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首页> 外文期刊>Molecular Microbiology >Nitrogen control of the glnN gene that codes for GS type III, the only glutamine synthetase in the cyanobacterium Pseudanabaena sp. PCC 6903.
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Nitrogen control of the glnN gene that codes for GS type III, the only glutamine synthetase in the cyanobacterium Pseudanabaena sp. PCC 6903.

机译:编码GS型III的glnN基因的氮控制,这是蓝细菌Pseudanabaena sp。中唯一的谷氨酰胺合成酶。 PCC 6903。

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摘要

Pseudanabaena sp. strain PCC 6903 is the first cyanobacteria lacking the typical prokaryotic glutamine synthetase type I encoded by the glnA gene. The glnN gene product, glutamine synthetase type III, is the only glutamine synthetase activity present in this cyanobacterium. Analysis of glnN expression clearly indicated a nitrogen-dependent regulation. Pseudanabaena glnN gene expression and GSIII activity were upregulated under nitrogen starvation or using nitrate as a nitrogen source, while low levels of transcript and activity were found in ammonium-containing medium. Primer extension analysis showed that the glnN gene promoter structure resembled that of the NtcA-related promoters. Mobility shift assays demonstrated that Synechocystis sp. PCC 6803 NtcA protein, expressed and purified from Escherichia coli, bound to the promoter of the Pseudanabaena 6903 glnN gene. The NtcA control of the glnN gene in this cyanobacterium suggested that, in the absence of a glnA gene, NtcA took control of the only glutamine synthetase gene in a fashion similar to the way the glnA gene is governed in those cyanobacteria harbouring a glnA gene.
机译:假单胞菌PCC 6903菌株是第一个缺少由glnA基因编码的典型原核生物谷氨酰胺合成酶I型的蓝细菌。 glnN基因产物谷氨酰胺合成酶III型是该蓝细菌中唯一存在的谷氨酰胺合成酶活性。对glnN表达的分析清楚地表明了氮依赖性调节。在氮饥饿或使用硝酸盐作为氮源的情况下,假单胞菌glnN基因表达和GSIII活性上调,而在含铵的培养基中发现较低的转录本和活性。引物延伸分析表明,glnN基因启动子的结构类似于NtcA相关启动子的结构。迁移率变化分析表明,集胞藻属。从大肠杆菌表达和纯化的PCC 6803 NtcA蛋白与Pseudanabaena 6903 glnN基因的启动子结合。该蓝细菌中对glnN基因的NtcA控制表明,在没有glnA基因的情况下,NtcA以与glnA基因在那些携带glnA基因的蓝细菌中的治理方式类似的方式控制了唯一的谷氨酰胺合成酶基因。

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