Lavander Moa, Ericsson Solveig K, Bröms Jeanette E, Forsberg Ake
Department of Molecular Biology, Umeå University, Sweden.
Adv Exp Med Biol. 2007;603:258-67. doi: 10.1007/978-0-387-72124-8_23.
Bacteria utilise Twin arginine translocation (Tat) to deliver folded proteins across the cytoplasmic membrane. Disruption of Tat typically results in pleiotropic effects on e.g. growth, stress resistance, bacterial membrane biogenesis, motility and cell morphology. Further, Tat is coupled to virulence in a range of pathogenic bacteria, including species of Pseudomonas, Legionella, Agrobacterium and Mycobacterium. We have investigated this, for Yersinia, previously unexplored system, and have shown that the Tat pathway is functional and absolutely required for virulence of Yersinia pseudotuberculosis. A range of putative Yersinia Tat substrates have been predicted in silico, which together with the Tat system itself may be interesting targets for future development of antimicrobial treatments. Here we present a brief review of bacterial Tat and discuss our results concerning this system in Yersinia.
细菌利用双精氨酸转运(Tat)系统将折叠好的蛋白质转运穿过细胞质膜。Tat系统的破坏通常会对例如生长、应激抗性、细菌膜生物合成、运动性和细胞形态等产生多效性影响。此外,Tat系统与一系列病原菌的毒力相关,包括假单胞菌属、军团菌属、农杆菌属和分枝杆菌属的一些菌种。我们已经对耶尔森菌属这个此前未被探索的系统进行了研究,并表明Tat途径具有功能,且对于假结核耶尔森菌的毒力是绝对必需的。通过计算机模拟预测了一系列假定的耶尔森菌属Tat底物,它们与Tat系统本身一起可能是未来抗菌治疗开发的有趣靶点。在此,我们简要综述细菌Tat系统,并讨论我们关于耶尔森菌属中该系统的研究结果。