Literature summary extracted from

Beigi, M.; Gauchenova, E.; Walter, L.; Waltzer, S.; Bonina, F.; Stillger, T.; Rother, D.; Pohl, M.; Mueller, M.
Regio- and stereoselective aliphatic-aromatic cross-benzoin reaction enzymatic divergent catalysis (2016), Chemistry, 22, 13999-14005 .

Application

EC Number	Application	Comment	Organism
4.1.1.72	synthesis	use of the enzyme for catalytic asymmetric synthesis of (R)-phenylacetylcarbinol derivatives	Lactococcus lactis

Organism

EC Number	Organism	UniProt	Comment	Textmining
4.1.1.72	Lactococcus lactis	-	-	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
4.1.1.72	3,5-dimethoxybenzaldehyde + 2-oxopropanoic acid	-	Lactococcus lactis	(1R)-1-(3,5-dimethoxyphenyl)-1-hydroxypropan-2-one + CO2	-	?
4.1.1.72	3-formylbenzonitrile + 2-oxobutanoic acid	-	Lactococcus lactis	3-[(1R)-1-hydroxy-2-oxobutyl]benzonitrile	-	?
4.1.1.72	additional information	enzyme additionallly catalyzes the asymmetric synthesis of chiral 2-hydroxy ketones with high stereochemical purity	Lactococcus lactis	?	-	?

Synonyms

EC Number	Synonyms	Comment	Organism
4.1.1.72	KdcA	-	Lactococcus lactis

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Release 2023.1 (January 2023)