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首页> 外文期刊>International Journal of Agriculture and Biology >Characterization of Pseudomonas tolaasii Isolates, Causing Brown Blotch Disease of Mushroom (Agaricus bisporus)
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Characterization of Pseudomonas tolaasii Isolates, Causing Brown Blotch Disease of Mushroom (Agaricus bisporus)

机译:造成蘑菇褐斑病的桃假单胞菌分离物的表征

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A total of 96 Pseudomonas tolaasii isolates were recovered from the suspected Brown blotch infected mushroom caps and cultured on King’s medium B. The LOPAT test results showed Levan and pectinolytic activity, positive oxidase, arginine dihydrolase and hypersensitivity on tobacco. The isolates was identified by the conventional PCR using Pt-1A/Pt 1D1 primers and Real-time PCR. The BLAST analysis of the PCR products showed 98–100% similarities with the strains recovered from the NCBI GenBank database. All the isolates were pathogenic on Agaricus bisporus and slices of potatoes. The Koch s postulates were fulfilled. This is the first record on the characterization of P. tolaasii isolates in west Mediterranean region of Turkey as well as rapid detection of this pathogen directly from the bacterial cell without DNA extraction and from the diseased tissue, respectively by the Real-time PCR.
机译:从疑似布朗斑点感染的蘑菇帽中回收了总共96株Tolaasii假单胞菌,并在King的B培养基上进行了培养。LOPAT测试结果显示了Levan和果胶分解活性,正氧化酶,精氨酸二水解酶和​​对烟草的超敏反应。通过常规PCR,使用Pt-1A / Pt 1D1引物和实时PCR鉴定分离株。 PCR产物的BLAST分析显示与从NCBI GenBank数据库中回收的菌株有98-100%的相似性。所有分离物对双孢蘑菇和马铃薯切片均具有致病性。科赫的假设得以实现。这是关于土耳其西地中海地区的tolaasii分离株的特征的首次记录,以及分别通过实时PCR直接从细菌细胞中快速检测到该病原体而无需提取DNA和从患病组织中进行的记录。

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