An extracytoplasmic function sigma factor, σ25, differentially regulates avermectin and oligomycin biosynthesis in Streptomyces avermitilis
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- 作者：Shuai Luo (1)
Di Sun (1)
Jianya Zhu (1)
Zhi Chen (1)
Ying Wen (1)
Jilun Li (1) - 关键词：Streptomyces avermitilis ; Avermectin ; ECF σ factor ; σ25
- 刊名：Applied Microbiology and Biotechnology
- 出版年：2014
- 出版时间：August 2014
- 年：2014
- 卷：98
- 期：16
- 页码：7097-7112
- 全文大小：4,084 KB
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Di Sun (1)
Jianya Zhu (1)
Zhi Chen (1)
Ying Wen (1)
Jilun Li (1)
1. State Key Laboratory of Agro-Biotechnology and MOA Key Laboratory of Soil Microbiology, College of Biological Sciences, China Agricultural University, Beijing, 100193, People’s Republic of China - ISSN：1432-0614
文摘
σ25 is an extracytoplasmic function (ECF) σ factor in the bacterium Streptomyces avermitilis that plays a differential regulatory role in avermectin and oligomycin biosynthesis. Gene deletion, complementation, and overexpression experiments showed that σ25 inhibited avermectin production but promoted oligomycin production. σ25 indirectly inhibited avermectin production by affecting the transcription of the pathway-specific activator gene aveR, whereas it directly activated oligomycin production by initiating transcription of the pathway-specific activator gene olmRI. The divergently transcribed genes smrAB are located upstream of sig25 and encode a putative two-component system (TCS). σ25 was found to initiate its own transcription, and its expression was directly activated by SmrA. The precise SmrA-binding sites in the region upstream of sig25 were determined by DNase I footprinting assays and identified two direct repeat sequences CTGTGA-n5-CTGTGA, suggesting that SmrA regulates sig25 transcription by binding to these direct repeats. The deletion of smrAB had the similar effect on avermectin and oligomycin A production to the deletion of sig25, indicating that σ25 and SmrAB function similarly in the regulation of antibiotic production. These findings helpfully clarify the regulation of antibiotic biosynthesis by an ECF σ factor-TCS signal transduction system in S. avermitilis.