TY - JOUR
T1 - Coordination of gene expression with cell size enables Escherichia coli to efficiently maintain motility across conditions
AU - Honda, Tomoya
AU - Cremer, Jonas
AU - Mancini, Leonardo
AU - Zhang, Zhongge
AU - Pilizota, Teuta
AU - Hwa, Terence
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Matteo Mori, Chenhao Wu, and Christina Ludwig for providing proteomic data and Angela Dawson and Ekaterina Krasno-peeva for providing the pTOF24 plasmids carrying S219C and sticky fliC. T.Honda acknowledges a JASSO (Japan Student Services Organization) long-term graduate fellowship and JSPS (Japan Society for the Promotion of Science) overseas research fellowship. L.M. and T.P. acknowledge the support of the Cunningham Trust award ACC/KWF/PhD1. Work in the T.Hwa lab is supported by the NIH through Grant No. R01GM109069 and by the NSF through Grant No. MCB 1818384.
Publisher Copyright:
© 2022 the Author(s). Published by PNAS.
PY - 2022/9/6
Y1 - 2022/9/6
N2 - To swim and navigate, motile bacteria synthesize a complex motility machinery involving flagella, motors, and a sensory system. A myriad of studies has elucidated the molecular processes involved, but less is known about the coordination of motility expression with cellular physiology: In Escherichia coli, motility genes are strongly up-regulated in nutrient-poor conditions compared to nutrient-replete conditions; yet a quantitative link to cellular motility has not been developed. Here, we systematically investigated gene expression, swimming behavior, cell growth, and available proteomics data across a broad spectrum of exponential growth conditions. Our results suggest that cells up-regulate the expression of motility genes at slow growth to compensate for reduction in cell size, such that the number of flagella per cell is maintained across conditions. The observed four or five flagella per cell is the minimum number needed to keep the majority of cells motile. This simple regulatory objective allows E. coli cells to remain motile across a broad range of growth conditions, while keeping the biosynthetic and energetic demands to establish and drive the motility machinery at the minimum needed. Given the strong reduction in flagella synthesis resulting from cell size increases at fast growth, our findings also provide a different physiological perspective on bacterial cell size control: A larger cell size at fast growth is an efficient strategy to increase the allocation of cellular resources to the synthesis of those proteins required for biomass synthesis and growth, while maintaining processes such as motility that are only needed on a per-cell basis.
AB - To swim and navigate, motile bacteria synthesize a complex motility machinery involving flagella, motors, and a sensory system. A myriad of studies has elucidated the molecular processes involved, but less is known about the coordination of motility expression with cellular physiology: In Escherichia coli, motility genes are strongly up-regulated in nutrient-poor conditions compared to nutrient-replete conditions; yet a quantitative link to cellular motility has not been developed. Here, we systematically investigated gene expression, swimming behavior, cell growth, and available proteomics data across a broad spectrum of exponential growth conditions. Our results suggest that cells up-regulate the expression of motility genes at slow growth to compensate for reduction in cell size, such that the number of flagella per cell is maintained across conditions. The observed four or five flagella per cell is the minimum number needed to keep the majority of cells motile. This simple regulatory objective allows E. coli cells to remain motile across a broad range of growth conditions, while keeping the biosynthetic and energetic demands to establish and drive the motility machinery at the minimum needed. Given the strong reduction in flagella synthesis resulting from cell size increases at fast growth, our findings also provide a different physiological perspective on bacterial cell size control: A larger cell size at fast growth is an efficient strategy to increase the allocation of cellular resources to the synthesis of those proteins required for biomass synthesis and growth, while maintaining processes such as motility that are only needed on a per-cell basis.
U2 - 10.1073/pnas.211034211
DO - 10.1073/pnas.211034211
M3 - Article
VL - 119
JO - Proceedings of the National Academy of Sciences (PNAS)
JF - Proceedings of the National Academy of Sciences (PNAS)
SN - 0027-8424
IS - 37
M1 - e2110342119
ER -