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Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent
Bacteria acquire phosphate (P(i)) by maintaining a periplasmic concentration below environmental levels. We recently described an extracellular P(i) buffer which appears to counteract the gradient required for P(i) diffusion. Here, we demonstrate that various treatments to outer membrane (OM) consti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250820/ https://www.ncbi.nlm.nih.gov/pubmed/32457313 http://dx.doi.org/10.1038/s41467-020-16428-w |
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author | Kamennaya, Nina A. Geraki, Kalotina Scanlan, David J. Zubkov, Mikhail V. |
author_facet | Kamennaya, Nina A. Geraki, Kalotina Scanlan, David J. Zubkov, Mikhail V. |
author_sort | Kamennaya, Nina A. |
collection | PubMed |
description | Bacteria acquire phosphate (P(i)) by maintaining a periplasmic concentration below environmental levels. We recently described an extracellular P(i) buffer which appears to counteract the gradient required for P(i) diffusion. Here, we demonstrate that various treatments to outer membrane (OM) constituents do not affect the buffered P(i) because bacteria accumulate P(i) in the periplasm, from which it can be removed hypo-osmotically. The periplasmic P(i) can be gradually imported into the cytoplasm by ATP-powered transport, however, the proton motive force (PMF) is not required to keep P(i) in the periplasm. In contrast, the accumulation of P(i) into the periplasm across the OM is PMF-dependent and can be enhanced by light energy. Because the conventional mechanism of P(i)-specific transport cannot explain P(i) accumulation in the periplasm we propose that periplasmic P(i) anions pair with chemiosmotic cations of the PMF and millions of accumulated P(i) pairs could influence the periplasmic osmolarity of marine bacteria. |
format | Online Article Text |
id | pubmed-7250820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72508202020-06-04 Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent Kamennaya, Nina A. Geraki, Kalotina Scanlan, David J. Zubkov, Mikhail V. Nat Commun Article Bacteria acquire phosphate (P(i)) by maintaining a periplasmic concentration below environmental levels. We recently described an extracellular P(i) buffer which appears to counteract the gradient required for P(i) diffusion. Here, we demonstrate that various treatments to outer membrane (OM) constituents do not affect the buffered P(i) because bacteria accumulate P(i) in the periplasm, from which it can be removed hypo-osmotically. The periplasmic P(i) can be gradually imported into the cytoplasm by ATP-powered transport, however, the proton motive force (PMF) is not required to keep P(i) in the periplasm. In contrast, the accumulation of P(i) into the periplasm across the OM is PMF-dependent and can be enhanced by light energy. Because the conventional mechanism of P(i)-specific transport cannot explain P(i) accumulation in the periplasm we propose that periplasmic P(i) anions pair with chemiosmotic cations of the PMF and millions of accumulated P(i) pairs could influence the periplasmic osmolarity of marine bacteria. Nature Publishing Group UK 2020-05-26 /pmc/articles/PMC7250820/ /pubmed/32457313 http://dx.doi.org/10.1038/s41467-020-16428-w Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kamennaya, Nina A. Geraki, Kalotina Scanlan, David J. Zubkov, Mikhail V. Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title | Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title_full | Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title_fullStr | Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title_full_unstemmed | Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title_short | Accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
title_sort | accumulation of ambient phosphate into the periplasm of marine bacteria is proton motive force dependent |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250820/ https://www.ncbi.nlm.nih.gov/pubmed/32457313 http://dx.doi.org/10.1038/s41467-020-16428-w |
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