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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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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. |
format | Online Article Text |
id | pubmed-4033308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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