• Title of article

    How the mode of Candida antarctica lipase B immobilization affects the continuous-flow kinetic resolution of racemic amines at various temperatures

  • Author/Authors

    Boros، نويسنده , , Zoltلn and Falus، نويسنده , , Péter and Mلrkus، نويسنده , , Mلria and Weiser، نويسنده , , Diلna and Olلh، نويسنده , , Mلrk and Hornyلnszky، نويسنده , , Gلbor and Nagy، نويسنده , , Jَzsef and Poppe، نويسنده , , Lلszlَ، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    7
  • From page
    119
  • To page
    125
  • Abstract
    The effect of temperature on enantiomeric ratio (E) and specific reaction rate (rflow) in the continuous-flow mode acetylation of (±)-1-phenylethanamine (rac-1a), (±)-4-phenylbutan-2-amine (rac-1b) and (±)-1,2,3,4-tetrahydro-1-naphthalenamine (rac-1c) by variously immobilized Candida antarctica lipase B biocatalysts was studied in the 0–70 °C range. In the continuous-flow kinetic resolutions with differently immobilized CaLB biocatalysts, the character of temperature effect depended significantly both on the substrate and on the mode of immobilization. Alteration of E in the kinetic resolutions of three differently flexible amines rac-1a–c as a function of temperature was rationalized by the various flexibility of the lipase in its different forms. Our results indicated that the optimal method of immobilization depended both on the nature of the substrate and the reaction conditions.
  • Keywords
    Lipase , Temperature effect , Immobilization , Amine , Enantiomer selectivity , Conformation
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Serial Year
    2013
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Record number

    1717572