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Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations

Bacillus subtilis and Escherichia coli are evolutionarily divergent model organisms whose analysis has enabled elucidation of fundamental differences between Gram-positive and Gram-negative bacteria, respectively. Despite their differences in cell cycle control at the molecular level, the two organi...

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Autores principales: Sauls, John T., Cox, Sarah E., Do, Quynh, Castillo, Victoria, Ghulam-Jelani, Zulfar, Jun, Suckjoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918070/
https://www.ncbi.nlm.nih.gov/pubmed/31848269
http://dx.doi.org/10.1128/mBio.02205-19
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author Sauls, John T.
Cox, Sarah E.
Do, Quynh
Castillo, Victoria
Ghulam-Jelani, Zulfar
Jun, Suckjoon
author_facet Sauls, John T.
Cox, Sarah E.
Do, Quynh
Castillo, Victoria
Ghulam-Jelani, Zulfar
Jun, Suckjoon
author_sort Sauls, John T.
collection PubMed
description Bacillus subtilis and Escherichia coli are evolutionarily divergent model organisms whose analysis has enabled elucidation of fundamental differences between Gram-positive and Gram-negative bacteria, respectively. Despite their differences in cell cycle control at the molecular level, the two organisms follow the same phenomenological principle, known as the adder principle, for cell size homeostasis. We thus asked to what extent B. subtilis and E. coli share common physiological principles in coordinating growth and the cell cycle. We measured physiological parameters of B. subtilis under various steady-state growth conditions with and without translation inhibition at both the population and single-cell levels. These experiments revealed core physiological principles shared between B. subtilis and E. coli. Specifically, both organisms maintain an invariant cell size per replication origin at initiation, under all steady-state conditions, and even during nutrient shifts at the single-cell level. Furthermore, the two organisms also inherit the same “hierarchy” of physiological parameters. On the basis of these findings, we suggest that the basic principles of coordination between growth and the cell cycle in bacteria may have been established early in evolutionary history.
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spelling pubmed-69180702019-12-23 Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations Sauls, John T. Cox, Sarah E. Do, Quynh Castillo, Victoria Ghulam-Jelani, Zulfar Jun, Suckjoon mBio Research Article Bacillus subtilis and Escherichia coli are evolutionarily divergent model organisms whose analysis has enabled elucidation of fundamental differences between Gram-positive and Gram-negative bacteria, respectively. Despite their differences in cell cycle control at the molecular level, the two organisms follow the same phenomenological principle, known as the adder principle, for cell size homeostasis. We thus asked to what extent B. subtilis and E. coli share common physiological principles in coordinating growth and the cell cycle. We measured physiological parameters of B. subtilis under various steady-state growth conditions with and without translation inhibition at both the population and single-cell levels. These experiments revealed core physiological principles shared between B. subtilis and E. coli. Specifically, both organisms maintain an invariant cell size per replication origin at initiation, under all steady-state conditions, and even during nutrient shifts at the single-cell level. Furthermore, the two organisms also inherit the same “hierarchy” of physiological parameters. On the basis of these findings, we suggest that the basic principles of coordination between growth and the cell cycle in bacteria may have been established early in evolutionary history. American Society for Microbiology 2019-12-17 /pmc/articles/PMC6918070/ /pubmed/31848269 http://dx.doi.org/10.1128/mBio.02205-19 Text en Copyright © 2019 Sauls et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Sauls, John T.
Cox, Sarah E.
Do, Quynh
Castillo, Victoria
Ghulam-Jelani, Zulfar
Jun, Suckjoon
Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title_full Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title_fullStr Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title_full_unstemmed Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title_short Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
title_sort control of bacillus subtilis replication initiation during physiological transitions and perturbations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918070/
https://www.ncbi.nlm.nih.gov/pubmed/31848269
http://dx.doi.org/10.1128/mBio.02205-19
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