Improved production of rifamycin SV by Amycolatopsis mediterranei MM2 by the feeding method of carbon source
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biomedical Engineering,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology
Link
http://link.springer.com/content/pdf/10.1007/s12257-008-0023-6.pdf
Reference14 articles.
1. Floss, H. G. and T.-W. Yu (2005) Rifamycin-mode of action, resistance, and biosynthesis. Chem. Rev. 105: 621–632.
2. Sanfilippo, A., C. Della Bruna, L. Marsili, E. Morvillo, C. R. Pasqualucci, G. Schioppacassi, and D. Ungheri (1980) Biological activity of a new class of rifamycins. Spiro-piperidyl-rifamycins. J. Antibiot. 33: 1193–1198.
3. Murali Krishna, P. S., G. Venkateswarlu, and L. V. Rao (1999) Production of rifamycin SV using mutant strains of Amycolatopsis mediterranei MTCC17. World J. Microbiol. Biotechnol. 15: 741–743.
4. Murali Krishna, P. S., G. Venkateswarlu, and L. Venkateswar Rao (2000) Effect of uracil on rifamycin SV production by Amycolatopsis mediterranei MV35R. Lett. Appl. Microbiol. 31: 73–76.
5. Krishna, P. S. M., G. Venkateswarlu, A. Pandey, and L. V. Rao (2003) Biosynthesis of rifamycin SV by Amycolatopsis mediterranei MTCC17 in solid cultures. Biotechnol. Appl. Biochem. 37: 311–315.
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