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首页> 外文期刊>Microbiological Research >HarpinPss-mediated enhancement in growth and biological control of late leaf spot in groundnut by a chlorothalonil-tolerant Bacillus thuringiensis SFC24.
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HarpinPss-mediated enhancement in growth and biological control of late leaf spot in groundnut by a chlorothalonil-tolerant Bacillus thuringiensis SFC24.

机译:Harpin Pss 介导的耐百菌清苏云金芽孢杆菌SFC24增强花生后期叶斑的生长和生物学控制。

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Chemical and biological approaches have been adopted to increase the growth and yield of crops and reduce loss due to diseases. We have adopted an integrated approach, where both direct antagonism and induced resistance were combined to reduce the incidence of late leaf spot (LLS) disease in groundnut caused by Phaeoisariopsis personata. Chitinolytic chlorothalonil-tolerant soil bacterium Bacillus thuringiensis SFC24 (Bt SFC24) was manipulated in vitro to express secretable form of elicitor protein harpinPss of Pseudomonas syringae pv. syringae. Severity of the LLS decreased by 65% when the leaves were sprayed with B. thuringiensis expressing harpinPss (Bt-pss). As seed treatment, there was an increase in growth of groundnut. Bt and Bt-pss accounted to 13% and 36% increase in shoot length. Expression of a secretable form of harpinPss thus improved the ability of B. thuringiensis SFC24 to promote growth and control LLS in groundnut. In this new approach a chlorothalonil-tolerant chitinolytic bacterium was genetically engineered to secrete elicitor harpinPss for dual benefit of growth promotion and disease control.Digital Object Identifier http://dx.doi.org/10.1016/j.micres.2011.07.002
机译:已经采用化学和生物学方法来增加农作物的生长和产量并减少由于疾病引起的损失。我们采用了一种综合方法,将直接拮抗作用和诱导抗性相结合,以减少花生由 Phaeoisariopsis personata 引起的晚叶斑病(LLS)发病率。 苏云金芽胞杆菌耐土壤几丁质的苏云金芽孢杆菌 SFC24(Bt SFC24)在体外进行表达,表达的分泌蛋白harpin Pss > Pseudomonas syringae pv。 丁香科。当用B喷洒叶子时,LLS的严重程度降低了65%。苏云金芽孢杆菌表达harpinPss(Bt-pss)。作为种子处理,花生的生长有所增加。 Bt和Bt-pss分别导致芽长增加13%和36%。因此,harpin Pss 的一种秘密形式的表达提高了 B的能力。苏云金 SFC24促进花生的生长并控制LLS。在这种新方法中,经过基因工程改造的耐百菌清的几丁质分解细菌可以分泌激发子harpin Pss ,从而具有促进生长和控制疾病的双重优势。数字对象标识符http://dx.doi.org/10.1016/ j.micres.2011.07.002

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