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Information on EC 2.4.1.121 - indole-3-acetate beta-glucosyltransferase
for references in articles please use BRENDA:EC2.4.1.121
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EC Tree 2 Transferases
2.4 Glycosyltransferases
2.4.1 Hexosyltransferases
2.4.1.121 indole-3-acetate beta-glucosyltransferase
The enzyme appears in viruses and cellular organisms
Reaction Schemes
showSynonyms
osiaglu, iaglc synthase, osiaaglu, indole-3-acetate beta-glucosyltransferase, indol-3-ylacetylglucose synthase, udp-glucose:indol-3-ylacetate glucosyl-transferase, iaa-glucose synthase, udpg-indol-3-ylacetyl glucosyl transferase, indole-3-acetic acid glucosyltransferase, more
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SYNONYM 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
glucosyltransferase, uridine diphosphoglucose-indoleacetate
-
-
-
-
IAA glucosyltransferase
IAA-glucose synthase
-
-
-
-
IAGlc synthase
IAGlu synthase
-
-
-
-
indol-3-ylacetylglucose synthase
-
-
-
-
UDP-glucose:indol-3-ylacetate glucosyl-transferase
-
-
-
-
UDP-glucose:indol-3-ylacetate glucosyltransferase
-
-
-
-
UDPG-indol-3-ylacetyl glucosyl transferase
-
-
-
-
UDPglucose:indole-3-acetate beta-D-glucosyltransferase
-
-
-
-
IAGlc synthase
-
-
-
-
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REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
UDP-glucose + (indol-3-yl)acetate = UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
-
-
-
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REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
hexosyl group transfer
-
-
-
-
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PATHWAY SOURCE
PATHWAYS
MetaCyc
indole-3-acetate inactivation IX, superpathway of indole-3-acetate conjugate biosynthesis
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SYSTEMATIC NAME
IUBMB Comments
UDP-glucose:(indol-3-yl)acetate beta-D-glucosyltransferase
-
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CAS REGISTRY NUMBER
COMMENTARY
74082-56-7
-
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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
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
UDP-glucose + (indol-3-yl)acetate
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)propionate
UDP + 1-O-(indol-3-yl)propionyl-beta-D-glucose
-
Substrates: 22% of the activity with (indol-3-yl)acetate
Products: -
Products: -
r
UDP-glucose + 1-naphtaleneacetic acid
UDP + ?
Substrates: 70% of the relative activity as compared to (indol-3-yl)acetate
Products: -
Products: -
?
UDP-glucose + 1-naphthalene acetate
UDP + 1-naphthalene acetyl-beta-D-glucose
-
Substrates: 24% of the activity with (indol-3-yl)acetate
Products: -
Products: -
r
UDP-glucose + cinnamic acid
UDP + cinnamoyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
r
UDP-glucose + gibberellin GA3
UDP + ?
-
Substrates: 1.9% of the activity with (indol-3-yl)acetate
Products: -
Products: -
r
UDP-glucose + indole-3-acetate
UDP + indole-3-acetyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
r
UDP-glucose + indole-3-butyric acid
UDP + ?
Substrates: 66% of the activity as compared to (indol-3-yl)acetate
Products: -
Products: -
?
UDP-glucose + indole-3-propionic acid
UDP + ?
Substrates: 49.7% of the activity as compared to (indol-3-yl)acetate
Products: -
Products: -
?
UDP-glucose + phenylacetic acid
UDP + ?
Substrates: 30% of the relative activity as compared to (indol-3-yl)acetate
Products: -
Products: -
?
UDP-glucose + phenylacetic acid
UDP + phenylacetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDPglucose + 2,5-dimethoxycinnamic acid
UDP + 2,5-dimethoxycinnamoyl-beta-1-D-glucose
-
Substrates: 4.3% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + 3,4-dimethoxycinnamic acid
UDP + 3,4-dimethoxycinnamoyl-beta-1-D-glucose
-
Substrates: 6.1% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + 3-hydroxy-4-methoxy cinnamic acid
UDP + 3-hydroxy-4-methoxycinnamoyl-beta-1-D-glucose
-
Substrates: 9.4% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + ferulic acid
UDP + feruloyl-beta-1-D-glucose
-
Substrates: 7.8% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + indole butyric acid
UDP + indole butanoyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
?
UDPglucose + indole propionic acid
UDP + indole propanoyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
?
UDPglucose + m-hydroxycinnamic acid
UDP + m-hydroxycinnamoyl-beta-1-D-glucose
-
Substrates: 4.3% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + o-hydroxycinnamic acid
UDP + o-hydroxycinnamoyl-beta-1-D-glucose
-
Substrates: 7.6% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + p-coumaric acid
UDP + p-coumaroyl-beta-1-D-glucose
-
Substrates: 10.2% of the activity with indole-3-acetate
Products: -
Products: -
?
UDPglucose + phenylacetic acid
UDP + phenylacetyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
?
additional information
?
-
Substrates: the enzyme shows no catalytic activity towards synthetic auxins, 2,4-dichlorophenoxyacetic acid, Picloram and Dicamba
Products: -
Products: -
-
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
Substrates: -
Products: -
Products: -
r
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
Substrates: best substrate
Products: -
Products: -
r
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: the enzyme catalyzes a reversible reaction with unfavourable equilibrium that delivers 1-O-(indol-3-yl)acetyl-beta-D-glucose for favourable transacylation to indole-3-acetic acid inositol
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: (indol-3-yl)acetate is a preferred substrate
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
r
UDP-glucose + indole-3-acetate
1-O-indole-3-acetyl-beta-D-glucose + UDP
-
Substrates: -
Products: -
Products: -
r
UDP-glucose + indole-3-acetate
1-O-indole-3-acetyl-beta-D-glucose + UDP
-
Substrates: -
Products: -
Products: -
r
UDPglucose + indole-3-acetate
?
-
Substrates: first enzyme in pathway synthesizing ester conjugates of indoleacetate, constitutive in maize vegetative tissue, can be increased by incubation of tissue with 1-naphthalene acetic acid
Products: -
Products: -
?
UDPglucose + indole-3-acetate
?
-
Substrates: first reaction in a series leading to the ester conjugates of indole-3-acetic acid
Products: -
Products: -
?
UDPglucose + indole-3-acetate
?
-
Substrates: first enzyme-catalyzed reaction leading from indole-3-acetic acid to the myo-inositol ester of indole-3-acetate
Products: -
Products: -
?
UDPglucose + indole-3-acetate
UDP + indole-3-acetyl-beta-1-D-glucose
-
Substrates: -
Products: -
Products: -
?
UDPglucose + indole-3-acetate
UDP + indole-3-acetyl-beta-1-D-glucose
-
Substrates: specific for UDPglucose
Products: -
Products: -
r
UDPglucose + indole-3-acetate
UDP + indole-3-acetyl-beta-1-D-glucose
-
Substrates: specific for UDPglucose
Products: i.e. 1-O-indol-3-ylacetyl-beta-D-glucose
Products: i.e. 1-O-indol-3-ylacetyl-beta-D-glucose
?
UDPglucose + indole-3-acetate
UDP + indole-3-acetyl-beta-1-D-glucose
-
Substrates: equilibrium away from ester formation and towards formation of indole-3-acetate
Products: -
Products: -
r
UDPglucose + naphthalene-1-acetic acid
UDP + naphthyl-1-acetyl-beta-1-D-glucose
-
Substrates: -
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
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
UDP-glucose + (indol-3-yl)acetate
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
Substrates: -
Products: -
Products: -
r
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
-
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: -
Products: -
Products: -
?
UDP-glucose + (indol-3-yl)acetate
UDP + 1-O-(indol-3-yl)acetyl-beta-D-glucose
Substrates: the enzyme catalyzes a reversible reaction with unfavourable equilibrium that delivers 1-O-(indol-3-yl)acetyl-beta-D-glucose for favourable transacylation to indole-3-acetic acid inositol
Products: -
Products: -
?
UDPglucose + indole-3-acetate
?
-
Substrates: first enzyme in pathway synthesizing ester conjugates of indoleacetate, constitutive in maize vegetative tissue, can be increased by incubation of tissue with 1-naphthalene acetic acid
Products: -
Products: -
?
UDPglucose + indole-3-acetate
?
-
Substrates: first reaction in a series leading to the ester conjugates of indole-3-acetic acid
Products: -
Products: -
?
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METALS and IONS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
Ca2+
Mg2+
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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
2,4-Dichlorophenoxyacetic acid
competitive inhibitor, 1.5-fold decrease in the enzyme affinity towards (indol-3-yl)acetate
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ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
ATP
activates at low concentrations and inhibites at higher concentrations (above 0.6)
D-gluconic acid lactone
-
the inhibitor of beta-glucosidase activity, potentiates the enzyme activity at the optimal concentration of 0.3 mM
Glucose-1-phosphate
activates at low concentrations and inhibites at higher concentrations (above 4 mM)
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KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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TURNOVER NUMBER [1/s]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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kcat/KM VALUE [1/mMs-1]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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Ki VALUE [mM]
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pH RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
30
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
additional information
expression pattern of OsIAGLU in various developmental and germination stages in rice using quantitative RT-PCR approach
brenda
quantitative RT-PCR enzyme expression analysis shows that the expression of OsIAGLU is relatively higher in the late developing and the early germinating seeds
brenda
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
transient expression of OsIAAGLU-GFP or GFP-OsIAAGLU in rice protoplasts is limited to the cytoplasm
brenda
Highest Expressing Human Cell Lines
Cell Line LinksPlease wait a moment until the data is sorted. This message will disappear when the data is sorted.
GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
malfunction
metabolism
physiological function
malfunction
disruption of OsIAGLU results in low seed vigour in rice, ABA-sensitive phenotypes during seed germination, overview
malfunction
Overexpression of OsIAAGLU results in altered plant architecture. The number of tillers and leaf angle is significantly increased with a concomitant decrease in plant height and panicle length in the transgenic rice lines overexpressing OsIAAGLU compared to the wild-type plants. Phenotypes of iaaglu mutants show no obvious differences with wild-type plants. Overexpression of OsIAAGLU results in reduced sensitivity to indole-3-acetic acid (IAA) and 1-naphthalene acetic acid (NAA) and altered gravitropic response of the roots in the transgenic plants. Free IAA contents in the leaves, root tips, and lamina joint of OsIAAGLU-overexpressing transgenic lines are lower than those of wild-type plants. The transgenic plants are shorter than the wild-type plants and exhibit exaggerated leaf angles at the 5-leaf stage compared to the wild-type plants
malfunction
significant increase in both the indole-3-acetic acid and phenylacetic acid levels in the ugt84b1 null mutants. No obvious developmental phenotypes were observed in the ugt84b1 mutants under laboratory growth conditions. Overexpression of UGT84B1 results in auxin-deficient root phenotypes and changes in the indole-3-acetic acid and phenylacetic acid levels
metabolism
-
the enzyme catalyzes the first step in the biosynthesis of indol-3-yl ester conjugates in monocotyledonous plants
metabolism
the enzyme is involved in biosynthesis pathway of indole-3-acetyl-myo-inositol during development of maize
physiological function
-
1-O-(indol-3-yl)acetyl-beta-D-glucose, synthesized by the enzyme, is the substrate for (indol-3-yl)acetate labeling of glycoproteins from pea seeds indicating a possible role of this enzyme in the covalent modification of a class of proteins by a plant hormone. Auxin is a key plant hormone that regulates many physiological processes in plants including organ morphogenesis (i.e. apical dominance, root development) and environmental responses (biotic and abiotic stress). The major auxin is indole-3-acetic acid (IAA), but other indole-derived carboxylic acids, i.e. indole-3-butyric acid, indole-3-propionic acid, 4-chloro-indole-3-acetic acid, and indole-3-pyruvic acid have also auxin activity. Auxin action is highly dependent on its concentration, which must be precisely controlled
physiological function
the enzyme plays a role on seed vigour in seeds. Transcriptome analysis reveals that the indole-3-acetic acid (IAA)- and abscisic acid (ABA)-related genes are involved in the OsIAGLU regulation of seed vigour in rice. The regulation of seed vigour by OsIAGLU accurs through modulating IAA and ABA levels to alert OsABIs expression in germinating seeds in rice. Based on analysis of single-nucleotide polymorphism data of rice accessions, two haplotypes of OsIAGLU that positively correlate with seed vigour are identified in Oryza sativa subsp. indica accessions. OsIAGLU regulates seed vigour involved in OsABIs expression
physiological function
indole-3-acetic acid glucosyltransferase (OsIAAGLU) catalyzes the reaction of free indole-3-acetic acid (IAA) with glucose to generate IAA-glucose. OsIAAGLU plays a regulatory role in IAA homeostasis and rice architecture
physiological function
the enzyme regulates the levels of indole-3-acetic acid and phenylacetic acid in Arabidopsis
physiological function
the enzyme glucosylates indole-3-acetic acid and thus abolishes its auxinic activity affecting plant hormonal homeostasis
physiological function
-
the enzyme (OsIAGLU) plays a critical role in regulating auxin homeostasis. Overexpression of OsIAGLU disrupts auxin homeostasis, thereby negatively impacting rice growth and development
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UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION
The reliability class of the localization prediction ranges from 1 (very reliable) to 5 (not reliable).
The reliability class of the localization prediction ranges from 1 (very reliable) to 5 (not reliable). IABG_MAIZE
471
0
49710
Swiss-Prot
other Location (Reliability: 2)
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MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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SUBUNIT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
additional information
additional information
higher levels of free indole-3-acetic acid (IAA) and abscisic acid (ABA) are identified in germinating seeds of osiaglu mutants compared to wild-type plants. When treated with exogenous IAA and ABA, the osiaglu mutants and wild-type plants show sensitivity to ABA while not IAA, but the exogenous IAA amplified ABA-induced reduction of seed vigour in rice. The continuously higher expressions of ABA-INSENSITIVE 3 (OsABI3) and OsABI5 occur in germinating seeds of osiaglu mutants compared to wild-type plants. ABSCISIC ACID-INSENSITIVE 3 (ABI3) is a major downstream component of ABA signalling, and it has been reported as a major regulator of seed dormancy and ABA inhibition of seed germination
additional information
overexpression of OsIAAGLU reveals a role for indole-3-acetic acid (IAA)-glucose conjugation in modulating rice plant architecture. Construction of iaaglu mutants using the CRISPR/Cas9 system. Construction of hybrids Dongjin as well as IAAGLUOE3 containing pDR5:GUS obtained by crossing pDR5:GUS plants as the male parent with wild-type, OsIAAGLU overexpression plants (IAAGLUOE3) as the female parent, respectively. OsIAAGLU-overexpressing plants are insensitive to exogenous IAA/NAA (1-naphthalene acetic acid) and exhibit reduced root gravitropism. Transgenic plant phenotypes, overview
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GENERAL STABILITY
ORGANISM
UNIPROT
LITERATURE
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STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
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PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
native enzyme from immature seeds by PEG fractionation, anion exchange chromatography, and preparative PAGE
-
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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
gene OsIAAGLU, sequence comparisons, quantitative real-time PCR enzyme expression analysis, recombinant expression of GFP-tagged wild-type and mutant enzymes in Oryza sativa plants using the Agrobacterium tumefaciens strain EHA105 transfection method
gene OsIAGLU, quantitative RT-PCR enzyme expression analysis
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EXPRESSION
ORGANISM
UNIPROT
LITERATURE
expression of OsIAAGLU can be induced by indole-3-acetic acid (IAA) and 1-naphthalene acetic acid (NAA). Quantitative RT-PCR analysis show that within 2-6 h of exogenous auxin (0.01 mM IAA or 0.001 mM NAA) treatment, the expression of OsIAAGLU is upregulated in the leaves of 14-day-old rice seedlings. The response to NAA is earlier and many times greater than IAA. The transgenic plants are shorter than the wild-type plants and exhibit exaggerated leaf angles at the 5-leaf stage compared to the wild-type plants
quantitative RT-PCR enzyme expression analysis shows that the expressions of OsIAGLU is significantly induced by indole-3-acetic acid (IAA) and abscisic acid (ABA). Induce transcription levels of OsIAGLU in response to GA3, ABA, and IAA treatments in germinating seeds conducted using quantitative RT-PCR approach
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REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Michalczuk, L.; Bandurski, R.S.
Enzymic synthesis of 1-O-indol-3-ylacetyl-beta-D-glucose and indol-3-ylacetyl-myo-inositol
Biochem. J.
207
273-281
1982
Zea mays
brenda
Kowalczyk, S.; Bandurski, R.S.
Isomerization of 1-O-indol-3-ylacetyl-beta-D-glucose. Enzymatic hydrolysis of 1-O-, 4-O-, and 6-O-indol-3-ylacetyl-beta-D-glucose and the enzymatic synthesis of indole-3-acetyl glycerol by a hormone metabolizing complex
Plant Physiol.
94
4-12
1990
Zea mays
brenda
Leznicki, A.J.; Bandurski, R.S.
Enzymic synthesis of indole-3-acetyl-1-O-beta-D-glucose
Plant Physiol.
88
1474-1480
1988
Zea mays
brenda
Leznicki, A.J.; Bandurski, R.S.
Enzymic synthesis of indole-3-acetyl-1-O-beta-D-glucose
Plant Physiol.
88
1481-1485
1988
Zea mays
brenda
Kowalczyk, S.; Bandurski, R.S.
Enzymic synthesis of 1-O-(indol-3-ylacetyl)-beta-D-glucose. Purification of the enzyme from Zea mays, and preparation of antibodies to the enzyme
Biochem. J.
279
509-514
1991
Zea mays
brenda
Kowalczyk, S.; Jakubowska, A.; Bandurski, R.S.
1-Naphtalene acetic acid induces indole-3-ylacetylglucose synthase in Zea mays seedling tissue
Plant Growth Regul.
38
127-134
2002
Zea mays
-
brenda
Jackson, R.G.; Lim, E.K.; Li, Y.; Kowalczyk, M.; Sandberg, G.; Hoggett, J.; Ashford, D.A.; Bowles, D.J.
Identification and biochemical characterization of an Arabidopsis indole-3-acetic acid glucosyltransferase
J. Biol. Chem.
276
4350-4356
2001
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brenda
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The auxin conjugate 1-O-indole-3-acetyl-beta-D-glucose is synthesized in immature legume seeds by IAGlc synthase and may be used for modification of some high molecular weight compounds
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Phytochemistry
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Lathyrus oleraceus
brenda
He, Y.; Zhao, J.; Yang, B.; Sun, S.; Peng, L.; Wang, Z.
Indole-3-acetate beta-glucosyltransferase OsIAGLU regulates seed vigour through mediating crosstalk between auxin and abscisic acid in rice
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2020
Oryza sativa Japonica Group (Q10RB7)
brenda
Yu, X.L.; Wang, H.Y.; Leung, D.W.M.; He, Z.D.; Zhang, J.J.; Peng, X.X.; Liu, E.E.
Overexpression of OsIAAGLU reveals a role for IAA-glucose conjugation in modulating rice plant architecture
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Oryza sativa Japonica Group (A0A0P0W2E0)
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Aoi, Y.; Hira, H.; Hayakawa, Y.; Liu, H.; Fukui, K.; Dai, X.; Tanaka, K.; Hayashi, K.I.; Zhao, Y.; Kasahara, H.
UDP-glucosyltransferase UGT84B1 regulates the levels of indole-3-acetic acid and phenylacetic acid in Arabidopsis
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Arabidopsis thaliana (O22182)
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Ciarkowska, A.; Ostrowski, M.; Kozakiewicz, A.
Biochemical characterization of recombinant UDPG-dependent IAA glucosyltransferase from maize (Zea mays)
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Zea mays (Q41819)
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Ostrowski, M.; Ciarkowska, A.; Dalka, A.; Wilmowicz, E.; Jakubowska, A.
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Zea mays (Q41819)
brenda
Chen, G.; Fu, X.; Ruan, X.; Yu, X.; Hou, D.; Xu, H.
Upregulation of an IAA-glucosyltransferase OsIAGLU in rice (Oryza sativa L.) impairs root gravitropism by disrupting starch granule homeostasis
Plants (Basel)
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Oryza sativa
brenda
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