Secondary metabolite biosynthetic diversity in the fungal family Hypoxylaceae and Xylaria hypoxylon

IF 14.1 1区 生物学 Q1 MYCOLOGY Studies in Mycology Pub Date : 2021-06-01 DOI:10.1016/j.simyco.2021.100118
E. Kuhnert , J.C. Navarro-Muñoz , K. Becker , M. Stadler , J. Collemare , R.J. Cox
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引用次数: 26

Abstract

To date little is known about the genetic background that drives the production and diversification of secondary metabolites in the Hypoxylaceae. With the recent availability of high-quality genome sequences for 13 representative species and one relative (Xylaria hypoxylon) we attempted to survey the diversity of biosynthetic pathways in these organisms to investigate their true potential as secondary metabolite producers. Manual search strategies based on the accumulated knowledge on biosynthesis in fungi enabled us to identify 783 biosynthetic pathways across 14 studied species, the majority of which were arranged in biosynthetic gene clusters (BGC). The similarity of BGCs was analysed with the BiG-SCAPE engine which organised the BGCs into 375 gene cluster families (GCF). Only ten GCFs were conserved across all of these fungi indicating that speciation is accompanied by changes in secondary metabolism. From the known compounds produced by the family members some can be directly correlated with identified BGCs which is highlighted herein by the azaphilone, dihydroxynaphthalene, tropolone, cytochalasan, terrequinone, terphenyl and brasilane pathways giving insights into the evolution and diversification of those compound classes. Vice versa, products of various BGCs can be predicted through homology analysis with known pathways from other fungi as shown for the identified ergot alkaloid, trigazaphilone, curvupallide, viridicatumtoxin and swainsonine BGCs. However, the majority of BGCs had no obvious links to known products from the Hypoxylaceae or other well-studied biosynthetic pathways from fungi. These findings highlight that the number of known compounds strongly underrepresents the biosynthetic potential in these fungi and that a tremendous number of unidentified secondary metabolites is still hidden. Moreover, with increasing numbers of genomes for further Hypoxylaceae species becoming available, the likelihood of revealing new biosynthetic pathways that encode new, potentially useful compounds will significantly improve. Reaching a better understanding of the biology of these producers, and further development of genetic methods for their manipulation, will be crucial to access their treasures.

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木霉科真菌和木霉次生代谢物生物合成多样性
迄今为止,人们对木香科植物次生代谢物产生和多样化的遗传背景知之甚少。随着13个代表性物种和一个近缘物种(Xylaria hypoxylon)的高质量基因组序列的获得,我们试图调查这些生物生物合成途径的多样性,以研究它们作为次生代谢物生产者的真正潜力。基于积累的真菌生物合成知识的人工搜索策略使我们能够在14个研究物种中确定783条生物合成途径,其中大多数排列在生物合成基因簇(BGC)中。利用BiG-SCAPE引擎对bgc进行相似性分析,将bgc组织为375个基因簇家族(GCF)。所有这些真菌中只有10个gcf是保守的,这表明物种形成伴随着次级代谢的变化。从家族成员产生的已知化合物中,一些可以与已鉴定的bgc直接相关,本文强调了氮唑啉、二羟基萘、tropolone、cytochalasan、terrequinone、terphenyl和brasilane途径,从而深入了解这些化合物类别的进化和多样化。反之,通过与其他真菌已知途径的同源性分析,可以预测各种bgc的产物,如鉴定出的麦角生物碱、trigazaphilone、弯曲肽、病毒毒素和苦马豆素bgc。然而,大多数bgc与已知的木氧根科产品或其他经过充分研究的真菌生物合成途径没有明显联系。这些发现强调了已知化合物的数量远远低于这些真菌的生物合成潜力,并且大量未识别的次级代谢物仍然被隐藏。此外,随着越来越多的藤本植物科物种的基因组变得可用,揭示新的生物合成途径编码新的、潜在有用的化合物的可能性将大大提高。更好地了解这些生产者的生物学,并进一步发展操纵它们的遗传方法,对于获取它们的宝藏至关重要。
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来源期刊
Studies in Mycology
Studies in Mycology 生物-真菌学
CiteScore
35.60
自引率
3.00%
发文量
7
期刊介绍: The international journal Studies in Mycology focuses on advancing the understanding of filamentous fungi, yeasts, and various aspects of mycology. It publishes comprehensive systematic monographs as well as topical issues covering a wide range of subjects including biotechnology, ecology, molecular biology, pathology, and systematics. This Open-Access journal offers unrestricted access to its content. Each issue of Studies in Mycology consists of around 5 to 6 papers, either in the form of monographs or special focused topics. Unlike traditional length restrictions, the journal encourages submissions of manuscripts with a minimum of 50 A4 pages in print. This ensures a thorough exploration and presentation of the research findings, maximizing the depth of the published work.
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