Enzymatic synthesis of L-ascorbyl linoleate in organic media

Bioprocess Biosyst Eng. 2006 Mar;28(4):211-5. doi: 10.1007/s00449-005-0006-3. Epub 2005 Nov 12.

Abstract

A novel L-ascorbyl fatty acid ester, L-ascorbyl linoleate was successfully prepared by enzymatic esterification and transesterification in a non-aqueous medium using immobilized lipase as biocatalyst. Changes in enzymatic activity and product yield were studied for the following variable: the nature of the fatty acid, the fatty acid concentration and water content. The yield of synthesis for the C18 unsaturated fatty acids were higher than for the C18 saturated fatty acid. Initial enzyme concentration does not affect the equilibrium of the reaction. And the product yield (33.5%) in the transesterification was higher than that of the esterification (21.8%) at a high-substrate concentration 0.3 M. The medium water content was found to have a distinct influence on the L-ascorbyl linoleate synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascorbic Acid / analogs & derivatives*
  • Ascorbic Acid / chemical synthesis
  • Ascorbic Acid / chemistry*
  • Enzymes, Immobilized / chemistry
  • Fungal Proteins
  • Linoleic Acid / chemistry*
  • Linoleic Acids / chemical synthesis*
  • Linoleic Acids / chemistry*
  • Lipase / chemistry*
  • Organic Chemicals / chemistry*
  • Solvents / chemistry*

Substances

  • Enzymes, Immobilized
  • Fungal Proteins
  • Linoleic Acids
  • Organic Chemicals
  • Solvents
  • methyl linoleate
  • Linoleic Acid
  • Lipase
  • lipase B, Candida antarctica
  • Ascorbic Acid
  • ascorbyl linoleate