Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 4.1.1.72 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 .
    View publication on PubMed

Application

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

Organism

Organism UniProt Comment Textmining
Lactococcus lactis
-
-
-

Substrates and Products (Substrate)

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

Synonyms

Synonyms Comment Organism
KdcA
-
Lactococcus lactis