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The NtrC Family Regulator AlgB, Which Controls Alginate Biosynthesis in Mucoid Pseudomonas aeruginosa, Binds Directly to the algD Promoter▿ †

机译:NtrC系列调节剂AlgB可直接控制algD启动子,从而控制铜绿粘液性铜绿假单胞菌中藻酸盐的生物合成。

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摘要

Alginate production in mucoid (MucA-defective) Pseudomonas aeruginosa is dependent upon several transcriptional regulators, including AlgB, a two-component response regulator belonging to the NtrC family. This role of AlgB was apparently independent of its sensor kinase, KinB, and even the N-terminal phosphorylation domain of AlgB was dispensable for alginate biosynthetic gene (i.e., algD operon) activation. However, it remained unclear whether AlgB stimulated algD transcription directly or indirectly. In this study, microarray analyses were used to examine a set of potential AlgB-dependent, KinB-independent genes in a PAO1 mucA background that overlapped with genes induced by d-cycloserine, which is known to activate algD expression. This set contained only the algD operon plus one other gene that was shown to be uninvolved in alginate production. This suggested that AlgB promotes alginate production by directly binding to the algD promoter (PalgD). Chromosome immunoprecipitation revealed that AlgB bound in vivo to PalgD but did not bind when AlgB had an R442E substitution that disrupted the DNA binding domain. AlgB also showed binding to PalgD fragments in an electrophoretic mobility shift assay at pH 4.5 but not at pH 8.0. A direct systematic evolution of ligands by exponential enrichment approach showed AlgB binding to a 50-bp fragment located at bp −224 to −274 relative to the start of PalgD transcription. Thus, AlgB belongs to a subclass of NtrC family proteins that can activate promoters which utilize a sigma factor other than σ54, in this case to stimulate transcription from the σ22-dependent PalgD promoter.
机译:粘液状(MucA缺陷型)铜绿假单胞菌中藻酸盐的产生取决于几种转录调节因子,包括AlgB(一种属于NtrC家族的两组分应答调节因子)。 AlgB的这种作用显然独立于其传感器激酶KinB,甚至AlgB的N末端磷酸化结构域对于藻酸盐生物合成基因(即algD操纵子)的激活也是必不可少的。但是,尚不清楚AlgB是直接还是间接刺激algD转录。在这项研究中,微阵列分析用于检查PAO1 mucA背景中一组潜在的AlgB依赖性,KinB依赖性基因,该基因与d-环丝氨酸诱导的基因重叠,后者已知可激活algD表达。该集合仅包含algD操纵子和一个其他基因,该基因被证明与藻酸盐生产无关。这表明AlgB通过直接结合到algD启动子(PalgD)来促进藻酸盐的产生。染色体免疫沉淀显示,AlgB在体内与PalgD结合,但是当AlgB具有破坏DNA结合结构域的R442E取代时却没有结合。 AlgB还显示在pH 4.5而不是pH 8.0的电泳迁移率迁移分析中与PalgD片段的结合。通过指数富集方法对配体的直接系统进化表明,相对于PalgD转录的开始,AlgB结合到位于bp -224至-274的50 bp片段。因此,AlgB属于NtrC家族蛋白的一个子类,可以激活利用σ54以外的σ因子的启动子,在这种情况下可以刺激依赖σ22的PalgD启动子转录。

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