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Novel Alkaloids from Aspergillus fumigatus VDL36, an Endophytic Fungus Associated with Vaccinium dunalianum .

Wei-Hua WangChu-Ran LiXu-Jie QinXiao-Qin YangSi-Da XieQian JiangLi-Hua ZouYing-Jun ZhangGuo-Lei ZhuPing Zhao
Published in: Journal of agricultural and food chemistry (2024)
Eleven alkaloids ( 1 - 11 ) including seven new ones, 1 - 7 , were isolated from the solid fermentation of Aspergillus fumigatus VDL36, an endophytic fungus isolated from the leaves of Vaccinium dunalianum Wight (Ericaceae), a perennial evergreen shrub distributed across the Southwest regions of China, Myanmar, and Vietnam. Their structures were elucidated on the basis of extensive spectroscopic methods. The isolates were evaluated for in vitro antifungal activities against five phytopathogenic fungi ( Fusarium oxysporum , Coriolus versicolor , Fusarium solani , Botrytis cinerea , Fusarium graminearum ). As a result, the new compounds fumigaclavine I ( 1 ), 13-ethoxycyclotryprostatin A ( 5 ), 13-dehydroxycyclotryprostatin A ( 6 ), and 12β-hydroxy-13-oxofumitremorgin C ( 7 ) exhibited antifungal activities with MIC values of 7.8-62.5 μg/mL which were comparable to the two positive controls ketoconazole (MIC = 7.8-31.25 μg/mL) and carbendazim (MIC = 1.95-7.8 μg/mL). Furthermore, compounds 1 and 5 demonstrated potent protective and curative effects against the tomato gray mold in vivo . Preliminary structure-activity relationships of the tested indole diketopiperazine alkaloids indicate that the introduction of a substituent group at position C-13 enhances their biological activities.
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