Nienaber A, Huber A, Göttfert M, Hennecke H, Fischer H M
Institut für Mikrobiologie, Eidgenössische Hochschule, CH-8092 Zürich, Switzerland.
J Bacteriol. 2000 Mar;182(6):1472-80. doi: 10.1128/JB.182.6.1472-1480.2000.
The so-called symbiotic region of the Bradyrhizobium japonicum chromosome (C. Kündig, H. Hennecke, and M. Göttfert, J. Bacteriol. 175:613-622, 1993) was screened for the presence of genes controlled by the nitrogen fixation regulatory protein NifA. Southern blots of restriction enzyme-digested cosmids that represent an ordered, overlapping library of the symbiotic region were competitively hybridized with in vitro-labeled RNA from anaerobically grown wild-type cells and an excess of RNA isolated either from anaerobically grown nifA and rpoN mutant cells or from aerobically grown wild-type cells. In addition to the previously characterized nif and fix gene clusters, we identified three new NifA-regulated genes that were named nrgA, nrgB, and nrgC (nrg stands for NifA-regulated gene). The latter two probably form an operon, nrgBC. The proteins encoded by nrgC and nrgA exhibited amino acid sequence similarity to bacterial hydroxylases and N-acetyltransferases, respectively. The product of nrgB showed no significant similarity to any protein with a database entry. Primer extension experiments and expression studies with translational lacZ fusions revealed the presence of a functional -24/-12-type promoter upstream of nrgA and nrgBC and proved the NifA- and RpoN (sigma(54))-dependent transcription of the respective genes. Null mutations introduced into nrgA and nrgBC resulted in mutant strains that exhibited wild-type-like symbiotic properties, including nitrogen fixation, when tested on soybean, cowpea, or mung bean host plants. Thus, the discovery of nrgA and nrgBC further emphasizes the previously suggested role of NifA as an activator of anaerobically induced genes other than the classical nitrogen fixation genes.
对日本慢生根瘤菌染色体的所谓共生区域(C. 昆迪格、H. 亨内克和M. 戈特费尔特,《细菌学杂志》175:613 - 622,1993年)进行筛选,以寻找受固氮调节蛋白NifA调控的基因。代表共生区域有序重叠文库的经限制性内切酶消化的黏粒的Southern印迹,与来自厌氧生长的野生型细胞的体外标记RNA以及过量的从厌氧生长的nifA和rpoN突变细胞或需氧生长的野生型细胞中分离的RNA进行竞争性杂交。除了先前已鉴定的nif和fix基因簇外,我们还鉴定出三个新的受NifA调控的基因,分别命名为nrgA、nrgB和nrgC(nrg代表受NifA调控的基因)。后两个基因可能形成一个操纵子,即nrgBC。由nrgC和nrgA编码的蛋白质分别与细菌羟化酶和N - 乙酰转移酶表现出氨基酸序列相似性。nrgB的产物与数据库中任何已录入条目的蛋白质均无明显相似性。引物延伸实验以及用翻译型lacZ融合体进行的表达研究表明,在nrgA和nrgBC上游存在一个功能性的 -24/-12型启动子,并证明了相应基因的转录依赖于NifA和RpoN(σ⁵⁴)。导入nrgA和nrgBC的缺失突变产生了突变菌株,当在大豆、豇豆或绿豆宿主植物上进行测试时,这些菌株表现出类似野生型的共生特性,包括固氮能力。因此,nrgA和nrgBC的发现进一步强调了先前提出的NifA作为经典固氮基因以外的厌氧诱导基因激活剂的作用。