首页> 外文期刊>Archives of Phytopathology and Plant Protection >PGPR MEDIATED MANAGEMENT OF STEM BLIGHT OF PHYLLANTHUS AMARUS (SCHUM AND THONN) CAUSED BY CORYNESPORA CASSIICOLA (BERK AND CURT) WEI
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PGPR MEDIATED MANAGEMENT OF STEM BLIGHT OF PHYLLANTHUS AMARUS (SCHUM AND THONN) CAUSED BY CORYNESPORA CASSIICOLA (BERK AND CURT) WEI

机译:PGPR介导的卡氏隐孢子虫(茎和茎)魏引起的空(茎和棘)枯萎病的管理

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摘要

Bacillus subtilis (BSCBE4), Pseudomonas chloror aphis (PA2.3), endophytic P fluorescent (ENPF1) inhibited the mycelial growth of stem blight pathogen Corynespora casiicola (Berk and Curt)Wei under in vitro. All these bacterial isolates produced both hydroxamate and carboxylate type of siderophores But the siderophore production was maximum with the isolate ENPF1. Delivering of talc based formulation of BSCBE4 through seedling dip and foliar application effectively reduced stem blight disease incidence and increased the dry matter production under pot culture and field conditions. Application of BSCBE4, PA23 and ENPF1 increased the defense related enzymes such as peroxidase, polyphenol oxidase, chitinase and beta-1,3 glucanase in P. amarus up to tendays after challenge inoculation with C. cassicola. Native gel electrophoretic analysis revealed that challenge inoculation of pathogen with BSCBE4 and PA23 induced both peroxidase and polyphnol oxidase isoforms.
机译:在体外,枯草芽孢杆菌(BSCBE4),绿脓杆菌(PA2.3),内生P荧光(ENPF1)抑制了枯萎病病原体Corynespora casiicola(Berk and Curt)Wei的菌丝生长。所有这些细菌分离物均产生异羟肟酸酯和羧酸盐类型的铁载体,但分离物ENPF1产生的铁载体最大。通过浸种和叶面施用基于滑石粉的BSCBE4制剂可有效降低茎叶枯病的发病率,并增加盆栽和田间条件下的干物质产量。 BSCBE4,PA23和ENPF1的使用可在挑战接种C. cassicola后的10天之内增加了防御性相关酶,如过氧化物酶,多酚氧化酶,几丁质酶和β-1,3葡聚糖酶。天然凝胶电泳分析表明,用BSCBE4和PA23挑战病原体接种可诱导过氧化物酶和多酚氧化酶同工型。

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