Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
- PMID: 32966800
- DOI: 10.1016/j.celrep.2020.108183
Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
Abstract
Cell size control emerges from a regulated balance between the rates of cell growth and division. In bacteria, simple quantitative laws connect cellular growth rate to ribosome abundance. However, it remains poorly understood how translation regulates bacterial cell size and shape under growth perturbations. Here, we develop a whole-cell model for growth dynamics of rod-shaped bacteria that links ribosomal abundance with cell geometry, division control, and the extracellular environment. Our study reveals that cell size maintenance under nutrient perturbations requires a balanced trade-off between ribosomes and division protein synthesis. Deviations from this trade-off relationship are predicted under translation inhibition, leading to distinct modes of cell morphological changes, in agreement with single-cell experimental data on Escherichia coli. Furthermore, by calibrating our model with experimental data, we predict how combinations of nutrient-, translational-, and shape perturbations can be chosen to optimize bacterial growth fitness and antibiotic resistance.
Keywords: Escherichia coli; antibiotics; bacterial growth control; cell shape; cell size regulation; translation; whole-cell model.
Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of Interests The authors declare no competing interests.
Similar articles
-
Invariance of Initiation Mass and Predictability of Cell Size in Escherichia coli.Curr Biol. 2017 May 8;27(9):1278-1287. doi: 10.1016/j.cub.2017.03.022. Epub 2017 Apr 13. Curr Biol. 2017. PMID: 28416114 Free PMC article.
-
A Numbers Game: Ribosome Densities, Bacterial Growth, and Antibiotic-Mediated Stasis and Death.mBio. 2017 Feb 7;8(1):e02253-16. doi: 10.1128/mBio.02253-16. mBio. 2017. PMID: 28174311 Free PMC article.
-
Selective protein synthesis by ribosomes with a drug-obstructed exit tunnel.Cell. 2012 Oct 26;151(3):508-20. doi: 10.1016/j.cell.2012.09.018. Cell. 2012. PMID: 23101624
-
The ribosome cycle in bacteria.Basic Life Sci. 1973;1:327-38. doi: 10.1007/978-1-4684-0877-5_27. Basic Life Sci. 1973. PMID: 4589685 Review. No abstract available.
-
ABC-F proteins in mRNA translation and antibiotic resistance.Res Microbiol. 2019 Nov-Dec;170(8):435-447. doi: 10.1016/j.resmic.2019.09.005. Epub 2019 Sep 26. Res Microbiol. 2019. PMID: 31563533 Review.
Cited by
-
A stochastic model of homeostasis: The roles of noise and nuclear positioning in deciding cell fate.iScience. 2021 Oct 2;24(10):103199. doi: 10.1016/j.isci.2021.103199. eCollection 2021 Oct 22. iScience. 2021. PMID: 34703995 Free PMC article.
-
Directed evolution of rRNA improves translation kinetics and recombinant protein yield.Nat Commun. 2021 Sep 24;12(1):5638. doi: 10.1038/s41467-021-25852-5. Nat Commun. 2021. PMID: 34561441 Free PMC article.
-
Gene Expression Tradeoffs Determine Bacterial Survival and Adaptation to Antibiotic Stress.PRX Life. 2024 Jan-Mar;2(1):013010. doi: 10.1103/prxlife.2.013010. Epub 2024 Feb 29. PRX Life. 2024. PMID: 39449977 Free PMC article.
-
Gene expression tradeoffs determine bacterial survival and adaptation to antibiotic stress.bioRxiv [Preprint]. 2024 Jan 23:2024.01.20.576495. doi: 10.1101/2024.01.20.576495. bioRxiv. 2024. Update in: PRX Life. 2024 Jan-Mar;2(1):013010. doi: 10.1103/prxlife.2.013010 PMID: 38328084 Free PMC article. Updated. Preprint.
-
Cellular resource allocation strategies for cell size and shape control in bacteria.FEBS J. 2022 Dec;289(24):7891-7906. doi: 10.1111/febs.16234. Epub 2021 Oct 30. FEBS J. 2022. PMID: 34665933 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
