scholarly journals Emergence of growth and dormancy from a kinetic model of the Escherichia coli central carbon metabolism

Author(s):  
Yusuke Himeoka ◽  
Namiko Mitarai

Abstract Physiological states of bacterial cells exhibit a wide spectrum of timescale. Under nutrient-rich conditions, most of the cells in an isogenic bacterial population grow at certain rates, while a small subpopulation sometimes stays in a dormant state where the growth rates slow down by orders of magnitude. For revealing the origins of such heterogeneity of timescales, we studied the kinetic model of Escherichia coli central carbon metabolism including the dynamics of the energy currency molecules. We found that the model robustly exhibits both the growing- and the dormant state. In order to unveil the mechanism of distinct behaviours, we developed a recursive method to simplify the model without changing the qualitative feature of the dynamics. Analytical and numerical studies of the 2-variable minimal model revealed the necessary conditions for the distinct behaviour, namely, the depletion of energy due to the futile cycle and its non-uniform impact on the kinetics because of the coexistence of the energy currency-coupled and uncoupled reactions as well as branching of the network. The result is consistent with the experimental reports that the dormant cells commonly exhibit low ATP levels, and provides a possible explanation for the appearance of dormant cells that causes antibiotic persistence.

2021 ◽  
Author(s):  
Yusuke Himeoka ◽  
Namiko Mitarai

Physiological states of bacterial cells exhibit a wide spectrum of timescale. Under the nutrient-rich conditions, most of the cells in an isogenic bacterial population grow at certain rates, while a small subpopulation sometimes stays in a dormant state where the growth rates slow down by orders of magnitude. What is the origin of such heterogeneity of timescales? Here we addressed this question by studying the kinetic model of Escherichia coli central carbon metabolism including the dynamics of the energy currency molecules, which have often been ignored. We found that the model robustly exhibits both the growing- and the dormant state. In order to unveil the mechanism of distinct behaviours, we developed a recursive method to simplify the model without changing the qualitative feature of the dynamics. Analytical and numerical studies of the 2-variable minimal model revealed the necessary conditions for the distinct behaviour, namely, the depletion of energy due to the futile cycle and its non-uniform impact to the kinetics because of the coexistence of the energy currency-coupled and uncoupled reactions as well as branching of the network. The result is consistent with the experimental evidences of the appearance of the futile cycle in mutants and provides a possible explanation for the appearance of dormant cells that causes antibiotic persistence.


2016 ◽  
Vol 15 (1) ◽  
Author(s):  
Nusrat Jahan ◽  
Kazuhiro Maeda ◽  
Yu Matsuoka ◽  
Yurie Sugimoto ◽  
Hiroyuki Kurata

2020 ◽  
Vol 45 (9) ◽  
pp. 5687-5696 ◽  
Author(s):  
Victor E. Balderas-Hernandez ◽  
Kathya P. Landeros Maldonado ◽  
Arturo Sánchez ◽  
Adam Smoliński ◽  
Antonio De Leon Rodriguez

2020 ◽  
Vol 163 ◽  
pp. 107753
Author(s):  
Fabián A. Ortega-Quintana ◽  
Mauricio A. Trujillo-Roldán ◽  
Héctor Botero-Castro ◽  
Hernan Alvarez

Genes ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 447
Author(s):  
Klaudyna Krause ◽  
Monika Maciąg-Dorszyńska ◽  
Anna Wosinski ◽  
Lidia Gaffke ◽  
Joanna Morcinek-Orłowska ◽  
...  

A direct link between DNA replication regulation and central carbon metabolism (CCM) has been previously demonstrated in Bacillus subtilis and Escherichia coli, as effects of certain mutations in genes coding for replication proteins could be specifically suppressed by particular mutations in genes encoding CCM enzymes. However, specific molecular mechanism(s) of this link remained unknown. In this report, we demonstrate that various CCM metabolites can suppress the effects of mutations in different replication genes of E. coli on bacterial growth, cell morphology, and nucleoid localization. This provides evidence that the CCM-replication link is mediated by metabolites rather than direct protein-protein interactions. On the other hand, action of metabolites on DNA replication appears indirect rather than based on direct influence on the replication machinery, as rate of DNA synthesis could not be corrected by metabolites in short-term experiments. This corroborates the recent discovery that in B. subtilis, there are multiple links connecting CCM to DNA replication initiation and elongation. Therefore, one may suggest that although different in detail, the molecular mechanisms of CCM-dependent regulation of DNA replication are similar in E. coli and B. subtilis, making this regulation an important and common constituent of the control of cell physiology in bacteria.


Sign in / Sign up

Export Citation Format

Share Document