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通过WggR(ExpG)、PhoB和MucR对两个启动子的差异依赖性调控来微调苜蓿中华根瘤菌中半乳葡聚糖的生物合成。

Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential WggR (ExpG)-, PhoB-, and MucR-dependent regulation of two promoters.

作者信息

Bahlawane Christelle, Baumgarth Birgit, Serrania Javier, Rüberg Silvia, Becker Anke

机构信息

Institute for Genome Research and Systems Biology, Center for Biotechnology, Bielefeld University, Universitätsstr. 25, 33594 Bielefeld, Germany.

出版信息

J Bacteriol. 2008 May;190(10):3456-66. doi: 10.1128/JB.00062-08. Epub 2008 Mar 14.

Abstract

Depending on the phosphate concentration encountered in the environment Sinorhizobium meliloti 2011 synthesizes two different exopolysaccharides (EPS). Galactoglucan (EPS II) is produced under phosphate starvation but also in the presence of extra copies of the transcriptional regulator WggR (ExpG) or as a consequence of a mutation in mucR. The galactoglucan biosynthesis gene cluster contains the operons wga (expA), wge (expE), wgd (expD), and wggR (expG). Two promoters, differentially controlled by WggR, PhoB, and MucR, were identified upstream of each of these operons. The proximal promoters of the wga, wge, and wgd transcription units were constitutively active when separated from the upstream regulatory sequences. Promoter activity studies and the positions of predicted PhoB and WggR binding sites suggested that the proximal promoters are cooperatively induced by PhoB and WggR. MucR was shown to strongly inhibit the distal promoters and bound to the DNA in the vicinity of the distal transcription start sites. An additional inhibitory effect on the distal promoter of the structural galactoglucan biosynthesis genes was identified as a new feature of WggR in a mucR mutant. A regulatory model of the fine-tuning of galactoglucan production is proposed.

摘要

根据在环境中遇到的磷酸盐浓度,苜蓿中华根瘤菌2011合成两种不同的胞外多糖(EPS)。半乳葡聚糖(EPS II)在磷酸盐饥饿条件下产生,也可在转录调节因子WggR(ExpG)有额外拷贝时产生,或者由于mucR突变而产生。半乳葡聚糖生物合成基因簇包含操纵子wga(expA)、wge(expE)、wgd(expD)和wggR(expG)。在这些操纵子的每一个上游都鉴定出了两个受WggR、PhoB和MucR差异控制的启动子。当与上游调控序列分离时,wga、wge和wgd转录单元的近端启动子具有组成型活性。启动子活性研究以及预测的PhoB和WggR结合位点的位置表明,近端启动子由PhoB和WggR协同诱导。结果表明,MucR强烈抑制远端启动子,并与远端转录起始位点附近的DNA结合。在mucR突变体中,WggR对结构半乳葡聚糖生物合成基因的远端启动子具有额外的抑制作用,这被确定为WggR的一个新特征。本文提出了一个半乳葡聚糖产生微调的调控模型。

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本文引用的文献

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Web services at the European bioinformatics institute.欧洲生物信息学研究所的网络服务。
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Microbiology (Reading). 2006 Jun;152(Pt 6):1751-1763. doi: 10.1099/mic.0.28743-0.

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