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Terpene biosynthesis in marine sponge animals
Sea sponges are the largest marine source of small-molecule natural products described to date. Sponge-derived molecules, such as the chemotherapeutic eribulin, the calcium-channel blocker manoalide, and antimalarial compound kalihinol A, are renowned for their impressive medicinal, chemical, and bi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992776/ https://www.ncbi.nlm.nih.gov/pubmed/36802428 http://dx.doi.org/10.1073/pnas.2220934120 |
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author | Wilson, Kayla de Rond, Tristan Burkhardt, Immo Steele, Taylor S. Schäfer, Rebecca J. B. Podell, Sheila Allen, Eric E. Moore, Bradley S. |
author_facet | Wilson, Kayla de Rond, Tristan Burkhardt, Immo Steele, Taylor S. Schäfer, Rebecca J. B. Podell, Sheila Allen, Eric E. Moore, Bradley S. |
author_sort | Wilson, Kayla |
collection | PubMed |
description | Sea sponges are the largest marine source of small-molecule natural products described to date. Sponge-derived molecules, such as the chemotherapeutic eribulin, the calcium-channel blocker manoalide, and antimalarial compound kalihinol A, are renowned for their impressive medicinal, chemical, and biological properties. Sponges contain microbiomes that control the production of many natural products isolated from these marine invertebrates. In fact, all genomic studies to date investigating the metabolic origins of sponge-derived small molecules concluded that microbes—not the sponge animal host—are the biosynthetic producers. However, early cell-sorting studies suggested the sponge animal host may play a role particularly in the production of terpenoid molecules. To investigate the genetic underpinnings of sponge terpenoid biosynthesis, we sequenced the metagenome and transcriptome of an isonitrile sesquiterpenoid-containing sponge of the order Bubarida. Using bioinformatic searches and biochemical validation, we identified a group of type I terpene synthases (TSs) from this sponge and multiple other species, the first of this enzyme class characterized from the sponge holobiome. The Bubarida TS-associated contigs consist of intron-containing genes homologous to sponge genes and feature GC percentage and coverage consistent with other eukaryotic sequences. We identified and characterized TS homologs from five different sponge species isolated from geographically distant locations, thereby suggesting a broad distribution amongst sponges. This work sheds light on the role of sponges in secondary metabolite production and speaks to the possibility that other sponge-specific molecules originate from the animal host. |
format | Online Article Text |
id | pubmed-9992776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99927762023-08-21 Terpene biosynthesis in marine sponge animals Wilson, Kayla de Rond, Tristan Burkhardt, Immo Steele, Taylor S. Schäfer, Rebecca J. B. Podell, Sheila Allen, Eric E. Moore, Bradley S. Proc Natl Acad Sci U S A Biological Sciences Sea sponges are the largest marine source of small-molecule natural products described to date. Sponge-derived molecules, such as the chemotherapeutic eribulin, the calcium-channel blocker manoalide, and antimalarial compound kalihinol A, are renowned for their impressive medicinal, chemical, and biological properties. Sponges contain microbiomes that control the production of many natural products isolated from these marine invertebrates. In fact, all genomic studies to date investigating the metabolic origins of sponge-derived small molecules concluded that microbes—not the sponge animal host—are the biosynthetic producers. However, early cell-sorting studies suggested the sponge animal host may play a role particularly in the production of terpenoid molecules. To investigate the genetic underpinnings of sponge terpenoid biosynthesis, we sequenced the metagenome and transcriptome of an isonitrile sesquiterpenoid-containing sponge of the order Bubarida. Using bioinformatic searches and biochemical validation, we identified a group of type I terpene synthases (TSs) from this sponge and multiple other species, the first of this enzyme class characterized from the sponge holobiome. The Bubarida TS-associated contigs consist of intron-containing genes homologous to sponge genes and feature GC percentage and coverage consistent with other eukaryotic sequences. We identified and characterized TS homologs from five different sponge species isolated from geographically distant locations, thereby suggesting a broad distribution amongst sponges. This work sheds light on the role of sponges in secondary metabolite production and speaks to the possibility that other sponge-specific molecules originate from the animal host. National Academy of Sciences 2023-02-21 2023-02-28 /pmc/articles/PMC9992776/ /pubmed/36802428 http://dx.doi.org/10.1073/pnas.2220934120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Wilson, Kayla de Rond, Tristan Burkhardt, Immo Steele, Taylor S. Schäfer, Rebecca J. B. Podell, Sheila Allen, Eric E. Moore, Bradley S. Terpene biosynthesis in marine sponge animals |
title | Terpene biosynthesis in marine sponge animals |
title_full | Terpene biosynthesis in marine sponge animals |
title_fullStr | Terpene biosynthesis in marine sponge animals |
title_full_unstemmed | Terpene biosynthesis in marine sponge animals |
title_short | Terpene biosynthesis in marine sponge animals |
title_sort | terpene biosynthesis in marine sponge animals |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992776/ https://www.ncbi.nlm.nih.gov/pubmed/36802428 http://dx.doi.org/10.1073/pnas.2220934120 |
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