Hirokawa K, Nagaya M, Aiba H, Mizuno T
Laboratory of Molecular Microbiology, School of Agriculture, Nagoya University, Japan.
Biosci Biotechnol Biochem. 1996 Feb;60(2):277-83. doi: 10.1271/bbb.60.277.
Synechococcus sp. PCC7942 is a phototrophic cyanobacterium. In this study we cloned a Synechococcus gene that has a striking effect on the production of the Escherichia coli outer membrane proteins, OmpC and OmpF, provided that this gene was introduced by a multicopy plasmid into the heterologous cells. This multicopy gene in E. coli cells was able to specifically shut off the production of both OmpC and OmpF at the level of transcription. The nucleotides were sequenced for this gene, named sis, and its gene product was purified from E. coli to near homogeneity. A computer-aided search found that the deduced amino acid sequence consisting of 138 residues is novel, with no significant similarity to any other protein in the databases. Since the transcription of ompC and ompF is regulated by the regulatory factors EnvZ and OmpR, through phosphotransfer signal transduction, we explored the inhibitory effect of Sis in various genetic backgrounds as to envZ and ompR. In particular, the inhibitory effect of Sis was observed even in an DeltaenvZ background, but was not observed in a certain background in which the ompC and ompF transcription was supported by a mutant OmpR that can function in a phosphorylation-independent manner. These results suggested that the EnvZ kinase may not be the direct target of Sis, but rather that the process(es) concerning the phosphorylation and/or dephosphorylation of the OmpR protein may be affected by Sis. However, no direct effect of Sis was seen in an in vitro OmpR-phosphorylation assay with the purified OmpR and Sis proteins. Based on these results, possible functions of Sis are discussed with special reference to the phosphotransfer signal transduction in E. coli.
聚球藻属PCC7942是一种光合蓝细菌。在本研究中,我们克隆了一个聚球藻基因,该基因对大肠杆菌外膜蛋白OmpC和OmpF的产生具有显著影响,前提是该基因通过多拷贝质粒导入异源细胞。大肠杆菌细胞中的这个多拷贝基因能够在转录水平特异性地关闭OmpC和OmpF的产生。对这个名为sis的基因进行了核苷酸测序,并从大肠杆菌中纯化了其基因产物,使其接近均一。计算机辅助搜索发现,由138个残基组成的推导氨基酸序列是新颖的,与数据库中的任何其他蛋白质都没有显著相似性。由于ompC和ompF的转录受调控因子EnvZ和OmpR通过磷酸转移信号转导的调节,我们探讨了Sis在各种envZ和ompR遗传背景下的抑制作用。特别是,即使在ΔenvZ背景下也观察到了Sis的抑制作用,但在ompC和ompF转录由一种可以以非磷酸化依赖方式发挥作用的突变OmpR支持的特定背景下未观察到。这些结果表明,EnvZ激酶可能不是Sis的直接靶点,而是OmpR蛋白的磷酸化和/或去磷酸化相关过程可能受到Sis的影响。然而,在使用纯化的OmpR和Sis蛋白进行的体外OmpR磷酸化试验中,未观察到Sis的直接作用。基于这些结果,并特别参考大肠杆菌中的磷酸转移信号转导,讨论了Sis的可能功能。