首页> 美国卫生研究院文献>Nucleic Acids Research >Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR glnA glnII and amtB expression by the response regulator PhoP
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Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR glnA glnII and amtB expression by the response regulator PhoP

机译:磷对天蓝色链霉菌中氮代谢的控制:响应调节器PhoP对glnRglnAglnII和amtB表达的直接和间接负控制

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摘要

Bacterial growth requires equilibrated concentration of C, N and P sources. This work shows a phosphate control over the nitrogen metabolism in the model actinomycete Streptomyces coelicolor. Phosphate control of metabolism in Streptomyces is exerted by the two component system PhoR-PhoP. The response regulator PhoP binds to well-known PHO boxes composed of direct repeat units (DRus). PhoP binds to the glnR promoter, encoding the major nitrogen regulator as shown by EMSA studies, but not to the glnRII promoter under identical experimental conditions. PhoP also binds to the promoters of glnA and glnII encoding two glutamine synthetases, and to the promoter of the amtB-glnK-glnD operon, encoding an ammonium transporter and two putative nitrogen sensing/regulatory proteins. Footprinting analyses revealed that the PhoP-binding sequence overlaps the GlnR boxes in both glnA and glnII. ‘Information theory’ quantitative analyses of base conservation allowed us to establish the structure of the PhoP-binding regions in the glnR, glnA, glnII and amtB genes. Expression studies using luxAB as reporter showed that PhoP represses the above mentioned nitrogen metabolism genes. A mutant deleted in PhoP showed increased expression of the nitrogen metabolism genes. The possible conservation of phosphate control over nitrogen metabolism in other microorganisms is discussed.
机译:细菌生长需要平衡浓度的C,N和P源。这项工作表明磷控制放线菌链霉菌模型的氮代谢。磷对链霉菌代谢的控制是由两组分系统PhoR-PhoP进行的。响应调节器PhoP绑定到由直接重复单元(DRus)组成的众所周知的PHO框。如EMSA研究所示,PhoP与glnR启动子结合,后者编码主要的氮调节剂,但在相同的实验条件下不与glnRII启动子结合。 PhoP还与编码两个谷氨酰胺合成酶的glnA和glnII的启动子以及编码铵转运蛋白和两个假定的氮感测/调节蛋白的amtB-glnK-glnD操纵子的启动子结合。足迹分析表明,PhoP结合序列在glnA和glnII中均与GlnR框重叠。 “信息理论”对碱基保守性的定量分析使我们能够确定glnR,glnA,glnII和amtB基因中PhoP结合区的结构。使用luxAB作为报告基因的表达研究表明,PhoP抑制上述氮代谢基因。 PhoP中缺失的突变体显示氮代谢基因的表达增加。讨论了可能的保护磷酸盐控制其他微生物中氮代谢的问题。

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