Cargando…

Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin

Secondary metabolites play essential roles in ecological interactions and nutrient acquisition, and are of interest for their potential uses in medicine and biotechnology. Genome mining for biosynthetic gene clusters (BGCs) can be used for the discovery of new compounds. Here, we use metagenomics an...

Descripción completa

Detalles Bibliográficos
Autores principales: Geller-McGrath, David, Mara, Paraskevi, Taylor, Gordon T., Suter, Elizabeth, Edgcomb, Virginia, Pachiadaki, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902471/
https://www.ncbi.nlm.nih.gov/pubmed/36746960
http://dx.doi.org/10.1038/s41467-023-36026-w
_version_ 1784883269040340992
author Geller-McGrath, David
Mara, Paraskevi
Taylor, Gordon T.
Suter, Elizabeth
Edgcomb, Virginia
Pachiadaki, Maria
author_facet Geller-McGrath, David
Mara, Paraskevi
Taylor, Gordon T.
Suter, Elizabeth
Edgcomb, Virginia
Pachiadaki, Maria
author_sort Geller-McGrath, David
collection PubMed
description Secondary metabolites play essential roles in ecological interactions and nutrient acquisition, and are of interest for their potential uses in medicine and biotechnology. Genome mining for biosynthetic gene clusters (BGCs) can be used for the discovery of new compounds. Here, we use metagenomics and metatranscriptomics to analyze BGCs in free-living and particle-associated microbial communities through the stratified water column of the Cariaco Basin, Venezuela. We recovered 565 bacterial and archaeal metagenome-assembled genomes (MAGs) and identified 1154 diverse BGCs. We show that differences in water redox potential and microbial lifestyle (particle-associated vs. free-living) are associated with variations in the predicted composition and production of secondary metabolites. Our results indicate that microbes, including understudied clades such as Planctomycetota, potentially produce a wide range of secondary metabolites in these anoxic/euxinic waters.
format Online
Article
Text
id pubmed-9902471
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-99024712023-02-08 Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin Geller-McGrath, David Mara, Paraskevi Taylor, Gordon T. Suter, Elizabeth Edgcomb, Virginia Pachiadaki, Maria Nat Commun Article Secondary metabolites play essential roles in ecological interactions and nutrient acquisition, and are of interest for their potential uses in medicine and biotechnology. Genome mining for biosynthetic gene clusters (BGCs) can be used for the discovery of new compounds. Here, we use metagenomics and metatranscriptomics to analyze BGCs in free-living and particle-associated microbial communities through the stratified water column of the Cariaco Basin, Venezuela. We recovered 565 bacterial and archaeal metagenome-assembled genomes (MAGs) and identified 1154 diverse BGCs. We show that differences in water redox potential and microbial lifestyle (particle-associated vs. free-living) are associated with variations in the predicted composition and production of secondary metabolites. Our results indicate that microbes, including understudied clades such as Planctomycetota, potentially produce a wide range of secondary metabolites in these anoxic/euxinic waters. Nature Publishing Group UK 2023-02-06 /pmc/articles/PMC9902471/ /pubmed/36746960 http://dx.doi.org/10.1038/s41467-023-36026-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Geller-McGrath, David
Mara, Paraskevi
Taylor, Gordon T.
Suter, Elizabeth
Edgcomb, Virginia
Pachiadaki, Maria
Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title_full Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title_fullStr Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title_full_unstemmed Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title_short Diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic Cariaco Basin
title_sort diverse secondary metabolites are expressed in particle-associated and free-living microorganisms of the permanently anoxic cariaco basin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902471/
https://www.ncbi.nlm.nih.gov/pubmed/36746960
http://dx.doi.org/10.1038/s41467-023-36026-w
work_keys_str_mv AT gellermcgrathdavid diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin
AT maraparaskevi diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin
AT taylorgordont diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin
AT suterelizabeth diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin
AT edgcombvirginia diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin
AT pachiadakimaria diversesecondarymetabolitesareexpressedinparticleassociatedandfreelivingmicroorganismsofthepermanentlyanoxiccariacobasin