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Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis

Carnobacterium maltaromaticum is a non-starter lactic acid bacterium (LAB) of interest in the dairy industry for biopreservation. This study investigated the interference competition network and the specialized metabolites biosynthetic gene clusters (BGCs) content in this LAB in order to explore the...

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Autores principales: Gontijo, Marco Túlio Pardini, Ramia, Nancy E., Dijamentiuk, Alexis, Elfassy, Annelore, Taha, Samir, Mangavel, Cécile, Revol-Junelles, Anne-Marie, Borges, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504619/
https://www.ncbi.nlm.nih.gov/pubmed/36144396
http://dx.doi.org/10.3390/microorganisms10091794
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author Gontijo, Marco Túlio Pardini
Ramia, Nancy E.
Dijamentiuk, Alexis
Elfassy, Annelore
Taha, Samir
Mangavel, Cécile
Revol-Junelles, Anne-Marie
Borges, Frédéric
author_facet Gontijo, Marco Túlio Pardini
Ramia, Nancy E.
Dijamentiuk, Alexis
Elfassy, Annelore
Taha, Samir
Mangavel, Cécile
Revol-Junelles, Anne-Marie
Borges, Frédéric
author_sort Gontijo, Marco Túlio Pardini
collection PubMed
description Carnobacterium maltaromaticum is a non-starter lactic acid bacterium (LAB) of interest in the dairy industry for biopreservation. This study investigated the interference competition network and the specialized metabolites biosynthetic gene clusters (BGCs) content in this LAB in order to explore the relationship between the antimicrobial properties and the genome content. Network analysis revealed that the potency of inhibition tended to increase when the inhibition spectrum broadened, but also that several strains exhibited a high potency and narrow spectrum of inhibition. The C. maltaromaticum strains with potent anti-L. monocytogenes were characterized by high potency and a wide intraspecific spectrum. Genome mining of 29 strains revealed the presence of 12 bacteriocin BGCs: four of class I and eight of class II, among which seven belong to class IIa and one to class IIc. Overall, eight bacteriocins and one nonribosomal peptide synthetase and polyketide synthase (NRPS-PKS) BGCs were newly described. The comparison of the antimicrobial properties resulting from the analysis of the network and the BGC genome content allowed us to delineate candidate BGCs responsible for anti-L. monocytogenes and anti-C. maltaromaticum activity. However, it also highlighted that genome analysis is not suitable in the current state of the databases for the prediction of genes involved in the antimicrobial activity of strains with a narrow anti-C. maltaromaticum activity.
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spelling pubmed-95046192022-09-24 Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis Gontijo, Marco Túlio Pardini Ramia, Nancy E. Dijamentiuk, Alexis Elfassy, Annelore Taha, Samir Mangavel, Cécile Revol-Junelles, Anne-Marie Borges, Frédéric Microorganisms Article Carnobacterium maltaromaticum is a non-starter lactic acid bacterium (LAB) of interest in the dairy industry for biopreservation. This study investigated the interference competition network and the specialized metabolites biosynthetic gene clusters (BGCs) content in this LAB in order to explore the relationship between the antimicrobial properties and the genome content. Network analysis revealed that the potency of inhibition tended to increase when the inhibition spectrum broadened, but also that several strains exhibited a high potency and narrow spectrum of inhibition. The C. maltaromaticum strains with potent anti-L. monocytogenes were characterized by high potency and a wide intraspecific spectrum. Genome mining of 29 strains revealed the presence of 12 bacteriocin BGCs: four of class I and eight of class II, among which seven belong to class IIa and one to class IIc. Overall, eight bacteriocins and one nonribosomal peptide synthetase and polyketide synthase (NRPS-PKS) BGCs were newly described. The comparison of the antimicrobial properties resulting from the analysis of the network and the BGC genome content allowed us to delineate candidate BGCs responsible for anti-L. monocytogenes and anti-C. maltaromaticum activity. However, it also highlighted that genome analysis is not suitable in the current state of the databases for the prediction of genes involved in the antimicrobial activity of strains with a narrow anti-C. maltaromaticum activity. MDPI 2022-09-06 /pmc/articles/PMC9504619/ /pubmed/36144396 http://dx.doi.org/10.3390/microorganisms10091794 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gontijo, Marco Túlio Pardini
Ramia, Nancy E.
Dijamentiuk, Alexis
Elfassy, Annelore
Taha, Samir
Mangavel, Cécile
Revol-Junelles, Anne-Marie
Borges, Frédéric
Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title_full Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title_fullStr Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title_full_unstemmed Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title_short Mining Biosynthetic Gene Clusters in Carnobacterium maltaromaticum by Interference Competition Network and Genome Analysis
title_sort mining biosynthetic gene clusters in carnobacterium maltaromaticum by interference competition network and genome analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504619/
https://www.ncbi.nlm.nih.gov/pubmed/36144396
http://dx.doi.org/10.3390/microorganisms10091794
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