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Bacterial motility depends on a critical flagellum length and energy-optimized assembly

Abstract:
The flagellum is the most complex macromolecular structure known in bacteria and is composed of around two dozen distinct proteins. The main building block of the long, external flagellar filament, flagellin, is secreted through the flagellar type-III secretion system at a remarkable rate of several tens of thousands of amino acids per second, significantly surpassing the rates achieved by other pore-based protein secretion systems. The evolutionary implications and potential benefits of this high secretion rate for flagellum assembly and function, however, have remained elusive. In this study, we provide both experimental and theoretical evidence that the flagellar secretion rate has been evolutionarily optimized to facilitate rapid and efficient construction of a functional flagellum. By synchronizing flagellar assembly, we found that a minimal filament length of 2.5 μm was required for swimming motility. Biophysical modeling revealed that this minimal filament length threshold resulted from an elasto-hydrodynamic instability of the whole swimming cell, dependent on the filament length. Furthermore, we developed a stepwise filament labeling method combined with electron microscopy visualization to validate predicted flagellin secretion rates of up to 10,000 amino acids per second. A biophysical model of flagellum growth demonstrates that the observed high flagellin secretion rate efficiently balances filament elongation and energy consumption, thereby enabling motility in the shortest amount of time. Taken together, these insights underscore the evolutionary pressures that have shaped the development and optimization of the flagellum and type-III secretion system, illuminating the intricate interplay and cost-benefit tradeoff between functionality and efficiency in assembly of large macromolecular structures
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1073/pnas.2413488122

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-9876-7493
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Role:
Author
ORCID:
0000-0002-7825-1550
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Role:
Author
ORCID:
0000-0003-4551-9239
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Role:
Author
ORCID:
0009-0001-2098-4997
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Role:
Author
ORCID:
0000-0003-1297-3312


Publisher:
National Academy of Sciences
Journal:
Proceedings of the National Academy of Sciences More from this journal
Volume:
122
Issue:
11
Pages:
e2413488122-e2413488122
Publication date:
2025-03-11
DOI:
EISSN:
1091-6490
ISSN:
0027-8424


Language:
English
Keywords:
Pubs id:
2370730
Local pid:
pubs:2370730
Source identifiers:
W4408323673
Deposit date:
2026-02-14
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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