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Decoupling of respiration rates and abundance in marine prokaryoplankton

The ocean–atmosphere exchange of CO(2) largely depends on the balance between marine microbial photosynthesis and respiration. Despite vast taxonomic and metabolic diversity among marine planktonic bacteria and archaea (prokaryoplankton)(1–3), their respiration usually is measured in bulk and treate...

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Autores principales: Munson-McGee, Jacob H., Lindsay, Melody R., Sintes, Eva, Brown, Julia M., D’Angelo, Timothy, Brown, Joe, Lubelczyk, Laura C., Tomko, Paxton, Emerson, David, Orcutt, Beth N., Poulton, Nicole J., Herndl, Gerhard J., Stepanauskas, Ramunas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771814/
https://www.ncbi.nlm.nih.gov/pubmed/36477536
http://dx.doi.org/10.1038/s41586-022-05505-3
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author Munson-McGee, Jacob H.
Lindsay, Melody R.
Sintes, Eva
Brown, Julia M.
D’Angelo, Timothy
Brown, Joe
Lubelczyk, Laura C.
Tomko, Paxton
Emerson, David
Orcutt, Beth N.
Poulton, Nicole J.
Herndl, Gerhard J.
Stepanauskas, Ramunas
author_facet Munson-McGee, Jacob H.
Lindsay, Melody R.
Sintes, Eva
Brown, Julia M.
D’Angelo, Timothy
Brown, Joe
Lubelczyk, Laura C.
Tomko, Paxton
Emerson, David
Orcutt, Beth N.
Poulton, Nicole J.
Herndl, Gerhard J.
Stepanauskas, Ramunas
author_sort Munson-McGee, Jacob H.
collection PubMed
description The ocean–atmosphere exchange of CO(2) largely depends on the balance between marine microbial photosynthesis and respiration. Despite vast taxonomic and metabolic diversity among marine planktonic bacteria and archaea (prokaryoplankton)(1–3), their respiration usually is measured in bulk and treated as a ‘black box’ in global biogeochemical models(4); this limits the mechanistic understanding of the global carbon cycle. Here, using a technology for integrated phenotype analyses and genomic sequencing of individual microbial cells, we show that cell-specific respiration rates differ by more than 1,000× among prokaryoplankton genera. The majority of respiration was found to be performed by minority members of prokaryoplankton (including the Roseobacter cluster), whereas cells of the most prevalent lineages (including Pelagibacter and SAR86) had extremely low respiration rates. The decoupling of respiration rates from abundance among lineages, elevated counts of proteorhodopsin transcripts in Pelagibacter and SAR86 cells and elevated respiration of SAR86 at night indicate that proteorhodopsin-based phototrophy(3,5–7) probably constitutes an important source of energy to prokaryoplankton and may increase growth efficiency. These findings suggest that the dependence of prokaryoplankton on respiration and remineralization of phytoplankton-derived organic carbon into CO(2) for its energy demands and growth may be lower than commonly assumed and variable among lineages.
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spelling pubmed-97718142022-12-23 Decoupling of respiration rates and abundance in marine prokaryoplankton Munson-McGee, Jacob H. Lindsay, Melody R. Sintes, Eva Brown, Julia M. D’Angelo, Timothy Brown, Joe Lubelczyk, Laura C. Tomko, Paxton Emerson, David Orcutt, Beth N. Poulton, Nicole J. Herndl, Gerhard J. Stepanauskas, Ramunas Nature Article The ocean–atmosphere exchange of CO(2) largely depends on the balance between marine microbial photosynthesis and respiration. Despite vast taxonomic and metabolic diversity among marine planktonic bacteria and archaea (prokaryoplankton)(1–3), their respiration usually is measured in bulk and treated as a ‘black box’ in global biogeochemical models(4); this limits the mechanistic understanding of the global carbon cycle. Here, using a technology for integrated phenotype analyses and genomic sequencing of individual microbial cells, we show that cell-specific respiration rates differ by more than 1,000× among prokaryoplankton genera. The majority of respiration was found to be performed by minority members of prokaryoplankton (including the Roseobacter cluster), whereas cells of the most prevalent lineages (including Pelagibacter and SAR86) had extremely low respiration rates. The decoupling of respiration rates from abundance among lineages, elevated counts of proteorhodopsin transcripts in Pelagibacter and SAR86 cells and elevated respiration of SAR86 at night indicate that proteorhodopsin-based phototrophy(3,5–7) probably constitutes an important source of energy to prokaryoplankton and may increase growth efficiency. These findings suggest that the dependence of prokaryoplankton on respiration and remineralization of phytoplankton-derived organic carbon into CO(2) for its energy demands and growth may be lower than commonly assumed and variable among lineages. Nature Publishing Group UK 2022-12-07 2022 /pmc/articles/PMC9771814/ /pubmed/36477536 http://dx.doi.org/10.1038/s41586-022-05505-3 Text en © The Author(s) 2022 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 Article
Munson-McGee, Jacob H.
Lindsay, Melody R.
Sintes, Eva
Brown, Julia M.
D’Angelo, Timothy
Brown, Joe
Lubelczyk, Laura C.
Tomko, Paxton
Emerson, David
Orcutt, Beth N.
Poulton, Nicole J.
Herndl, Gerhard J.
Stepanauskas, Ramunas
Decoupling of respiration rates and abundance in marine prokaryoplankton
title Decoupling of respiration rates and abundance in marine prokaryoplankton
title_full Decoupling of respiration rates and abundance in marine prokaryoplankton
title_fullStr Decoupling of respiration rates and abundance in marine prokaryoplankton
title_full_unstemmed Decoupling of respiration rates and abundance in marine prokaryoplankton
title_short Decoupling of respiration rates and abundance in marine prokaryoplankton
title_sort decoupling of respiration rates and abundance in marine prokaryoplankton
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771814/
https://www.ncbi.nlm.nih.gov/pubmed/36477536
http://dx.doi.org/10.1038/s41586-022-05505-3
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