Chen Shuangshuang, Zheng Guosong, Zhu Hong, He Huiqi, Chen Lei, Zhang Weiwen, Jiang Weihong, Lu Yinhua
Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China Key Laboratory of Synthetic Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 300 Fenglin Road, Shanghai 200032, PR China.
Key Laboratory of Synthetic Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 300 Fenglin Road, Shanghai 200032, PR China.
FEMS Microbiol Lett. 2016 Aug;363(15). doi: 10.1093/femsle/fnw160. Epub 2016 Jun 15.
We previously demonstrated that in Streptomyces coelicolor two-component system AfsQ1/Q2 activates the production of the yellow-colored coelimycin P2 (also named as yCPK) on glutamate-supplemented minimal medium, and the response regulator AfsQ1 could specifically bind to the intergenic region between two structural genes, cpkA and cpkD Here, a more in-depth investigation was performed to elucidate the mechanism underlying the role of AfsQ1/Q2 in regulating coelimycin P2 biosynthesis. Deletion of afsQ1/Q2 resulted in markedly decreased expression of the whole coelimycin P2 biosynthetic gene cluster. Electrophoretic mobility shift assays revealed that AfsQ1 bound only to the target site identified previously, but not to any other promoters in the gene cluster. Mutations of AfsQ1-binding motif only resulted in drastically reduced transcription of the cpkA/B/C operon (encoding three type I polyketide synthases) and intriguingly, led to enhanced expression of some coelimcyin P2 genes, particularly accA1 and scF These results suggested the direct role of AfsQ1/Q2 in regulating coelimycin production, which is directly mediated by the structural genes, but not the cluster-situated regulatory genes, and also implied that other unknown mechanisms may be involved in AfsQ1/Q2-mediated regulation of coelimycin P2 biosynthesis.
我们之前证明,在天蓝色链霉菌中,双组分系统AfsQ1/Q2在添加谷氨酸的基本培养基上激活黄色的天蓝色菌素P2(也称为yCPK)的产生,并且应答调节因子AfsQ1可以特异性结合两个结构基因cpkA和cpkD之间的基因间区域。在此,我们进行了更深入的研究,以阐明AfsQ1/Q2在调节天蓝色菌素P2生物合成中作用的潜在机制。缺失afsQ1/Q2导致整个天蓝色菌素P2生物合成基因簇的表达明显降低。电泳迁移率变动分析表明,AfsQ1仅与先前鉴定的靶位点结合,而不与基因簇中的任何其他启动子结合。AfsQ1结合基序的突变仅导致cpkA/B/C操纵子(编码三种I型聚酮合酶)的转录大幅降低,有趣的是,导致一些天蓝色菌素P2基因的表达增强,特别是accA1和scF。这些结果表明AfsQ1/Q2在调节天蓝色菌素产生中起直接作用,这是由结构基因直接介导的,而不是由位于基因簇中的调节基因介导的,并且还暗示其他未知机制可能参与AfsQ1/Q2介导的天蓝色菌素P2生物合成调节。