Affinity adsorbents for the vancomycin group of antibiotics

Biotechnol Appl Biochem. 2000 Feb;31(1):15-20. doi: 10.1042/ba19990039.

Abstract

The vancomycin group of antibiotics kill Gram-positive bacteria by binding to nascent bacterial cell-wall peptidoglycan bearing the C-terminal sequence-D-Ala-D-Ala. In this paper, affinity adsorbents for the vancomycin group of antibiotics were prepared by immobilizing the peptidoglycan analogues -D-Ala-D-Ala, -succinyl-D-Ala and -succinyl-Gly on to crosslinked poly(N, N-dimethylacrylamide). The adsorption capacities of the three adsorbents for demethylvancomycin were 0.59, 0.35 and 0.29 mmol/g, respectively. The adsorption capacity of the adsorbent with-D-Ala-D-Ala for vancomycin was 0.53 mmol/g. In contrast, the adsorbent bearing -succinyl-L-Ala hardly adsorbed demethylvancomycin. Aqueous sodium carbonate (0.4 M)/acetonitrile (7/3, v/v) completely desorbed demethylvancomycin adsorbed on the adsorbents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / metabolism
  • Biotechnology / methods
  • Cell Wall / chemistry
  • Cross-Linking Reagents / chemistry
  • Peptides / chemical synthesis*
  • Peptides / metabolism
  • Peptidoglycan / chemistry*
  • Peptidoglycan / metabolism
  • Vancomycin / analogs & derivatives
  • Vancomycin / chemistry*
  • Vancomycin / metabolism

Substances

  • Anti-Bacterial Agents
  • Cross-Linking Reagents
  • Peptides
  • Peptidoglycan
  • Vancomycin
  • N-demethylvancomycin