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Transcription of the glnB and glnA genes in the photosynthetic bacterium Rhodospirillum rubrum

机译:在光合菌罗达螺旋中的GLNB和GLNA基因的转录

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The P11 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 P11 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 s54-dependent promoter consensus sequence. A putative s70 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.
机译:通过GLNB编码的P11蛋白在氮气固定原核生物中的氮代谢控制方面具有重要作用。 rhodospirillum rubrum的Glnb基因被分离并测序。推导的氨基酸序列对其他P11蛋白质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下游的135bp,部分测序。 GLNB与具有高相似性的启动子与S54依赖性启动子共有序列的启动子进行COTASED。调用的S70启动子也在GLNB的上游鉴定。 Northern印迹分析表明,在未识别的启动子或更可能的情况下,加工GlnBA转录物以产生GlNA mRNA的GlNA可以转录。氮素固定细胞的两种转录物的总水平高于氨生长细胞。

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