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Prenylated Flavonoids Isolated from the Root of Sophora flavescens as Potent Antifungal Agents against Botrytis cinerea .

Jun-Xia AnRui WangAn-Ping LiWen ZhangZhibiao NanWei-Qi JiangShao-Yong ZhangZhi-Jun ZhangXiong-Fei LuoHong-Jie LiangYing-Qian Liu
Published in: Journal of agricultural and food chemistry (2024)
Sophora flavescens , a traditional Chinese herb, produces a wide range of secondary metabolites with a broad spectrum of biological activities. In this study, we isolated six isopentenyl flavonoids (1-6) from the roots of S. flavescens and evaluated their activities against phytopathogenic fungi. In vitro activities showed that kurarinone and sophoraflavanone G displayed broad spectrum and superior activities, among which sophoraflavanone G displayed excellent activity against tested fungi, with EC 50 values ranging from 4.76 to 13.94 μg/mL. Notably, kurarinone was easily purified and showed potential activity against Rhizoctonia solani , Botrytis cinerea , and Fusarium graminearum with EC 50 values of 16.12, 16.55, and 16.99 μg/mL, respectively. Consequently, we initially investigated the mechanism of kurarinone against B. cinerea . It was found that kurarinone disrupted cell wall components, impaired cell membrane integrity, increased cell membrane permeability, and affected cellular energy metabolism, thereby exerting its effect against B. cinerea . Therefore, kurarinone is expected to be a potential candidate for the development of plant fungicides.
Keyphrases
  • cell wall
  • ms ms
  • candida albicans
  • endothelial cells
  • atomic force microscopy
  • high speed