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Literature summary for 4.1.2.10 extracted from

  • Effenberger, F.; Foerster, S.; Wajant, H.
    Hydroxynitrile lyases in stereoselective catalysis (2000), Curr. Opin. Biotechnol., 11, 532-539.
    View publication on PubMed

Application

Application Comment Organism
synthesis used as a catalyst in the preparation of optically active cyanohydrins Prunus sp.

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
55000 80000
-
Prunus sp.

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
cyanide + benzaldehyde Prunus sp.
-
(R)-mandelonitrile
-
r

Organism

Organism UniProt Comment Textmining
Prunus sp.
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
cyanide + benzaldehyde
-
Prunus sp. (R)-mandelonitrile
-
r
cyanide + benzaldehyde (R)-specific Prunus sp. (R)-mandelonitrile
-
?

Subunits

Subunits Comment Organism
monomer 1 * 55000-80000 Prunus sp.

Synonyms

Synonyms Comment Organism
Hydroxynitrile lyase
-
Prunus sp.

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
5 6
-
Prunus sp.