Stewart V, Cali B M
Section of Microbiology, Cornell University, Ithaca, New York 14853-8101.
J Bacteriol. 1990 Aug;172(8):4482-8. doi: 10.1128/jb.172.8.4482-4488.1990.
We cloned the narL gene, required for nitrate induction of respiratory nitrate reductase synthesis, from Klebsiella pneumoniae. The E. coli narL gene product shares sequence similarity with the response regulator proteins of two-component regulatory systems. We found that narL(+)-containing plasmids restored nitrate regulation of anaerobic respiratory gene expression in appropriate Escherichia coli hosts. The K. pneumoniae narL region encoded a protein whose migration in Laemmli gels was indistinguishable from that of the narL product of E. coli. We constructed a narL::Km mutant of K. pneumoniae. This mutation abolished nitrate induction of respiratory nitrate reductase synthesis but had no effect on nitrate induction of assimilatory nitrate and nitrite reductase synthesis. We conclude that K. pneumoniae has distinct nitrate-responsive regulators for controlling respiratory and assimilatory gene expression.
我们从肺炎克雷伯菌中克隆了呼吸性硝酸还原酶合成的硝酸盐诱导所需的narL基因。大肠杆菌narL基因产物与双组分调节系统的应答调节蛋白具有序列相似性。我们发现,含有narL(+)的质粒可恢复合适的大肠杆菌宿主中厌氧呼吸基因表达的硝酸盐调节。肺炎克雷伯菌的narL区域编码一种蛋白质,其在Laemmli凝胶中的迁移与大肠杆菌的narL产物无法区分。我们构建了肺炎克雷伯菌的narL::Km突变体。该突变消除了呼吸性硝酸还原酶合成的硝酸盐诱导,但对同化性硝酸和亚硝酸还原酶合成的硝酸盐诱导没有影响。我们得出结论,肺炎克雷伯菌具有不同的硝酸盐应答调节因子,用于控制呼吸和同化基因的表达。