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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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 |
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