Hong Chang Soo, Shitashiro Maiko, Kuroda Akio, Ikeda Tsukasa, Takiguchi Noboru, Ohtake Hisao, Kato Junichi
Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8530, Japan.
FEMS Microbiol Lett. 2004 Feb 16;231(2):247-52. doi: 10.1016/S0378-1097(04)00009-6.
It was previously shown that the chemotaxis gene cluster 1 (cheYZABW) was required for chemotaxis. In this study, the involvement of the same cluster in aerotaxis is described and two transducer genes for aerotaxis are identified. Aerotaxis assays of a number of deletion-insertion mutants of Pseudomonas aeruginosa PAO1 revealed that the chemotaxis gene cluster 1 and cheR are required for aerotaxis. Mutant strains which contained deletions in the methyl-accepting chemotaxis protein-like genes tlpC and tlpG showed decreased aerotaxis. A double mutant deficient in tlpC and tlpG was negative for aerotaxis. TlpC has 45% amino acid identity with the Escherichia coli aerotactic transducer Aer. The TlpG protein has a predicted C-terminal segment with 89% identity to the highly conserved domain of the E. coli serine chemoreceptor Tsr. A hydropathy plot of TlpG indicated that hydrophobic membrane-spanning regions are missing in TlpG. A PAS motif was found in the N-terminal domains of TlpC and TlpG. On this basis, the tlpC and tlpG genes were renamed aer and aer-2, respectively. No significant homology other than the PAS motif was detected in the N-terminal domains between Aer and Aer-2.
先前的研究表明趋化基因簇1(cheYZABW)是趋化作用所必需的。在本研究中,描述了同一基因簇在趋氧性中的作用,并鉴定了两个趋氧性转导基因。对铜绿假单胞菌PAO1的多个缺失插入突变体进行趋氧性分析,结果显示趋化基因簇1和cheR是趋氧性所必需的。在甲基接受趋化蛋白样基因tlpC和tlpG中存在缺失的突变菌株表现出趋氧性降低。tlpC和tlpG双缺失突变体的趋氧性为阴性。TlpC与大肠杆菌趋氧性转导蛋白Aer的氨基酸同一性为45%。TlpG蛋白的预测C末端片段与大肠杆菌丝氨酸化学感受器Tsr的高度保守结构域的同一性为89%。TlpG的亲水性图谱表明TlpG中缺少疏水跨膜区域。在TlpC和TlpG的N末端结构域中发现了一个PAS基序。在此基础上,将tlpC和tlpG基因分别重新命名为aer和aer-2。在Aer和Aer-2的N末端结构域之间,除了PAS基序外未检测到明显的同源性。