Molecular Microbiology and Structural Biochemistry, UMR 5086, Université Lyon 1, CNRS, IBCP building, 7 passage du Vercors, 69367 Lyon Cedex 07, France.
Trends Microbiol. 2016 Sep;24(9):713-724. doi: 10.1016/j.tim.2016.04.004. Epub 2016 Apr 26.
Over the past decade, Streptococcus pneumoniae (the pneumococcus) has gained prominence as a model for studying the bacterial cell cycle. This important human pathogen possesses a characteristic diplo-ovococcal cell shape and produces a protective polysaccharide capsule required for virulence, and it has been used to investigate natural genetic transformation. Recent advances have demonstrated that the pneumococcus has evolved phosphorylation-dependent regulatory mechanisms dedicated to controlling cell division and ensuring the concealment of the newborn cells by the capsule. In this review, I survey the role of the only two serine/threonine- (StkP) and tyrosine-kinases (CpsD) of the pneumococcus and discuss the existence of interconnected phosphorylation networks coordinating cell division and morphogenesis with key aspects of the cell cycle.
在过去的十年中,肺炎链球菌(肺炎球菌)作为研究细菌细胞周期的模型而备受关注。这种重要的人类病原体具有典型的双球菌细胞形状,并产生保护性多糖荚膜,这是其毒力所必需的,并且已被用于研究自然遗传转化。最近的进展表明,肺炎球菌已经进化出依赖于磷酸化的调节机制,专门用于控制细胞分裂,并确保新生细胞被荚膜隐藏。在这篇综述中,我调查了肺炎球菌中仅有的两个丝氨酸/苏氨酸激酶(StkP)和酪氨酸激酶(CpsD)的作用,并讨论了相互连接的磷酸化网络的存在,这些网络协调细胞分裂和形态发生与细胞周期的关键方面。