{"title":"Characterization of Indigoidine Biosynthetic Genes in Erwinia chrysanthemi and Role of This Blue Pigment in Pathogenicity","authors":"S. Reverchon, C. Rouanet, D. Expert, W. Nasser","doi":"10.1128/JB.184.3.654-665.2002","DOIUrl":null,"url":null,"abstract":"ABSTRACT 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.","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":"119 1","pages":"654 - 665"},"PeriodicalIF":2.7000,"publicationDate":"2002-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1128/JB.184.3.654-665.2002","citationCount":"196","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/JB.184.3.654-665.2002","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 196
Abstract
ABSTRACT 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.
植物致病菌菊花Erwinia的果胶酸裂解酶是主要的毒力决定因素,它的产生是由一个涉及多种调节蛋白的复杂网络调节的。其中一种调节因子PecS也控制一种被称为靛蓝素的蓝色色素的合成。由于这种色素的产生在野生型菌株中是隐秘的,因此通过筛选pecS突变体中Tn5-B21插入文库,分离出缺乏靛蓝素合成的菊花E. d .突变体。这些突变位于pecM的下游,靠近pecS-pecM的调控位点。该DNA区域的序列分析显示了三个开放阅读框,indA, indB和indC,参与靛蓝苷的生物合成。没有特定的功能可以分配给IndA。相比之下,IndB与参与抗生素合成的各种磷酸酶具有相似性,而IndC与许多非核糖体肽合成酶(NRPS)具有显著的同源性。IndC产物包含一个腺苷化结构域,显示谷氨酰胺识别的特征序列DAWCFGLI和一个类似于各种噻唑形成NRPS的氧化结构域。这些数据表明,谷氨酰胺是靛蓝素的前体。我们假设靛蓝素是由两个谷氨酰胺分子缩合而成的,这两个谷氨酰胺分子先前通过分子内酰胺键形成环化,然后脱氢。在pecS背景下,ind基因的表达被强烈抑制,表明pecS是这种次生代谢物合成的主要调节剂。DNA带移分析支持PecS蛋白通过结合indA和indC启动子区域抑制indA和indC表达的模型。通过pecS,靛蓝素与毒力因子产生之间的调控联系使我们探索了靛蓝素在菊花致病性中的潜在作用。靛蓝素生产受损的突变体不能引起盆栽圣保利亚的系统性入侵。此外,靛蓝素的产生增加了对氧化应激的抵抗力,这表明靛蓝素可以保护细菌免受植物防御反应过程中产生的活性氧的侵害。
期刊介绍:
The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.