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Efficient Tandem Biocatalytic Process for the Kinetic Resolution of Aromatic β-Amino Acids

By Bian Wu, Wiktor Szymański, Stefaan de Wildeman, Gerrit J. Poelarends, Ben L. Feringa and Dick B. Janssen

Abstract

We describe a simple and efficient enzymatic tandem reaction for the preparation of enantiomerically pure β-phenylalanine and its analogues from the corresponding racemates. In this process, phenylalanine aminomutase (PAM) catalyzes the stereoselective isomerization of (R)-β-phenylalanines to (S)-α-phenylalanines, which are in situ transformed to cinnamic acids by phenylalanine ammonia lyase (PAL). Preparative scale conversions are done with a mutated PAM with enhanced catalytic activity.

Year: 2010
OAI identifier: oai:ub.rug.nl:dbi/4c34408013296
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