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Literature summary for 1.14.13.22 extracted from

  • Carrea, G.; Redigolo, B.; Riva, S.; Colonna, S.; Gaggero, N.; Battistel, E.; Bianchi, D.
    Effects of substrate structure on the enantioselectivity and stereochemical course of sulfoxidation catalyzed by cyclohexanone monooxygenase (1992), Tetrahedron, 3, 1063-1068.
No PubMed abstract available
Search for more literature for 1.14.13.22

Organism

Organism UniProt Comment Textmining
Acinetobacter sp.
-
 NCIB 9871
-

Reaction

Reaction Comment Organism Reaction ID
cyclohexanone + NADPH + H+ + O2 = hexano-6-lactone + NADP+ + H2O stereochemistry and enantioselectivity of the oxidation reaction depends strongly on the structure and stereochemistry of the substrates Acinetobacter sp.
a

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
cyclohexanone + NADPH + O2
-
 Acinetobacter sp. 6-hexanolide + NADP+ + H2O
-
 ?
ethyl p-tolyl sulfide + NADPH + O2
-
 Acinetobacter sp. (S)-ethyl p-tolyl sulfoxide + NADP+ + H2O
-
 ?
additional information active with diverse alkyl aryl sulfides, dialkyl sulfides and dialkyldisulfides Acinetobacter sp. ?
-
 ?
additional information high enantioselectivity in oxidation of sulfides Acinetobacter sp. ?
-
 ?