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首页> 外文期刊>Current Microbiology: An International Journal >Antifungal Action of Antifungalmycin N2 Against Rhizoctonia solani by Disrupting Cell Membrane and Inhibiting Succinate Dehydrogenase
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Antifungal Action of Antifungalmycin N2 Against Rhizoctonia solani by Disrupting Cell Membrane and Inhibiting Succinate Dehydrogenase

机译:抗细胞膜抗血红素酰基菌菌抗氨基霉素的抗真菌作用及抑制琥珀酸脱氢酶

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摘要

Antifungalmycin N2 (3-methyl-3,5-amino-4-vinyl-2-pyrone, C6H7O2N) was a novel structural antifungal metabolite produced by Streptomyces sp. strain N2. Our previous study reported that the antagonistic interaction between antifungalmycin N2 and Rhizoctonia solani was accompanied by an oxidative stress in R. solani cell, indicating a probable damage occurred in the cell membranes and mitochondria. To verify this, the present study focused on investigating the effects of antifungalmycin N2 on the structure and function of cell membranes and mitochondria of R. solani. Morphological observations in transmission electron microscopy and fluorescence microscope showed that cell membranes of R. solani were damaged, and its cytoplasmic organelles were disorganized when treated with antifungalmycin N2. Meanwhile, the kinetics of membrane-related physiological and biochemical parameters, such as the increased malondialdehyde level, dropped ergosterol formation, and enhanced electrical conductivity in R. solani mycelia, further confirmed that antifungalmycin N2 would disrupt the cell membrane structure and function. More significantly, antifungalmycin N2 had a significantly inhibitory effect on the succinate dehydrogenase (SDH) activity of R. solani, and indicated that the mode and site of action of antifungalmycin N2 against R. solani might be similar to the existing succinate dehydrogenase inhibitors fungicides by binding in the ubiquinone-binding site. In conclusion, the above results demonstrated that the mode and site of action of antifungalmycin N2 targeted to cell membrane and SDH of R. solani, thus exerting the antifungal activity by damaging cell membrane structure and function, together with inhibiting the SDH activity.
机译:抗真菌霉素N 2(3-甲基-3,5-氨基-4-乙烯基-2-吡喃酮,C6H7O2N)是由Streptomyces SP产生的新型结构抗真菌代谢物。菌株N2。我们以前的研究报道说,抗真菌霉素N 2和Rhizoctonia Solani之间的拮抗相互作用伴随着R.Solani细胞中的氧化应激,表明细胞膜和线粒体发生的可能损伤。为了验证这一点,本研究旨在研究抗氨苄青素N2对茄膜细胞膜和线粒体的结构和功能的影响。透射电子显微镜和荧光显微镜中的形态学观察表明,R.Solani的细胞膜损坏,并且当用抗真菌霉素N 2处理时,其细胞质细胞细胞被混乱。同时,膜相关的生理和生化参数的动力学,例如丙二醛水平增加,替代的Ergosterol形成和R.Solani Mycelia中增强的导电性,进一步证实了抗真菌霉素N2会破坏细胞膜结构和功能。更重要的是,抗胆霉素N2对R.索尔甘油的琥珀酸脱氢酶(SDH)活性具有显着的抑制作用,并表明抗胺霉素N2对R.Solani的作用模式和部位可能与现有的琥珀酸脱氢酶抑制剂杀菌剂相似在泛醌结合位点中结合。总之,上述结果证明,抗氨基霉素N 2的靶向细胞膜和R.Solani的SDH的方法和部位,从而通过损害细胞膜结构和抑制SDH活性来施加抗真菌活性。

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