首页> 美国卫生研究院文献>Journal of Bacteriology >Complex Transcriptional Control of the Antibiotic Regulator afsS in Streptomyces: PhoP and AfsR Are Overlapping Competitive Activators
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Complex Transcriptional Control of the Antibiotic Regulator afsS in Streptomyces: PhoP and AfsR Are Overlapping Competitive Activators

机译:链霉菌中抗生素调节剂afsS的复杂转录控制:PhoP和AfsR重叠竞争性激活剂

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摘要

The afsS gene of several Streptomyces species encodes a small sigma factor-like protein that acts as an activator of several pathway-specific regulatory genes (e.g., actII-ORF4 and redD in Streptomyces coelicolor). The two pleiotropic regulators AfsR and PhoP bind to overlapping sequences in the −35 region of the afsS promoter and control its expression. Using mutated afsS promoters containing specific point mutations in the AfsR and PhoP binding sequences, we proved that the overlapping recognition sequences for AfsR and PhoP are displaced by 1 nucleotide. Different nucleotide positions are important for binding of AfsR or PhoP, as shown by electrophoretic mobility shift assays and by reporter studies using the luxAB gene coupled to the different promoters. Mutant promoter M5 (with a nucleotide change at position 5 of the consensus box) binds AfsR but not PhoP with high affinity (named “superAfsR”). Expression of the afsS gene from this promoter led to overproduction of actinorhodin. Mutant promoter M16 binds PhoP with extremely high affinity (“superPhoP”). Studies with ΔafsR and ΔphoP mutants (lacking AfsR and PhoP, respectively) showed that both global regulators are competitive transcriptional activators of afsS. AfsR has greater influence on expression of afsS than PhoP, as shown by reverse transcriptase PCR (RT-PCR) and promoter reporter (luciferase) studies. These two high-level regulators appear to integrate different nutritional signals (particularly phosphate limitation sensed by PhoR), S-adenosylmethionine, and other still unknown environmental signals (leading to AfsR phosphorylation) for the AfsS-mediated control of biosynthesis of secondary metabolites.
机译:几种链霉菌种的afsS基因编码一个小的sigma因子样蛋白,可作为多种途径特异性调控基因(例如链霉菌中的actII-ORF4和redD)的激活剂。两个多效性调节剂AfsR和PhoP与afsS启动子的-35区域中的重叠序列结合并控制其表达。使用在AfsR和PhoP结合序列中包含特定点突变的突变afsS启动子,我们证明了AfsR和PhoP的重叠识别序列被1个核苷酸取代。如电泳迁移率迁移分析和使用偶联至不同启动子的luxAB基因进行的报道研究所表明的,不同的核苷酸位置对于结合AfsR或PhoP很重要。突变启动子M5(在共有框的第5位具有核苷酸改变)以高亲和力结合AfsR,但不结合PhoP(称为“ superAfsR”)。来自该启动子的afsS基因的表达导致肌动蛋白的过量生产。突变启动子M16以极高的亲和力结合PhoP(“ superPhoP”)。对ΔafsR和ΔphoP突变体(分别缺少AfsR和PhoP)的研究表明,这两个全局调节因子都是afsS的竞争性转录激活因子。如逆转录酶PCR(RT-PCR)和启动子报告基因(萤光素酶)研究所示,AfsR对AfsS的表达比PhoP具有更大的影响。这两个高级调节剂似乎整合了不同的营养信号(尤其是PhoR检测到的磷酸盐限制),S-腺苷甲硫氨酸和其他仍未知的环境信号(导致AfsR磷酸化),用于AfsS介导的次级代谢产物生物合成的控制。

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