Ramakrishnan G, Ikenaka K, Inouye M
J Bacteriol. 1985 Jul;163(1):82-7. doi: 10.1128/jb.163.1.82-87.1985.
The expression of the genes for the Escherichia coli K-12 outer membrane proteins, ompF and ompC, is subject to osmoregulation and responds to changes in the osmolarity of the growth medium. The transcription of these genes is dependent on the products of the regulatory locus ompB (comprising the genes ompR and envZ). The native promoter of ompF was replaced with an inducible lpp promoter to eliminate this transcriptional dependence of ompF expression on ompB. As a result, it was possible for the OmpF protein to be produced in an ompB mutant strain that does not normally express ompF. Surprisingly, the expression of ompF under the lpp promoter was still osmoregulated not only in the ompB+ strain but also in two ompB strains tested. These results indicate the involvement of a factor(s) besides the ompR and envZ gene products in the osmoregulation of OmpF production. This factor may interact with a sequence downstream of the ompF promoter. In addition, we show that the expression of ompF under the lpp promoter has no direct effect on ompC expression.
大肠杆菌K-12外膜蛋白ompF和ompC的基因表达受渗透压调节,并对生长培养基渗透压的变化做出反应。这些基因的转录依赖于调节位点ompB的产物(由基因ompR和envZ组成)。ompF的天然启动子被可诱导的lpp启动子取代,以消除ompF表达对ompB的这种转录依赖性。结果,在通常不表达ompF的ompB突变菌株中也有可能产生OmpF蛋白。令人惊讶的是,不仅在ompB+菌株中,而且在所测试的两个ompB菌株中,lpp启动子控制下的ompF表达仍然受渗透压调节。这些结果表明,除了ompR和envZ基因产物外,还有一个因子参与了OmpF产生的渗透压调节。该因子可能与ompF启动子下游的序列相互作用。此外,我们表明,lpp启动子控制下的ompF表达对ompC表达没有直接影响。