Mizuno T, Mizushima S
J Biochem. 1987 Feb;101(2):387-96. doi: 10.1093/oxfordjournals.jbchem.a121923.
Expression of the ompC and ompF genes coding for the major outer membrane proteins, OmpC and OmpF, respectively, is known to be controlled by at least two regulatory genes, ompR and envZ, which together comprise a single ompB operon. We constructed chromosomal mutants with either ompR-envZ deletion or envZ deletion. Characterization of these deletion strains showed that the OmpR protein is necessary for transcription of the ompC and ompF genes, and the EnvZ protein is essential for normal regulation of the ompC and ompF expression, which is affected by the medium osmolarity. We also constructed several plasmids carrying different portions of the ompB operon. Characterization of these plasmids allowed us to identify the OmpR protein with an apparent molecular weight of 29 kilodaltons (kDa) and the EnvZ protein with an apparent molecular weight of 50 kDa. The initiation codon for EnvZ translation appeared to overlap with the termination codon for OmpR translation. It was also found that a truncated EnvZ polypeptide (44 kDa) which lacks the N-terminal 55 amino acid residues can complement the envZ deletion mutant. Based on these results, the structure and function of the ompB operon are discussed in relation to the regulation of ompC and ompF expression.
分别编码主要外膜蛋白OmpC和OmpF的ompC和ompF基因的表达,已知受至少两个调控基因ompR和envZ控制,它们共同构成一个单一的ompB操纵子。我们构建了ompR - envZ缺失或envZ缺失的染色体突变体。对这些缺失菌株的特性分析表明,OmpR蛋白是ompC和ompF基因转录所必需的,而EnvZ蛋白对于ompC和ompF表达的正常调控至关重要,这种调控受培养基渗透压影响。我们还构建了携带ompB操纵子不同部分的几种质粒。对这些质粒的特性分析使我们能够鉴定出表观分子量为29千道尔顿(kDa)的OmpR蛋白和表观分子量为50 kDa的EnvZ蛋白。EnvZ翻译的起始密码子似乎与OmpR翻译的终止密码子重叠。还发现一种缺少N端55个氨基酸残基的截短EnvZ多肽(44 kDa)可以互补envZ缺失突变体。基于这些结果,结合ompC和ompF表达的调控对ompB操纵子的结构和功能进行了讨论。