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Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis

Microorganisms possess diverse mechanisms to regulate investment into individual cellular processes according to their environment. How these regulatory strategies reflect the inherent trade-off between the benefit and cost of resource investment remains largely unknown, particularly for many cellul...

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Autores principales: Ni, Bin, Colin, Remy, Link, Hannes, Endres, Robert G., Sourjik, Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955288/
https://www.ncbi.nlm.nih.gov/pubmed/31871173
http://dx.doi.org/10.1073/pnas.1910849117
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author Ni, Bin
Colin, Remy
Link, Hannes
Endres, Robert G.
Sourjik, Victor
author_facet Ni, Bin
Colin, Remy
Link, Hannes
Endres, Robert G.
Sourjik, Victor
author_sort Ni, Bin
collection PubMed
description Microorganisms possess diverse mechanisms to regulate investment into individual cellular processes according to their environment. How these regulatory strategies reflect the inherent trade-off between the benefit and cost of resource investment remains largely unknown, particularly for many cellular functions that are not immediately related to growth. Here, we investigate regulation of motility and chemotaxis, one of the most complex and costly bacterial behaviors, as a function of bacterial growth rate. We show with experiment and theory that in poor nutritional conditions, Escherichia coli increases its investment in motility in proportion to the reproductive fitness advantage provided by the ability to follow nutrient gradients. Since this growth-rate dependent regulation of motility genes occurs even when nutrient gradients are absent, we hypothesize that it reflects an anticipatory preallocation of cellular resources. Notably, relative fitness benefit of chemotaxis could be observed not only in the presence of imposed gradients of secondary nutrients but also in initially homogeneous bacterial cultures, suggesting that bacteria can generate local gradients of carbon sources and excreted metabolites, and subsequently use chemotaxis to enhance the utilization of these compounds. This interplay between metabolite excretion and their chemotaxis-dependent reutilization is likely to play an important general role in microbial communities.
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spelling pubmed-69552882020-01-14 Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis Ni, Bin Colin, Remy Link, Hannes Endres, Robert G. Sourjik, Victor Proc Natl Acad Sci U S A Biological Sciences Microorganisms possess diverse mechanisms to regulate investment into individual cellular processes according to their environment. How these regulatory strategies reflect the inherent trade-off between the benefit and cost of resource investment remains largely unknown, particularly for many cellular functions that are not immediately related to growth. Here, we investigate regulation of motility and chemotaxis, one of the most complex and costly bacterial behaviors, as a function of bacterial growth rate. We show with experiment and theory that in poor nutritional conditions, Escherichia coli increases its investment in motility in proportion to the reproductive fitness advantage provided by the ability to follow nutrient gradients. Since this growth-rate dependent regulation of motility genes occurs even when nutrient gradients are absent, we hypothesize that it reflects an anticipatory preallocation of cellular resources. Notably, relative fitness benefit of chemotaxis could be observed not only in the presence of imposed gradients of secondary nutrients but also in initially homogeneous bacterial cultures, suggesting that bacteria can generate local gradients of carbon sources and excreted metabolites, and subsequently use chemotaxis to enhance the utilization of these compounds. This interplay between metabolite excretion and their chemotaxis-dependent reutilization is likely to play an important general role in microbial communities. National Academy of Sciences 2020-01-07 2019-12-23 /pmc/articles/PMC6955288/ /pubmed/31871173 http://dx.doi.org/10.1073/pnas.1910849117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ni, Bin
Colin, Remy
Link, Hannes
Endres, Robert G.
Sourjik, Victor
Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title_full Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title_fullStr Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title_full_unstemmed Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title_short Growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
title_sort growth-rate dependent resource investment in bacterial motile behavior quantitatively follows potential benefit of chemotaxis
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955288/
https://www.ncbi.nlm.nih.gov/pubmed/31871173
http://dx.doi.org/10.1073/pnas.1910849117
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