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Literature summary for 4.1.2.38 extracted from

  • Dominguez de Maria, P.; Pohl, M.; Gocke, D.; Groeger, H.; Trauthwein, H.; Stillger, T.; Walter, L.; Mueller, M.
    Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes (2007), Eur. J. Org. Chem., 2007, 2940-2944.
No PubMed abstract available

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+
-
Pseudomonas fluorescens

Organism

Organism UniProt Comment Textmining
Pseudomonas fluorescens
-
strain biovar I
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
acetaldehyde
-
Pseudomonas fluorescens (R)-acetoin
-
?
benzoin
-
Pseudomonas fluorescens benzaldehyde + benzaldehyde
-
?
cyclohexylaldehyde + acetaldehyde
-
Pseudomonas fluorescens 1-cyclohexyl 2-hydroxypropanone
-
?
isovaleraldehyde
-
Pseudomonas fluorescens (R)-5-hydroxy-2,7-dimethyloctan-4-one
-
?
additional information isobutyraldehyde, pivalaldehyde, and tert-butylacetaldehyde are no substrates Pseudomonas fluorescens ?
-
?
n-butanal
-
Pseudomonas fluorescens (R)-5-hydroxyoctan-4-one
-
?
n-pentanal
-
Pseudomonas fluorescens (R)-6-hydroxydecan-5-one
-
?
propanal
-
Pseudomonas fluorescens 4-hydroxyhexan-3-one
-
?

Synonyms

Synonyms Comment Organism
BAL
-
Pseudomonas fluorescens

Cofactor

Cofactor Comment Organism Structure
thiamine diphosphate dependent Pseudomonas fluorescens