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Enantioselective alpha-hydroxylation of 2-arylacetic acid derivatives and buspirone catalyzed by engineered cytochrome P450 BM-3.


ABSTRACT: Here we report that an engineered microbial cytochrome P450 BM-3 (CYP102A subfamily) efficiently catalyzes the alpha-hydroxylation of phenylacetic acid esters. This P450 BM-3 variant also produces the authentic human metabolite of buspirone, R-6-hydroxybuspirone, with 99.5% ee.

SUBMITTER: Landwehr M 

PROVIDER: S-EPMC2551755 | biostudies-literature | 2006 May

REPOSITORIES: biostudies-literature

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Enantioselective alpha-hydroxylation of 2-arylacetic acid derivatives and buspirone catalyzed by engineered cytochrome P450 BM-3.

Landwehr Marco M   Hochrein Lisa L   Otey Christopher R CR   Kasrayan Alex A   Bäckvall Jan-E JE   Arnold Frances H FH  

Journal of the American Chemical Society 20060501 18


Here we report that an engineered microbial cytochrome P450 BM-3 (CYP102A subfamily) efficiently catalyzes the alpha-hydroxylation of phenylacetic acid esters. This P450 BM-3 variant also produces the authentic human metabolite of buspirone, R-6-hydroxybuspirone, with 99.5% ee. ...[more]

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