Document Type

Article

Publication Date

2005

Abstract

Leaf spots and root rots are major fungal diseases in Camptotheca acuminata that limit cultivation of the plant for camptothecin (CPT), a promising anticancer and antiviral alkaloid. Bioassays showed that pure CPT and flavonoids (trifolin and hyperoside) isolated from Camptotheca effectively control fungal pathogens in vitro, including Alternaria alternata, Epicoccum nigrum, Pestalotia guepinii, Drechslera sp., and Fusarium avenaceum, although antifungal activity of these compounds in the plant is limited. CPT inhibited mycelial growth by approximately 50% (EC50) at 10−30 μg/mL and fully inhibited growth at 75−125 μg/mL. The flavonoids were less effective than CPT at 50 μg/mL, particularly within 20 days after treatment, but more effective at 100 or 150 μg/mL. CPT, trifolin, and hyperoside may serve as leads for the development of fungicides.

Comments

Li, Shiyou, Zhizhen Zhang, Abigail Cain, Bo Wang, Melissa Long, and Josephine Taylor. "Antifungal activity of camptothecin, trifolin, and hyperoside isolated from Camptotheca acuminata." Journal of agricultural and food chemistry 53, no. 1 (2005): 32-37.

Posted with permission from the American Chemical Society.

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