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首页> 外文期刊>Journal of bacteriology >Characterization of Indigoidine Biosynthetic Genes in Erwinia chrysanthemi and Role of This Blue Pigment in Pathogenicity
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Characterization of Indigoidine Biosynthetic Genes in Erwinia chrysanthemi and Role of This Blue Pigment in Pathogenicity

机译:菊花欧文氏菌中靛蓝生物合成基因的鉴定及其在致病性中的作用

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In the plant-pathogenic bacterium Erwinia chrysanthemi production of pectate lyases, the main virulence determinant, is modulated by a complex network involving several regulatory proteins. One of these regulators, PecS, also controls the synthesis of a blue pigment identified as indigoidine. Since production of this pigment is cryptic in the wild-type strain, E. chrysanthemi ind mutants deficient in indigoidine synthesis were isolated by screening a library of Tn5-B21 insertions in a pecS mutant. These ind mutations were localized close to the regulatory pecS-pecM locus, immediately downstream of pecM. Sequence analysis of this DNA region revealed three open reading frames, indA, indB, and indC, involved in indigoidine biosynthesis. No specific function could be assigned to IndA. In contrast, IndB displays similarity to various phosphatases involved in antibiotic synthesis and IndC reveals significant homology with many nonribosomal peptide synthetases (NRPS). The IndC product contains an adenylation domain showing the signature sequence DAWCFGLI for glutamine recognition and an oxidation domain similar to that found in various thiazole-forming NRPS. These data suggest that glutamine is the precursor of indigoidine. We assume that indigoidine results from the condensation of two glutamine molecules that have been previously cyclized by intramolecular amide bond formation and then dehydrogenated. Expression of ind genes is strongly derepressed in the pecS background, indicating that PecS is the main regulator of this secondary metabolite synthesis. DNA band shift assays support a model whereby the PecS protein represses indA and indC expression by binding to indA and indC promoter regions. The regulatory link, via pecS, between indigoidine and virulence factor production led us to explore a potential role of indigoidine in E. chrysanthemi pathogenicity. Mutants impaired in indigoidine production were unable to cause systemic invasion of potted Saintpaulia ionantha. Moreover, indigoidine production conferred an increased resistance to oxidative stress, indicating that indigoidine may protect the bacteria against the reactive oxygen species generated during the plant defense response.
机译:在植物致病细菌中,果胶酸裂解酶的生产主要是由果胶酸裂解酶(Erwinia chrysanthemi )产生,而果胶酸裂解酶是由涉及几种调控蛋白的复杂网络调节的。这些调节剂之一,PecS,也控制着蓝色靛蓝素的合成。由于这种色素的产生在野生型菌株 E中是隐性的。通过筛选 pecS 突变体中Tn 5 -B21插入的文库,分离出缺乏靛蓝定合成的chrysanthemi ind 突变体。这些 ind 突变位于 pecM 下游的调控 pecS-pecM 位点附近。该DNA区域的序列分析显示了三个开放阅读框,分别是 indA indB indC ,它们参与了靛蓝的生物合成。没有特定功能可以分配给IndA。相反,IndB显示与参与抗生素合成的各种磷酸酶相似,IndC显示与许多非核糖体肽合成酶(NRPS)具有显着同源性。 IndC产品包含一个腺苷酸化域,该域显示出用于谷氨酰胺识别的签名序列DAWCFGLI,其氧化域与各种形成噻唑的NRPS中的氧化域相似。这些数据表明谷氨酰胺是茚满丁的前体。我们假定靛蓝定是由两个谷氨酰胺分子的缩合产生的,这两个谷氨酰胺分子先前已通过分子内酰胺键的形成而环化,然后脱氢。 ind 基因的表达在 pecS 背景中被强烈抑制,这表明PecS是这种次级代谢产物合成的主要调节剂。 DNA带移分析支持PecS蛋白通过结合 indA indC 抑制 indA indC 表达的模型启动子区域。通过 pecS 在靛蓝定和毒力因子产生之间的调控联系使我们探索了靛蓝定在 E中的潜在作用。菊花的致病性。靛靛苷生产受损的突变体无法引起盆栽的 Saintpaulia ionantha 的全身入侵。此外,靛蓝苷的产生赋予对氧化应激的增加的抵抗力,这表明靛蓝苷可以保护细菌免受植物防御反应期间产生的活性氧的影响。

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