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Literature summary extracted from

  • Latham, J.A.; Walsh, C.
    Retention of configuration in oxidation of a chiral boronic acid by the flavoenzyme cyclihexanone oxygenase (1986), J. Chem. Soc. Chem. Commun., 1986, 527-528.
No PubMed abstract available

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
1.14.13.22 additional information
-
 additional information
-
 Acinetobacter sp.
1.14.13.22 0.07
-
 2-methylcyclohexyl boronic acid
-
 Acinetobacter sp.

Organism

EC Number Organism UniProt Comment Textmining
1.14.13.22 Acinetobacter sp.
-
 NCIB 9871
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.13.22 2-methylcyclohexyl boronic acid + NADPH + O2 racemic substrate Acinetobacter sp. 2-methylcyclohexanol + BO3- + NADP+ + H2O
-
 ?
1.14.13.22 additional information peroxide-like oxidation catalyzed Acinetobacter sp. ?
-
 ?
1.14.13.22 additional information ability to convert aryl and alkyl boronic acids into phenols and alcohols, racemic 2-methylcyclohexyl boronic acid is processed to 2-methylcyclohexanol Acinetobacter sp. ?
-
 ?

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
1.14.13.22 additional information
-
 additional information
-
 Acinetobacter sp.
1.14.13.22 8.4
-
 2-methylcyclohexyl boronic acid
-
 Acinetobacter sp.

Cofactor

EC Number Cofactor Comment Organism Structure
1.14.13.22 FAD enzyme-bound FAD-4a-OOH is the actual oxygenation reagent Acinetobacter sp.
1.14.13.22 NADPH
-
 Acinetobacter sp.