Yamamoto Kaneyoshi, Hirao Kiyo, Oshima Taku, Aiba Hirofumi, Utsumi Ryutaro, Ishihama Akira
Department of Agricultural Chemistry, Kinki University, Nakamachi 3327-204, Nara 631-8505, Japan.
J Biol Chem. 2005 Jan 14;280(2):1448-56. doi: 10.1074/jbc.M410104200. Epub 2004 Nov 2.
Bacteria possess a signal transduction system, referred to as a two-component system, for adaptation to external stimuli. Each two-component system consists of a sensor protein-histidine kinase (HK) and a response regulator (RR), together forming a signal transduction pathway via histidyl-aspartyl phospho-relay. A total of 30 sensor HKs, including as yet uncharacterized putative HKs (BaeS, BasS, CreC, CusS, HydH, RstB, YedV, and YfhK), and a total of 34 RRs, including putative RRs (BaeR, BasR, CreB, CusR, HydG, RstA, YedW, YfhA, YgeK, and YhjB), have been suggested to exist in Escherichia coli. We have purified the carboxyl-terminal catalytic domain of 27 sensor HKs and the full-length protein of all 34 RRs to apparent homogeneity. Self-phosphorylation in vitro was detected for 25 HKs. The rate of self-phosphorylation differed among HKs, whereas the level of phosphorylation was generally co-related with the phosphorylation rate. However, the phosphorylation level was low for ArcB, HydH, NarQ, and NtrB even though the reaction rate was fast, whereas the level was high for the slow phosphorylation species BasS, CheA, and CreC. By using the phosphorylated HKs, we examined trans-phosphorylation in vitro of RRs for all possible combinations. Trans-phosphorylation of presumed cognate RRs by HKs was detected, for the first time, for eight pairs, BaeS-BaeR, BasS-BasR, CreC-CreB, CusS-CusR, HydH-HydG, RstB-RstA, YedV-YedW, and YfhK-YfhA. All trans-phosphorylation took place within less than 1/2 min, but the stability of phosphorylated RRs differed, indicating the involvement of de-phosphorylation control. In addition to the trans-phosphorylation between the cognate pairs, we detected trans-phosphorylation between about 3% of non-cognate HK-RR pairs, raising the possibility that the cross-talk in signal transduction takes place between two-component systems.
细菌拥有一种信号转导系统,称为双组分系统,用于适应外部刺激。每个双组分系统由一个传感器蛋白 - 组氨酸激酶(HK)和一个响应调节器(RR)组成,它们通过组氨酰 - 天冬氨酰磷酸中继共同形成一条信号转导途径。在大肠杆菌中,共发现了30种传感器HK,包括尚未鉴定的假定HK(BaeS、BasS、CreC、CusS、HydH、RstB、YedV和YfhK),以及34种RR,包括假定的RR(BaeR、BasR、CreB、CusR、HydG、RstA、YedW、YfhA、YgeK和YhjB)。我们已经将27种传感器HK的羧基末端催化结构域和所有34种RR的全长蛋白纯化至表观均一性。检测到25种HK在体外发生自磷酸化。HK之间的自磷酸化速率不同,而磷酸化水平通常与磷酸化速率相关。然而,尽管反应速率很快,但ArcB、HydH、NarQ和NtrB的磷酸化水平较低,而对于磷酸化较慢的BasS、CheA和CreC,其磷酸化水平较高。通过使用磷酸化的HK,我们检测了RR在体外针对所有可能组合的转磷酸化。首次检测到8对HK对假定的同源RR的转磷酸化,即BaeS - BaeR、BasS - BasR、CreC - CreB、CusS - CusR、HydH - HydG、RstB - RstA、YedV - YedW和YfhK - YfhA。所有转磷酸化均在不到1/2分钟内发生,但磷酸化RR的稳定性不同,表明存在去磷酸化控制。除了同源对之间的转磷酸化外,我们还检测到约3%的非同源HK - RR对之间的转磷酸化,这增加了信号转导中的串扰可能发生在双组分系统之间的可能性。