| Literature DB >> 27126098 |
Jun Shi1, Jian Pan1, Ling Liu1, Dong Yang2, Songquan Lu3, Xiangcheng Zhu1,3, Ben Shen2,4,5, Yanwen Duan6,7,8, Yong Huang9,10.
Abstract
Platensimycin (PTM) and platencin (PTN), isolated from several strains of Streptomyces platensis are potent antibiotics against multi-drug resistant bacteria. PTM was also shown to have antidiabetic and antisteatotic activities in mouse models. Through a novel genome-mining method, we have recently identified six PTM and PTN dual-producing strains, and generated several mutants with improved production of PTM or PTN by inactivating the pathway-specific transcriptional repressor gene ptmR1. Among them, S. platensis SB12026 gave the highest titer of 310 mg/L for PTM. In this study, we now report titer improvement by medium and fermentation optimization and pilot-scale production and isolation of PTM from SB12026. The fermentation medium optimization was achieved by manipulating the carbon and nitrogen sources, as well as the inorganic salts. The highest titer of 1560 mg/L PTM was obtained in 15-L fermentors, using a formulated medium mainly containing soluble starch, soybean flour, morpholinepropanesulfonic acid sodium salt and CaCO3. In addition, a polyamide chromatographic step was applied to facilitate the purification and 45.14 g of PTM was successfully obtained from a 60 L scale fermentation. These results would speed up the future development of PTM as human medicine.Entities:
Keywords: Fermentation medium optimization; Platensimycin; Polyamide chromatography; Streptomyces platensis SB12026
Mesh:
Substances:
Year: 2016 PMID: 27126098 PMCID: PMC5056013 DOI: 10.1007/s10295-016-1769-z
Source DB: PubMed Journal: J Ind Microbiol Biotechnol ISSN: 1367-5435 Impact factor: 3.346