Enantioselective acetylation of (R,S)-atenolol: The use of Candidarugosa lipases immobilized onto magnetic chitosan nanoparticles inenzyme-catalyzed biotransformation
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Abstract
tThis paper describes the enzyme immobilization protocol as well as the enzymatic method for the directresolution of (R,S)-atenolol. The used magnetic enzyme carriers possess on their surface new-synthetizedchitosan derivatives with free amine groups distanced by ethyl or butyl chain. Additionally the cat-alytic activity of two types of commercially available lipases from Candida rugosa immobilized onto twodifferent magnetic nanoparticles were compared. The highest values of enantioselectivity (E = 66.9), enan-tiomeric excess of product (eep= 94.1%) and conversion (c = 41.84%) were obtained by using lipase fromCandida rugosa OF immobilized onto Fe3O4-CS-EtNH2. The study confirmed that even after 5 reactioncycles the immobilized lipase maintain its high catalytic activity.
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Enantioselective acetylation, (R,S)-atenolol, Magnetic nanoparticles, Lipases
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Journal of Molecular Catalysis. B, Enzymatic, 134, 2016, pp. 43-50.
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Except where otherwised noted, this item's license is described as CC0 1.0 Universal