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Method For Screening Pseudomonas Protegens Mutant Strain, And Application Thereof In Biological Control

机译:假单胞菌蛋白突变株的筛选方法及其在生物防治中的应用

摘要

Provided are Pseudomonas protegens mutant strain Pf5-NiF, Pf5-ΔretS, or Pf5-ΔretS-NiF, and a screening method therefor and an application thereof. By means of Red/ET recombination and direct cloning technologies, the NiF nitrogen fixation gene island in the genome of Pseudomonas stutzeri DSM4166, taken as a whole, is cloned into the genome of Pseudomonas protegens Pf5, so as to heterologously express the same successfully to obtain a genetically engineered strain Pf5-NiF, thereby bringing a biological nitrogen fixation function to Pseudomonas protegens Pf5 which does not own a biological nitrogen fixation function. In addition, gene-directed markerless knockout of retS gene in the genome of Pseudomonas protegens Pf5 is performed to obtain a genetically engineered strain Pf5-ΔretS. Thus, the expression levels of an antibiotic 2,4-diacetylphloroglucinol and red pigment are increased, and a mutant strain of Pseudomonas protegens Pf5 having a stronger bactericidal activity is obtained.
机译:提供了假单胞菌蛋白突变株Pf5-NiF,Pf5-ΔretS或Pf5-ΔretS-NiF及其筛选方法和应用。通过Red / ET重组和直接克隆技术,将 Putudomonas stutzeri DSM4166基因组中的NiF固氮基因岛作为一个整体克隆到 Pseudomonas protegens < / I> Pf5,以便成功地异源表达以获得基因工程菌株Pf5-NiF,从而为不具有生物固氮功能的假单胞菌蛋白 Pf5带来生物固氮功能。另外,进行了

假单胞菌蛋白质 5基因组中retS基因的基因指导的无标记敲除,以获得基因工程菌株Pf5-ΔretS。因此,增加了抗生素2,4-二乙酰基间苯三酚和红色色素的表达水平,并获得了具有更强杀菌活性的假单胞菌蛋白Pf5的突变菌株。

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