Johansson Magnus, Nordlund Stefan
Department of Biochemistry, Arrhenius Laboratories for Natural Sciences, Stockholm University, S-10691 Stockholm, Sweden.
Microbiology (Reading). 1996 May;142 ( Pt 5):1265-1272. doi: 10.1099/13500872-142-5-1265.
The PII protein, encoded by glnB, has a central role in the control of nitrogen metabolism in nitrogen-fixing prokaryotes. The glnB gene of Rhodospirillum rubrum was isolated and sequenced. The deduced amino acid sequence had very high sequence identity to other PII proteins. The glnA gene, encoding glutamine synthetase, was located 135 bp downstream of glnB and was partially sequenced. glnB is cotranscribed with glnA from a promoter with high similarity to the sigma 54-dependent promoter consensus sequence. A putative sigma 70 promoter was also identified further upstream of glnB. Northern blotting analyses showed that in addition glnA is either transcribed from an unidentified promoter or, more likely, that the glnBA transcript is processed to give the glnA mRNA. The total level of the two transcripts was much higher in nitrogen-fixing cells than in ammonia-grown cells.
由glnB编码的PII蛋白在固氮原核生物的氮代谢控制中起核心作用。对红螺菌的glnB基因进行了分离和测序。推导的氨基酸序列与其他PII蛋白具有非常高的序列同一性。编码谷氨酰胺合成酶的glnA基因位于glnB下游135 bp处,并进行了部分测序。glnB与glnA从一个与σ54依赖型启动子共有序列高度相似的启动子共转录。在glnB的更上游还鉴定出一个推定的σ70启动子。Northern印迹分析表明,此外,glnA要么从未知启动子转录,要么更有可能是glnBA转录本经过加工产生glnA mRNA。这两种转录本的总水平在固氮细胞中比在氨培养细胞中高得多。