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Microbial acetone oxidation in coastal seawater

Acetone is an important oxygenated volatile organic compound (OVOC) in the troposphere where it influences the oxidizing capacity of the atmosphere. However, the air-sea flux is not well quantified, in part due to a lack of knowledge regarding which processes control oceanic concentrations, and, spe...

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Autores principales: Dixon, Joanna L., Beale, Rachael, Sargeant, Stephanie L., Tarran, Glen A., Nightingale, Philip D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033308/
https://www.ncbi.nlm.nih.gov/pubmed/24904556
http://dx.doi.org/10.3389/fmicb.2014.00243
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author Dixon, Joanna L.
Beale, Rachael
Sargeant, Stephanie L.
Tarran, Glen A.
Nightingale, Philip D.
author_facet Dixon, Joanna L.
Beale, Rachael
Sargeant, Stephanie L.
Tarran, Glen A.
Nightingale, Philip D.
author_sort Dixon, Joanna L.
collection PubMed
description Acetone is an important oxygenated volatile organic compound (OVOC) in the troposphere where it influences the oxidizing capacity of the atmosphere. However, the air-sea flux is not well quantified, in part due to a lack of knowledge regarding which processes control oceanic concentrations, and, specifically whether microbial oxidation to CO(2) represents a significant loss process. We demonstrate that (14)C labeled acetone can be used to determine microbial oxidation to (14)CO(2). Linear microbial rates of acetone oxidation to CO(2) were observed for between 0.75-3.5 h at a seasonally eutrophic coastal station located in the western English Channel (L4). A kinetic experiment in summer at station L4 gave a V(max) of 4.1 pmol L(-1) h(-1), with a K(m) constant of 54 pM. We then used this technique to obtain microbial acetone loss rates ranging between 1.2 and 42 pmol L(-1) h(-1.)(monthly averages) over an annual cycle at L4, with maximum rates observed during winter months. The biological turnover time of acetone (in situ concentration divided by microbial oxidation rate) in surface waters varied from ~3 days in February 2011, when in situ concentrations were 3 ± 1 nM, to >240 days in June 2011, when concentrations were more than twofold higher at 7.5 ± 0.7 nM. These relatively low marine microbial acetone oxidation rates, when normalized to in situ concentrations, suggest that marine microbes preferentially utilize other OVOCs such as methanol and acetaldehyde.
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spelling pubmed-40333082014-06-05 Microbial acetone oxidation in coastal seawater Dixon, Joanna L. Beale, Rachael Sargeant, Stephanie L. Tarran, Glen A. Nightingale, Philip D. Front Microbiol Microbiology Acetone is an important oxygenated volatile organic compound (OVOC) in the troposphere where it influences the oxidizing capacity of the atmosphere. However, the air-sea flux is not well quantified, in part due to a lack of knowledge regarding which processes control oceanic concentrations, and, specifically whether microbial oxidation to CO(2) represents a significant loss process. We demonstrate that (14)C labeled acetone can be used to determine microbial oxidation to (14)CO(2). Linear microbial rates of acetone oxidation to CO(2) were observed for between 0.75-3.5 h at a seasonally eutrophic coastal station located in the western English Channel (L4). A kinetic experiment in summer at station L4 gave a V(max) of 4.1 pmol L(-1) h(-1), with a K(m) constant of 54 pM. We then used this technique to obtain microbial acetone loss rates ranging between 1.2 and 42 pmol L(-1) h(-1.)(monthly averages) over an annual cycle at L4, with maximum rates observed during winter months. The biological turnover time of acetone (in situ concentration divided by microbial oxidation rate) in surface waters varied from ~3 days in February 2011, when in situ concentrations were 3 ± 1 nM, to >240 days in June 2011, when concentrations were more than twofold higher at 7.5 ± 0.7 nM. These relatively low marine microbial acetone oxidation rates, when normalized to in situ concentrations, suggest that marine microbes preferentially utilize other OVOCs such as methanol and acetaldehyde. Frontiers Media S.A. 2014-05-26 /pmc/articles/PMC4033308/ /pubmed/24904556 http://dx.doi.org/10.3389/fmicb.2014.00243 Text en Copyright © 2014 Dixon, Beale, Sargeant, Tarran and Nightingale. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Dixon, Joanna L.
Beale, Rachael
Sargeant, Stephanie L.
Tarran, Glen A.
Nightingale, Philip D.
Microbial acetone oxidation in coastal seawater
title Microbial acetone oxidation in coastal seawater
title_full Microbial acetone oxidation in coastal seawater
title_fullStr Microbial acetone oxidation in coastal seawater
title_full_unstemmed Microbial acetone oxidation in coastal seawater
title_short Microbial acetone oxidation in coastal seawater
title_sort microbial acetone oxidation in coastal seawater
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033308/
https://www.ncbi.nlm.nih.gov/pubmed/24904556
http://dx.doi.org/10.3389/fmicb.2014.00243
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AT nightingalephilipd microbialacetoneoxidationincoastalseawater