Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth

Summary: 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 gro...

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Main Authors: Diana Serbanescu, Nikola Ojkic, Shiladitya Banerjee
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124720311724
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spelling doaj-344c6ea999c14da9bb4dd3f8a6e3d6182020-11-25T02:02:17ZengElsevierCell Reports2211-12472020-09-013212108183Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and GrowthDiana Serbanescu0Nikola Ojkic1Shiladitya Banerjee2Department of Physics and Astronomy, University College London, London WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, London WC1E 6BT, UKDepartment of Physics and Astronomy, University College London, London WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, London WC1E 6BT, UKDepartment of Physics, Carnegie Mellon University, Pittsburgh, PA 15213, USA; Corresponding authorSummary: 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.http://www.sciencedirect.com/science/article/pii/S2211124720311724whole-cell modelbacterial growth controlcell size regulationtranslationantibioticscell shape
collection DOAJ
language English
format Article
sources DOAJ
author Diana Serbanescu
Nikola Ojkic
Shiladitya Banerjee
spellingShingle Diana Serbanescu
Nikola Ojkic
Shiladitya Banerjee
Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
Cell Reports
whole-cell model
bacterial growth control
cell size regulation
translation
antibiotics
cell shape
author_facet Diana Serbanescu
Nikola Ojkic
Shiladitya Banerjee
author_sort Diana Serbanescu
title Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
title_short Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
title_full Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
title_fullStr Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
title_full_unstemmed Nutrient-Dependent Trade-Offs between Ribosomes and Division Protein Synthesis Control Bacterial Cell Size and Growth
title_sort nutrient-dependent trade-offs between ribosomes and division protein synthesis control bacterial cell size and growth
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2020-09-01
description Summary: 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.
topic whole-cell model
bacterial growth control
cell size regulation
translation
antibiotics
cell shape
url http://www.sciencedirect.com/science/article/pii/S2211124720311724
work_keys_str_mv AT dianaserbanescu nutrientdependenttradeoffsbetweenribosomesanddivisionproteinsynthesiscontrolbacterialcellsizeandgrowth
AT nikolaojkic nutrientdependenttradeoffsbetweenribosomesanddivisionproteinsynthesiscontrolbacterialcellsizeandgrowth
AT shiladityabanerjee nutrientdependenttradeoffsbetweenribosomesanddivisionproteinsynthesiscontrolbacterialcellsizeandgrowth
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