甘蓝链格孢菌
索拉尼链格孢菌
尖孢镰刀菌
灰葡萄孢菌
链格孢
化学
内生真菌在植物防御中的应用
黑斑病
多菌灵
植物
微生物学
生物
生物化学
杀菌剂
拟南芥
突变体
基因
作者
Weihua Wang,Xulu Luo,Xu‐Jie Qin,Jiandong Tang,Sida Xie,Kai‐Ze Shen,Guo‐Lei Zhu,Ping Zhao
标识
DOI:10.1002/cbdv.202502391
摘要
ABSTRACT Co‐culturing the endophytic fungus Clonostachys rosea VDGF806 from Vaccinium dunalianum Wight with Alternaria brassicicola on solid rice medium resulted in the production of two new compounds, altenarizine C ( 1 ) and clonbrasterol A ( 2 ), along with three known ones ( 3 – 5 ). Their structures were identified based on extensive spectroscopic analyses and electronic circular dichroism experiments. The isolated compounds were evaluated for in vitro antifungal activities against five phytopathogenic fungi ( Fusarium oxysporum , Alternaria brassicae , F. solani , Botrytis cinerea , and F. graminearum ). Clonbrasterol A ( 2 ) and nafuredin ( 3 ) showed antifungal activity, with minimum inhibitory concentration (MIC) values of 7.8–62.5 µg/mL. In comparison, the positive controls thiabendazole and carbendazim had MIC values of 0.98–3.9 and 1.95–3.9 µg/mL, respectively. Molecular docking analysis suggests that clonbrasterol A ( 2 ) targets CYP51, while nafuredin ( 3 ) inhibits fatty acid synthase to exert antifungal activity. These findings validate fungal co‐cultivation as an effective strategy for discovering novel bioactive metabolites.
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