Heterologous Expression of an Abandoned Termite Mound Fungus Gene Cluster Reveals a Protective Aldehyde–Alcohol Cycle and a Candidate Termiticidal Metabolite

IF 4.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2026-08-21 Epub Date: 2026-07-06 DOI:10.1021/acssynbio.6c00101
Yize Cai, Hongling Yan, Jiaxu Qin, Yaxiong Qiang, Guo-Qiang Lin, Haiying Wang, Qing-Li He, Qunfei Zhao
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引用次数: 0

Abstract

The medicinal fungus Wulingshen, comprising multiple Xylaria species, inhabits deserted termite mounds as sclerotia. To explore the molecular basis of its niche adaptation, we employed a synthetic biology-driven approach. Metagenomic and transcriptomic mining of wild specimens identified a conserved biosynthetic gene cluster. Its heterologous reconstruction in the fungal host Aspergillus oryzae enabled the characterization of a family of α-pyrone metabolites and, crucially, the elucidation of a spatially separated aldehyde–alcohol cycle. In this self-protection system, an extracellular oxidase (WlsA) converts an alcohol precursor to a reactive aldehyde, while an intracellular reductase (WlsE) catalyzes the reverse reaction. The aldehyde product exhibits potent toxicity against termites in vitro, suggesting a potential role in ecological interactions. This work establishes a functional genomics platform that decodes cryptic ecological metabolism by integrating multiomics with heterologous pathway expression, providing a generalizable strategy for discovering and mechanistically understanding niche-specific natural products.

废弃白蚁丘真菌基因簇的异源表达揭示了保护醛-醇循环和候选杀蚁代谢物。
药用真菌武灵神,由多种木耳组成,作为菌核栖息在废弃的白蚁丘上。为了探索其生态位适应的分子基础,我们采用了合成生物学驱动的方法。野生标本的宏基因组和转录组挖掘鉴定出一个保守的生物合成基因簇。它在真菌宿主米曲霉(Aspergillus oryzae)中的异源重建使α-吡酮代谢产物家族的表征成为可能,更重要的是,阐明了空间分离的醛-醇循环。在这个自我保护系统中,细胞外氧化酶(WlsA)将醇前体转化为活性醛,而细胞内还原酶(WlsE)催化逆向反应。甲醛产物在体外对白蚁表现出强大的毒性,表明其在生态相互作用中具有潜在的作用。这项工作建立了一个功能基因组学平台,通过整合多组学和异源通路表达来解码神秘的生态代谢,为发现和机制理解特定生态位的天然产物提供了一种通用策略。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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