Patriarca E J, Riccio A, Taté R, Colonna-Romano S, Iaccarino M, Defez R
International Institute of Genetics and Biophysics, CNR, Naples, Italy.
Mol Microbiol. 1993 Aug;9(3):569-77. doi: 10.1111/j.1365-2958.1993.tb01717.x.
We report here that ntrB and ntrC genes of Rhizobium leguminosarum biovar phaseoli are cotranscribed with an open reading frame (called ORF1) of unknown function. The promoter region of the ORF1-ntrB-ntrC operon was mapped immediately upstream of ORF1 and two in vivo transcription initiation sites were identified, both preceded by -35/-10 promoter consensus sequences. Some major aspects differentiate R. leguminosarum from the enteric nitrogen regulatory system: the ntrBC genes are cotranscribed with ORF1 which is homologous to an ORF located upstream of ntrBC of R. capsulatus and to the ORF1 located upstream of the fis gene of Escherichia coli; ntrBC are not transcribed from a -24/-12 promoter and are only autogenously repressed. Moreover, the intracellular concentration of the NtrC protein increases when the bacterium is grown on ammonium salts, while under the same conditions the promoter of one of its target genes, glnII, is 12 times less active.
我们在此报告,菜豆根瘤菌生物变种的ntrB和ntrC基因与一个功能未知的开放阅读框(称为ORF1)共转录。ORF1-ntrB-ntrC操纵子的启动子区域定位在ORF1的紧邻上游,并且鉴定出两个体内转录起始位点,两者之前均有-35/-10启动子共有序列。菜豆根瘤菌与肠道氮调节系统在一些主要方面存在差异:ntrBC基因与ORF1共转录,ORF1与荚膜红细菌ntrBC上游的一个ORF以及大肠杆菌fis基因上游的ORF1同源;ntrBC并非从-24/-12启动子转录,且仅受自身抑制。此外,当细菌在铵盐上生长时,NtrC蛋白的细胞内浓度会增加,而在相同条件下,其一个靶基因glnII的启动子活性降低12倍。