首页> 美国卫生研究院文献>Journal of Bacteriology >The ggpS Gene from Synechocystis sp. Strain PCC 6803 Encoding Glucosyl-Glycerol-Phosphate Synthase Is Involved in Osmolyte Synthesis
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The ggpS Gene from Synechocystis sp. Strain PCC 6803 Encoding Glucosyl-Glycerol-Phosphate Synthase Is Involved in Osmolyte Synthesis

机译:来自集胞藻种的ggpS基因。编码葡萄糖基-甘油-磷酸合酶的PCC 6803菌株参与渗透液的合成

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摘要

A salt-sensitive mutant of Synechocystis sp. strain PCC 6803 defective in the synthesis of the compatible solute glucosylglycerol (GG) was used to search for the gene encoding GG-phosphate synthase (GGPS), the key enzyme in GG synthesis. Cloning and sequencing of the mutated region and the corresponding wild-type region revealed that a deletion of about 13 kb occurred in the genome of mutant 11. This deletion affected at least 10 open reading frames, among them regions coding for proteins showing similarities to trehalose (otsA homolog)- and glycerol-3-phosphate-synthesizing enzymes. After construction and characterization of mutants defective in these genes, it became obvious that an otsA homolog (sll1566) (T. Kaneko et al., DNA Res. 3:109–136, 1996) encodes GGPS, since only the mutant affected in sll1566 showed salt sensitivity combined with a complete absence of GG accumulation. Furthermore, the overexpression of sll1566 in Escherichia coli led to the appearance of GGPS activity in the heterologous host. The overexpressed protein did not show the salt dependence that is characteristic for the GGPS in crude protein extracts of Synechocystis.
机译:盐敏感的集胞藻的突变体。相容溶质葡萄糖基甘油(GG)合成中有缺陷的PCC 6803菌株用于搜索编码GG合成的关键酶GG-磷酸合酶(GGPS)的基因。突变区和相应的野生型区的克隆和测序表明,突变体11的基因组中发生了约13 kb的缺失。该缺失影响了至少10个开放阅读框,其中编码与海藻糖相似的蛋白质的区域(otsA同源物)和3磷酸甘油合成酶。在构建并鉴定了这些基因中有缺陷的突变体后,很明显,一个otsA同源物(sll1566)(T. Kaneko等人,DNA Res。3:109–136,1996)编码GGPS,因为只有受影响的突变体才受sll1566影响显示出对盐的敏感性以及完全不存在GG积累。此外,sll1566在大肠杆菌中的过表达导致异源宿主中出现GGPS活性。过表达的蛋白质没有显示出盐依赖性,而盐依赖性是集胞藻粗蛋白提取物中GGPS的特征。

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