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Literature summary extracted from

  • Purkarthofer, T.; Skranc, W.; Schuster, C.; Griengl, H.
    Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry (2007), Appl. Microbiol. Biotechnol., 76, 309-320.
    View publication on PubMed

Application

EC Number Application Comment Organism
4.1.2.47 drug development industrial processes Hevea brasiliensis

Cloned(Commentary)

EC Number Cloned (Comment) Organism
4.1.2.47 cloned and produced by heterologous expression in different microbial hosts Hevea brasiliensis

Crystallization (Commentary)

EC Number Crystallization (Comment) Organism
4.1.2.47 three-dimensional structure analysis, catalytic triad consisting of serine, histidine and aspartic acid Hevea brasiliensis

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
4.1.2.47 2-hydroxy-2-methylpropanenitrile Hevea brasiliensis
-
acetone + HCN
-
r

Organism

EC Number Organism UniProt Comment Textmining
4.1.2.47 Hevea brasiliensis
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.1.2.47 (1S)-1-furan-2-yl-2-nitroethanol enantiomeric excess: ~90%, yield: 60-70% Hevea brasiliensis furan-2-carbaldehyde + CH3NO2
-
r
4.1.2.47 (1S)-2-nitro-1-(4-nitrophenyl)ethanol enantiomeric excess: ~90%, yield: 60-70% Hevea brasiliensis 4-nitrobenzaldehyde + CH3NO2
-
r
4.1.2.47 (1S)-2-nitro-1-phenylethanol enantiomeric excess: ~90%, yield: 60-70% Hevea brasiliensis benzaldehyde + CH3NO2
-
r
4.1.2.47 (1S,2R)-2-nitro-1-phenyl-propanol 4 diastereomers, enantiomeric excess: 95%, yield: 67% Hevea brasiliensis benzaldehyde + C2H5NO2
-
r
4.1.2.47 (2S)-1-nitrooctan-2-ol enantiomeric excess: ~90%, yield: 60-70% Hevea brasiliensis heptanal + CH3NO2
-
r
4.1.2.47 (R)-2-(2-furyl)-2-hydroxyacetonitrile enantiomeric excess: > 99%, yield: 90% Hevea brasiliensis furan-2-carbaldehyde + HCN
-
r
4.1.2.47 (S)-3-phenoxybenzaldehyde cyanohydrin enantiomeric excess: > 98.5%, yield: 95.5%, used for insecticide synthesis Hevea brasiliensis m-phenoxybenzaldyhyde + HCN
-
r
4.1.2.47 (S)-mandelonitrile enantiomeric excess: > 99%, yield: 90% Hevea brasiliensis benzaldehyde + HCN
-
r
4.1.2.47 2-hydroxy-2-methylpropanenitrile
-
Hevea brasiliensis acetone + HCN
-
r
4.1.2.47 3-[(1S)-1-hydroxy-2-nitroethyl]phenol enantiomeric excess: ~90%, yield: 60-70% Hevea brasiliensis 3-hydroxybenzaldehyde + CH3NO2
-
r

Synonyms

EC Number Synonyms Comment Organism
4.1.2.47 HbHNL
-
Hevea brasiliensis
4.1.2.47 HNL
-
Hevea brasiliensis
4.1.2.47 Hydroxynitrile lyase
-
Hevea brasiliensis