首页> 美国卫生研究院文献>Journal of Bacteriology >nodO a new nod gene of the Rhizobium leguminosarum biovar viciae sym plasmid pRL1JI encodes a secreted protein.
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nodO a new nod gene of the Rhizobium leguminosarum biovar viciae sym plasmid pRL1JI encodes a secreted protein.

机译:nodO是豆科根瘤菌生物变种蚕豆sym质粒pRL1JI的新nod基因它编码一种分泌的蛋白质。

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摘要

The region of the Rhizobium leguminosarum biovar viciae Sym plasmid pRL1JI, responsible for the production and secretion of a previously described 50-kilodalton protein (R. A. de Maagd, C. A. Wijffelman, E. Pees, and B. J. J. Lugtenberg, J. Bacteriol. 170:4424-4427, 1988), was cloned and its nucleotide sequence was determined. A new nod gene, nodO, preceded by a poorly conserved nod box, was identified and its transcriptional start site was determined. Comparison of its predicted protein product with the N-terminal amino acid sequence of the isolated secreted protein showed that nodO is the structural gene of this protein, although the nucleotide sequence predicted a protein only 30,002 daltons in size. This comparison also showed that the secreted protein is not the product of N-terminal processing of a larger precursor. A conventional N-terminal signal sequence was not detected in the NodO protein. The NodO protein has significant homology with a part (residues 720 to 920) of the hemolysin protein (HlyA) of Escherichia coli. Analysis of the transcriptional regulation of the nodO gene revealed that, in contrast with other nod promoters in this species, activity of the nodO promoter is greatly enhanced in the presence of multiple copies of the nodD gene.
机译:豆根瘤菌生物变种蚕豆Sym质粒pRL1JI的区域,该区域负责产生和分泌先前描述的50千达尔顿蛋白质(RA de Maagd,CA Wijffelman,E。Pees和BJJ Lugtenberg,J。Bacteriol。170:4424-克隆了4427,1988),并确定了其核苷酸序列。鉴定了一个新的nod基因nodO,其后是保守性很差的nod盒,并确定了其转录起始位点。将其预测的蛋白质产物与分离的分泌蛋白质的N端氨基酸序列进行比较表明,nodO是该蛋白质的结构基因,尽管核苷酸序列预测的蛋白质大小仅为30,002道尔顿。该比较还表明,分泌的蛋白质不是较大前体的N末端加工的产物。在NodO蛋白中未检测到常规的N端信号序列。 NodO蛋白与大肠杆菌的溶血素蛋白(HlyA)的一部分(残基720至920)具有显着同源性。对nodO基因转录调控的分析表明,与该物种中的其他nod启动子相反,在存在多个nodD基因拷贝的情况下,nodO启动子的活性大大增强。

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