Vancomycin production is enhanced in chemostat culture with biomass-recycle

Citation
Jj. Mcintyre et al., Vancomycin production is enhanced in chemostat culture with biomass-recycle, BIOTECH BIO, 62(5), 1999, pp. 576-582
Citations number
23
Categorie Soggetti
Biotecnology & Applied Microbiology",Microbiology
Journal title
BIOTECHNOLOGY AND BIOENGINEERING
ISSN journal
00063592 → ACNP
Volume
62
Issue
5
Year of publication
1999
Pages
576 - 582
Database
ISI
SICI code
0006-3592(19990305)62:5<576:VPIEIC>2.0.ZU;2-9
Abstract
Production of the glycopeptide antibiotic vancomycin by Amycolatopsis orien talis ATCC 19795 was examined in phosphate-limited chemostat cultures with biomass-recycle, employing an oscillating membrane separator, at a constant dilution rate (D = 0.14 h(-1)). Experiments made under low agitation condi tions (600 rpm) showed that the biomass concentration could be increased 3. 9-fold with vancomycin production kinetics very similar to that of chemosta t culture without biomass-recycle. The specific production rate (q(vancomyc in)) was maximal when the biomass-recycle ratio (R) was 0.13 (D = 0.087 h(- 1)). When the dissolved oxygen tension dropped below 20% (air saturation), the biomass and vancomycin concentrations decreased and an unidentified red metabolite was released into the culture medium. Using increased agitation (850 rpm), used to maintain the dissolved oxygen tension above 20% air sat uration, maximum increases in biomass concentration (7.9-fold) and vancomcy in production 1.6-fold (0.6 mg/g dry weight/h) were obtained when R was 0.4 4(D = 0.056 h(-1)) compared to chemostat culture without biomass-recycle. M oreover, at this latter recycle ratio the volumetric vancomycin production rate was 14.7 mg/L/h (a 7-fold increase compared to chemostat culture witho ut biomass-recycle). These observations encourage further research on bioma ss-recycling as a means of optimising the production of antibiotics. (C) 19 99 John Wiley & Sons, Inc.