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首页> 外文期刊>Journal of bacteriology >Regulation of pelZ, a gene of the pelB-pelC cluster encoding a new pectate lyase of Erwinia chrysanthemi 3937.
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Regulation of pelZ, a gene of the pelB-pelC cluster encoding a new pectate lyase of Erwinia chrysanthemi 3937.

机译:pelZ的调节,pelZ是pelB-pelC簇的一个基因,编码一个新的果糖菊欧文氏菌3937的果胶酸裂合酶。

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The phytopathogenic enterobacterium Erwinia chrysanthemi 3937 produces five major and several secondary endo-pectate lyases encoded by the pel genes. Most of these genes are arranged in clusters on the bacterial chromosome. The genomic region surrounding the pelB-pelC cluster was supposed to be involved in the regulation of PelB and PelC synthesis. We demonstrated that the variation of pelB expression resulted from the titration of a regulatory protein by the gene adjacent to pelC. This gene was renamed pelZ since it encodes a protein of 420 amino acids with an endo-pectate lyase activity. Regulation of pelZ expression was investigated by using transcriptional fusions and a study of mRNA synthesis. Its transcription depends on different environmental conditions. It is induced in planta and in the presence of pectic catabolite products. This induction seems to be partially mediated by the KdgR protein but does not result from a direct interaction of KdgR with the pelZ 5' region. The transcription of pelZ leads to the synthesis of a monocistronic mRNA. However, the synthesis of a polycistronic mRNA from the pelC promoter, regulated by KdgR, is responsible for increased production of PelZ under inducing conditions. pelZ transcription is also controlled by pecT, which regulates some other pel genes, but it is independent of the pecS regulatory locus. The pelZ gene appears to be widespread in different strains of E. chrysanthemi. Moreover, a gene homologous to pelZ exists in Erwinia carotovora subsp. atroseptica adjacent to the cluster containing the pectate lyase-encoding genes pel1, pel2, and pel3. This conservation could reflect a significant role of PelZ in the pectinolytic system of Erwiniae. We showed pelZ is not a predominant virulence factor of E. chrysanthemi but is involved in host specificity.
机译:植物病原性肠杆菌欧文氏杆菌3937产生由pel基因编码的五种主要的和几种继发的果胶内切酶。这些基因大多数都排列在细菌染色体上的簇中。 pelB-pelC簇周围的基因组区域应该参与了PelB和PelC合成的调控。我们证明了pelB表达的变化是由邻近pelC的基因滴定调节蛋白引起的。该基因被命名为pelZ,因为它编码具有果胶内切酶活性的420个氨基酸的蛋白质。通过使用转录融合和mRNA合成研究来研究pelZ表达的调控。其转录取决于不同的环境条件。它在植物和果胶分解代谢产物的存在下被诱导。这种诱导似乎部分由KdgR蛋白介导,但不是KdgR与pelZ 5'区域的直接相互作用导致的。 pelZ的转录导致单顺反子mRNA的合成。但是,由pelC启动子合成的多顺反子mRNA,受KdgR调节,可在诱导条件下增加PelZ的产量。 pelZ转录也受pecT控制,后者可调节其他一些pel基因,但与pecS调节位点无关。 pelZ基因似乎广泛分布在不同的金黄色葡萄球菌菌株中。此外,在胡萝卜欧文氏菌亚种中存在与pelZ同源的基因。与含有果胶酸裂解酶编码基因pel1,pel2和pel3的簇相邻的atroseptica。这种保守性可能反映了PelZ在欧文氏菌的果胶分解系统中的重要作用。我们显示pelZ不是菊花大肠杆菌的主要毒力因子,但与宿主特异性有关。

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