
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289
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Nostoc punctiforme (B2J5P3)
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Bruehlmann, F.; Bosijokovic, B.; Ullmann, C.; Auffray, P.; Fourage, L.; Wahler, D.
Directed evolution of a 13-hydroperoxide lyase (CYP74B) for improved process performance
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163
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Psidium guajava
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Hoffmann, I.; Oliw, E.H.
Discovery of a linoleate 9S-dioxygenase and an allene oxide synthase in a fusion protein of Fusarium oxysporum
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54
3471-3480
2013
Fusarium oxysporum (F9F4K7), Fusarium oxysporum, Fusarium oxysporum Fo5176 (F9F4K7)
brenda
Hosur Gnanaprakash, P.; Jogaiah, S.; Sreedhara, A.P.; Nagraj Prashanth, G.; Kini, R.K.; Shetty, S.H.
Association between accumulation of allene oxide synthase activity and development of resistance against downy mildew disease of pearl millet
Mol. Biol. Rep.
40
6821-6829
2013
Cenchrus americanus
brenda
Padilla, M.N.; Hernandez, M.L.; Sanz, C.; Martinez-Rivas, J.M.
Stress-dependent regulation of 13-lipoxygenases and 13-hydroperoxide lyase in olive fruit mesocarp
Phytochemistry
102
80-88
2014
Olea europaea
brenda
Huang, F.C.; Schwab, W.
Overexpression of hydroperoxide lyase, peroxygenase and epoxide hydrolase in tobacco for the biotechnological production of flavours and polymer precursors
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10
1099-1109
2012
Cucumis melo
brenda
Tong, X.; Qi, J.; Zhu, X.; Mao, B.; Zeng, L.; Wang, B.; Li, Q.; Zhou, G.; Xu, X.; Lou, Y.; He, Z.
The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway
Plant J.
71
763-775
2012
Oryza sativa
brenda
Knopf, R.R.; Feder, A.; Mayer, K.; Lin, A.; Rozenberg, M.; Schaller, A.; Adam, Z.
Rhomboid proteins in the chloroplast envelope affect the level of allene oxide synthase in Arabidopsis thaliana
Plant J.
72
559-571
2012
Arabidopsis thaliana (Q96242), Arabidopsis thaliana
brenda
Panagakou, I.; Touloupakis, E.; Ghanotakis, D.F.
Structural characterization of hydroperoxide lyase in dodecyl maltoside by using circular dichroism
Protein J.
32
1-6
2013
Capsicum annuum
brenda
Teder, T.; Boeglin, W.E.; Schneider, C.; Brash, A.R.
A fungal catalase reacts selectively with the 13S fatty acid hydroperoxide products of the adjacent lipoxygenase gene and exhibits 13S-hydroperoxide-dependent peroxidase activity
Biochim. Biophys. Acta
1862
706-715
2017
Fusarium graminearum (I1REW2), Fusarium graminearum, Fusarium graminearum PH-1 (I1REW2)
brenda
Jacopini, S.; Mariani, M.; de Caraffa, V.B.; Gambotti, C.; Vincenti, S.; Desjobert, J.M.; Muselli, A.; Costa, J.; Berti, L.; Maury, J.
Olive recombinant hydroperoxide lyase, an efficient biocatalyst for synthesis of green leaf volatiles
Appl. Biochem. Biotechnol.
179
671-683
2016
Olea europaea (G8XQN2)
brenda
Jacopini, S.; Vincenti, S.; Mariani, M.; Brunini-Bronzini de Caraffa, V.; Gambotti, C.; Desjobert, J.M.; Muselli, A.; Costa, J.; Tomi, F.; Berti, L.; Maury, J.
Activation and stabilization of olive recombinant 13-hydroperoxide lyase using selected additives
Appl. Biochem. Biotechnol.
182
1000-1013
2017
Olea europaea (G8XQN2)
brenda
Toporkova, Y.Y.; Gorina, S.S.; Bessolitsyna, E.K.; Smirnova, E.O.; Fatykhova, V.S.; Bruehlmann, F.; Ilyina, T.M.; Mukhtarova, L.S.; Grechkin, A.N.
Double function hydroperoxide lyases/epoxyalcohol synthases (CYP74C) of higher plants identification and conversion into allene oxide synthases by site-directed mutagenesis
Biochim. Biophys. Acta
1863
369-378
2018
Cucumis sativus (U5YTM6), Cucumis sativus (A0A0A0K2U8), Glycine max (M4WFN0), Solanum tuberosum (C7ENW3), Cucumis melo (Q93XR3), Medicago truncatula (Q7X9B3)
brenda
Liu, Q.; Hua, Y.
Continuous synthesis of hexanal by immobilized hydroperoxide lyase in packed-bed reactor
Bioprocess Biosyst. Eng.
38
2439-2449
2015
Amaranthus tricolor
brenda
Santiago-Gomez, P.M.; Vergely, C.; Policar, C.; Nicaud, J.-M.; Belin, J.-M.; Rochette, L.; Husson, F.
Characterization of purified green bell pepper hydroperoxide lyase expressed by Yarrowia lipolytica radicals detection during catalysis
Enzyme Microb. Technol.
41
13-18
2007
Capsicum annuum (Q39443)
-
brenda
Li, J.; Avila, C.A.; Tieman, D.M.; Klee, H.J.; Goggin, F.L.
A Comparison of the effects of fatty acid desaturase and hydroperoxide lyase on plant-aphid interactions
Int. J. Mol. Sci.
19
E1077
2018
Solanum lycopersicum (Q9XGI8)
brenda
Deng, W.W.; Wu, Y.L.; Li, Y.Y.; Tan, Z.; Wei, C.L.
Molecular Cloning and characterization of hydroperoxide lyase gene in the leaves of tea plant (Camellia sinensis)
J. Agric. Food Chem.
64
1770-1776
2016
Camellia sinensis
brenda
Gargouri, M.; Drouet, P.; Legoy, M.-D.
Hydroperoxide-lyase activity in mint leaves volatile C6-aldehyde production from hydroperoxy-fatty acids
J. Biotechnol.
111
59-65
2004
Mentha spicata, Mentha pulegium
brenda
Nilsson, A.K.; Fahlberg, P.; Johansson, O.N.; Hamberg, M.; Andersson, M.X.; Ellerstroem, M.
The activity of hydroperoxide lyase 1 regulates accumulation of galactolipids containing 12-oxo-phytodienoic acid in Arabidopsis
J. Exp. Bot.
67
5133-5144
2016
Arabidopsis thaliana (B3LF83)
brenda
Ono, E.; Handa, T.; Koeduka, T.; Toyonaga, H.; Tawfik, M.M.; Shiraishi, A.; Murata, J.; Matsui, K.
CYP74B24 is the 13-hydroperoxide lyase involved in biosynthesis of green leaf volatiles in tea (Camellia sinensis)
Plant Physiol. Biochem.
98
112-118
2016
Camellia sinensis (G4VV60), Camellia sinensis
brenda
Savchenko, T.; Yanykin, D.; Khorobrykh, A.; Terentyev, V.; Klimov, V.; Dehesh, K.
The hydroperoxide lyase branch of the oxylipin pathway protects against photoinhibition of photosynthesis
Planta
245
1179-1192
2017
Arabidopsis thaliana (B3LF83), Arabidopsis thaliana, Spinacia oleracea, Arabidopsis thaliana Col-0 (B3LF83)
brenda
Gorina, S.S.; Smirnova, E.O.; Mukhtarova, L.S.; Toporkova, Y.Y.; Grechkin, A.N.
Conversion of tomato allene oxide synthase LeAOS3 (CYP74C3) into epoxyalcohol synthase by site-directed mutagenesis
Dokl. Biochem. Biophys.
483
329-332
2018
Solanum lycopersicum (K4BV52)
brenda
Peng, Q.; Zhou, Y.; Liao, Y.; Zeng, L.; Xu, X.; Jia, Y.; Dong, F.; Li, J.; Tang, J.; Yang, Z.
Functional characterization of an allene oxide synthase involved in biosynthesis of jasmonic acid and its influence on metabolite profiles and ethylene formation in tea (Camellia sinensis) flowers
Int. J. Mol. Sci.
19
2440
2018
Camellia sinensis (A0A023UKW8)
brenda
Dumin, W.; Rostas, M.; Winefield, C.
Identification and functional characterisation of an allene oxide synthase from grapevine (Vitis vinifera L. Sauvignon blanc)
Mol. Biol. Rep.
45
263-277
2018
Vitis vinifera
brenda
Toporkova, Y.Y.; Smirnova, E.O.; Mukhtarova, L.S.; Gorina, S.S.; Grechkin, A.N.
Catalysis by allene oxide synthases (CYP74A and CYP74C) Alterations by the Phe/Leu mutation at the SRS-1 region
Phytochemistry
169
112152
2020
Linum usitatissimum (P48417), Zea mays (Q6RW10), Solanum lycopersicum (K4BV52), Physcomitrium patens
brenda
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