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PubMed	članci
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(S)-limonen 3-monooksigenaza
(S)-limonen 3-monooksigenaza
Identifikatori
EC broj	1.14.13.47
CAS broj	138066-92-9
Baze podataka
IntEnz	IntEnz pregled
BRENDA	BRENDA pristup
ExPASy	NiceZyme pregled
KEGG	KEGG pristup
MetaCyc	metabolički put
PRIAM	profil
Strukture PBP	RCSB PDB PDBe PDBj PDBsum
PMC
Pretraga
PMC	članci
PubMed	članci
NCBI	proteini

(S)-limonen 3-monooksigenaza (EC 1.14.13.47, (-)-limonenska 3-hidroksilaza, (-)-limonenska 3-monooksigenaza, (-)-limonen,NADPH:kiseonik oksidoreduktaza (3-hidroksilacija)) je enzim sa sistematskim imenom (S)-limonen,NADPH:kiseonik oksidoreduktaza (3-hidroksilacija).^[1] Ovaj enzim katalizuje sledeću hemijsku reakciju

(S)-limonen + NADPH + H⁺ + O₂

\rightleftharpoons

(-)-trans-izopiperitenol + NADP⁺ + H₂O

Ovaj enzim ima visoku specifičnost. On može da koristi NADH umesto NADPH, ali je reakcija spora. On je hem-tiolatni protein (P-450).

Reference

^ Karp, F., Mihaliak, C.A., Harris, J.L. and Croteau, R. (1990). „Monoterpene biosynthesis: specificity of the hydroxylations of (-)-limonene by enzyme preparations from peppermint (Mentha piperita), spearmint (Mentha spicata), and perilla (Perilla frutescens) leaves”. Arch. Biochem. Biophys. 276: 219—226. PMID 2297225.

Literatura

Nicholas C. Price; Lewis Stevens (1999). Fundamentals of Enzymology: The Cell and Molecular Biology of Catalytic Proteins (Third изд.). USA: Oxford University Press. ISBN 019850229X.
Eric J. Toone (2006). Advances in Enzymology and Related Areas of Molecular Biology, Protein Evolution (Volume 75 изд.). Wiley-Interscience. ISBN 0471205036.
Branden C; Tooze J. Introduction to Protein Structure. New York, NY: Garland Publishing. ISBN 0-8153-2305-0.
Irwin H. Segel. Enzyme Kinetics: Behavior and Analysis of Rapid Equilibrium and Steady-State Enzyme Systems (Book 44 изд.). Wiley Classics Library. ISBN 0471303097.
William P. Jencks (1987). Catalysis in Chemistry and Enzymology. Dover Publications. ISBN 0486654605.

Spoljašnje veze

(S)-limonene+3-monooxygenase на US National Library of Medicine Medical Subject Headings (MeSH)

[1] Karp, F., Mihaliak, C.A., Harris, J.L. and Croteau, R. (1990). „Monoterpene biosynthesis: specificity of the hydroxylations of (-)-limonene by enzyme preparations from peppermint (Mentha piperita), spearmint (Mentha spicata), and perilla (Perilla frutescens) leaves”. Arch. Biochem. Biophys. 276: 219—226. PMID 2297225.

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