Enhanced rifamycin SV production by submerged fermentation using Amycolatopsis mediterranei

Verfasser / Beitragende:
[M. Nagavalli, S. Ponamgi, V. Girijashankar, L. Rao]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/18(2015-09-01), 7505-7513
Format:
Artikel (online)
ID: 605501246
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024 7 0 |a 10.1007/s00253-015-6682-2  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6682-2 
245 0 0 |a Enhanced rifamycin SV production by submerged fermentation using Amycolatopsis mediterranei  |h [Elektronische Daten]  |c [M. Nagavalli, S. Ponamgi, V. Girijashankar, L. Rao] 
520 3 |a Rifamycin is a broad-spectrum antimicrobial drug produced commercially by submerged fermentation where the yields are far less in comparison to its demand in human drug therapy. Addressing the need, sequential mutational strain improvement was carried using UV and EtBr that resulted in improved strain yielding rifamycin SV up to 4.32g/L. Further optimization of six important fermentation factors was followed which include temperature, agitation, inoculum level, period of fermentation, inorganic nitrogen source and amino acids. For the first time, we report a maximum yield of 5.32g/L of rifamycin SV. Among the amino acids, proline known for its slowest assimilation by Amycolatopsis mediterranei produced the highest improvement in antibiotic yields. Following mutational strain improvement and process optimization, a total of 3.8-fold increase in antibiotic titre was achieved. Following a conventional procedure of mutational strain improvement, highest yield of rifamycin SV was reported by optimizing submerged fermentation process. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Rifamycin SV  |2 nationallicence 
690 7 |a Amycolatopsis mediterranei  |2 nationallicence 
690 7 |a Mutational strain improvement  |2 nationallicence 
690 7 |a Submerged fermentation optimization  |2 nationallicence 
690 7 |a Proline  |2 nationallicence 
700 1 |a Nagavalli  |D M.  |u Department of Microbiology, Osmania University, 500 007, Hyderabad, India  |4 aut 
700 1 |a Ponamgi  |D S.  |u Center for Biotechnology, Jawaharlal Nehru Technological University, IST, Kukatpally, Hyderabad, India  |4 aut 
700 1 |a Girijashankar  |D V.  |u Scientist C, Department of Science and Technology, DST, New Mehrauli, New Delhi, India  |4 aut 
700 1 |a Rao  |D L.  |u Department of Microbiology, Osmania University, 500 007, Hyderabad, India  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/18(2015-09-01), 7505-7513  |x 0175-7598  |q 99:18<7505  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6682-2  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-015-6682-2  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Nagavalli  |D M.  |u Department of Microbiology, Osmania University, 500 007, Hyderabad, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ponamgi  |D S.  |u Center for Biotechnology, Jawaharlal Nehru Technological University, IST, Kukatpally, Hyderabad, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Girijashankar  |D V.  |u Scientist C, Department of Science and Technology, DST, New Mehrauli, New Delhi, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Rao  |D L.  |u Department of Microbiology, Osmania University, 500 007, Hyderabad, India  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/18(2015-09-01), 7505-7513  |x 0175-7598  |q 99:18<7505  |1 2015  |2 99  |o 253