Enzymatic synthesis of (R)-cyanohydrins by a novel (R)-oxynitrilase from Vicia sativa L

Biotechnol Lett. 2006 Dec;28(23):1909-12. doi: 10.1007/s10529-006-9175-7. Epub 2006 Sep 26.

Abstract

The defatted seed meal of common vetch (Vicia sativa L.) served as a source of (R)-oxynitrilase which catalyzed the enantioselective addition of HCN to aromatic, heteroaromatic, fluoro-substituted aromatic aldehydes to produce the corresponding enantiomeric pure cyanohydrins in yields of 52-100% and 88-99% ee at 12 degrees C under micro-aqueous medium (diisopropyl ether) without addition of buffer solution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde-Lyases / chemical synthesis
  • Aldehyde-Lyases / chemistry*
  • Biotechnology / methods
  • Biotransformation
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Nitriles / chemical synthesis
  • Nitriles / chemistry*
  • Plant Extracts / chemistry*
  • Plants / metabolism
  • Stereoisomerism
  • Temperature
  • Vicia sativa / enzymology*

Substances

  • Nitriles
  • Plant Extracts
  • cyanohydrin
  • Aldehyde-Lyases
  • mandelonitrile lyase