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Salt-Dependent Expression of Glucosylglycerol-Phosphate Synthase, Involved in Osmolyte Synthesis in the Cyanobacterium Synechocystis sp. Strain PCC 6803†

机译:盐依赖性表达的葡萄糖基甘油-磷酸合酶,参与蓝藻蓝藻属中的渗透压合成。应变PCC 6803†

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摘要

The cyanobacterium Synechocystis sp. strain PCC 6803 is able to acclimate to levels of salinity ranging from freshwater to twice the seawater concentrations of salt by accumulating the compatible solute glucosylglycerol (GG). Expression of the ggpS gene coding for the key enzyme (glucosylglycerol-phosphate synthase) in GG synthesis was examined in detail. Under control conditions, the GgpS protein is stable, so that weak constitutive transcription of the ggpS gene resulted in a significant protein content. However, the enzyme activity was biochemically switched off, and no GG was detectable. After a salt shock, an immediate increase in mRNA content proportional to the salt content occurred, while the GgpS protein and GG contents rose in a linear manner. Furthermore, the stability of the ggpS mRNA increased transiently. In salt-acclimated cells expression of the ggpS gene, the GgpS protein content, and the amount of accumulated GG depended linearly on the external salt concentration. Mapping of the 5′ end of the ggpS transcript revealed a long nontranslated 5′ sequence and a putative typical cyanobacterial promoter, which did not show any obvious salt-regulatory element. The alternative σ factor σF was found to be involved in salt-dependent regulation of ggpS, since in a σF mutant induction of this gene was strongly reduced. The present study demonstrated that in addition to biochemical regulation of GgpS activity, alterations of ggpS expression are involved in regulation of GG synthesis in Synechocystis sp. strain PCC 6803. A model showing the interaction of the two regulatory levels is presented.
机译:蓝藻集胞藻PCC 6803菌株能够通过积累相容的溶质葡萄糖基甘油(GG)来适应盐度水平,从淡水到海水盐浓度的两倍。详细检查了GG合成中编码关键酶(葡萄糖基甘油磷酸合酶)的ggpS基因的表达。在控制条件下,GgpS蛋白是稳定的,因此ggpS基因的弱组成型转录导致大量蛋白质含量。然而,酶活性被生化关闭,并​​且没有检测到GG。盐冲击后,与盐含量成正比的mRNA含量立即增加,而GgpS蛋白和GG含量呈线性增加。此外,ggpS mRNA的稳定性瞬时增加。在盐适应的细胞中,ggpS基因的表达,GgpS蛋白含量和GG的积累量线性依赖于外部盐浓度。 ggpS转录本的5'末端的图谱显示了一个长的非翻译的5'序列和一个推定的典型蓝细菌启动子,该启动子没有显示任何明显的盐调节元件。发现替代的σ因子σF参与了ggpS的盐依赖性调控,因为在σF突变体中该基因的诱导被大大降低。本研究表明,除了对GgpS活性的生化调节外,ggpS表达的改变还与集胞藻(Synechocystis sp。)GG的合成有关。菌株PCC6803。提出了显示两个调节水平相互作用的模型。

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