An Improved Racemase/Acylase Biotransformation for the Preparation of Enantiomerically Pure Amino Acids

Scott Baxter, Sylvain Royer, Gideon Grogan, Fraser Brown, Karen E Holt-Tiffin, Ian N Taylor, Ian G Fotheringham, Dominic J Campopiano

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Using directed evolution, a variant N-acetyl amino acid racemase (NAAAR G291D/F323Y) has been developed with up to 6-fold higher activity than the wild-type on a range of N-acetylated amino acids. The variant has been coupled with an enantiospecific acylase to give a preparative scale dynamic kinetic resolution which allows 98% conversion of N-acetyl-DL-allylglycine into D-allylglycine in 18 h at high substrate concentrations (50 g L(-1)). This is the first example of NAAAR operating under conditions which would allow it to be successfully used on an industrial scale for the production of enantiomerically pure α-amino acids. X-ray crystal analysis of the improved NAAAR variant allowed a comparison with the wild-type enzyme. We postulate that a network of novel interactions that result from the introduction of the two side chains is the source of improved catalytic performance.
Original languageEnglish
Pages (from-to)19310-19313
Number of pages4
JournalJournal of the American Chemical Society
Volume134
Issue number47
DOIs
Publication statusPublished - Nov 2012

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