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Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis

An important factor dictating coral fitness is the quality of bacteria associated with corals and coral reefs. One way that bacteria benefit corals is by stimulating the larval to juvenile life cycle transition of settlement and metamorphosis. Tetrabromopyrrole (TBP) is a small molecule produced by...

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Autores principales: Alker, Amanda T., Farrell, Morgan V., Demko, Alyssa M., Purdy, Trevor N., Adak, Sanjoy, Moore, Bradley S., Sneed, Jennifer M., Paul, Valerie J., Shikuma, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509201/
https://www.ncbi.nlm.nih.gov/pubmed/37726481
http://dx.doi.org/10.1038/s43705-023-00309-6
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author Alker, Amanda T.
Farrell, Morgan V.
Demko, Alyssa M.
Purdy, Trevor N.
Adak, Sanjoy
Moore, Bradley S.
Sneed, Jennifer M.
Paul, Valerie J.
Shikuma, Nicholas J.
author_facet Alker, Amanda T.
Farrell, Morgan V.
Demko, Alyssa M.
Purdy, Trevor N.
Adak, Sanjoy
Moore, Bradley S.
Sneed, Jennifer M.
Paul, Valerie J.
Shikuma, Nicholas J.
author_sort Alker, Amanda T.
collection PubMed
description An important factor dictating coral fitness is the quality of bacteria associated with corals and coral reefs. One way that bacteria benefit corals is by stimulating the larval to juvenile life cycle transition of settlement and metamorphosis. Tetrabromopyrrole (TBP) is a small molecule produced by bacteria that stimulates metamorphosis with and without attachment in a range of coral species. A standing debate remains, however, about whether TBP biosynthesis from live Pseudoalteromonas bacteria is the primary stimulant of coral metamorphosis. In this study, we create a Pseudoalteromonas sp. PS5 mutant lacking the TBP brominase gene, bmp2. Using this mutant, we confirm that the bmp2 gene is critical for TBP biosynthesis in Pseudoalteromonas sp. PS5. Mutation of this gene ablates the bacterium’s ability in live cultures to stimulate the metamorphosis of the stony coral Porites astreoides. We further demonstrate that expression of TBP biosynthesis genes is strongest in stationary and biofilm modes of growth, where Pseudoalteromonas sp. PS5 might exist within surface-attached biofilms on the sea floor. Finally, we create a modular transposon plasmid for genomic integration and fluorescent labeling of Pseudoalteromonas sp. PS5 cells. Our results functionally link a TBP biosynthesis gene from live bacteria to a morphogenic effect in corals. The genetic techniques established here provide new tools to explore coral-bacteria interactions and could help to inform future decisions about utilizing marine bacteria or their products for coral restoration.
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spelling pubmed-105092012023-09-21 Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis Alker, Amanda T. Farrell, Morgan V. Demko, Alyssa M. Purdy, Trevor N. Adak, Sanjoy Moore, Bradley S. Sneed, Jennifer M. Paul, Valerie J. Shikuma, Nicholas J. ISME Commun Brief Communication An important factor dictating coral fitness is the quality of bacteria associated with corals and coral reefs. One way that bacteria benefit corals is by stimulating the larval to juvenile life cycle transition of settlement and metamorphosis. Tetrabromopyrrole (TBP) is a small molecule produced by bacteria that stimulates metamorphosis with and without attachment in a range of coral species. A standing debate remains, however, about whether TBP biosynthesis from live Pseudoalteromonas bacteria is the primary stimulant of coral metamorphosis. In this study, we create a Pseudoalteromonas sp. PS5 mutant lacking the TBP brominase gene, bmp2. Using this mutant, we confirm that the bmp2 gene is critical for TBP biosynthesis in Pseudoalteromonas sp. PS5. Mutation of this gene ablates the bacterium’s ability in live cultures to stimulate the metamorphosis of the stony coral Porites astreoides. We further demonstrate that expression of TBP biosynthesis genes is strongest in stationary and biofilm modes of growth, where Pseudoalteromonas sp. PS5 might exist within surface-attached biofilms on the sea floor. Finally, we create a modular transposon plasmid for genomic integration and fluorescent labeling of Pseudoalteromonas sp. PS5 cells. Our results functionally link a TBP biosynthesis gene from live bacteria to a morphogenic effect in corals. The genetic techniques established here provide new tools to explore coral-bacteria interactions and could help to inform future decisions about utilizing marine bacteria or their products for coral restoration. Nature Publishing Group UK 2023-09-19 /pmc/articles/PMC10509201/ /pubmed/37726481 http://dx.doi.org/10.1038/s43705-023-00309-6 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 Brief Communication
Alker, Amanda T.
Farrell, Morgan V.
Demko, Alyssa M.
Purdy, Trevor N.
Adak, Sanjoy
Moore, Bradley S.
Sneed, Jennifer M.
Paul, Valerie J.
Shikuma, Nicholas J.
Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title_full Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title_fullStr Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title_full_unstemmed Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title_short Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
title_sort linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509201/
https://www.ncbi.nlm.nih.gov/pubmed/37726481
http://dx.doi.org/10.1038/s43705-023-00309-6
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