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Phosphate control of phoA, phoC and phoD gene expression in Streptomyces coelicolor reveals significant differences in binding of PhoP to their promoter regions

机译:磷酸盐对链霉菌中的磷酸肽,PHOC和Phod基因表达的磷酸盐控制揭示了疗法结合对其启动子区的显着差异

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Three putative alkaline phosphatase genes, phoA, phoC and phoD, were identified in the genome of Streptomyces coelicolor by homology with the amino acid sequence obtained from the PhoA protein of Streptomyces griseus. PhoA and PhoC correspond to broad-spectrum alkaline phosphatases whereas PhoD is similar to a Ca2+-dependent phospholipase D of Streptomyces chromofuscus. The phoA and phoD genes were efficiently expressed in R5 medium under phosphate-limited conditions, as shown by studies using the xylE reporter gene, whereas phoC was poorly transcribed under the same conditions. Expression of phoA was clearly PhoP-dependent since it was not transcribed in the S. coelicolor ΔphoP mutant and was strongly activated under low phosphate concentrations. Similarly, expression of phoD was PhoP-dependent and highly sensitive to phosphate availability. By contrast, expression of phoC was not PhoP-dependent. Electrophoretic mobility shift assays showed that PhoP binds to the phoA and phoD promoters, but not to that of phoC. Footprinting studies with GST–PhoP revealed the presence of a PHO box (two direct 11?nt repeats) in the phoA promoter and two PHO boxes in the promoter of phoD. The transcription start points of the three promoters were identified by primer extension. The transcription start point of phoD coincides with the G of its translation start codon, indicating that this gene is transcribed as a leaderless mRNA. The deduced ?10 and ?35 regions of phoD (but not those of phoA) overlapped with the PHO boxes in this promoter, suggesting that an excess of PhoP interferes with binding of the RNA polymerase to this promoter. In summary, the three promoters showed clear differences in the modulation of their expression by PhoP.
机译:通过与从链霉菌Griseus的Phoa蛋白获得的氨基酸序列的同源性,在Streptomyces共孔的基因组中鉴定了三个推定的碱性磷酸酶基因,肽,PHOC和PHOD。 PHOA和PHOC对应于广谱碱性磷酸酶,而PHOD类似于CA2 +依赖性磷脂脂酶D的链霉菌染色体。在磷酸盐有限的条件下,在R5培养基下在R5培养基中有效地在R5培养基中在磷酸盐的条件下有效地表达PHOD基因,如使用XYLE报道基因的研究所示,而PHOC在相同条件下差。 Phoa的表达显然依赖于Phop依赖性,因为它未在S.的Δphop突变体中转录,并且在低磷酸盐浓度下强烈激活。类似地,PROD的表达是依赖性依赖性,对磷酸盐可用性高敏感。相比之下,PHOC的表达不是依赖的。电泳迁移率移位测定显示PHOP与PHOA和PHOD启动子结合,但不与PHOC的磷酸盐启动子结合。具有GST-PHOP的脚印研究显示Phoa启动子的PHO盒(两种直接11〜NT重复)和Phod启动子的两个Pho盒。通过引物延伸来鉴定三个启动子的转录起点。 PROD的转录开始点与其翻译开始密码子的G一致,表明该基因被作为无领导的mRNA转录。推导出的?10和?35个授权(但不是Phoa)的Phod(但不是Phoa)在该启动子中的Pho盒重叠,表明过量的PHOP干扰RNA聚合酶对该启动子的结合。总之,三个启动子表现出通过PHOP调节其表达的显然差异。

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