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Literature summary extracted from

  • Resnick, S.M.; Torok, D.S.; Lee, K.; Brand, J.M.; Gibson, D.T.
    Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase (1994), Appl. Environ. Microbiol., 60, 3323-3328.
    View publication on PubMedView publication on EuropePMC

Organism

EC Number Organism UniProt Comment Textmining
1.14.12.11 Pseudomonas putida
-
 F39D
-
1.14.12.11 Pseudomonas putida F39D
-
 F39D
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.12.11 2-indanone + NADH + O2 no reaction with 1-indanone Pseudomonas putida (S)-2-hydroxy-1-indanone + NAD+ 95% S-enantiomer, product is formed by incorporation of a single atom of molecular oxygen rather than by dioxygenation of enol tautomers of the ketone substrate ?
1.14.12.11 2-indanone + NADH + O2 no reaction with 1-indanone Pseudomonas putida F39D (S)-2-hydroxy-1-indanone + NAD+ 95% S-enantiomer, product is formed by incorporation of a single atom of molecular oxygen rather than by dioxygenation of enol tautomers of the ketone substrate ?
1.14.12.11 additional information no reaction with 1-indanone Pseudomonas putida ?
-
 ?
1.14.12.11 additional information no reaction with 1-indanone Pseudomonas putida F39D ?
-
 ?
1.14.12.11 toluene + NADH + O2
-
 Pseudomonas putida (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?
1.14.12.11 toluene + NADH + O2
-
 Pseudomonas putida F39D (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?

Cofactor

EC Number Cofactor Comment Organism Structure
1.14.12.11 NADH
-
 Pseudomonas putida