Genome Mining Leads to Diverse Sesquiterpenes with Anti-inflammatory Activity from an Arctic-Derived Fungus

• Published in: Journal of natural products (Washington, D.C.) Vol. 87; no. 5; pp. 1426 - 1440
• Main Authors: Ning, Yaodong, Gu, Qinwufeng, Zheng, Te, Xu, Yao, Li, Song, Zhu, Yuping, Hu, Bo, Yu, Haobing, Liu, Xiaoyu, Zhang, Yun, Jiao, Binghua, Lu, Xiaoling
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society and American Society of Pharmacognosy 24.05.2024; Amer Chemical Soc
• Subjects: Animals; Anti-Inflammatory Agents - chemistry; Anti-Inflammatory Agents - pharmacology; Chemistry, Medicinal; Life Sciences & Biomedicine; Lipopolysaccharides - pharmacology; Mice; Molecular Structure; Nitric Oxide - biosynthesis; Pharmacology & Pharmacy; Plant Sciences; RAW 264.7 Cells; Science & Technology; Sesquiterpenes - chemistry; Sesquiterpenes - pharmacology; Zebrafish; SECONDARY METABOLITES; SIGNALING PATHWAYS; CYTOKINES; NATURAL-PRODUCTS; BIOSYNTHESIS; PIMARANE DITERPENES; NLRP3 INFLAMMASOME; MAPK; EUTYPELLA
• ISSN: 0163-3864; 1520-6025
• DOI: 10.1021/acs.jnatprod.4c00237

With the advancement of bioinformatics, the integration of genome mining with efficient separation technology enables the discovery of a greater number of novel bioactive compounds. The deletion of the key gene responsible for triterpene cyclase biosynthesis in the polar strain Eutypella sp. D-1 instigated metabolic shunting, resulting in the activation of dormant genes and the subsequent production of detectable, new compounds. Fifteen sesquiterpenes were isolated from the mutant strain, with eight being new compounds. The structural elucidation of these compounds was obtained through a combination of HRESIMS, NMR spectroscopy, and ECD calculations, revealing six distinct skeleton types. Compound 7 possessed a unique skeleton of 5/10 macrocyclic ether structure. Based on the gene functions and newly acquired secondary metabolites, the metabolic shunting pathway in the mutant strain was inferred. Compounds 6, 8, 11, 14, and 15 exhibited anti-inflammatory effects without cytotoxicity through the release of nitric oxide from lipopolysaccharide-stimulated RAW264.7 cells. Notably, acorane-type sesquiterpene 8 inhibited nitric oxide production and modulated the MAPK and NLRP3/caspase-1 signaling pathways. Compound 8 also alleviated the CuSO4-induced systemic neurological inflammation symptoms in a transgenic fluorescent zebrafish model.