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将一个聚酮合酶基因簇与6-戊基-α-吡喃酮相联系,6-戊基-α-吡喃酮是一种具有多种生物活性的木霉代谢产物。

Linking a polyketide synthase gene cluster to 6-pentyl-alpha-pyrone, a Trichoderma metabolite with diverse bioactivities.

作者信息

Flatschacher Daniel, Eschlböck Alexander, Pierson Siebe, Schreiner Ulrike, Stock Valentina, Schiller Arne, Ruso David, Doppler Maria, Ruzsanyi Veronika, Gründlinger Mario, Büschl Christoph, Schuhmacher Rainer, Zeilinger Susanne

机构信息

Department of Microbiology, University of Innsbruck, Technikerstrasse 25, Innsbruck, 6020, Austria.

Institute for Breath Research, University of Innsbruck, Innsbruck, Austria.

出版信息

Microb Cell Fact. 2025 Apr 21;24(1):89. doi: 10.1186/s12934-025-02718-9.

Abstract

BACKGROUND

Members of the fungal genus Trichoderma are well-known for their mycoparasitic and plant protecting activities, rendering them important biocontrol agents. One of the most significant specialized metabolites (SMs) produced by various Trichoderma species is the unsaturated lactone 6-pentyl-alpha-pyrone (6-PP). Although first identified more than 50 years ago and having pronounced antifungal and plant growth-promoting properties, the biosynthetic pathway of 6-PP still remains unresolved.

RESULTS

Here, we demonstrate that 6-PP is biosynthesized via the polyketide biosynthesis pathway. We identified Pks1, an iterative type I polyketide synthase, as crucial for its biosynthesis in Trichoderma atroviride, a species recognized for its prominent 6-PP production abilities. Phylogenetic and comparative genomic analyses revealed that the pks1 gene is part of a biosynthetic gene cluster conserved in those Trichoderma species that are known to produce 6-PP. Deletion of pks1 caused a complete loss of 6-PP production in T. atroviride and a significant reduction in antifungal activity against Botrytis cinerea and Rhizoctonia solani. Surprisingly, the absence of pks1 led to enhanced lateral root formation in Arabidopsis thaliana during interaction with T. atroviride. Transcriptomic analysis revealed co-regulation of pks1 with adjacent genes, including candidates coding for a C3H1-type zinc finger protein and lytic polysaccharide monooxygenase, suggesting coordination between 6-PP biosynthesis and environmental response mechanisms.

CONCLUSION

Our findings establish pks1 as an essential gene for 6-PP biosynthesis in T. atroviride, providing novel insights into the production of one of the most significant compounds of this mycoparasite. These findings may pave the way for the development of improved biocontrol agents and the application of 6-PP as potent biopesticide contributing to an eco-friendly and sustainable way of plant disease management.

摘要

背景

木霉属真菌成员以其真菌寄生和植物保护活性而闻名,使其成为重要的生物防治剂。各种木霉菌种产生的最重要的特殊代谢产物(SMs)之一是不饱和内酯6-戊基-α-吡喃酮(6-PP)。尽管6-PP在50多年前就已首次被鉴定出来,并且具有显著的抗真菌和促进植物生长的特性,但其生物合成途径仍未得到解决。

结果

在这里,我们证明6-PP是通过聚酮生物合成途径生物合成的。我们鉴定出迭代型I聚酮合酶Pks1对其在深绿木霉中的生物合成至关重要,深绿木霉是一种以其突出的6-PP生产能力而闻名的物种。系统发育和比较基因组分析表明,pks1基因是已知产生6-PP的那些木霉菌种中保守的生物合成基因簇的一部分。pks1的缺失导致深绿木霉中6-PP的产生完全丧失,并且对灰葡萄孢和立枯丝核菌的抗真菌活性显著降低。令人惊讶的是,pks1的缺失导致拟南芥在与深绿木霉相互作用期间侧根形成增强。转录组分析揭示了pks1与相邻基因的共调控,包括编码C3H1型锌指蛋白和裂解多糖单加氧酶的候选基因,表明6-PP生物合成与环境响应机制之间的协调。

结论

我们的研究结果确定pks1是深绿木霉中6-PP生物合成的必需基因,为这种真菌寄生物最重要的化合物之一的生产提供了新的见解。这些发现可能为开发改良的生物防治剂以及将6-PP用作有效的生物农药铺平道路,有助于以生态友好和可持续的方式进行植物病害管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01d/12010586/6b65ee6381d1/12934_2025_2718_Fig1_HTML.jpg

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