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Literature summary for 4.1.2.38 extracted from

  • Maugeri, Z.; Dominguez De Maria, P.
    Benzaldehyde lyase (BAL)-catalyzed enantioselective CC bond formation in deep-eutectic-solvents-buffer mixtures (2014), J. Mol. Catal. B, 107, 120-123 .
No PubMed abstract available
Search for more literature for 4.1.2.38

Cloned(Commentary)

Cloned (Comment) Organism
expressed in Escherichia coli Pseudomonas fluorescens

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ required Pseudomonas fluorescens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2-hydroxy-1,2-diphenylethanone Pseudomonas fluorescens
-
 2 benzaldehyde
-
 ?

Organism

Organism UniProt Comment Textmining
Pseudomonas fluorescens P51853
-
-

Purification (Commentary)

Purification (Comment) Organism
-
 Pseudomonas fluorescens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2 benzaldehyde 95% conversion Pseudomonas fluorescens 2-hydroxy-1,2-diphenylethanone
-
 ?
2 butyraldehyde 96% conversion Pseudomonas fluorescens (R)-5-hydroxy-4-octanone
-
 ?
2 valeraldehyde 98% conversion Pseudomonas fluorescens (R)-6-hydroxy-5-decanone
-
 ?
2-furaldehyde 75% conversion Pseudomonas fluorescens (R)-furoin
-
 ?
2-hydroxy-1,2-diphenylethanone
-
 Pseudomonas fluorescens 2 benzaldehyde
-
 ?

Synonyms

Synonyms Comment Organism
BAL
-
 Pseudomonas fluorescens
benzaldehyde lyase
-
 Pseudomonas fluorescens

Cofactor

Cofactor Comment Organism Structure
thiamine diphosphate dependent on Pseudomonas fluorescens