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Efficient Enzymic Production of Enantiomerically Pure Amino Acids

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Enzymes as Catalysts in Organic Synthesis

Abstract

A generally applicable process for the production of enan-tioraerically pure amino acids is described. The method is based upon an enzymic resolution of DL-amino acid amides. As a biocatalyst aminopep-tidase from Pseudomonas putida is used, which will stereospecifically hydrolyze the L-from of the amino acid amide. Efficient methods for the synthesis of substrates, the separation of L-amino acid from D-amino acid amide and the racemization and recycling of the unwanted isomer have been developed.

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References

  1. See for reviews: a. G. Schmidt-Kastner and P. Egerer, in H.J. Rehra and G. Reed (Eds). Biotechnology Vol 6a, Verlag Chemie, Florida-Basel, p. 387–421 (1984) b. E.M. Meijer, W.H.J. Boesten, H.E. Schoemaker and J.A.M. van Balken. Symposium Biocatalysts in organic syntheses, Noordwijkerhout, The Netherlands, Elsevler Science Publishers, in press (1985)

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© 1986 D. Reidel Publishing Company

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Boesten, W.H.J. et al. (1986). Efficient Enzymic Production of Enantiomerically Pure Amino Acids. In: Schneider, M.P. (eds) Enzymes as Catalysts in Organic Synthesis. NATO ASI Series, vol 178. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-4686-6_24

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  • DOI: https://doi.org/10.1007/978-94-009-4686-6_24

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-8583-0

  • Online ISBN: 978-94-009-4686-6

  • eBook Packages: Springer Book Archive

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