Lipase-catalyzed condensation of p-methoxyphenethyl alcohol and carboxylic acids with different steric and electrical properties in acetonitrile

Biotechnol Lett. 2003 Jan;25(1):3-7. doi: 10.1023/a:1021799825272.

Abstract

The substrate selectivity of Candida antarctica lipase for various carboxylic acids was systematically investigated for their condensation with p-methoxyphenethyl alcohol in acetonitrile. The electron density of a carboxylic carbon and the projection area of an acid molecule were numerical indicators for evaluating the substrate selectivity. Both the electron density and projection area had an influence on the V/Km value, while only the projection area affected the Km value. The presence of conjugation with a carboxyl group in an acid and a branched structure in the non-carboxylic region independently lowered the V/Km value by an order of 1.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Acetonitriles / chemistry*
  • Carboxylic Acids / chemistry*
  • Carboxylic Acids / classification
  • Catalysis
  • Electrochemistry / methods*
  • Enzyme Activation
  • Fungal Proteins
  • Kinetics
  • Lipase / chemistry*
  • Models, Molecular
  • Structure-Activity Relationship
  • Substrate Specificity

Substances

  • Acetonitriles
  • Carboxylic Acids
  • Fungal Proteins
  • Lipase
  • lipase B, Candida antarctica
  • acetonitrile