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Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere
ABSTRACT: The biocatalysis of β-myrcene into value-added compounds, with enhanced organoleptic/therapeutic properties, may be performed by resorting to specialized enzymatic machinery of β-myrcene-biotransforming bacteria. Few β-myrcene-biotransforming bacteria have been studied, limiting the divers...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386936/ https://www.ncbi.nlm.nih.gov/pubmed/37405434 http://dx.doi.org/10.1007/s00253-023-12650-w |
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author | Soares-Castro, Pedro Soares, Filipa Reis, Francisca Lino-Neto, Teresa Santos, Pedro M. |
author_facet | Soares-Castro, Pedro Soares, Filipa Reis, Francisca Lino-Neto, Teresa Santos, Pedro M. |
author_sort | Soares-Castro, Pedro |
collection | PubMed |
description | ABSTRACT: The biocatalysis of β-myrcene into value-added compounds, with enhanced organoleptic/therapeutic properties, may be performed by resorting to specialized enzymatic machinery of β-myrcene-biotransforming bacteria. Few β-myrcene-biotransforming bacteria have been studied, limiting the diversity of genetic modules/catabolic pathways available for biotechnological research. In our model Pseudomonas sp. strain M1, the β-myrcene catabolic core-code was identified in a 28-kb genomic island (GI). The lack of close homologs of this β-myrcene-associated genetic code prompted a bioprospection of cork oak and eucalyptus rhizospheres, from 4 geographic locations in Portugal, to evaluate the environmental diversity and dissemination of the β-myrcene-biotransforming genetic trait (Myr(+)). Soil microbiomes were enriched in β-myrcene-supplemented cultures, from which β-myrcene-biotransforming bacteria were isolated, belonging to Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, and Sphingobacteriia classes. From a panel of representative Myr(+) isolates that included 7 bacterial genera, the production of β-myrcene derivatives previously reported in strain M1 was detected in Pseudomonas spp., Cupriavidus sp., Sphingobacterium sp., and Variovorax sp. A comparative genomics analysis against the genome of strain M1 found the M1-GI code in 11 new Pseudomonas genomes. Full nucleotide conservation of the β-myrcene core-code was observed throughout a 76-kb locus in strain M1 and all 11 Pseudomonas spp., resembling the structure of an integrative and conjugative element (ICE), despite being isolated from different niches. Furthermore, the characterization of isolates not harboring the Myr(+)-related 76-kb locus suggested that they may biotransform β-myrcene via alternative catabolic loci, being thereby a novel source of enzymes and biomolecule catalogue for biotechnological exploitation. KEY POINTS: • The isolation of 150 Myr(+) bacteria hints the ubiquity of such trait in the rhizosphere. • The Myr(+) trait is spread across different bacterial taxonomic classes. • The core-code for the Myr(+) trait was detected in a novel ICE, only found in Pseudomonas spp. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-023-12650-w. |
format | Online Article Text |
id | pubmed-10386936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103869362023-07-31 Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere Soares-Castro, Pedro Soares, Filipa Reis, Francisca Lino-Neto, Teresa Santos, Pedro M. Appl Microbiol Biotechnol Genomics, Transcriptomics, Proteomics ABSTRACT: The biocatalysis of β-myrcene into value-added compounds, with enhanced organoleptic/therapeutic properties, may be performed by resorting to specialized enzymatic machinery of β-myrcene-biotransforming bacteria. Few β-myrcene-biotransforming bacteria have been studied, limiting the diversity of genetic modules/catabolic pathways available for biotechnological research. In our model Pseudomonas sp. strain M1, the β-myrcene catabolic core-code was identified in a 28-kb genomic island (GI). The lack of close homologs of this β-myrcene-associated genetic code prompted a bioprospection of cork oak and eucalyptus rhizospheres, from 4 geographic locations in Portugal, to evaluate the environmental diversity and dissemination of the β-myrcene-biotransforming genetic trait (Myr(+)). Soil microbiomes were enriched in β-myrcene-supplemented cultures, from which β-myrcene-biotransforming bacteria were isolated, belonging to Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, and Sphingobacteriia classes. From a panel of representative Myr(+) isolates that included 7 bacterial genera, the production of β-myrcene derivatives previously reported in strain M1 was detected in Pseudomonas spp., Cupriavidus sp., Sphingobacterium sp., and Variovorax sp. A comparative genomics analysis against the genome of strain M1 found the M1-GI code in 11 new Pseudomonas genomes. Full nucleotide conservation of the β-myrcene core-code was observed throughout a 76-kb locus in strain M1 and all 11 Pseudomonas spp., resembling the structure of an integrative and conjugative element (ICE), despite being isolated from different niches. Furthermore, the characterization of isolates not harboring the Myr(+)-related 76-kb locus suggested that they may biotransform β-myrcene via alternative catabolic loci, being thereby a novel source of enzymes and biomolecule catalogue for biotechnological exploitation. KEY POINTS: • The isolation of 150 Myr(+) bacteria hints the ubiquity of such trait in the rhizosphere. • The Myr(+) trait is spread across different bacterial taxonomic classes. • The core-code for the Myr(+) trait was detected in a novel ICE, only found in Pseudomonas spp. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-023-12650-w. Springer Berlin Heidelberg 2023-07-05 2023 /pmc/articles/PMC10386936/ /pubmed/37405434 http://dx.doi.org/10.1007/s00253-023-12650-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 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 | Genomics, Transcriptomics, Proteomics Soares-Castro, Pedro Soares, Filipa Reis, Francisca Lino-Neto, Teresa Santos, Pedro M. Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title | Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title_full | Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title_fullStr | Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title_full_unstemmed | Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title_short | Bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
title_sort | bioprospection of the bacterial β-myrcene-biotransforming trait in the rhizosphere |
topic | Genomics, Transcriptomics, Proteomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386936/ https://www.ncbi.nlm.nih.gov/pubmed/37405434 http://dx.doi.org/10.1007/s00253-023-12650-w |
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