Abstract

The bacterial flagellar filament is an extracellular tubular protein structure that acts as a propeller for bacterial swimming motility. It is connected to the membrane-anchored rotary bacterial flagellar motor through a short hook. The bacterial flagellar filament consists of approximately 20,000 flagellins and can be several micrometers long. In this article, we reviewed the experimental works and models of flagellar filament construction and the recent findings of flagellar filament ejection during the cell cycle. The length-dependent decay of flagellar filament growth data supports the injection-diffusion model. The decay of flagellar growth rate is due to reduced transportation of long-distance diffusion and jamming. However, the filament is not a permeant structure. Several bacterial species actively abandon their flagella under starvation. Flagellum is disassembled when the rod is broken, resulting in an ejection of the filament with a partial rod and hook. The inner membrane component is then diffused on the membrane before further breakdown. These new findings open a new field of bacterial macro-molecule assembly, disassembly, and signal transduction.

Highlights

  • Since Antonie van Leeuwenhoek observed animalcules by using his single-lens microscope in the 18th century, we have entered a new era of microbiology

  • The motility of single-cell organisms is fascinating, but it took a long period of time to develop tools to determine the underlying mechanisms. Among these single-cell organisms, many bacterial species swim by using flagella consisting of a long extracellular filament, a hook, and a rotary bacterial flagellar motor anchored on the cell envelope (Figure 1) [1]

  • The flagellum consists of a thin helical flagellar filament that acts as a propeller, a reversible rotary molecular motor embedded on the envelope, and a hook that acts as a universal connection joint between the motor and the flagellar filament [2] (Figure 1)

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Summary

Introduction

Since Antonie van Leeuwenhoek observed animalcules by using his single-lens microscope in the 18th century, we have entered a new era of microbiology. The motility of single-cell organisms is fascinating, but it took a long period of time to develop tools to determine the underlying mechanisms Among these single-cell organisms, many bacterial species swim by using flagella consisting of a long extracellular filament, a hook, and a rotary bacterial flagellar motor anchored on the cell envelope (Figure 1) [1]. Flagellar distribution on the cell surface varies on different bacterial species Peritrichous bacteria, such as Escherichia coli and Salmonella enterica, can produce multiple flagella distributed around the cell body. A flagellar filament is typically about 5–20 μm (2–10 times the cell body length) and is a hollow cylinder with outer and inner diameters of 20 and 2 nm, respectively [21] This long extracellular component is self-assembled with several thousand flagellin monomers [21]. Whereas molecular triggering and the activation mechanism remain unknown, the novel finding of the active ejection of the flagellar filament provides a new direction of cellular adaptation to external stimuli

Architecture of the Type-III Secretion System
Strcture of the Flagellin
Substrates Accumulation and Delivery
Milestones of Flagellar Filament Growth Measurements
Models for Flagellin Transport and Filament Growth
Loss of Flagella
Concluding Remarks and Future Perspective
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