Huergo Luciano F, Souza Emanuel M, Steffens M Berenice R, Yates M Geoffrey, Pedrosa Fabio O, Chubatsu Leda S
Department of Biochemistry and Molecular Biology, Universidade Federal do Paraná, CP 19046, 81531-990, PR, Curitiba, Brazil.
FEMS Microbiol Lett. 2003 Jun 6;223(1):33-40. doi: 10.1016/S0378-1097(03)00346-X.
In Azospirillum brasilense the glnB and glnA genes are clustered in an operon regulated by three different promoters: two located upstream of glnB (glnBp1-sigma(70), and glnBp2-sigma(N)) and one as yet unidentified promoter, in the glnBA intergenic region. We have investigated the expression of the glnB gene promoter using glnB-lacZ gene fusions, mutation analysis, heterologous expression and DNA band-shift assays. Deletion of the glnB promoter region showed that NtrC-binding sequences were essential for glnB expression under nitrogen limitation. The A. brasilense NtrC protein activated transcription of glnB-lacZ fusions in the heterologous genetic background of Escherichia coli. Expression of glnB-lacZ fusions in two A. brasilense ntrC mutants differed from that in the wild-type strain. In vitro studies also indicated that the purified NtrC protein from E. coli was able to bind to the glnB promoter region of A. brasilense. Our results show that the NtrC protein activates glnBglnA expression under nitrogen limitation in A. brasilense.
在巴西固氮螺菌中,glnB和glnA基因聚集在一个由三个不同启动子调控的操纵子中:两个位于glnB上游(glnBp1 - σ⁷⁰和glnBp2 - σᴺ),另一个位于glnBA基因间区域,尚未鉴定。我们使用glnB - lacZ基因融合、突变分析、异源表达和DNA条带迁移分析研究了glnB基因启动子的表达。glnB启动子区域的缺失表明,NtrC结合序列对于氮限制条件下glnB的表达至关重要。巴西固氮螺菌的NtrC蛋白在大肠杆菌的异源遗传背景中激活了glnB - lacZ融合基因的转录。在两个巴西固氮螺菌ntrC突变体中,glnB - lacZ融合基因的表达与野生型菌株不同。体外研究还表明,从大肠杆菌中纯化的NtrC蛋白能够结合到巴西固氮螺菌的glnB启动子区域。我们的结果表明,NtrC蛋白在氮限制条件下激活巴西固氮螺菌中glnBglnA的表达。