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北极海洋宏基因组中的次生代谢物生物合成多样性。

Secondary metabolite biosynthetic diversity in Arctic Ocean metagenomes.

机构信息

Interdisciplinary Centre of Marine and Environmental Research (CIIMAR), University of Porto, Matosinhos, Portugal.

Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, 4050-313 Porto, Portugal.

出版信息

Microb Genom. 2021 Dec;7(12). doi: 10.1099/mgen.0.000731.

DOI:10.1099/mgen.0.000731
PMID:34904945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8767328/
Abstract

Polyketide synthases (PKSs) and non-ribosomal peptide synthetases (NRPSs) are mega enzymes responsible for the biosynthesis of a large fraction of natural products (NPs). Molecular markers for biosynthetic genes, such as the ketosynthase (KS) domain of PKSs, have been used to assess the diversity and distribution of biosynthetic genes in complex microbial communities. More recently, metagenomic studies have complemented and enhanced this approach by allowing the recovery of complete biosynthetic gene clusters (BGCs) from environmental DNA. In this study, the distribution and diversity of biosynthetic genes and clusters from Arctic Ocean samples (NICE-2015 expedition), was assessed using PCR-based strategies coupled with high-throughput sequencing and metagenomic analysis. In total, 149 KS domain OTU sequences were recovered, 36 % of which could not be assigned to any known BGC. In addition, 74 bacterial metagenome-assembled genomes were recovered, from which 179 BGCs were extracted. A network analysis identified potential new NP families, including non-ribosomal peptides and polyketides. Complete or near-complete BGCs were recovered, which will enable future heterologous expression efforts to uncover the respective NPs. Our study represents the first report of biosynthetic diversity assessed for Arctic Ocean metagenomes and highlights the potential of Arctic Ocean planktonic microbiomes for the discovery of novel secondary metabolites. The strategy employed in this study will enable future bioprospection, by identifying promising samples for bacterial isolation efforts, while providing also full-length BGCs for heterologous expression.

摘要

聚酮合酶(PKSs)和非核糖体肽合酶(NRPSs)是负责生物合成大量天然产物(NPs)的巨型酶。生物合成基因的分子标记物,如 PKS 的酮合酶(KS)结构域,已被用于评估复杂微生物群落中生物合成基因的多样性和分布。最近,宏基因组学研究通过允许从环境 DNA 中恢复完整的生物合成基因簇(BGCs),补充和增强了这一方法。在这项研究中,使用基于 PCR 的策略结合高通量测序和宏基因组分析,评估了来自北极海洋样本(NICE-2015 考察)的生物合成基因和簇的分布和多样性。总共回收了 149 个 KS 结构域 OTU 序列,其中 36%无法分配到任何已知的 BGC。此外,还回收了 74 个细菌宏基因组组装基因组,从中提取了 179 个 BGC。网络分析确定了潜在的新型 NP 家族,包括非核糖体肽和聚酮。回收了完整或近乎完整的 BGC,这将使未来的异源表达努力能够揭示各自的 NPs。我们的研究代表了对北极海洋宏基因组进行生物合成多样性评估的首次报告,并强调了北极海洋浮游微生物组在发现新型次生代谢物方面的潜力。本研究中采用的策略将通过识别有希望进行细菌分离的样本,同时为异源表达提供全长 BGC,从而实现未来的生物勘探。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/a66449a9e7bc/mgen-7-0731-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/cdb75abb8c95/mgen-7-0731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/bda116414d38/mgen-7-0731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/c9b494231b44/mgen-7-0731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/2aee04785b9d/mgen-7-0731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/bdd855042f05/mgen-7-0731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/f29fc11d3503/mgen-7-0731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/a66449a9e7bc/mgen-7-0731-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/cdb75abb8c95/mgen-7-0731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/bda116414d38/mgen-7-0731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/c9b494231b44/mgen-7-0731-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/f29fc11d3503/mgen-7-0731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec4/8767328/a66449a9e7bc/mgen-7-0731-g007.jpg

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