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首页> 外文期刊>Journal of applied microbiology >Use of green fluorescent protein-based reporters to monitor balanced production of antifungal compounds in the biocontrol agent Pseudomonas fluorescens CHA0
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Use of green fluorescent protein-based reporters to monitor balanced production of antifungal compounds in the biocontrol agent Pseudomonas fluorescens CHA0

机译:使用基于绿色荧光蛋白的报道分子监测生物防治剂荧光假单胞菌CHA0中抗真菌化合物的平衡产生

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Aims: To develop reporter constructs based on stable and unstable variants of the green fluorescent protein ( GFP) for monitoring balanced production of antifungal compounds that are crucial for the capacity of the root- colonizing Pseudomonas fluorescens strain CHA0 to control plant diseases caused by soil- borne pathogenic fungi.Methods and Results: Pseudomonas fluorescens CHA0 produces the three antifungal metabolites 2,4- diacetylphloroglucinol ( DAPG), pyoluteorin ( PLT) and pyrrolnitrin ( PRN). The gfp[ mut3] and gfp[ AAV] reporter genes were fused to the promoter regions of the DAPG, PLT and PRN biosynthetic genes. The reporter fusions were then used to follow the kinetics of expression of the three antifungal metabolites in a microplate assay. DAPG and PLT were found to display an inverse relationship in which each metabolite activates its own biosynthesis while repressing the synthesis of the other metabolite. PRN appears not to be involved in this balance. However, the microbial and plant phenolic metabolite salicylate was found to interfere with the expression of both DAPG and PLT.Conclusions: The results obtained provide evidence that P. fluorescens CHA0 may keep the antifungal compounds DAPG and PLT at a fine- tuned balance that can be affected by certain microbial and plant phenolics. Significance and Impact of the Study: To our knowledge, the present study is the first to use stable and unstable GFP variants to study antibiotic gene expression in a biocontrol pseudomonad. The developed reporter fusions will be a highly valuable tool to study in situ expression of this bacterial biocontrol trait on plant roots, i. e. at the site of pathogen suppression.
机译:目的:开发基于绿色荧光蛋白(GFP)稳定和不稳定变体的报告基因构建体,以监测抗真菌化合物的均衡产生,这些真菌合成物对于生根的荧光假单胞菌CHA0控制由土壤致病的植物病害的能力至关重要方法和结果:荧光假单胞菌CHA0产生3种抗真菌代谢物2,4-二乙酰基间苯三酚(DAPG),脓黄素(PLT)和吡咯硝菌素(PRN)。将gfp [mut3]和gfp [AAV]报告基因融合到DAPG,PLT和PRN生物合成基因的启动子区域。然后,在微孔板测定中,使用报告基因融合物追踪三种抗真菌代谢物表达的动力学。发现DAPG和PLT显示反比关系,其中每种代谢物激活其自身的生物合成,同时抑制另一种代谢物的合成。 PRN似乎不参与此平衡。然而,发现微生物和植物酚类代谢产物水杨酸酯会干扰DAPG和PLT的表达。结论:所得结果提供了荧光假单胞菌CHA0可以使抗真菌化合物DAPG和PLT保持微调的平衡,从而可以受到某些微生物和植物酚类物质的影响。研究的意义和影响:据我们所知,本研究是第一个使用稳定和不稳定的GFP变体研究生物控制假单胞菌中抗生素基因表达的研究。开发的报道基因融合蛋白将是研究这种细菌生物防治性状在植物根系上原位表达的极有价值的工具。 e。在病原体抑制部位。

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