Cell and Molecular Microbiology Division, Institute of Microbiology of the ASCR, v.v.i., Academy of Sciences of the Czech Republic, Vídenská 1083, 142 20 Prague 4, Czech Republic.
J Bacteriol. 2010 Jul;192(14):3629-38. doi: 10.1128/JB.01564-09. Epub 2010 May 7.
Monitoring the external environment and responding to its changes are essential for the survival of all living organisms. The transmission of extracellular signals in prokaryotes is mediated mainly by two-component systems. In addition, genomic analyses have revealed that many bacteria contain eukaryotic-type Ser/Thr protein kinases. The human pathogen Streptococcus pneumoniae encodes 13 two-component systems and has a single copy of a eukaryotic-like Ser/Thr protein kinase gene designated stkP. Previous studies demonstrated the pleiotropic role of the transmembrane protein kinase StkP in pneumococcal physiology. StkP regulates virulence, competence, and stress resistance and plays a role in the regulation of gene expression. To determine the intracellular signaling pathways controlled by StkP, we used a proteomic approach for identification of its substrates. We detected six proteins phosphorylated on threonine by StkP continuously during growth. We identified three new substrates of StkP: the Mn-dependent inorganic pyrophosphatase PpaC, the hypothetical protein spr0334, and the cell division protein DivIVA. Contrary to the results of a previous study, we did not confirm that the alpha-subunit of RNA polymerase is a target of StkP. We showed that StkP activation and substrate recognition depend on the presence of a peptidoglycan-binding domain comprising four extracellular penicillin-binding protein- and Ser/Thr kinase-associated domain (PASTA domain) repeats. We found that StkP is regulated in a growth-dependent manner and likely senses intracellular peptidoglycan subunits present in the cell division septa. In addition, stkP inactivation results in cell division defects. Thus, the data presented here suggest that StkP plays an important role in the regulation of cell division in pneumococcus.
监测外部环境并对其变化做出响应是所有生物生存的关键。原核生物细胞外信号的传递主要是通过双组分系统来介导的。此外,基因组分析表明,许多细菌含有真核型丝氨酸/苏氨酸蛋白激酶。人类病原体肺炎链球菌编码 13 个双组分系统,并且具有一个单一拷贝的真核样丝氨酸/苏氨酸蛋白激酶基因 stkP。先前的研究表明,跨膜蛋白激酶 StkP 在肺炎球菌生理学中具有多效性作用。StkP 调节毒力、感受态和应激抗性,并在基因表达调控中发挥作用。为了确定 StkP 控制的细胞内信号通路,我们使用蛋白质组学方法鉴定其底物。我们检测到在生长过程中 StkP 连续磷酸化六个 Thr 残基的蛋白质。我们鉴定了 StkP 的三个新底物:Mn 依赖性无机焦磷酸酶 PpaC、假定蛋白 spr0334 和细胞分裂蛋白 DivIVA。与先前研究的结果相反,我们没有确认 RNA 聚合酶的α亚基是 StkP 的靶标。我们表明,StkP 的激活和底物识别依赖于存在一个由四个细胞外青霉素结合蛋白和丝氨酸/苏氨酸激酶相关结构域(PASTA 结构域)重复组成的肽聚糖结合结构域。我们发现 StkP 以生长依赖性方式受到调节,并且可能感知存在于细胞分裂隔膜中的细胞内肽聚糖亚单位。此外,stkP 的失活导致细胞分裂缺陷。因此,这里呈现的数据表明 StkP 在肺炎球菌细胞分裂的调节中发挥重要作用。