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Literature summary for 1.14.14.99 extracted from

  • Wust, M.; Little, D.B.; Schalk, M.; Croteau, R.
    Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from Mint (Mentha) species: Evidence for catalysis within sterically constrained active sites (2001), Arch. Biochem. Biophys., 387, 125-136.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Mentha x piperita
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-
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(+)-limonene + [reduced NADPH-hemoprotein reductase] + O2
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Mentha x piperita (+)-trans-isopiperitenol + [oxidized NADPH-hemoprotein reductase] + H2O
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?
(-)-(4S)-limonene + [reduced NADPH-hemoprotein reductase] + O2 highly specific, regiospecific and stereospecific reaction Mentha x piperita (-)-trans-(3S,4R)-isopiperitenol + [oxidized NADPH-hemoprotein reductase] + H2O
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?