Department of Biology, McMaster University, Hamilton, Ontario L8S 4K1, Canada.
Department of Biology, McMaster University, Hamilton, Ontario L8S 4K1, Canada
Genetics. 2017 Nov;207(3):961-974. doi: 10.1534/genetics.117.300212. Epub 2017 Aug 29.
The order Rhizobiales contains numerous agriculturally, biotechnologically, and medically important bacteria, including the rhizobia, and the genera , , and , among others. These organisms tend to be metabolically versatile, but there has been relatively little investigation into the regulation of their central carbon metabolic pathways. Here, RNA-sequencing and promoter fusion data are presented to show that the PckR protein is a key regulator of central carbon metabolism in ; during growth with gluconeogenic substrates, PckR represses expression of the complete Entner-Doudoroff glycolytic pathway and induces expression of the and gluconeogenic genes. Electrophoretic mobility shift assays indicate that PckR binds an imperfect palindromic sequence that overlaps the promoter or transcriptional start site in the negatively regulated promoters, or is present in tandem upstream the promoter motifs in the positively regulated promoters. Genetic and electrophoretic mobility shift assay experiments suggest that elevated concentrations of a PckR effector ligand results in the dissociation of PckR from its target binding site, and evidence is presented that suggests phosphoenolpyruvate may function as the effector. Characterization of missense alleles identified three conserved residues important for increasing the affinity of PckR for its cognate effector molecule. Bioinformatics analyses illustrates that PckR is limited to a narrow phylogenetic range consisting of the , , , and families. These data provide novel insights into the regulation of the core carbon metabolic pathways of this pertinent group of α-proteobacteria.
根瘤菌目包含许多农业、生物技术和医学上重要的细菌,包括根瘤菌,以及 、 和 等属。这些生物体往往具有代谢多样性,但对其中心碳代谢途径的调控相对较少研究。这里提出了 RNA 测序和启动子融合数据,表明 PckR 蛋白是 中中心碳代谢的关键调节剂;在以生糖基质生长时,PckR 抑制完整的 Entner-Doudoroff 糖酵解途径的表达,并诱导 和 生糖基因的表达。电泳迁移率变动分析表明,PckR 结合一个不完美的回文序列,该序列与负调控启动子中的启动子或转录起始位点重叠,或存在于正调控启动子中启动子基序的串联上游。遗传和电泳迁移率变动分析实验表明,PckR 效应配体浓度的升高导致 PckR 与其靶结合位点解离,并提出磷酸烯醇丙酮酸可能作为效应物发挥作用。错义 等位基因的表征确定了三个对增加 PckR 与其同源效应分子亲和力很重要的保守残基。生物信息学分析表明,PckR 仅限于一个狭窄的进化范围,包括 、 、 和 科。这些数据为这组相关的α-变形菌核心碳代谢途径的调控提供了新的见解。