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Indole prevents Escherichia coli cell division by modulating membrane potential

Indole is a bacterial signalling molecule that blocks E. coli cell division at concentrations of 3–5 mM. We have shown that indole is a proton ionophore and that this activity is key to the inhibition of division. By reducing the electrochemical potential across the cytoplasmic membrane of E. coli,...

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Detalles Bibliográficos
Autores principales: Chimerel, Catalin, Field, Christopher M., Piñero-Fernandez, Silvia, Keyser, Ulrich F., Summers, David K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793866/
https://www.ncbi.nlm.nih.gov/pubmed/22387460
http://dx.doi.org/10.1016/j.bbamem.2012.02.022
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author Chimerel, Catalin
Field, Christopher M.
Piñero-Fernandez, Silvia
Keyser, Ulrich F.
Summers, David K.
author_facet Chimerel, Catalin
Field, Christopher M.
Piñero-Fernandez, Silvia
Keyser, Ulrich F.
Summers, David K.
author_sort Chimerel, Catalin
collection PubMed
description Indole is a bacterial signalling molecule that blocks E. coli cell division at concentrations of 3–5 mM. We have shown that indole is a proton ionophore and that this activity is key to the inhibition of division. By reducing the electrochemical potential across the cytoplasmic membrane of E. coli, indole deactivates MinCD oscillation and prevents formation of the FtsZ ring that is a prerequisite for division. This is the first example of a natural ionophore regulating a key biological process. Our findings have implications for our understanding of membrane biology, bacterial cell cycle control and potentially for the design of antibiotics that target the cell membrane.
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spelling pubmed-37938662013-10-10 Indole prevents Escherichia coli cell division by modulating membrane potential Chimerel, Catalin Field, Christopher M. Piñero-Fernandez, Silvia Keyser, Ulrich F. Summers, David K. Biochim Biophys Acta Article Indole is a bacterial signalling molecule that blocks E. coli cell division at concentrations of 3–5 mM. We have shown that indole is a proton ionophore and that this activity is key to the inhibition of division. By reducing the electrochemical potential across the cytoplasmic membrane of E. coli, indole deactivates MinCD oscillation and prevents formation of the FtsZ ring that is a prerequisite for division. This is the first example of a natural ionophore regulating a key biological process. Our findings have implications for our understanding of membrane biology, bacterial cell cycle control and potentially for the design of antibiotics that target the cell membrane. Elsevier Pub. Co 2012-07 /pmc/articles/PMC3793866/ /pubmed/22387460 http://dx.doi.org/10.1016/j.bbamem.2012.02.022 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Chimerel, Catalin
Field, Christopher M.
Piñero-Fernandez, Silvia
Keyser, Ulrich F.
Summers, David K.
Indole prevents Escherichia coli cell division by modulating membrane potential
title Indole prevents Escherichia coli cell division by modulating membrane potential
title_full Indole prevents Escherichia coli cell division by modulating membrane potential
title_fullStr Indole prevents Escherichia coli cell division by modulating membrane potential
title_full_unstemmed Indole prevents Escherichia coli cell division by modulating membrane potential
title_short Indole prevents Escherichia coli cell division by modulating membrane potential
title_sort indole prevents escherichia coli cell division by modulating membrane potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793866/
https://www.ncbi.nlm.nih.gov/pubmed/22387460
http://dx.doi.org/10.1016/j.bbamem.2012.02.022
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