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Literature summary for 4.1.2.47 extracted from

  • Wajant, H.; Foerster, S.; Spauer, A.; Effenberger, F.; Pfizenmaier, K.
    Enantioselective synthesis of aliphatic (S)-cyanohydrins in organic solvents using hydroxynitrile lyase from Manihot esculenta (1996), Ann. N. Y. Acad. Sci., 799, 771-776.
    View publication on PubMed
Search for more literature for 4.1.2.47

Organism

Organism UniProt Comment Textmining
Manihot esculenta
-
-
-

Purification (Commentary)

Purification (Comment) Organism
recombinant enzyme Manihot esculenta

Source Tissue

Source Tissue Comment Organism Textmining
leaf
-
 Manihot esculenta
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
86
-
-
 Manihot esculenta

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-Furylaldehyde + cyanide
-
 Manihot esculenta Furan-3-yl-hydroxyacetonitrile
-
 ?
2-Pentanone + cyanide
-
 Manihot esculenta 3-Hydroxyhexanonitrile
-
 ?
2-Thienylaldehyde + cyanide
-
 Manihot esculenta Hydroxythiophen-3-yl-acetonitrile
-
 ?
4-Methoxybenzaldehyde + cyanide
-
 Manihot esculenta 4-Methoxymandelonitrile
-
 ?
Acetophenone + cyanide
-
 Manihot esculenta 3-Hydroxy-3-phenylpropionitrile
-
 ?
Benzaldehyde + cyanide
-
 Manihot esculenta (S)-Mandelonitrile
-
 ?
Isobutyraldehyde + cyanide
-
 Manihot esculenta 2-Hydroxy-3-methylbutyronitrile
-
 ?
n-Butyraldehyde + cyanide
-
 Manihot esculenta (S)-2-Hydroxyvaleronitrile
-
 ?