Wray L V, Atkinson M R, Fisher S H
Department of Microbiology, Boston University School of Medicine, Massachusetts 02118.
J Bacteriol. 1994 Jan;176(1):108-14. doi: 10.1128/jb.176.1.108-114.1994.
Expression of beta-galactosidase encoded by the nrg-29::Tn917-lacZ insertion increases 4,000-fold during nitrogen-limited growth (M.R. Atkinson and S. H. Fisher, J. Bacteriol. 173:23-27, 1991). The chromosomal DNA adjacent to the nrg-29::Tn917-lacZ insertion was cloned and sequenced. Analysis of the resulting nucleotide sequence revealed that the Tn917-lacZ transposon was inserted into the first gene of a dicistronic operon, nrgAB. The nrgA gene encodes a 43-kDa hydrophobic protein that is likely to be an integral membrane protein. The nrgB gene encodes a 13-kDa protein that has significant sequence similarity with the Escherichia coli glnB-encoded PII protein. Primer extension analysis revealed that the nrgAB operon is transcribed from a single promoter. The nucleotide sequence of this promoter has significant similarity with the -10 region, but not the -35 region, of the consensus sequence for Bacillus subtilis sigma A-dependent promoters.
由nrg - 29::Tn917 - lacZ插入所编码的β - 半乳糖苷酶的表达在氮限制生长期间增加了4000倍(M.R. 阿特金森和S.H. 费舍尔,《细菌学杂志》173:23 - 27,1991年)。与nrg - 29::Tn917 - lacZ插入相邻的染色体DNA被克隆并测序。对所得核苷酸序列的分析表明,Tn917 - lacZ转座子插入到了一个双顺反子操纵子nrgAB的第一个基因中。nrgA基因编码一种43 kDa的疏水蛋白,可能是一种整合膜蛋白。nrgB基因编码一种13 kDa的蛋白,与大肠杆菌glnB编码的PII蛋白具有显著的序列相似性。引物延伸分析表明nrgAB操纵子从单个启动子转录。该启动子的核苷酸序列与枯草芽孢杆菌σA依赖型启动子的共有序列的 - 10区域有显著相似性,但与 - 35区域没有相似性。