ABSTRACT
Bacterial flagellar motor (BFM) is a large membrane-spanning molecular rotary machine for swimming motility. Torque is generated by the interaction between the rotor and multiple stator units powered by ion-motive force (IMF). The number of bound stator units is dynamically changed in response to the external load and the IMF. However, the detailed dynamics of stator unit exchange process remains unclear. Here, we directly measured the speed changes of sodium-driven chimeric BFMs under fast perfusion of different sodium concentration conditions using computer-controlled, high-throughput microfluidic devices. We found the sodium-driven chimeric BFMs maintained constant speed over a wide range of sodium concentrations by adjusting stator units in compensation to the sodium-motive force (SMF) changes. The BFM has the maximum number of stator units and is most stable at 5 mM sodium concentration rather than higher sodium concentration. Upon rapid exchange from high to low sodium concentration, the number of functional stator units shows a rapidly excessive reduction and then resurrection that is different from predictions of simple absorption model. This may imply the existence of a metastable hidden state of the stator unit during the sudden loss of sodium ions.
ABSTRACT
The dynamic assembly of the cell wall is key to the maintenance of cell shape during bacterial growth. Here, we present a method for the analysis of Escherichia coli cell wall growth at high spatial and temporal resolution, which is achieved by tracing the movement of fluorescently labeled cell wall-anchored flagellar motors. Using this method, we clearly identify the active and inert zones of cell wall growth during bacterial elongation. Within the active zone, the insertion of newly synthesized peptidoglycan occurs homogeneously in the axial direction without twisting of the cell body. Based on the measured parameters, we formulate a Bernoulli shift map model to predict the partitioning of cell wall-anchored proteins following cell division.
Subject(s)
Cell Wall/metabolism , Escherichia coli Proteins/metabolism , Escherichia coli/metabolism , Multiprotein Complexes/metabolism , Cell Division , Escherichia coli/growth & development , Flagella/metabolism , Fluorescence , Peptidoglycan/metabolismABSTRACT
Bacterial flagellar motor (BFM) is a protein complex used for bacterial motility and chemotaxis that involves in energy transformation, torque generation and switching. FliL is a single-transmembrane protein associated with flagellar motor function. We performed biochemical and biophysical approaches to investigate the functional roles of FliL associated with stator-units. Firstly, we found the periplasmic region of FliL is crucial for its polar localization. Also, the plug mutation in stator-unit affected the polar localization of FliL implying the activation of stator-unit is important for FliL recruitment. Secondly, we applied single-molecule fluorescent microscopy to study the role of FliL in stator-unit assembly. Using molecular counting by photobleaching, we found the stoichiometry of stator-unit and FliL protein would be 1:1 in a functional motor. Moreover, the turnover time of stator-units are slightly increased in the absence of FliL. By further investigation of protein dynamics on membrane, we found the diffusions of stator-units and FliL are independent. Surprisingly, the FliL diffusion rate without stator-units is unexpectedly slow indicating a protein-complex forming event. Our results suggest that FliL plays a supporting role to the stator in the BFM.
Subject(s)
Bacterial Proteins/metabolism , Flagella/physiology , Membrane Proteins/metabolism , Sodium/metabolism , Vibrio alginolyticus/physiology , Bacterial Proteins/genetics , Cell Membrane Permeability , Cell Movement/physiology , Cell Polarity/physiology , Gene Deletion , Microscopy, Fluorescence , Molecular Motor Proteins , Mutation , Periplasm/metabolism , Photobleaching , Sodium Channels/genetics , Sodium Channels/metabolism , Torque , Vibrio alginolyticus/geneticsABSTRACT
Cells need energy to survive. Ion-motive force (IMF) is one of the most important biological energy formats in bacterial cells. Essentially, the ion-motive force is the sum of electrical and chemical potential differences across the cell membrane. For bacteria, the ion-motive force is involved not only in ATP production but also in flagellar motility. The bacterial flagellar motor is driven either by proton or sodium ion. The ion-motive force measurement therefore requires the measurement of membrane potential, proton concentration, or sodium ion concentration. The bacterial flagellar motor is the most powerful molecular machine we have known so far. To understand the energetic condition of bacterial flagellar motors, together with single-motor torque measurement, methods for single-cell ion-motive force measurement have been developed. Here, we describe fluorescent approaches to measure the components of ion-motive force.
