Nonequivalence of membrane voltage and ion-gradient as driving forces for the bacterial flagellar motor at low load.

Biophys J 93:1 (2007) 294-302

Authors:

Chien-Jung Lo, Mark C Leake, Teuta Pilizota, Richard M Berry

Abstract:

Many bacterial species swim using flagella. The flagellar motor couples ion flow across the cytoplasmic membrane to rotation. Ion flow is driven by both a membrane potential (V(m)) and a transmembrane concentration gradient. To investigate their relation to bacterial flagellar motor function we developed a fluorescence technique to measure V(m) in single cells, using the dye tetramethyl rhodamine methyl ester. We used a convolution model to determine the relationship between fluorescence intensity in images of cells and intracellular dye concentration, and calculated V(m) using the ratio of intracellular/extracellular dye concentration. We found V(m) = -140 +/- 14 mV in Escherichia coli at external pH 7.0 (pH(ex)), decreasing to -85 +/- 10 mV at pH(ex) 5.0. We also estimated the sodium-motive force (SMF) by combining single-cell measurements of V(m) and intracellular sodium concentration. We were able to vary the SMF between -187 +/- 15 mV and -53 +/- 15 mV by varying pH(ex) in the range 7.0-5.0 and extracellular sodium concentration in the range 1-85 mM. Rotation rates for 0.35-microm- and 1-microm-diameter beads attached to Na(+)-driven chimeric flagellar motors varied linearly with V(m). For the larger beads, the two components of the SMF were equivalent, whereas for smaller beads at a given SMF, the speed increased with sodium gradient and external sodium concentration.

A programmable optical angle clamp for rotary molecular motors

BIOPHYS J (2007) 372A-372A

Authors:

T Pilizota, T Bilyard, F Bai, RM Berry

Single-molecule fluorescence microscopy of the twin-arginine translocation (Tat) system

BIOPHYS J (2007) 527A-527A

Authors:

MC Leake, NP Greene, RM Godun, T Palmer, RM Berry, BC Berks

Stoichiometry and turnover in single, functioning membrane protein complexes

Nature 443 (2006) 355-358

Authors:

RM Berry, Armitage JP, Chandler JH, Leake MC

The maximum number of torque-generating units in the flagellar motor of Escherichia coli is at least 11

Proceedings of the National Academy of Sciences of the United States of America 103:21 (2006) 8066-8071

Authors:

SW Reid, MC Leake, JH Chandler, CJ Lo, JP Armitage, RM Berry

Abstract:

Torque is generated in the rotary motor at the base of the bacterial flagellum by ion translocating stator units anchored to the peptidoglycan cell wall. Stator units are composed of the proteins MotA and MotB in proton-driven motors, and they are composed of PomA and PomB in sodium-driven motors. Strains of Escherichia coli lacking functional stator proteins produce flagella that do not rotate, and induced expression of the missing proteins leads to restoration of motor rotation in discrete speed increments, a process known as "resurrection." Early work suggested a maximum of eight units. More recent indications that WT motors may contain more than eight units, based on recovery of disrupted motors, are inconclusive. Here we demonstrate conclusively that the maximum number of units in a motor is at least 11. Using back-focal-plane interferometry of 1-μm polystyrene beads attached to flagella, we observed at least 11 distinct speed increments during resurrection with three different combinations of stator proteins in E. coli. The average torques generated by a single unit and a fully induced motor were lower than previous estimates. Speed increments at high numbers of units are smaller than those at low numbers, indicating that not all units in a fully induced motor are equivalent. © 2006 by The National Academy of Sciences of the USA.