Modulating the synthetase activity of penicillin G acylase in organic media by addition of N-methylimidazole: using vinyl acetate as activated acyl donor

J Biotechnol. 2011 May 20;153(3-4):111-5. doi: 10.1016/j.jbiotec.2011.03.009. Epub 2011 Mar 17.

Abstract

This paper reported the modulation of enzyme activity by organic small molecule. The esterification activity of Penicillin G acylase (PGA) was improved more than 70-fold by the addition of 10% N-methylimidazole. Some control experiments have been designed to demonstrate the catalytic specificity of PGA. The structure and the amount of additive were optimized to improve the product yield. The influence of N-methylimidazole on the PGA conformation was investigated by FTIR and autodock simulation. Seven substrates were used to evaluate the effect of structure on the PGA-catalyzed transesterification. A series of products were successfully synthesized with the yield ranged from 56% to 84% and PGA showed specific recognition on the substrate with phenyl group in the presence of 10% N-methylimidazole.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Bioengineering
  • Enzymes, Immobilized / chemistry*
  • Enzymes, Immobilized / metabolism
  • Esterification
  • Guaifenesin / analogs & derivatives
  • Guaifenesin / chemistry
  • Guaifenesin / metabolism
  • Imidazoles / chemistry
  • Imidazoles / pharmacology*
  • Ligases / chemistry
  • Ligases / metabolism
  • Models, Molecular
  • Penicillin Amidase / chemistry*
  • Penicillin Amidase / metabolism
  • Spectrophotometry, Infrared
  • Substrate Specificity
  • Vinyl Compounds / chemistry*
  • Vinyl Compounds / metabolism

Substances

  • Enzymes, Immobilized
  • Imidazoles
  • Vinyl Compounds
  • Guaifenesin
  • Penicillin Amidase
  • Ligases
  • vinyl acetate
  • 1-methylimidazole