• Title of article

    Kinetic resolution of racemic 5,6-epoxy-bicyclo[2.2.1]heptane-2-one using genetically engineered Saccharomyces cerevisiae

  • Author/Authors

    Carlquist، نويسنده , , Magnus G. Olsson، نويسنده , , Cecilia and Bergdahl، نويسنده , , Basti and van Niel، نويسنده , , Ed W.J. and Gorwa-Grauslund، نويسنده , , Marie F. and Frejd، نويسنده , , Torbjِrn، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2009
  • Pages
    5
  • From page
    98
  • To page
    102
  • Abstract
    (+)-5,6-Epoxy-bicyclo[2.2.1]heptane-2-one, (+)-1, and endo-(−)-5,6-epoxy-bicyclo[2.2.1]heptane-2-ol, endo-(−)-2, were obtained by kinetic resolution of rac-1 by asymmetric bioreduction catalyzed by whole cells of a genetically engineered Saccharomyces cerevisiae yeast strain. The strain, TMB4100, had 1% phosphoglucose isomerase (PGI) activity and overexpressed a specific short-chain dehydrogenase, encoded by the gene YMR226c. The whole cell biocatalyst was demonstrated to be significantly inactivated within 24 h, thus restricting the reaction to low concentration. Despite this, the resolution method could be used to produce optically pure (+)-1 and endo-(−)-2 from the racemic mixture at 5 g/L substrate. At optimal conditions, 1 g of rac-1 was kinetically resolved to give (+)-1 in 95% ee and 28% yield and endo-(−)-2 in 74% ee, 80% de and 45% yield.
  • Keywords
    kinetic resolution , Bioreduction , Racemic epoxy ketone , epoxide , Kinetic model , Enantiomeric ratio , Bakerיs yeast , Saccharomyces cerevisiae , Asymmetric carbonyl reduction
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Serial Year
    2009
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Record number

    1713828