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

BRENDA support

Literature summary extracted from

  • Kuehl, S.; Zehentgruber, D.; Pohl, M.; Mueller, M.; Luetz, S.
    Process development for enzyme catalysed asymmetric C-C-bond formation (2007), Chem. Eng. Sci., 62, 5201-5205.
No PubMed abstract available

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
4.1.2.38 0.06
-
 (R)-3,3'-dimethoxybenzoin in 50 mM potassium phosphate buffer (pH 8), containing 0.5 mM thiamine diphosphate and 0.5 mM MgCl2 Pseudomonas fluorescens
4.1.2.38 2.1
-
 3-Methoxybenzaldehyde in 50 mM potassium phosphate buffer (pH 8), containing 0.5 mM thiamine diphosphate and 0.5 mM MgCl2 Pseudomonas fluorescens

Organism

EC Number Organism UniProt Comment Textmining
4.1.2.38 Pseudomonas fluorescens
-
 strain biovar I
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.1.2.38 3-methoxybenzaldehyde
-
 Pseudomonas fluorescens (R)-3,3'-dimethoxybenzoin
-
 r
4.1.2.38 3-methoxybenzaldehyde + 2-chlorobenzaldehyde
-
 Pseudomonas fluorescens (R)-3-methoxy-2'-chlorobenzoin
-
 r
4.1.2.38 benzoin
-
 Pseudomonas fluorescens benzaldehyde + benzaldehyde
-
 r

Synonyms

EC Number Synonyms Comment Organism
4.1.2.38 BAL
-
 Pseudomonas fluorescens

Cofactor

EC Number Cofactor Comment Organism Structure
4.1.2.38 thiamine diphosphate dependent Pseudomonas fluorescens