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Literature summary extracted from

  • Resnick, S.M.; Gibson, D.T.
    Oxidation of 6,7-dihydro-5H-benzocycloheptene by bacterial strains expressing naphthalene dioxygenase, biphenyl dioxygenase, and toluene dioxygenase yields homochiral mono-ol or cis-diol enantiomers as major products (1996), Appl. Environ. Microbiol., 62, 1364-1368.
    View publication on PubMedView publication on EuropePMC

Organism

EC Number Organism UniProt Comment Textmining
1.14.12.12 Pseudomonas sp.
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 strain NCIB 9816/11, naphthalene dihydrogenase mutant derived from strain NCIB 9816-4 oxidizing naphthalene to cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene
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1.14.12.18 Sphingobium yanoikuyae
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 former name Beijerinckia sp.
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1.14.12.18 Sphingobium yanoikuyae B8/36
-
 former name Beijerinckia sp.
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.12.12 6,7-dihydro-5H-benzocycloheptene + NADH + O2 naphthalene dioxygenase activity in cells induced by salicylate Pseudomonas sp. (1R,2S)-cis-dihydroxybenzocycloheptane + NAD+ enantiomeric excess greater than 98% ?
1.14.12.18 6,7-dihydro-5H-benzocycloheptene + NAD(P)H + O2
-
 Sphingobium yanoikuyae (-)-cis-(1R,2S)-dihydroxybenzocycloheptane + NAD(P)+
-
 ?
1.14.12.18 6,7-dihydro-5H-benzocycloheptene + NAD(P)H + O2
-
 Sphingobium yanoikuyae B8/36 (-)-cis-(1R,2S)-dihydroxybenzocycloheptane + NAD(P)+
-
 ?