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Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake

Lakes are a significant component of the global carbon cycle. Respiration exceeds net primary production in most freshwater lakes, making them a source of CO(2) to the atmosphere. Driven by heterotrophic microorganisms, respiration is assumed to be unaffected by light, thus it is measured in the dar...

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Autores principales: Piwosz, Kasia, Villena-Alemany, Cristian, Mujakić, Izabela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941148/
https://www.ncbi.nlm.nih.gov/pubmed/34802055
http://dx.doi.org/10.1038/s41396-021-01142-2
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author Piwosz, Kasia
Villena-Alemany, Cristian
Mujakić, Izabela
author_facet Piwosz, Kasia
Villena-Alemany, Cristian
Mujakić, Izabela
author_sort Piwosz, Kasia
collection PubMed
description Lakes are a significant component of the global carbon cycle. Respiration exceeds net primary production in most freshwater lakes, making them a source of CO(2) to the atmosphere. Driven by heterotrophic microorganisms, respiration is assumed to be unaffected by light, thus it is measured in the dark. However, photoheterotrophs, such as aerobic anoxygenic photoheterotrophic (AAP) bacteria that produce ATP via photochemical reactions, substantially reduce respiration in the light. They are an abundant and active component of bacterioplankton, but their photoheterotrophic contribution to microbial community metabolism remains unquantified. We showed that the community respiration rate in a freshwater lake was reduced by 15.2% (95% confidence interval (CI): 6.6–23.8%) in infrared light that is usable by AAP bacteria but not by primary producers. Moreover, significantly higher assimilation rates of glucose (18.1%; 7.8–28.4%), pyruvate (9.5%; 4.2–14.8%), and leucine (5.9%; 0.1–11.6%) were measured in infrared light. At the ecosystem scale, the amount of CO(2) from respiration unbalanced by net primary production was by 3.69 × 10(9) g CO(2) lower over these two sampling seasons when measured in the infrared light. Our results demonstrate that dark measurements of microbial activity significantly bias the carbon fluxes, providing a new paradigm for their quantification in aquatic environments.
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spelling pubmed-89411482022-04-08 Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake Piwosz, Kasia Villena-Alemany, Cristian Mujakić, Izabela ISME J Article Lakes are a significant component of the global carbon cycle. Respiration exceeds net primary production in most freshwater lakes, making them a source of CO(2) to the atmosphere. Driven by heterotrophic microorganisms, respiration is assumed to be unaffected by light, thus it is measured in the dark. However, photoheterotrophs, such as aerobic anoxygenic photoheterotrophic (AAP) bacteria that produce ATP via photochemical reactions, substantially reduce respiration in the light. They are an abundant and active component of bacterioplankton, but their photoheterotrophic contribution to microbial community metabolism remains unquantified. We showed that the community respiration rate in a freshwater lake was reduced by 15.2% (95% confidence interval (CI): 6.6–23.8%) in infrared light that is usable by AAP bacteria but not by primary producers. Moreover, significantly higher assimilation rates of glucose (18.1%; 7.8–28.4%), pyruvate (9.5%; 4.2–14.8%), and leucine (5.9%; 0.1–11.6%) were measured in infrared light. At the ecosystem scale, the amount of CO(2) from respiration unbalanced by net primary production was by 3.69 × 10(9) g CO(2) lower over these two sampling seasons when measured in the infrared light. Our results demonstrate that dark measurements of microbial activity significantly bias the carbon fluxes, providing a new paradigm for their quantification in aquatic environments. Nature Publishing Group UK 2021-11-20 2022-04 /pmc/articles/PMC8941148/ /pubmed/34802055 http://dx.doi.org/10.1038/s41396-021-01142-2 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Piwosz, Kasia
Villena-Alemany, Cristian
Mujakić, Izabela
Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title_full Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title_fullStr Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title_full_unstemmed Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title_short Photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
title_sort photoheterotrophy by aerobic anoxygenic bacteria modulates carbon fluxes in a freshwater lake
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941148/
https://www.ncbi.nlm.nih.gov/pubmed/34802055
http://dx.doi.org/10.1038/s41396-021-01142-2
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