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海洋来源真菌F1-1的基因组挖掘发现了佛手柑烯型倍半萜类化合物。

Genome Mining of the Marine-Derived Fungus F1-1 Unearths Bergamotene-Type Sesquiterpenoids.

作者信息

Yang Wencong, Tian Shurong, Du Yi-Fan, Zeng Xian-Liang, Liang Jia-Jing, Lan Wen-Jian, Li Hang

机构信息

State Key Laboratory of Anti-Infective Drug Discovery and Development, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, 510006, China.

出版信息

J Nat Prod. 2024 Dec 27;87(12):2746-2756. doi: 10.1021/acs.jnatprod.4c00905. Epub 2024 Dec 2.

Abstract

Terpenoids are a vast group of natural products known for their remarkable biological properties and structural diversity. UbiA terpene synthases are increasingly recognized for producing various terpenoids. In this study, we identified a biosynthetic gene cluster () encoding a UbiA terpene synthase BgtA in the genome of the marine-derived fungus F1-1. The gene was validated to encode the biosynthesis of (-)-α--bergamotene (). Heterologous expression of the gene cluster in the characterized host LO8030 activated the biosynthetic pathway, leading to the isolation of eight previously undocumented bergamotene-derived sesquiterpenoids (-). Their structures, including the absolute configurations, were elucidated by a combination of spectroscopic analysis, ECD spectra, chemical hydrolysis, single-crystal X-ray diffraction, and biosynthetic considerations. We further demonstrated that the production of these structurally intricate sesquiterpenoids in heterologous expression is attributable to the concerted action of the UbiA terpene synthase BgtA, the cytochrome P450 BgtC, and endogenous enzymes. This study underscores the immense biosynthetic potential of fungal UbiA terpene synthase gene clusters and shows genome mining is a promising strategy for the discovery of novel terpenoids from fungi.

摘要

萜类化合物是一大类天然产物,以其卓越的生物学特性和结构多样性而闻名。泛醌A萜烯合酶越来越被认为能够产生各种萜类化合物。在本研究中,我们在海洋来源真菌F1-1的基因组中鉴定出一个编码泛醌A萜烯合酶BgtA的生物合成基因簇()。该基因被证实编码(-)-α-佛手柑烯()的生物合成。该基因簇在特征明确的宿主LO8030中的异源表达激活了生物合成途径,从而分离出8种以前未记录的佛手柑烯衍生的倍半萜(-)。通过光谱分析、ECD光谱、化学水解、单晶X射线衍射以及生物合成方面的综合考虑,阐明了它们的结构,包括绝对构型。我们进一步证明,在异源表达中这些结构复杂的倍半萜的产生归因于泛醌A萜烯合酶BgtA、细胞色素P450 BgtC和内源性酶的协同作用。本研究强调了真菌泛醌A萜烯合酶基因簇巨大的生物合成潜力,并表明基因组挖掘是从真菌中发现新型萜类化合物的一种有前途的策略。

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