Area de Microbiología, Departamento de Biología Molecular, Universidad de León, León, Spain.
PLoS One. 2018 Dec 6;13(12):e0208278. doi: 10.1371/journal.pone.0208278. eCollection 2018.
The biosynthesis of the antifungal filipin in Streptomyces filipinensis is very sensitive to phosphate regulation. Concentrations as low as 2.5 mM block filipin production. This effect is, at least in part, produced by repression of the transcription of most filipin biosynthetic genes. The role of the two-component PhoRP system in this process was investigated. The phoRP system of S. filipinensis was cloned and transcriptionally characterised. PhoP binds to two PHO boxes present in one of its two promoters. Filipin production was greatly increased in ΔphoP and ΔphoRP mutants, in agreement with a higher transcription of the fil genes, and the effect of phosphate repression on the antibiotic production of these strains was significantly reduced. No PhoP binding was observed by electrophoretic mobility gel shift assays (EMSAs) with the promoter regions of the fil gene cluster thus suggesting an indirect effect of mutations. Binding assays with cell-free extracts from the wild-type and mutant strains on fil genes promoters revealed retardation bands in the parental strain that were absent in the mutants, thus suggesting that binding of the putative transcriptional regulator or regulators controlled by PhoP was PhoP dependent. Noteworthy, PhoP or PhoRP deletion also produced a dramatic decrease in sporulation ability, thus indicating a clear relationship between the phosphate starvation response mediated by PhoP and the sporulation process in S. filipinensis. This effect was overcome upon gene complementation, but also by phosphate addition, thus suggesting that alternative pathways take control in the absence of PhoRP.
菲律宾链霉菌中抗真菌菲律宾菌素的生物合成对磷酸盐调控非常敏感。低至 2.5mM 的浓度就可以阻断菲律宾菌素的产生。这种效应至少部分是通过抑制大多数菲律宾菌素生物合成基因的转录产生的。本研究调查了双组分 PhoRP 系统在此过程中的作用。克隆并转录分析了菲律宾链霉菌的 phoRP 系统。PhoP 与两个启动子之一的两个 PHO 盒结合。在 ΔphoP 和 ΔphoRP 突变体中,菲律宾菌素的产量大大增加,与 fil 基因的转录增加一致,并且磷酸盐对这些菌株抗生素产量的抑制作用显著降低。通过与 fil 基因簇启动子区域的电泳迁移率凝胶阻滞实验(EMSA)观察到没有 PhoP 结合,这表明突变具有间接影响。与野生型和突变菌株的无细胞提取物在 fil 基因启动子上的结合实验表明,亲本菌株中存在阻滞带,而在突变体中不存在,这表明假定的转录调节剂或由 PhoP 控制的调节剂的结合是 PhoP 依赖性的。值得注意的是,PhoP 或 PhoRP 的缺失也导致了明显的孢子形成能力下降,这表明 PhoP 介导的磷酸盐饥饿反应与菲律宾链霉菌的孢子形成过程之间存在明显的关系。这种效应通过基因互补得到克服,但也可以通过添加磷酸盐得到克服,这表明在没有 PhoRP 的情况下,替代途径会进行控制。