Literature summary 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.

Organism

EC Number	Organism	UniProt	Comment	Textmining
4.1.2.47	Manihot esculenta	-	-	-

Purification (Commentary)

EC Number	Purification (Comment)	Organism
4.1.2.47	recombinant enzyme	Manihot esculenta

Source Tissue

EC Number	Source Tissue	Comment	Organism	Textmining
4.1.2.47	leaf	-	Manihot esculenta	-

Specific Activity [micromol/min/mg]

EC Number	Specific Activity Minimum [µmol/min/mg]	Specific Activity Maximum [µmol/min/mg]	Comment	Organism
4.1.2.47	86	-	-	Manihot esculenta

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
4.1.2.47	2-Furylaldehyde + cyanide	-	Manihot esculenta	Furan-3-yl-hydroxyacetonitrile	-	?
4.1.2.47	2-Pentanone + cyanide	-	Manihot esculenta	3-Hydroxyhexanonitrile	-	?
4.1.2.47	2-Thienylaldehyde + cyanide	-	Manihot esculenta	Hydroxythiophen-3-yl-acetonitrile	-	?
4.1.2.47	4-Methoxybenzaldehyde + cyanide	-	Manihot esculenta	4-Methoxymandelonitrile	-	?
4.1.2.47	Acetophenone + cyanide	-	Manihot esculenta	3-Hydroxy-3-phenylpropionitrile	-	?
4.1.2.47	Benzaldehyde + cyanide	-	Manihot esculenta	(S)-Mandelonitrile	-	?
4.1.2.47	Isobutyraldehyde + cyanide	-	Manihot esculenta	2-Hydroxy-3-methylbutyronitrile	-	?
4.1.2.47	n-Butyraldehyde + cyanide	-	Manihot esculenta	(S)-2-Hydroxyvaleronitrile	-	?

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)