Chemical Modification of Lipase for Rational Enhancement of Enantioselectivity

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  • Tadashi Ema
    Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
  • Hiroki Inoue
    Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University

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<jats:title>Abstract</jats:title> <jats:p>Chemical modifications of the I287C mutant of a Burkholderia cepacia lipase afforded various I287C-X conjugates, among which I287C-PAA bearing an N-phenylacetamide (PAA) moiety showed excellent enantioselectivity and catalytic activity for secondary alcohols. Site-directed chemical modifications are powerful tools to control enantioselective biocatalysis.</jats:p>

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  • Chemistry Letters

    Chemistry Letters 44 (10), 1374-1376, 2015-10

    Oxford University Press (OUP)

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