Ramamurthy V, Dapíc V, Oliver D
Department of Molecular Biology and Biochemistry, Wesleyan University, Middletown, Connecticut 06459, USA.
J Bacteriol. 1998 Dec;180(23):6419-23. doi: 10.1128/JB.180.23.6419-6423.1998.
SecA is a dynamic protein that undergoes ATP-dependent membrane cycling to drive protein translocation across the Escherichia coli inner membrane. To understand more about this process, azide-resistant (azi) and signal sequence suppressor (prlD) alleles of secA were studied. We found that azide resistance is cold sensitive because of a direct effect on protein export, suggesting that SecA-membrane interaction is regulated by an endothermic step that is azide inhibitable. secG function is required for expression of azide-resistant and signal sequence suppressor activities of azi and prlD alleles, and in turn, these alleles suppress cold-sensitive and export-defective phenotypes of a secG null mutant. These remarkable genetic observations support biochemical data indicating that SecG promotes SecA membrane cycling and that this process is dependent on an endothermic change in SecA conformation.
SecA是一种动态蛋白,它通过ATP依赖的膜循环来驱动蛋白质穿过大肠杆菌内膜进行转运。为了更深入了解这一过程,我们研究了secA的叠氮化物抗性(azi)和信号序列抑制子(prlD)等位基因。我们发现叠氮化物抗性对温度敏感,因为它直接影响蛋白质输出,这表明SecA与膜的相互作用受一个可被叠氮化物抑制的吸热步骤调控。secG的功能对于azi和prlD等位基因的叠氮化物抗性及信号序列抑制子活性的表达是必需的,反过来,这些等位基因可抑制secG缺失突变体的温度敏感型和输出缺陷型表型。这些显著的遗传学观察结果支持了生化数据,这些数据表明SecG促进SecA膜循环,且这一过程依赖于SecA构象的吸热变化。