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首页> 外文期刊>Microbiological Research >Differential expression of pectolytic enzyme genes in Xanthomonas citri subsp citri and demonstration that pectate lyase Pel3 is required for the formation of citrus canker
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Differential expression of pectolytic enzyme genes in Xanthomonas citri subsp citri and demonstration that pectate lyase Pel3 is required for the formation of citrus canker

机译:柑橘黄单胞菌中的果胶分解酶基因的差异表达,并证明果胶裂解酶Pel3是柑桔溃疡病形成所必需的

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Bacterial canker, caused by Xanthomonas citri subsp. citri (Xcc), is one of the most destructive diseases of citrus. The pectolytic enzymes produced by phytobacteria are important virulence factors involved in tissue maceration, electrolyte loss and cell death of host plants. In this study, the promoter activity of the pectolytic enzyme genes pell, pel2, pel3, pgIA, and peh-1 were investigated in Xcc XW19 strain using the beta-glucuronidase (GUS) gene as a reporter. GUS activity expressed under the control of the pell, pel3, pglA, and peh-1 gene promoters positively correlated with bacterial growth. These gene promoters displayed high GUS activity in the presence of sodium polypectate. In addition, the four genes were induced in XVM2 minimal medium. However, only pell was subjected to catabolite repression by glucose. GUS activity was significantly enhanced in the XW19-derived reporter strains after they were inoculated into the leaves of Mexican lime and grapefruit, suggesting the involvement of the pell pel3, pglA, and peh-1 genes in XW19 pathogenesis. The pel3 promoter produced the highest GUS activity under all test conditions, whereas no GUS activity was detected using the pel2 promoter in vitro and in planta. In comparison with wild type Xcc, a pel3 mutant generated from Xcc XW19 using unmarked mutagenesis displayed reduced growth and induced smaller canker lesions on the leaves of Mexican lime, demonstrating that Pel3 of Xcc strain XI/V19 is a virulence factor. (C) 2016 Published by Elsevier GmbH.
机译:Xanthomonas citri subsp。引起的细菌性溃疡病。柠檬(Xcc)是柑橘最具破坏性的疾病之一。植物细菌产生的果胶分解酶是重要的毒力因子,参与宿主植物的组织浸润,电解质损失和细胞死亡。在这项研究中,使用β-葡糖醛酸糖苷酶(GUS)基因作为报告基因,研究了Xcc XW19菌株中果胶分解酶基因pell,pel2,pel3,pgIA和peh-1的启动子活性。在pell,pel3,pglA和peh-1基因启动子的控制下表达的GUS活性与细菌生长呈正相关。在聚果酸钠存在下,这些基因启动子显示出高的GUS活性。此外,在XVM2基本培养基中诱导了这四个基因。但是,只有法术受到葡萄糖的分解代谢物抑制。在将XW19衍生的报告菌株接种到墨西哥石灰和葡萄柚的叶子中后,GUS活性显着增强,表明pell pel3,pglA和peh-1基因参与了XW19的发病机理。 pel3启动子在所有测试条件下均产生最高的GUS活性,而在体外和植物中使用pel2启动子均未检测到GUS活性。与野生型Xcc相比,使用无标记诱变从Xcc XW19产生的pel3突变体显示出生长减慢,并在墨西哥石灰的叶片上引起较小的溃疡病,表明Xcc菌株XI / V19的Pel3是一种致病因子。 (C)2016由Elsevier GmbH发布。

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