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  • Research PapersAsymmetric bioreduction of (2-(4-nitro-phenyl)-N-(2-oxo-2-pyridin-3-yl-ethyl)-acetamide) to its corresponding (R) alcohol [(R)-N- (2-hydroxy-2-pyridin-3-yl-ethyl)-2-(4-nitro-phenyl)-acetamide] by using Candida sorbophila MY 1833
  • Add time:09/09/2019         Source:sciencedirect.com

    A microbial screen identified the yeast Candida sorbophila MY 1833 as a suitable biocatalyst for the asymmetric bioreduction of a ketone (2-(4-nitro-phenyl)-N-(2-oxo-2-pyridin-3-yl-ethyl)-acetamide) to its corresponding (R) alcohol [(R)-N-(2-hydroxy-2-pyridin-3-yl-ethyl)-2-(4-nitro-phenyl)-acetamide]. Studies yielded the formulation of a chemically defined cultivation medium that supported excellent growth and bioconversion activity. Process development showed that the optimization of the bioreduction environmental conditions (pH, temperature), the timing of ketone addition, and the implementation of a nutrient feeding strategy were key factors in achieving increased bioreduction rates. The optimized process achieved a 10-fold bioreduction rate improvement over the original process, while reaching final product concentrations of up to 60 g/l. When scaled up in Pilot Plant bioreactors (280 l), the bioreduction process supported the production of several kilograms of highly optically pure (R) alcohol (enantiomeric excess > 98%).

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    Prev:Excited states of selected hydrazo-compounds on the example of 5-nitro-2-(2-phenylhydrazinyl)pyridine and its 3-, 4- or 6-methyl isomers
    Next: Crystal structure and Hirshfeld surface analysis of bis (2-(2-(1H-benzo[d]imidazol-2-yl)hydrazono)propan-1-ol) nickel(II) chloride)

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