Cargando…

Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner

Bacterial cells are critically dependent upon pH regulation. Here we demonstrate that indole plays a critical role in the regulation of the cytoplasmic pH of Escherichia coli. Indole is an aromatic molecule with diverse signalling roles. Two modes of indole signalling have been described: persistent...

Descripción completa

Detalles Bibliográficos
Autores principales: Zarkan, Ashraf, Caño-Muñiz, Santiago, Zhu, Jinbo, Al Nahas, Kareem, Cama, Jehangir, Keyser, Ulrich F., Summers, David K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405993/
https://www.ncbi.nlm.nih.gov/pubmed/30846797
http://dx.doi.org/10.1038/s41598-019-40560-3
_version_ 1783401198558117888
author Zarkan, Ashraf
Caño-Muñiz, Santiago
Zhu, Jinbo
Al Nahas, Kareem
Cama, Jehangir
Keyser, Ulrich F.
Summers, David K.
author_facet Zarkan, Ashraf
Caño-Muñiz, Santiago
Zhu, Jinbo
Al Nahas, Kareem
Cama, Jehangir
Keyser, Ulrich F.
Summers, David K.
author_sort Zarkan, Ashraf
collection PubMed
description Bacterial cells are critically dependent upon pH regulation. Here we demonstrate that indole plays a critical role in the regulation of the cytoplasmic pH of Escherichia coli. Indole is an aromatic molecule with diverse signalling roles. Two modes of indole signalling have been described: persistent and pulse signalling. The latter is illustrated by the brief but intense elevation of intracellular indole during stationary phase entry. We show that under conditions permitting indole production, cells maintain their cytoplasmic pH at 7.2. In contrast, under conditions where no indole is produced, the cytoplasmic pH is near 7.8. We demonstrate that pH regulation results from pulse, rather than persistent, indole signalling. Furthermore, we illustrate that the relevant property of indole in this context is its ability to conduct protons across the cytoplasmic membrane. Additionally, we show that the effect of the indole pulse that occurs normally during stationary phase entry in rich medium remains as a “memory” to maintain the cytoplasmic pH until entry into the next stationary phase. The indole-mediated reduction in cytoplasmic pH may explain why indole provides E. coli with a degree of protection against stresses, including some bactericidal antibiotics.
format Online
Article
Text
id pubmed-6405993
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64059932019-03-12 Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner Zarkan, Ashraf Caño-Muñiz, Santiago Zhu, Jinbo Al Nahas, Kareem Cama, Jehangir Keyser, Ulrich F. Summers, David K. Sci Rep Article Bacterial cells are critically dependent upon pH regulation. Here we demonstrate that indole plays a critical role in the regulation of the cytoplasmic pH of Escherichia coli. Indole is an aromatic molecule with diverse signalling roles. Two modes of indole signalling have been described: persistent and pulse signalling. The latter is illustrated by the brief but intense elevation of intracellular indole during stationary phase entry. We show that under conditions permitting indole production, cells maintain their cytoplasmic pH at 7.2. In contrast, under conditions where no indole is produced, the cytoplasmic pH is near 7.8. We demonstrate that pH regulation results from pulse, rather than persistent, indole signalling. Furthermore, we illustrate that the relevant property of indole in this context is its ability to conduct protons across the cytoplasmic membrane. Additionally, we show that the effect of the indole pulse that occurs normally during stationary phase entry in rich medium remains as a “memory” to maintain the cytoplasmic pH until entry into the next stationary phase. The indole-mediated reduction in cytoplasmic pH may explain why indole provides E. coli with a degree of protection against stresses, including some bactericidal antibiotics. Nature Publishing Group UK 2019-03-07 /pmc/articles/PMC6405993/ /pubmed/30846797 http://dx.doi.org/10.1038/s41598-019-40560-3 Text en © The Author(s) 2019 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
Zarkan, Ashraf
Caño-Muñiz, Santiago
Zhu, Jinbo
Al Nahas, Kareem
Cama, Jehangir
Keyser, Ulrich F.
Summers, David K.
Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title_full Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title_fullStr Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title_full_unstemmed Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title_short Indole Pulse Signalling Regulates the Cytoplasmic pH of E. coli in a Memory-Like Manner
title_sort indole pulse signalling regulates the cytoplasmic ph of e. coli in a memory-like manner
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405993/
https://www.ncbi.nlm.nih.gov/pubmed/30846797
http://dx.doi.org/10.1038/s41598-019-40560-3
work_keys_str_mv AT zarkanashraf indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT canomunizsantiago indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT zhujinbo indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT alnahaskareem indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT camajehangir indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT keyserulrichf indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner
AT summersdavidk indolepulsesignallingregulatesthecytoplasmicphofecoliinamemorylikemanner