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A novel rhizobacterium Bk7 for biological control of brown sheath rot of rice caused by Pseudomonas fuscovaginae and its mode of action

机译:一种新型的根瘤菌Bk7,用于生物防治褐斑假单胞菌引起的水稻褐鞘腐烂及其作用方式

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The study presents the first report on biocontrol of brown sheath rot disease of rice caused by Pseudomonas fuscovaginae using rhizo-bacterial isolate Bacillus amyloliquefaciens Bk7. Four potential bioactive antagonists were selected from 120 Bacillus isolates. Results obtained from in vitro laboratory assay showed that rhizosphere bacterial strain Bk7 and its metabolites significantly suppressed the growth of Pseudomonas fuscovaginae with 93 % efficacy. In glasshouse experiments, strain Bk7 exhibited biocontrol efficacy of 76.6 % by reducing the disease incidence to 16.9 %, compared to 72.8 % observed in control treatment. In addition, the isolate Bk7 showed the growth promotion efficacy of plant height (GPE, 46.4 %) and fresh weight (GPE, 84.3 %). Characterization of isolate Bk7 revealed its strong capability for biofilm formation, inorganic phosphate solubilization and production of high amounts of Indole-3 acetic acid, siderophores and ammonia in vitro. Results obtained from multiplex PCR assay confirmed the presence of five lipopeptide biosynthetic gene markers (srfAA, fenD, bmyB, bacA and ituC) in the genome of strain Bk7. Moreover, Real-time qPCR of these genes demonstrated that surfactin, iturin and bacylisin coding genes were highly expressed in response to P. fuscovaginae exposure in vitro. Rhizosphere bacterial strain Bk7 was identified as B. amyloliquefaciens strain Bk7 based on the analysis of 16S rDNA internal transcribed spacer sequences and a fatty acid methyl ester analysis. The results obtained from this study showed the potential usefulness of Bk7 as a biocontrol agent in disease control of rice brown sheath rot.
机译:该研究首次报道了根瘤菌分离的芽孢杆菌芽孢杆菌Bk7对褐褐假单胞菌引起的水稻褐鞘腐病的生物防治。从120种芽孢杆菌分离物中选择了四种潜在的生物活性拮抗剂。从体外实验室测定获得的结果表明,根际细菌菌株Bk7及其代谢产物显着抑制褐藻假单胞菌的生长,功效为93%。在温室实验中,菌株Bk7通过将疾病发生率降低到16.9%,显示出76.6%的生物防治效力,而对照处理中观察到的为72.8%。另外,分离株Bk7显示出株高(GPE,46.4%)和鲜重(GPE,84.3%)的生长促进功效。分离物Bk7的表征显示了其强大的生物膜形成能力,无机磷酸盐增溶能力以及体外大量Indole-3乙酸,铁载体和氨的产生。从多重PCR分析获得的结果证实了菌株Bk7的基因组中存在五个脂肽生物合成基因标记(srfAA,fenD,bmyB,bacA和ituC)。此外,这些基因的实时qPCR显示,在体外响应褐藻假单胞菌暴露后,surfactin,iturin和bacylisin编码基因高度表达。基于对16S rDNA内部转录间隔区序列的分析和脂肪酸甲酯分析,将根际细菌菌株Bk7鉴定为解淀粉芽孢杆菌菌株Bk7。这项研究获得的结果表明,Bk7作为生物防治剂在水稻褐皮腐烂病害防治中的潜在用途。

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