Improved specific productivity in cephalexin synthesis by immobilized PGA in silica magnetic micro-particles

Biotechnol Bioeng. 2010 Dec 1;107(5):753-62. doi: 10.1002/bit.22867.

Abstract

There is a marked trend in pharmaceutical industry towards the replacement of classical organic methods by "green" alternatives that minimize or eliminate the generation of waste and avoid, where possible, the use of toxic and/or hazardous reagents and solvents. In this work the kinetically controlled synthesis of cephalexin by soluble and penicillin G acylase immobilized in sol-gel micro-particles with magnetic properties was performed in aqueous media with PGME and 7-ADCA as substrates, at different concentrations of substrate, temperature, pH, enzyme to substrate ratio and acyl donor to nucleophile ratio. Excess acyl donor had a strong effect on cephalexin productivity. A PGME/7-ADCA ratio of 3 was considered optimum. A maximum specific productivity of 5.9 mmol h(-1), gbiocatalyst(-1) at 160 mM 7-ADCA, 480 mM PGME and low enzyme to substrate ratio at 32.5 U mmol(-1) 7-ADCA was obtained with immobilized PGA in full aqueous medium, suggesting that diffusional limitations were minimized when compared with other commercial biocatalysts. A half-life of 133 h for the immobilized biocatalyst was estimated during cephalexin synthesis in the presence of 100 mM 7-ADCA and 300 mM PGME, in 50 mM Tris/HCl at pH 7.2 and 14°C. These results compare quite favorably with those previously reported for the kinetically controlled synthesis of cephalexin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / metabolism*
  • Biotechnology / methods
  • Cephalexin / metabolism*
  • Enzymes, Immobilized / metabolism*
  • Half-Life
  • Hydrogen-Ion Concentration
  • Magnetics*
  • Microspheres*
  • Penicillin Amidase / metabolism*
  • Silicon Dioxide*
  • Technology, Pharmaceutical / methods
  • Temperature

Substances

  • Anti-Bacterial Agents
  • Enzymes, Immobilized
  • Silicon Dioxide
  • Penicillin Amidase
  • Cephalexin