Trichocomaceae

Yang, Guang-Yu, Dai, Jia-Meng, Mi, Qi-Li, Li, Zhen-Jie, Li, Xue-Mei, Zhang, Jian-Duo, Wang, Jin, Li, Yin-Ke, Wang, Wei-Guang, Zhou, Min & Hu, Qiu-Fen, 2022, Cyclopiazonic acid type indole alkaloids from Nicotiana tabacum-derived fungus Aspergillus versicolor and their anti-tobacco mosaic virus activities, Phytochemistry (113137) 198, pp. 1-7 : 1

publication ID

https://doi.org/ 10.1016/j.phytochem.2022.113137

persistent identifier

https://treatment.plazi.org/id/03868791-5151-FFC7-FFC5-FCE0FC006CEC

treatment provided by

Felipe

scientific name

Trichocomaceae
status

 

Family Trichocomaceae View in CoL View at ENA Aspergillus versicolor

Nicotiana tabacum derived Fungus CPA-Type indole alkaloids Anti-TMV activities

A B S T R A C T

Indole alkaloids have attracted widespread attention of chemists and biologists. Therefore, the aim of this study is to screen more bioactivities indole alkaloids from the microorganisms. In this study, five undescribed CPA-type indole alkaloids, aspergillines F–J, and three known CPA-type indole alkaloids, aspergilline A, aspergilline C, and cyclopiamide E, were obtained from the Nicotiana tabacum - derived fungus Aspergillus versicolor . Notably, aspergillines F and G represent the first examples of indole alkaloids with a benzo[cd]indol-2(1 H)-one skeleton, and aspergilline J is also the firstly obtained indole alkaloids bearing a N -1-(2-(1 H -imidazole-5-yl)ethyl) moiety. Aspergillines F–J and cyclopiamide E were tested for their anti-TMV activities, and the results revealed that aspergillines G and J exhibited obvious anti-TMV activities with inhibition rates of 41.2 and 56.8% at the concentration of 20 μ M, respectively. These rates are high than that of positive control (with inhibition rate of 32.5%). In addition, the molecular docking studies for the isolated CPA-type indole alkaloids may also reveal that the benzo[cd]indol-2(1 H)-one substructure is the fundamental for anti-TMV activity and the oxygen-containing substituent groups at C-19 also increases the inhibitory activity. This study of structure-activity relationship is helpful to find new anti-TMV activity inhibitors.

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