Identification of a terpene synthase arsenal using long-read sequencing and genome assembly of Aspergillus wentii.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Richard Olumakaiye, Christophe Corre, Fabrizio Alberti
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引用次数: 0

Abstract

Background: Fungi are talented producers of secondary metabolites with applications in the pharmaceutical and agrochemical sectors. Aspergillus wentii CBS 141173 has gathered research interest due to its ability to produce high-value norditerpenoid compounds, including anticancer molecules. In this study, we aimed to expand the genomic information available for A. wentii to facilitate the identification of terpenoid biosynthetic genes that may be involved in the production of bioactive molecules.

Results: Long-read genome sequencing of Aspergillus wentii CBS 141173 was conducted using Oxford Nanopore Technologies (ONT) MinION MK1C. In addition, paired-end stranded RNA-seq data from two time points, 7 days and 30 days, was used for functional annotation of the assembled genome. Overall, we assembled a genome of approximately 31.2 Mb and identified 66 biosynthetic gene clusters from the annotated genome. Metabolic extracts of A. wentii were analysed and the production of the bioactive terpenoid asperolide A was confirmed. We further mined the assembled and annotated genome for BGCs involved in terpenoid pathways using a combination of antiSMASH and local BlastP and identified 16 terpene synthases. Phylogenetic analysis was conducted and allowed us to establish relationships with other characterised terpene synthases. We identified two terpene clusters potentially involved in pimarane-like diterpenoid biosynthesis. Finally, the analysis of the 16 terpene synthases in our 7-day and 30-day transcriptomic data suggested that only four of them were constitutively expressed under laboratory conditions.

Conclusion: These results provide a scaffold for the future exploration of terpenoid biosynthetic pathways for bioactive molecules in A. wentii. The terpenoid clusters identified in this study are candidates for heterologous gene expression and/or gene disruption experiments. The description and availability of the long-read genome assembly of A. wentii CBS 141173 further provides the basis for downstream genome analysis and biotechnological exploitation of this species.

利用长线程测序和文曲霉基因组组装鉴定萜烯合成酶库。
背景:真菌是二次代谢产物的天才生产者,可应用于制药和农用化学品领域。文氏曲霉(Aspergillus wentii)CBS 141173 由于能够产生高价值的北萜类化合物(包括抗癌分子)而引起了研究兴趣。在这项研究中,我们的目的是扩大文曲霉的基因组信息,以便于鉴定可能参与生产生物活性分子的萜类化合物生物合成基因:结果:使用牛津纳米孔技术公司(ONT)的 MinION MK1C 对文曲霉 CBS 141173 进行了长读程基因组测序。此外,我们还利用 7 天和 30 天两个时间点的成对链 RNA-seq 数据对组装好的基因组进行了功能注释。总之,我们组装了一个约 31.2 Mb 的基因组,并从注释的基因组中鉴定出 66 个生物合成基因簇。我们对 wentii 的代谢提取物进行了分析,并确认了生物活性萜类物质阿斯佩罗内酯 A 的生产。我们使用反SMASH和本地BlastP相结合的方法,进一步从组装和注释的基因组中挖掘参与萜类化合物途径的BGCs,结果发现了16个萜类化合物合成酶。通过系统进化分析,我们确定了萜烯合成酶与其他萜烯合成酶之间的关系。我们还发现了两个可能参与类茚二萜生物合成的萜类群。最后,我们对 7 天和 30 天转录组数据中的 16 个萜烯合成酶进行了分析,结果表明其中只有 4 个萜烯合成酶在实验室条件下是组成型表达的:这些结果为今后探索文竹属植物生物活性分子的萜类化合物生物合成途径提供了一个支架。本研究中发现的萜类化合物群是异源基因表达和/或基因干扰实验的候选对象。A. wentii CBS 141173 的长线程基因组组装的描述和可用性进一步为该物种的下游基因组分析和生物技术利用提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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