Minder A C, Narberhaus F, Babst M, Hennecke H, Fischer H M
Mikrobiologisches Institut, Eidgenossische Technische Hochschule, Zurich, Switzerland.
Mol Gen Genet. 1997 Mar 26;254(2):195-206. doi: 10.1007/s004380050408.
The dnaKJ genes of Bradyrhizobium japonicum were cloned and sequenced. They map adjacent to each other, as in other proteobacteria of the alpha and gamma subgroups. Primer extension experiments identified two strongly heat-inducible transcripts starting 99 bp (T1) and 204 bp (T2) upstream of dnaK. Synthesis of the shorter transcript T1 in Escherichia coli required the presence of a recently characterized sigma32 homologue (RpoH1) from B. japonicum. The -35 and -10 regions of the promoters associated with the transcription start sites T1 and T2 displayed nucleotide sequence motifs that are characteristic for sigma32-dependent promoters in E. coli and alpha-proteobacteria. Heat shock regulation of dnaK expression was confirmed by immunoblot analysis of DnaK protein. All of these results put dnaK into the sigma32-dependent class, not the CIRCE-dependent class, of heat shock genes in B. japonicum. At normal growth temperature dnaK was expressed at a significant basal level. All attempts to eliminate dnaK function by insertion or deletion mutagenesis failed. By contrast, dnaJ null mutants and insertions in the dnaKJ intergenic region were easily obtained. The growth rate of dnaJ mutants was reduced but the final cell density reached in rich medium and their symbiotic properties were indistinguishable from the wild type.
慢生根瘤菌的dnaKJ基因被克隆并测序。它们彼此相邻定位,就像在α和γ亚群的其他变形菌中一样。引物延伸实验确定了两个强烈受热诱导的转录本,分别起始于dnaK上游99 bp(T1)和204 bp(T2)处。在大肠杆菌中合成较短的转录本T1需要存在慢生根瘤菌中最近鉴定出的sigma32同源物(RpoH1)。与转录起始位点T1和T2相关的启动子的-35和-10区域显示出核苷酸序列基序,这些基序是大肠杆菌和α-变形菌中sigma32依赖性启动子的特征。通过对DnaK蛋白的免疫印迹分析证实了dnaK表达的热休克调节。所有这些结果将dnaK归入慢生根瘤菌热休克基因的sigma32依赖性类别,而非CIRCE依赖性类别。在正常生长温度下,dnaK以显著的基础水平表达。通过插入或缺失诱变消除dnaK功能的所有尝试均失败。相比之下,很容易获得dnaJ缺失突变体和dnaKJ基因间区域的插入突变体。dnaJ突变体的生长速率降低,但在丰富培养基中达到的最终细胞密度以及它们的共生特性与野生型没有区别。