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Volumn 387, Issue 1, 2001, Pages 125-136

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

(4) Ẅst, Matthias a,b Little, Dawn B a Schalk, Michel a Croteau, Rodney a

a WASHINGTON STATE UNIVERSITY (United States)

b GOETHE UNIVERSITY (Germany)

Author keywords

Carveol; Cytochrome P450 monooxygenase; Fluorinated substrate analogs; Isopiperitenol; Lamiaceae; Mentha piperita; Mentha spicata; Monoterpene biosynthesis

Indexed keywords

CARVEOL; LIMONENE; LIMONENE 3 HYDROXYLASE; LIMONENE 6 HYDROXYLASE; OXYGENASE; PEPPERMINT; TERPENE; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CATALYSIS; ENANTIOMER; ENZYME ACTIVE SITE; ENZYME MECHANISM; HYDROPHOBICITY; HYDROXYLATION; PLANT; PRIORITY JOURNAL; REACTION ANALYSIS; SPEARMINT; STEREOSPECIFICITY;

LAMIACEAE; MENTHA; MENTHA SPICATA; MENTHA X PIPERITA;

EID: 0035264179 PISSN: 00039861 EISSN: None Source Type: Journal
DOI: 10.1006/abbi.2000.2248 Document Type: Article

Times cited : (50)

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