Expression of a Colletotrichum polyketide synthase gene in Aspergillus nidulans leads to unexpected conjugates with a host metabolite

IF 2.6 3区 生物学 Q3 MICROBIOLOGY Archives of Microbiology Pub Date : 2025-02-06 DOI:10.1007/s00203-025-04258-7
David Breyer, Leyao Chen, Jenny Zhou, Zhang-Hai Li, Shu-Ming Li
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Abstract

Heterologous expression of the putative 1,3,6,8-tetrahydroxynaphthalene synthase gene ChPKS from Colletotrichum higginsianum in Aspergillus nidulans led to the formation of at least eight new compounds. LC-MS analysis proved them as coupling products of 1,3,6,8-tetrahydroxynaphthalene with an intermediate of the cichorine biosynthetic pathway. Comprehensive NMR analysis confirmed the structures of the two predominant products higginidulans A and B. Deletion of the backbone gene of the cichorine pathway in host strain Aspergillus nidulans abolished the formation of higginidulans. Heterologous expression of ChPKS in the alternative Penicillium crustosum expression host resulted in the formation of the expected product 1,3,6,8-tetrahydroxynaphthalene, which was confirmed by acetylation and structural elucidation. This study provides an additional example of unexpected natural product formation by crosstalk of biosynthetic pathways derived from different species. Moreover, it highlights the importance of using alternative host systems for gene expression.

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炭疽菌多酮合成酶基因在灰曲霉中的表达导致与宿主代谢物意想不到的结合
从炭黑菌中提取的1,3,6,8-四羟基萘合成酶基因ChPKS在细粒曲霉中的异源表达导致至少8个新化合物的形成。LC-MS分析证实它们是1,3,6,8-四羟基萘与蝉碱生物合成途径中间体的偶联产物。综合核磁共振分析证实了两种主要产物higginidulans A和b的结构。在寄主菌株Aspergillus nidulans中,cichorine通路主干基因的缺失使higginidulans的形成中断。ChPKS在褐皮青霉备选表达宿主中的异源表达可形成预期产物1,3,6,8-四羟基萘,经乙酰化和结构解析证实。这项研究提供了一个额外的例子,通过来自不同物种的生物合成途径的串扰产生意想不到的天然产物。此外,它强调了使用替代宿主系统进行基因表达的重要性。
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来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
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