Li Rui, Xie Zhoujie, Tian Yuqing, Yang Haihua, Chen Wenqing, You Delin, Liu Gang, Deng Zixin, Tan Huarong
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Laboratory of Microbial Metabolism and School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200030, China.
Microbiology (Reading). 2009 Jun;155(Pt 6):1819-1831. doi: 10.1099/mic.0.028639-0. Epub 2009 Apr 21.
The polyoxin (POL) biosynthetic gene cluster (pol) was recently cloned from Streptomyces cacaoi subsp. asoensis. A 3.3 kb DNA fragment carrying an obvious open reading frame (polR), whose deduced product shows sequence similarity to SanG of Streptomyces ansochromogenes and PimR of Streptomyces natalensis, was revealed within the pol gene cluster. Disruption of polR abolished POL production, which could be complemented by the integration of a single copy of polR into the chromosome of the non-producing mutant. The introduction of an extra copy of polR in the wild-type strain resulted in increased production of POLs. The transcription start point (tsp) of polR was determined by S1 mapping. Reverse transcriptase PCR experiments showed that PolR is required for the transcription of 18 structural genes in the pol gene cluster. Furthermore, we showed that polC and polB, the respective first genes of two putative operons (polC-polQ2 and polA-polB) consisting of 16 and 2 of these 18 genes, have similar promoter structures. Gel retardation assays indicated that PolR has specific DNA-binding activity for the promoter regions of polC and polB. Our data suggest that PolR acts in a positive manner to regulate POL production by activating the transcription of at least two putative operons in the pol gene cluster.
多氧霉素(POL)生物合成基因簇(pol)最近从可可链霉菌亚种恶疫霉中克隆得到。在pol基因簇中发现了一个3.3 kb的DNA片段,其携带一个明显的开放阅读框(polR),其推导产物与暗产色链霉菌的SanG和纳塔尔链霉菌的PimR具有序列相似性。polR的破坏消除了POL的产生,通过将单拷贝的polR整合到不产生突变体的染色体中可以互补。在野生型菌株中引入额外拷贝的polR导致POL产量增加。通过S1作图确定了polR的转录起始点(tsp)。逆转录酶PCR实验表明,PolR是pol基因簇中18个结构基因转录所必需的。此外,我们发现polC和polB分别是由这18个基因中的16个和2个组成的两个假定操纵子(polC-polQ2和polA-polB)的第一个基因,具有相似的启动子结构。凝胶阻滞试验表明,PolR对polC和polB的启动子区域具有特异性DNA结合活性。我们的数据表明,PolR通过激活pol基因簇中至少两个假定操纵子的转录,以正向方式调节POL的产生。