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Slr1670 from Synechocystis sp. PCC 6803 Is Required for the Re-assimilation of the Osmolyte Glucosylglycerol.

机译:来自集胞藻属的Srl1670。 Osmolyte葡萄糖基甘油的重新同化需要PCC 6803。

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摘要

When subjected to mild salt stress, the cyanobacterium Synechocystis sp. PCC 6803 produces small amounts of glycerol through an as of yet unidentified pathway. Here, we show that this glycerol is a degradation product of the main osmolyte of this organism, glucosylglycerol (GG). Inactivation of ggpS, encoding the first step of GG-synthesis, abolished de novo synthesis of glycerol, while the ability to hydrolyze exogenously supplied glucoslylglycerol was unimpaired. Inactivation of glpK, encoding glycerol kinase, had no effect on glycerol synthesis. Inactivation of slr1670, encoding a GHL5-type putative glycoside hydrolase, abolished de novo synthesis of glycerol, as well as hydrolysis of GG, and led to increased intracellular concentrations of this osmolyte. Slr1670 therefore presumably displays GG hydrolase activity. A gene homologous to the one encoded by slr1670 occurs in a wide range of cyanobacteria, proteobacteria, and archaea. In cyanobacteria, it co-occurs with genes involved in GG-synthesis.
机译:受到轻度盐胁迫时,蓝藻集胞藻(Synechocystis sp。)。 PCC 6803通过迄今尚未确定的途径产生少量甘油。在这里,我们表明该甘油是该生物体主要渗透压物质葡萄糖基甘油(GG)的降解产物。编码GG合成第一步的ggpS失活消除了甘油的从头合成,而水解外源提供的糖基甘油的能力没有受到损害。编码甘油激酶的glpK的失活对甘油合成没有影响。编码GHL5型推定的糖苷水解酶的slr1670的失活,废除了甘油的从头合成以及GG的水解,并导致该渗透液的细胞内浓度增加。因此,Srl1670可能显示GG水解酶活性。与slr1670编码的基因同源的基因广泛存在于蓝细菌,变形杆菌和古细菌中。在蓝细菌中,它与参与GG合成的基因共存。

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