首页> 外文会议>International Conference on Pseudomonas Syringae Pathovars and Related Pathogens >Characterisation of an Inhibitory Strainof Pseudomonas syringae pv. syringaewith Potential as a Biocontrol Agentfor Bacterial Blight on Soybean
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Characterisation of an Inhibitory Strainof Pseudomonas syringae pv. syringaewith Potential as a Biocontrol Agentfor Bacterial Blight on Soybean

机译:抑制抑制菌毒素乳香菌菌菌毒素PV的特征。用于细菌对大豆的细菌枯萎的毒剂作为生物控制潜力

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The soybean epiphyte Pseudomonas syringae pv. syringae 22d/93(Pss22d) exhibits strong potential to control Pseudomonas syringae pv. glycinea(Psg), the causal agent of bacterial blight. Under greenhouse and field conditions theantagonism has been proven, but the underlying mechanisms are unclear, up to now.The secondary metabolites are of particular interest for this antagonism. We focus ourinvestigation on the influence of produced toxins of the biological control system. The antagonist produces the well-known syringomycin, syringopeptin and oneunknown toxin, which inhibits the pathogen in vitro. The unknown toxin wasdetected by an agar diffusion bioassay using Psg as indicator strain. This growthinhibition was reversed by arginine and not by argininosuccinate, suggesting that theunknown toxin could interfere with this step of citrulline/arginine biosynthesis. Via marker exchange mutagenesis in genes coding for nonribosomal proteinsynthesis responsible for initial steps in biosynthesis of syringomycin (syrE) andsyringopeptin (sypA), toxin negative mutants were constructed. Subsequently, adouble mutant in which both genes were deleted was constructed, as well. In plantacoinoculation experiments with the double mutant of Pss22d and the pathogenindicated that syringomycin and syringopeptin did not affect the antagonism.
机译:大豆骨骺假单胞菌皂苷PV。 Syringae 22d / 93(pss22d)表现出强大的潜力来控制假单胞菌皂苷PV。甘氨酸(PSG),细菌枯萎病剂。在温室和现场条件下,据证明,潜在的机制目前尚不清楚。次级代谢产物对这种拮抗作用特别感兴趣。我们将OutInveRation重点放弃了生物控制系统产生的毒素的影响。拮抗剂产生了众所周知的倾向霉素,槲皮素和oneunknown毒素,其抑制体外病原体。通过琼脂扩散生物测定使用PSG作为指示菌株的未知毒素。这种增长抑制因素是由精氨酸而不是精氨酸源逆转,这表明南京毒素可能会干扰瓜氨酸/精氨酸生物合成的这一步骤。通过标记交换诱变在编码非纤维素蛋白质合成的基因中,其负责掺量霉素(SYRE)和过敏肽(SYPA)的生物合成中的初始步骤,构建毒素负突变体。随后,构建缺失两个基因的双突变体。在PersacoInculation实验中,PSS22D的双突变体和含入霉素和槲皮素的病原体不影响拮抗作用。

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