Polycyclic meroterpenoids, talaromyolides E - K for antiviral activity against pseudorabies virus from the endophytic fungus Talaromyces purpureogenus

被引:17
|
作者
Cao, Xun [1 ]
Shi, Yutong [3 ]
Wu, Shanhu [6 ]
Wu, Xiaodan [1 ]
Wang, Kuiwu [4 ]
Sun, Hongxiang [5 ]
He, Shan [3 ]
Dickschat, Jeroen S. [2 ]
Wu, Bin [1 ]
机构
[1] Zhejiang Univ, Ocean Coll, Hangzhou 310058, Peoples R China
[2] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[3] Ningbo Univ, Coll Food & Pharmaceut Sci, Li Dak Sum Yip Yio Chin Kenneth Li Marine Biophar, Ningbo 315832, Peoples R China
[4] Zhejiang Gongshang Univ, Dept Appl Chem, Hangzhou 310058, Peoples R China
[5] Zhejiang Univ, Coll Anim Sci, Hangzhou 310058, Peoples R China
[6] ThermoFisher Sci, Life Sci & Mass Spectrc, Shanghai 200000, Peoples R China
基金
国家重点研发计划;
关键词
OSMAC fermentation; Talaromyces purpureogenus; Endophytic fungus; Polycyclic meroterpenoids; Pseudorabies virus; STEREOCHEMISTRY; METABOLITES; ISOLATE;
D O I
10.1016/j.tet.2020.131349
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Anti-pseudorabies virus (PRV) activity-guided isolation of an endophytic fungus Talaromyces purpureogenus resulted in seven rare polycyclic meroterpenoids talaromyolides E-K, together with two known compounds preaustinoid and austinolide. Their structures and absolute configurations were elucidated by HRESIMS, extensive NMR spectroscopic analyses, time-dependent density functional theory (TDDFT) calculations of ECD spectra, and single crystal X-ray diffraction. Talaromyolides I and K showed a dose-dependent inhibition of PRV, of which talaromyolide K had the most potent inhibition effect rate (60.11%), blocking effect rate (53.24%) and killing effect rate (62.16%) at a concentration of 50 mu g/mL. A plausible biosynthetic pathway for talaromyolides E-K was proposed. (C) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:9
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