关键词: 1,3,4-oxadiazole thioether 4-substituted mandelic acid derivatives antifungal activity cell membrane integrity morphological study

Mesh : Antifungal Agents / chemistry Fungicides, Industrial / pharmacology Mandelic Acids / pharmacology Oxadiazoles Structure-Activity Relationship

来  源:   DOI:10.3390/ijms24108898   PDF(Pubmed)

Abstract:
Plant diseases caused by phytopathogenic fungi are a serious threat in the process of crop production and cause large economic losses to global agriculture. To obtain high-antifungal-activity compounds with novel action mechanisms, a series of 4-substituted mandelic acid derivatives containing a 1,3,4-oxadiazole moiety were designed and synthesized. In vitro bioassay results revealed that some compounds exhibited excellent activity against the tested fungi. Among them, the EC50 values of E13 against Gibberella saubinetii (G. saubinetii), E6 against Verticillium dahlia (V. dahlia), and E18 against Sclerotinia sclerotiorum (S. sclerotiorum) were 20.4, 12.7, and 8.0 mg/L, respectively, which were highly superior to that of the commercialized fungicide mandipropamid. The morphological studies of G. saubinetii with a fluorescence microscope (FM) and scanning electron microscope (SEM) indicated that E13 broke the surface of the hyphae and destroyed cell membrane integrity with increased concentration, thereby inhibiting fungal reproduction. Further cytoplasmic content leakage determination results showed a dramatic increase of the nucleic acid and protein concentrations in mycelia with E13 treatment, which also indicated that the title compound E13 could destroy cell membrane integrity and affect the growth of fungi. These results provide important information for further study of the mechanism of action of mandelic acid derivatives and their structural derivatization.
摘要:
植物病原真菌引起的植物病害是作物生产过程中的严重威胁,给全球农业造成巨大的经济损失。为了获得具有新作用机制的高抗真菌活性化合物,设计并合成了一系列含有1,3,4-恶二唑部分的4-取代扁桃酸衍生物。体外生物测定结果表明,一些化合物对测试的真菌表现出优异的活性。其中,E13对赤霉素的EC50值(G.saubinetii),E6抗黄萎病菌大丽花(V.大丽花),和E18抗菌核病(S.硬核)分别为20.4、12.7和8.0mg/L,分别,其高度优于商业化的杀菌剂反式丙酰胺。用荧光显微镜(FM)和扫描电子显微镜(SEM)对G.saubinetii的形态学研究表明,E13破坏了菌丝的表面并破坏了细胞膜的完整性,随着浓度的增加,从而抑制真菌繁殖。进一步的细胞质含量泄漏测定结果表明,E13处理后,菌丝体中的核酸和蛋白质浓度急剧增加,这也表明标题化合物E13可以破坏细胞膜的完整性并影响真菌的生长。这些结果为进一步研究扁桃酸衍生物的作用机理及其结构衍生化提供了重要信息。
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