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Issue 2, 2017
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Biocatalytic stereoinversion of d-para-bromophenylalanine in a one-pot three-enzyme reaction

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Halogenated derivatives of phenylalanine can be used as cross-coupling reagents for making drug-like molecules, and pure enantiomers of these precursors are therefore highly desirable. In our exploration of enzymatic routes to simplify the deracemisation process, the application of two enzymes, D-amino acid transaminase and phenylalanine dehydrogenase, both from Lysinibacillus sphaericus, has given promising results for the stereo-inversion of D-enantiomers of para-bromophenylalanine as the model substrate and also p-chloro/fluorophenylalanine and tyrosine. The addition of a coenzyme recycling system using ethanol and alcohol dehydrogenase reduced the amount of coenzyme needed for the reaction catalysed by phenylalanine dehydrogenase, reducing cost and permitting efficient and complete conversion of the racemic amino acids to the L-enantiomer. Relative proportions of the enzymes were optimized. The high purity of the L-enantiomer, with an ee over 99%, and the ease of the process make it an ideal alternative for deracemisation of the studied compounds.

Graphical abstract: Biocatalytic stereoinversion of d-para-bromophenylalanine in a one-pot three-enzyme reaction

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The article was received on 14 Jul 2016, accepted on 07 Oct 2016 and first published on 07 Oct 2016

Article type: Paper
DOI: 10.1039/C6GC01922F
Green Chem., 2017,19, 503-510

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    Biocatalytic stereoinversion of D-para-bromophenylalanine in a one-pot three-enzyme reaction

    F. Khorsand, C. D. Murphy, A. J. Whitehead and P. C. Engel, Green Chem., 2017, 19, 503
    DOI: 10.1039/C6GC01922F

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