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The P aracoccus denitrificans NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms
Nitrate and nitrite transport across biological membranes is often facilitated by protein transporters that are members of the major facilitator superfamily. Paracoccus denitrificans contains an unusual arrangement whereby two of these transporters, NarK1 and NarK2, are fused into a single protein,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217062/ https://www.ncbi.nlm.nih.gov/pubmed/27696579 http://dx.doi.org/10.1111/mmi.13546 |
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author | Goddard, Alan D. Bali, Shilpa Mavridou, Despoina A.I. Luque‐Almagro, Victor M. Gates, Andrew J. Dolores Roldán, M. Newstead, Simon Richardson, David J. Ferguson, Stuart J. |
author_facet | Goddard, Alan D. Bali, Shilpa Mavridou, Despoina A.I. Luque‐Almagro, Victor M. Gates, Andrew J. Dolores Roldán, M. Newstead, Simon Richardson, David J. Ferguson, Stuart J. |
author_sort | Goddard, Alan D. |
collection | PubMed |
description | Nitrate and nitrite transport across biological membranes is often facilitated by protein transporters that are members of the major facilitator superfamily. Paracoccus denitrificans contains an unusual arrangement whereby two of these transporters, NarK1 and NarK2, are fused into a single protein, NarK, which delivers nitrate to the respiratory nitrate reductase and transfers the product, nitrite, to the periplasm. Our complementation studies, using a mutant lacking the nitrate/proton symporter NasA from the assimilatory nitrate reductase pathway, support that NarK1 functions as a nitrate/proton symporter while NarK2 is a nitrate/nitrite antiporter. Through the same experimental system, we find that Escherichia coli NarK and NarU can complement deletions in both narK and nasA in P. denitrificans, suggesting that, while these proteins are most likely nitrate/nitrite antiporters, they can also act in the net uptake of nitrate. Finally, we argue that primary sequence analysis and structural modelling do not readily explain why NasA, NarK1 and NarK2, as well as other transporters from this protein family, have such different functions, ranging from net nitrate uptake to nitrate/nitrite exchange. |
format | Online Article Text |
id | pubmed-5217062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52170622017-01-25 The P aracoccus denitrificans NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms Goddard, Alan D. Bali, Shilpa Mavridou, Despoina A.I. Luque‐Almagro, Victor M. Gates, Andrew J. Dolores Roldán, M. Newstead, Simon Richardson, David J. Ferguson, Stuart J. Mol Microbiol Research Articles Nitrate and nitrite transport across biological membranes is often facilitated by protein transporters that are members of the major facilitator superfamily. Paracoccus denitrificans contains an unusual arrangement whereby two of these transporters, NarK1 and NarK2, are fused into a single protein, NarK, which delivers nitrate to the respiratory nitrate reductase and transfers the product, nitrite, to the periplasm. Our complementation studies, using a mutant lacking the nitrate/proton symporter NasA from the assimilatory nitrate reductase pathway, support that NarK1 functions as a nitrate/proton symporter while NarK2 is a nitrate/nitrite antiporter. Through the same experimental system, we find that Escherichia coli NarK and NarU can complement deletions in both narK and nasA in P. denitrificans, suggesting that, while these proteins are most likely nitrate/nitrite antiporters, they can also act in the net uptake of nitrate. Finally, we argue that primary sequence analysis and structural modelling do not readily explain why NasA, NarK1 and NarK2, as well as other transporters from this protein family, have such different functions, ranging from net nitrate uptake to nitrate/nitrite exchange. John Wiley and Sons Inc. 2016-10-27 2017-01 /pmc/articles/PMC5217062/ /pubmed/27696579 http://dx.doi.org/10.1111/mmi.13546 Text en © 2016 The Authors. Molecular Microbiology Published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Goddard, Alan D. Bali, Shilpa Mavridou, Despoina A.I. Luque‐Almagro, Victor M. Gates, Andrew J. Dolores Roldán, M. Newstead, Simon Richardson, David J. Ferguson, Stuart J. The P aracoccus denitrificans NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title | The P
aracoccus denitrificans
NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title_full | The P
aracoccus denitrificans
NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title_fullStr | The P
aracoccus denitrificans
NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title_full_unstemmed | The P
aracoccus denitrificans
NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title_short | The P
aracoccus denitrificans
NarK‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
title_sort | p
aracoccus denitrificans
nark‐like nitrate and nitrite transporters—probing nitrate uptake and nitrate/nitrite exchange mechanisms |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217062/ https://www.ncbi.nlm.nih.gov/pubmed/27696579 http://dx.doi.org/10.1111/mmi.13546 |
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