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Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria
BACKGROUND: Cyanobacteria are well known for the production of a range of secondary metabolites. Whilst recent genome sequencing projects has led to an increase in the number of publically available cyanobacterial genomes, the secondary metabolite potential of many of these organisms remains elusive...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558948/ https://www.ncbi.nlm.nih.gov/pubmed/26335778 http://dx.doi.org/10.1186/s12864-015-1855-z |
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author | Micallef, Melinda L. D’Agostino, Paul M. Sharma, Deepti Viswanathan, Rajesh Moffitt, Michelle C. |
author_facet | Micallef, Melinda L. D’Agostino, Paul M. Sharma, Deepti Viswanathan, Rajesh Moffitt, Michelle C. |
author_sort | Micallef, Melinda L. |
collection | PubMed |
description | BACKGROUND: Cyanobacteria are well known for the production of a range of secondary metabolites. Whilst recent genome sequencing projects has led to an increase in the number of publically available cyanobacterial genomes, the secondary metabolite potential of many of these organisms remains elusive. Our study focused on the 11 publically available Subsection V cyanobacterial genomes, together with the draft genomes of Westiella intricata UH strain HT-29-1 and Hapalosiphon welwitschii UH strain IC-52-3, for their genetic potential to produce secondary metabolites. The Subsection V cyanobacterial genomes analysed in this study are reported to produce a diverse range of natural products, including the hapalindole-family of compounds, microcystin, hapalosin, mycosporine-like amino acids and hydrocarbons. RESULTS: A putative gene cluster for the cyclic depsipeptide hapalosin, known to reverse P-glycoprotein multiple drug resistance, was identified within three Subsection V cyanobacterial genomes, including the producing cyanobacterium H. welwitschii UH strain IC-52-3. A number of orphan NRPS/PKS gene clusters and ribosomally-synthesised and post translationally-modified peptide gene clusters (including cyanobactin, microviridin and bacteriocin gene clusters) were identified. Furthermore, gene clusters encoding the biosynthesis of mycosporine-like amino acids, scytonemin, hydrocarbons and terpenes were also identified and compared. CONCLUSIONS: Genome mining has revealed the diversity, abundance and complex nature of the secondary metabolite potential of the Subsection V cyanobacteria. This bioinformatic study has identified novel biosynthetic enzymes which have not been associated with gene clusters of known classes of natural products, suggesting that these cyanobacteria potentially produce structurally novel secondary metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1855-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4558948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45589482015-09-04 Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria Micallef, Melinda L. D’Agostino, Paul M. Sharma, Deepti Viswanathan, Rajesh Moffitt, Michelle C. BMC Genomics Research Article BACKGROUND: Cyanobacteria are well known for the production of a range of secondary metabolites. Whilst recent genome sequencing projects has led to an increase in the number of publically available cyanobacterial genomes, the secondary metabolite potential of many of these organisms remains elusive. Our study focused on the 11 publically available Subsection V cyanobacterial genomes, together with the draft genomes of Westiella intricata UH strain HT-29-1 and Hapalosiphon welwitschii UH strain IC-52-3, for their genetic potential to produce secondary metabolites. The Subsection V cyanobacterial genomes analysed in this study are reported to produce a diverse range of natural products, including the hapalindole-family of compounds, microcystin, hapalosin, mycosporine-like amino acids and hydrocarbons. RESULTS: A putative gene cluster for the cyclic depsipeptide hapalosin, known to reverse P-glycoprotein multiple drug resistance, was identified within three Subsection V cyanobacterial genomes, including the producing cyanobacterium H. welwitschii UH strain IC-52-3. A number of orphan NRPS/PKS gene clusters and ribosomally-synthesised and post translationally-modified peptide gene clusters (including cyanobactin, microviridin and bacteriocin gene clusters) were identified. Furthermore, gene clusters encoding the biosynthesis of mycosporine-like amino acids, scytonemin, hydrocarbons and terpenes were also identified and compared. CONCLUSIONS: Genome mining has revealed the diversity, abundance and complex nature of the secondary metabolite potential of the Subsection V cyanobacteria. This bioinformatic study has identified novel biosynthetic enzymes which have not been associated with gene clusters of known classes of natural products, suggesting that these cyanobacteria potentially produce structurally novel secondary metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1855-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-03 /pmc/articles/PMC4558948/ /pubmed/26335778 http://dx.doi.org/10.1186/s12864-015-1855-z Text en © Micallef et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Micallef, Melinda L. D’Agostino, Paul M. Sharma, Deepti Viswanathan, Rajesh Moffitt, Michelle C. Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title | Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title_full | Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title_fullStr | Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title_full_unstemmed | Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title_short | Genome mining for natural product biosynthetic gene clusters in the Subsection V cyanobacteria |
title_sort | genome mining for natural product biosynthetic gene clusters in the subsection v cyanobacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558948/ https://www.ncbi.nlm.nih.gov/pubmed/26335778 http://dx.doi.org/10.1186/s12864-015-1855-z |
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