4.8 Article

A highly regioselective route to arbutin esters by immobilized lipase from Penicillium expansum

Journal

BIORESOURCE TECHNOLOGY
Volume 101, Issue 1, Pages 1-5

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2009.07.067

Keywords

Lipase from Penicillium expansum; Immobilization; Arbutin; Regioselective acylation; Acyl donor specificity

Funding

  1. National Natural Science Foundation of China [20676043, 20876059]
  2. Science and Technology Project of Guangzhou city [2007Z3-E4101]
  3. Major State Basic Research Development Program [2010CB732201]

Ask authors/readers for more resources

Immobilized lipase from Penicillium expansum, a novel and inexpensive enzyme preparation that we immobilized in our laboratory, was an excellent catalyst for highly regioselective acylation of arbutin with fatty acid vinyl esters. For the enzymatic butanoylation of arbutin, under the optimal conditions, initial reaction rate was 75.1 mM/h, and substrate conversion and regioselectivity were greater than 99%. In addition, a variety of 6'-esters of arbutin were prepared with high conversion (>99%) and excellent regioselectivity (>99%). It was found that the enzymatic reaction rate varied widely with different acyl donors, presumably owing to their different interactions with the active site of the lipase. The immobilized lipase from A expansum displayed highest catalytic activity with medium-length straight-chain acyl donors. Acyl donors bearing a substituent or a conjugate double bond gave reduced reaction rates. (C) 2009 Elsevier Ltd. All rights reserved.

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