Discovery of antifungal secondary metabolites from an intestinal fungus Fusarium sp.

被引:2
|
作者
Zhang, Mingkai [1 ,2 ]
Chen, Baosong [2 ]
Dai, Huanqin [2 ]
Sun, Jingzu [2 ]
Liu, Hongwei [1 ,2 ,3 ]
Han, Junjie [2 ]
机构
[1] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Coll Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, State Key Lab Mycol, Beijing 100101, Peoples R China
[3] Univ Chinese Acad Sci, Savaid Med Sch, Beijing 100049, Peoples R China
来源
JOURNAL OF ANTIBIOTICS | 2024年 / 77卷 / 03期
基金
中国国家自然科学基金;
关键词
D-MANNOPYRANOSIDES; STEROL;
D O I
10.1038/s41429-023-00692-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Intestinal fungi, which are important parts of the gut microbiota, have the ability to produce specialized metabolites that significantly contribute to maintaining the balance of the gut microbiota and promoting the health of the host organism. In the present study, two new glycosides, including fusintespyrone A (1) and cerevisterolside A (4), as well as ten known compounds were isolated from the intestinal fungus Fusarium sp. LE06. The structures of the new compounds were elucidated by a combination of spectroscopic methods, such as mass spectrometry (MS) and nuclear magnetic resonance (NMR), along with chemical reactions and calculations of NMR and ECD spectra. Compounds 1-3 showed significant growth inhibition against Aspergillus fumigatus, Fusarium oxysporum, and Verticillium dahliae with MIC values in the range of 1.56-6.25 mu g ml(-1).
引用
收藏
页码:163 / 169
页数:7
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