首页> 外文期刊>Molecular Plant-Microbe Interactions >Cloning and Characterization of a Cyclic Peptide Synthetase Gene from Alternaria alternata Apple Pathotype Whose Product Is Involved in AM-Toxin Synthesis and Pathogenicity
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Cloning and Characterization of a Cyclic Peptide Synthetase Gene from Alternaria alternata Apple Pathotype Whose Product Is Involved in AM-Toxin Synthesis and Pathogenicity

机译:苹果黑粉病病原菌参与AM-毒素合成及致病性的环肽合成酶基因的克隆与鉴定

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Alternaria alternata apple pathotype causes Alternaria blotch of susceptible apple cultivars through the production of a cyclic peptide host-specific toxin, AM-toxin. PCR (polymerase chain reaction), with primers designed to conserved domains of peptide synthetase genes, amplified several products from A. alternata apple pathotype that showed high similarity to other fungal peptide synthetases and were specific to the apple pathotype. Screening of a Lambda Zap genomic library with these PCR-generated probes identified overlapping clones containing a complete cyclic peptide synthetase gene of 13.1 kb in length with no introns. Disruption of this gene, designated AM-toxin synthetase ( AMT ), by transformation of wild-type A. alternata apple pathotype with disruption vectors resulted in toxin-minus mutants, which were also unable to cause disease symptoms on susceptible apple cultivars. AM-toxin synthetase is therefore a primary determinant of virulence and specificity in the A. alternata apple pathotype/apple interaction.
机译:交链孢霉苹果病原体通过产生环状肽宿主特异性毒素AM毒素而引起易感苹果品种的交链孢菌斑。 PCR(聚合酶链反应)使用设计用于保守肽合成酶基因结构域的引物,扩增了来自互生曲霉苹果病理型的几种产物,这些产物与其他真菌肽合成酶具有高度相似性,并且对苹果病理型具有特异性。用这些PCR产生的探针筛选Lambda Zap基因组文库,鉴定出重叠的克隆,这些克隆包含长度为13.1 kb的完整环肽合成酶基因,没有内含子。通过用破坏载体转化野生型苹果交链孢菌苹果病原型来破坏该基因,称为AM毒素合成酶(AMT),导致产生了毒素减号突变体,该突变体也无法在易感苹果品种上引起疾病症状。因此,AM-毒素合成酶是交替链球菌苹果病原型/苹果相互作用中毒力和特异性的主要决定因素。

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