The State Key Laboratory of Microbial Technology, Shandong University, Qingdao, China.
College of Biomedical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, China.
Appl Environ Microbiol. 2020 Oct 1;86(20). doi: 10.1128/AEM.01201-20.
Regulation of antibiotic production by is complex. We report that the response regulator MtrA is a master regulator for antibiotic production in Deletion of MtrA altered production of actinorhodin, undecylprodigiosin, calcium-dependent antibiotic, and the yellow-pigmented type I polyketide and resulted in altered expression of the corresponding gene clusters in Integrated and analyses identified MtrA binding sites upstream of , , and and between and MtrA disruption also led to marked changes in chloramphenicol and jadomycin production and in transcription of their biosynthetic gene clusters ( and , respectively) in , and MtrA sites were identified within and MtrA also recognized predicted sites within the avermectin and oligomycin pathways in and in the validamycin gene cluster of The regulator GlnR competed for several MtrA sites and impacted production of some antibiotics, but its effects were generally less dramatic than those of MtrA. Additional potential MtrA sites were identified in a range of other antibiotic biosynthetic gene clusters in species and other actinobacteria. Overall, our study suggests a universal role for MtrA in antibiotic production in and potentially other actinobacteria. In natural environments, the ability to produce antibiotics helps the producing host to compete with surrounding microbes. In , increasing evidence suggests that the regulation of antibiotic production is complex, involving multiple regulatory factors. The regulatory factor MtrA is known to have additional roles beyond controlling development, and using bioassays, transcriptional studies, and DNA-binding assays, our study identified MtrA recognition sequences within multiple antibiotic pathways and indicated that MtrA directly controls the production of multiple antibiotics. Our analyses further suggest that this role of MtrA is evolutionarily conserved in species, as well as in other actinobacterial species, and also suggest that MtrA is a major regulatory factor in antibiotic production and in the survival of actinobacteria in nature.
调控抗生素产生的机制十分复杂。我们的研究表明,应答调节子 MtrA 是调控 产生抗生素的主要调节子。MtrA 的缺失会改变放线紫红素、十一烷吡咯并红菌素、钙依赖性抗生素和黄色物质 I 型聚酮化合物的产生,导致相应基因簇在 中的表达发生改变。整合分析确定了 MtrA 在 、 、 和 上游的结合位点,以及 在 之间的结合位点。MtrA 的破坏也导致氯霉素和贾地霉素的产生以及它们生物合成基因簇(分别为 和 )的转录发生显著变化。在 中鉴定了 MtrA 位点和 内的 ,MtrA 还识别了 中的阿维菌素和寡霉素途径以及 中的井冈霉素基因簇中的预测位点。调控因子 GlnR 与几个 MtrA 位点竞争,并影响一些抗生素的产生,但它的影响通常不如 MtrA 显著。在 种和其他放线菌的其他抗生素生物合成基因簇中也鉴定出了其他潜在的 MtrA 位点。总的来说,我们的研究表明 MtrA 在 中抗生素的产生中具有普遍作用,并且可能在其他放线菌中也是如此。在自然环境中,产生抗生素的能力有助于产生宿主与周围微生物竞争。在 中,越来越多的证据表明抗生素产生的调控是复杂的,涉及多个调控因子。调节因子 MtrA 除了控制发育外,还有其他作用,通过生物测定、转录研究和 DNA 结合测定,我们在多个抗生素途径中鉴定了 MtrA 识别序列,并表明 MtrA 直接控制多种抗生素的产生。我们的分析进一步表明,MtrA 在 种以及其他放线菌物种中的这一作用是进化保守的,并且还表明 MtrA 是抗生素产生和放线菌在自然界中生存的主要调控因子。