首页> 外文期刊>Plant and Cell Physiology >A Response Regulator Rre37 and an RNA Polymerase Sigma Factor SigE Represent Two Parallel Pathways to Activate Sugar Catabolismn in a Cyanobacterium Synechocystis sp. PCC 6803
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A Response Regulator Rre37 and an RNA Polymerase Sigma Factor SigE Represent Two Parallel Pathways to Activate Sugar Catabolismn in a Cyanobacterium Synechocystis sp. PCC 6803

机译:响应调节器Rre37和RNA聚合酶西格玛因子SigE代表两个并行的途径来激活蓝藻蓝藻中的糖分解代谢。 PCC 6803

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Sugar catabolic genes are induced during nitrogen starvation in a cyanobacterium Synechocystis sp. PCC 6803, but the underlying regulatory mechanism still remains to be completely characterized. In this study, we showed by molecular genetics and transcriptome analyses that a response regulator Rre37 (encoded by sll1330), whose expression is enhanced by nitrogen depletion under the control of NtcA, activates transcript accumulation of sugar catabolic genes, such as gap1, pfkA (sll1196), glgP (slr1367) and glgX (slr1857), mainly during nitrogen starvation. Previously, we reported that a group-2 sigma factor SigE also positively regulates sugar catabolic genes in this strain. Phenotypic analyses using a single or double mutant lacking rre37 and/or sigE indicated that both SigE and Rre37 positively regulate sugar catabolic genes independently. These findings substantiated a regulatory network of sugar catabolic genes in this cyanobacterium.
机译:糖分解代谢基因是在蓝藻蓝藻属(Sychochocystis sp。)的氮饥饿期间诱导的。 PCC 6803,但基本的调节机制仍然有待完全表征。在这项研究中,我们通过分子遗传学和转录组分析表明,响应调节剂Rre37(由sll1330编码)在NtcA的控制下通过氮耗竭而增强了其表达,从而激活了糖代谢基因(如gap1,pfkA( sll1196),glgP(slr1367)和glgX(slr1857),主要是在氮饥饿期间。先前,我们报道了2型西格玛因子SigE也正调节此菌株中的糖代谢基因。使用缺少rre37和/或sigE的单个或双重突变体进行的表型分析表明,SigE和Rre37均独立地积极调节糖代谢基因。这些发现证实了该蓝细菌中糖分解代谢基因的调控网络。

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