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A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes

ABSTRACT: Culture-independent metagenomic approaches offer a promising solution to the discovery of therapeutically relevant compounds such as antibiotics by enabling access to the hidden biosynthetic potential of microorganisms. These strategies, however, often entail laborious, multi-step, and tim...

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Autores principales: Negri, Timo, Mantri, Shrikant, Angelov, Angel, Peter, Silke, Muth, Günther, Eustáquio, Alessandra S., Ziemert, Nadine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064862/
https://www.ncbi.nlm.nih.gov/pubmed/35435454
http://dx.doi.org/10.1007/s00253-022-11917-y
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author Negri, Timo
Mantri, Shrikant
Angelov, Angel
Peter, Silke
Muth, Günther
Eustáquio, Alessandra S.
Ziemert, Nadine
author_facet Negri, Timo
Mantri, Shrikant
Angelov, Angel
Peter, Silke
Muth, Günther
Eustáquio, Alessandra S.
Ziemert, Nadine
author_sort Negri, Timo
collection PubMed
description ABSTRACT: Culture-independent metagenomic approaches offer a promising solution to the discovery of therapeutically relevant compounds such as antibiotics by enabling access to the hidden biosynthetic potential of microorganisms. These strategies, however, often entail laborious, multi-step, and time-consuming procedures to recover the biosynthetic gene clusters (BGCs) from soil metagenomes for subsequent heterologous expression. Here, we developed an efficient method we called single Nanopore read cluster mining (SNRCM), which enables the fast recovery of complete BGCs from a soil metagenome using long- and short-read sequencing. A metagenomic fosmid library of 83,700 clones was generated and sequenced using Nanopore as well as Illumina technologies. Hybrid assembled contigs of the sequenced fosmid library were subsequently analyzed to identify BGCs encoding secondary metabolites. Using SNRCM, we aligned the identified BGCs directly to Nanopore long-reads and were able to detect complete BGCs on single fosmids. This enabled us to select for and recover BGCs of interest for subsequent heterologous expression attempts. Additionally, the sequencing data of the fosmid library and its corresponding metagenomic DNA enabled us to assemble and recover a large nonribosomal peptide synthetase (NRPS) BGC from three different fosmids of our library and to directly amplify and recover a complete lasso peptide BGC from the high-quality metagenomic DNA. Overall, the strategies presented here provide a useful tool for accelerating and facilitating the identification and production of potentially interesting bioactive compounds from soil metagenomes. KEY POINTS: • An efficient approach for the recovery of BGCs from soil metagenomes was developed to facilitate natural product discovery. • A fosmid library was constructed from soil metagenomic HMW DNA and sequenced via Illumina and Nanopore. • Nanopore long-reads enabled the direct identification and recovery of complete BGCs on single fosmids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11917-y.
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spelling pubmed-90648622022-05-07 A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes Negri, Timo Mantri, Shrikant Angelov, Angel Peter, Silke Muth, Günther Eustáquio, Alessandra S. Ziemert, Nadine Appl Microbiol Biotechnol Methods and Protocols ABSTRACT: Culture-independent metagenomic approaches offer a promising solution to the discovery of therapeutically relevant compounds such as antibiotics by enabling access to the hidden biosynthetic potential of microorganisms. These strategies, however, often entail laborious, multi-step, and time-consuming procedures to recover the biosynthetic gene clusters (BGCs) from soil metagenomes for subsequent heterologous expression. Here, we developed an efficient method we called single Nanopore read cluster mining (SNRCM), which enables the fast recovery of complete BGCs from a soil metagenome using long- and short-read sequencing. A metagenomic fosmid library of 83,700 clones was generated and sequenced using Nanopore as well as Illumina technologies. Hybrid assembled contigs of the sequenced fosmid library were subsequently analyzed to identify BGCs encoding secondary metabolites. Using SNRCM, we aligned the identified BGCs directly to Nanopore long-reads and were able to detect complete BGCs on single fosmids. This enabled us to select for and recover BGCs of interest for subsequent heterologous expression attempts. Additionally, the sequencing data of the fosmid library and its corresponding metagenomic DNA enabled us to assemble and recover a large nonribosomal peptide synthetase (NRPS) BGC from three different fosmids of our library and to directly amplify and recover a complete lasso peptide BGC from the high-quality metagenomic DNA. Overall, the strategies presented here provide a useful tool for accelerating and facilitating the identification and production of potentially interesting bioactive compounds from soil metagenomes. KEY POINTS: • An efficient approach for the recovery of BGCs from soil metagenomes was developed to facilitate natural product discovery. • A fosmid library was constructed from soil metagenomic HMW DNA and sequenced via Illumina and Nanopore. • Nanopore long-reads enabled the direct identification and recovery of complete BGCs on single fosmids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11917-y. Springer Berlin Heidelberg 2022-04-18 2022 /pmc/articles/PMC9064862/ /pubmed/35435454 http://dx.doi.org/10.1007/s00253-022-11917-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Methods and Protocols
Negri, Timo
Mantri, Shrikant
Angelov, Angel
Peter, Silke
Muth, Günther
Eustáquio, Alessandra S.
Ziemert, Nadine
A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title_full A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title_fullStr A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title_full_unstemmed A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title_short A rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
title_sort rapid and efficient strategy to identify and recover biosynthetic gene clusters from soil metagenomes
topic Methods and Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064862/
https://www.ncbi.nlm.nih.gov/pubmed/35435454
http://dx.doi.org/10.1007/s00253-022-11917-y
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