Schöffler H, Braun V
Mikrobiologie II, Universität Tübingen, Federal Republic of Germany.
Mol Gen Genet. 1989 Jun;217(2-3):378-83. doi: 10.1007/BF02464907.
Point mutations in the "TonB box" of fhuA were suppressed by point mutations in the tonB gene, suggesting both a functional and physical interaction between the FhuA receptor protein in the outer membrane and the TonB protein in the cytoplasmic membrane of Escherichia coli K12. Mutations in fhuA were classified into four types according to the extent by which they impaired mutant cells in their growth on ferrichrome as sole iron source and in their sensitivity to the antibiotic albomycin and to colicin M. The tonB mutation with a glutamine to leucine replacement at position 165 was less efficient in restoring the FhuA functions than the glutamine to lysine exchange at the same position. The better the coupling between FhuA and TonB the poorer was the inhibition of phage T1 binding to FhuA by ferrichrome. A working model is proposed in which the TonB protein assumes different conformations in response to the energized state of the cytoplasmic membrane and thereby allosterically regulates the activity of the FhuA receptor. This model implies an intermembrane coupling between two proteins in adjacent membranes.
fhuA基因“TonB框”中的点突变被tonB基因中的点突变所抑制,这表明大肠杆菌K12外膜中的FhuA受体蛋白与细胞质膜中的TonB蛋白之间存在功能和物理相互作用。根据fhuA突变对突变细胞以高铁载体作为唯一铁源生长以及对抗生素白霉素和大肠菌素M敏感性的损害程度,fhuA突变可分为四种类型。在第165位由谷氨酰胺替换为亮氨酸的tonB突变在恢复FhuA功能方面不如在同一位置由谷氨酰胺替换为赖氨酸有效。FhuA与TonB之间的偶联越好,高铁载体对噬菌体T1与FhuA结合的抑制作用就越弱。提出了一个工作模型,其中TonB蛋白根据细胞质膜的能量状态呈现不同构象,从而变构调节FhuA受体的活性。该模型意味着相邻膜中两种蛋白质之间的跨膜偶联。