• Title of article

    Understanding water effect on Candida antarctica lipase B activity and enantioselectivity towards secondary alcohols

  • Author/Authors

    Léonard-Nevers، نويسنده , , Valérie and Marton، نويسنده , , Zsuzsanna and Lamare، نويسنده , , Sylvain and Hult، نويسنده , , Karl and Graber، نويسنده , , Marianne، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2009
  • Pages
    6
  • From page
    90
  • To page
    95
  • Abstract
    The effect of water activity (aW) on Candida antarctica lipase B (CALB) activity and enantioselectivity towards secondary alcohols was assessed. Experimental results for the resolution of racemic pentan-2-ol, hexan-3-ol, butan-2-ol and octan-4-ol by immobilized CALB-catalyzed acylation with methyl propanoate were obtained by using a solid/gas reactor. Water and substrate adsorption mechanism on immobilized CALB were then studied using moisture sorption analyzer and inverse gas chromatography, and the effective hydration state of the biocatalyst when varying aW was defined. The data showed a pronounced aW effect on both activity and enantioselectivity. If secondary alcohol follows the steric rules for being efficiently resolved, water at very low aW increased enantioselectivity by acting predominantly as an enantioselective inhibitor, making the stereospecificity pocket smaller. When increasing aW, water decreased enantioselectivity, due to an unfavourable increase of the entropic term TΔR−SΔS‡ of the differential free energy of activation. The “turning point” at which water changed from one predominant role to another would correspond to aW allowing full coverage of polar groups of the immobilized biocatalyst by water molecules.
  • Keywords
    Thermodynamics , Thermodynamic activity of water , Water adsorption , Lipase , Stereoselective catalysis
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Serial Year
    2009
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Record number

    1713926