Optimized enzymatic synthesis of hesperidin fatty acid esters in a two-phase system containing ionic liquid

Molecules. 2011 Aug 23;16(8):7171-82. doi: 10.3390/molecules16087171.

Abstract

Response surface methodology (RSM) based on a five-level, three-variable central composite design (CCD) was employed for modeling and optimizing the conversion yield of the enzymatic acylation of hesperidin with decanoic acid using immobilized Candida antarctica lipase B (CALB) in a two-phase system containing [bmim]BF(4). The three variables studied (molar ratio of hesperidin to decanoic acid, [bmim]BF(4)/acetone ratio and lipase concentration) significantly affected the conversion yield of acylated hesperidin derivative. Verification experiments confirmed the validity of the predicted model. The lipase showed higher conversion degree in a two-phase system using [bmim]BF(4) and acetone compared to that in pure acetone. Under the optimal reaction conditions carried out in a single-step biocatalytic process when the water content was kept lower than 200 ppm, the maximum acylation yield was 53.6%.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Biocatalysis*
  • Candida / enzymology
  • Decanoic Acids / chemical synthesis*
  • Enzymes, Immobilized / chemistry*
  • Esters
  • Fungal Proteins
  • Hesperidin / analogs & derivatives*
  • Hesperidin / chemical synthesis
  • Imidazoles / chemistry
  • Ionic Liquids / chemistry*
  • Kinetics
  • Lipase / chemistry*

Substances

  • 1-butyl-3-methylimidazolium tetrafluoroborate
  • Decanoic Acids
  • Enzymes, Immobilized
  • Esters
  • Fungal Proteins
  • Imidazoles
  • Ionic Liquids
  • Hesperidin
  • Lipase
  • lipase B, Candida antarctica