Asymmetric Bioreduction of Benzyl Acetoacetate to Its Corresponding Alcohol, Benzyl (S)-(+)-3-Hydroxybutyrate by the Yeast Candida schatavii MY 1831

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概要

• 論文の詳細を見る

• The screening of 35 microbial strains yielded 13 of them as suitable biocatalysts for the asymmetric bioreduction of benzyl acetoacetate to its corresponding alcohol benzyl (S)-(+)-3-hydroxybutyrate. The production of benzyl (S)-(+)-3-hydroxybutyrate with an elevated optical purity of 93% was achieved when employing the yeast Candida schatavii strain MY 1831.

• 公益社団法人日本生物工学会の論文
• 1996-11-25

著者

• CHARTRAIN MICHEL

  Merck Research Laboratories

• GREASHAM RANDOLPH

  Merck Research Laboratories

• Chartrain Michel

  Merck Research Laboratories Department Of Bioprocess Research

• Greasham Randolph

  Merck Research Laboratories Department Of Bioprocess Research

• McNAMARA JAMES

  Department of Process Research

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• Asymmetric Bioreduction of a β-Tetralone to Its Corresponding (S)-Alcohol by the Yeast Trichosporon capitatum NY 1890
• Asymmetric Bioreduction of a β-Ketoester to (R)-β-Hydroxyester by the Fungus Mortierella alpina MF 5534
• Asymmetric Bioreduction of Benzyl Acetoacetate to Its Corresponding Alcohol, Benzyl (S)-(+)-3-Hydroxybutyrate by the Yeast Candida schatavii MY 1831

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