Issue 31, 2014

A novel P450-based biocatalyst for the selective production of chiral 2-alkanols

Abstract

A P450 monooxygenase from Nocardia farcinica (CYP154A8) catalyses the stereo- and regioselective hydroxylation of n-alkanes, still a challenging task in chemical catalysis. In a biphasic reaction system, the regioselectivity for the C2-position of C7–C9 alkanes was over 90%. The enzyme showed strict S-selectivity for all tested substrates, with enantiomeric excess (ee) of up to 91%.

Graphical abstract: A novel P450-based biocatalyst for the selective production of chiral 2-alkanols

Supplementary files

Article information

Article type
Communication
Submitted
24 Jan 2014
Accepted
24 Feb 2014
First published
25 Feb 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2014,50, 4089-4091

A novel P450-based biocatalyst for the selective production of chiral 2-alkanols

C. J. von Bühler and V. B. Urlacher, Chem. Commun., 2014, 50, 4089 DOI: 10.1039/C4CC00647J

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