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A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress
Resistance to high concentrations of bile salts in the human intestinal tract is vital for the survival of enteric bacteria such as E scherichia coli. Although the tripartite AcrAB–TolC efflux system plays a significant role in this resistance, it is purported that other efflux pumps must also be in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235344/ https://www.ncbi.nlm.nih.gov/pubmed/24684269 http://dx.doi.org/10.1111/mmi.12597 |
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author | Paul, Stephanie Alegre, Kamela O Holdsworth, Scarlett R Rice, Matthew Brown, James A McVeigh, Paul Kelly, Sharon M Law, Christopher J |
author_facet | Paul, Stephanie Alegre, Kamela O Holdsworth, Scarlett R Rice, Matthew Brown, James A McVeigh, Paul Kelly, Sharon M Law, Christopher J |
author_sort | Paul, Stephanie |
collection | PubMed |
description | Resistance to high concentrations of bile salts in the human intestinal tract is vital for the survival of enteric bacteria such as E scherichia coli. Although the tripartite AcrAB–TolC efflux system plays a significant role in this resistance, it is purported that other efflux pumps must also be involved. We provide evidence from a comprehensive suite of experiments performed at two different pH values (7.2 and 6.0) that reflect pH conditions that E . coli may encounter in human gut that MdtM, a single-component multidrug resistance transporter of the major facilitator superfamily, functions in bile salt resistance in E . coli by catalysing secondary active transport of bile salts out of the cell cytoplasm. Furthermore, assays performed on a chromosomal ΔacrB mutant transformed with multicopy plasmid encoding MdtM suggested a functional synergism between the single-component MdtM transporter and the tripartite AcrAB–TolC system that results in a multiplicative effect on resistance. Substrate binding experiments performed on purified MdtM demonstrated that the transporter binds to cholate and deoxycholate with micromolar affinity, and transport assays performed on inverted vesicles confirmed the capacity of MdtM to catalyse electrogenic bile salt/H(+) antiport. |
format | Online Article Text |
id | pubmed-4235344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42353442014-12-19 A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress Paul, Stephanie Alegre, Kamela O Holdsworth, Scarlett R Rice, Matthew Brown, James A McVeigh, Paul Kelly, Sharon M Law, Christopher J Mol Microbiol Research Articles Resistance to high concentrations of bile salts in the human intestinal tract is vital for the survival of enteric bacteria such as E scherichia coli. Although the tripartite AcrAB–TolC efflux system plays a significant role in this resistance, it is purported that other efflux pumps must also be involved. We provide evidence from a comprehensive suite of experiments performed at two different pH values (7.2 and 6.0) that reflect pH conditions that E . coli may encounter in human gut that MdtM, a single-component multidrug resistance transporter of the major facilitator superfamily, functions in bile salt resistance in E . coli by catalysing secondary active transport of bile salts out of the cell cytoplasm. Furthermore, assays performed on a chromosomal ΔacrB mutant transformed with multicopy plasmid encoding MdtM suggested a functional synergism between the single-component MdtM transporter and the tripartite AcrAB–TolC system that results in a multiplicative effect on resistance. Substrate binding experiments performed on purified MdtM demonstrated that the transporter binds to cholate and deoxycholate with micromolar affinity, and transport assays performed on inverted vesicles confirmed the capacity of MdtM to catalyse electrogenic bile salt/H(+) antiport. BlackWell Publishing Ltd 2014-05 2014-04-13 /pmc/articles/PMC4235344/ /pubmed/24684269 http://dx.doi.org/10.1111/mmi.12597 Text en © 2014 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Paul, Stephanie Alegre, Kamela O Holdsworth, Scarlett R Rice, Matthew Brown, James A McVeigh, Paul Kelly, Sharon M Law, Christopher J A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title | A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title_full | A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title_fullStr | A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title_full_unstemmed | A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title_short | A single-component multidrug transporter of the major facilitator superfamily is part of a network that protects E scherichia coli from bile salt stress |
title_sort | single-component multidrug transporter of the major facilitator superfamily is part of a network that protects e scherichia coli from bile salt stress |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235344/ https://www.ncbi.nlm.nih.gov/pubmed/24684269 http://dx.doi.org/10.1111/mmi.12597 |
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