From the Cover: Bacterial flagellum as a propeller and as a rudder for efficient chemotaxis.

We investigate swimming and chemotactic behaviors of the polarly flagellated marine bacteria Vibrio alginolyticus in an aqueous medium. Our observations show that V. alginolyticus execute a cyclic, three-step (forward, reverse, and flick) swimming pattern that is distinctively different from the run-tumble pattern adopted by Escherichia coli. Specifically, the bacterium backtracks its forward swimming path when the motor reverses. However, upon resuming forward swimming, the flagellum flicks and a new swimming direction is selected at random. In a chemically homogeneous medium (no attractant or repellent), the consecutive forward t(f) and backward t(b) swimming times are uncorrelated. Interestingly, although t(f) and t(b) are not distributed in a Poissonian fashion, their difference Δt = |t(f) - t(b)| is. Near a point source of attractant, on the other hand, t(f) and t(b) are found to be strongly correlated, and Δt obeys a bimodal distribution. These observations indicate that V. alginolyticus exploit the time-reversal symmetry of forward and backward swimming by using the time difference to regulate their chemotactic behavior. By adopting the three-step cycle, cells of V. alginolyticus are able to quickly respond to a chemical gradient as well as to localize near a point source of attractant.

The effect of long-range hydrodynamic interaction on the swimming of a single bacterium.

It has been theoretically suggested that when a bacterium swims in a fluid, the disturbance it creates is long-ranged and can influence its locomotion. The contribution of these long-range hydrodynamic interactions to swimming cells is examined herein for a number of bacterial strains with well-defined flagellar geometries. We show experimentally for the first time that long-range hydrodynamic interactions are important for an accurate description of the swimming of a single cell, and the effect is more pronounced for bacteria with a large cell body. The commonly used local resistive force theory assumes a stationary background fluid while ignoring flows induced due to other moving parts of the cell. Although pedagogically attractive, resistive force theory is not generally applicable to experiment.

Bacterial chemotaxis in an optical trap.

An optical trapping technique is implemented to investigate the chemotactic behavior of a marine bacterial strain Vibrio alginolyticus. The technique takes the advantage that the bacterium has only a single polar flagellum, which can rotate either in the counter-clock-wise or clock-wise direction. The two rotation states of the motor can be readily and instantaneously resolved in the optical trap, allowing the flagellar motor switching rate S(t) to be measured under different chemical stimulations. In this paper the focus will be on the bacterial response to an impulsive change of chemoattractant serine. Despite different propulsion apparati and motility patterns, cells of V. alginolyticus apparently use a similar response as Escherichia coli to regulate their chemotactic behavior. Specifically, we found that the switching rate S(t) of the bacterial motor exhibits a biphasic behavior, showing a fast initial response followed by a slow relaxation to the steady-state switching rate S0. The measured S(t) can be mimicked by a model that has been recently proposed for chemotaxis in E. coli. The similarity in the response to the brief chemical stimulation in these two different bacteria is striking, suggesting that the biphasic response may be evolutionarily conserved. This study also demonstrated that optical tweezers can be a useful tool for chemotaxis studies and should be applicable to other polarly flagellated bacteria.

Swimming efficiency of bacterium Escherichia coli.

We use measurements of swimming bacteria in an optical trap to determine fundamental properties of bacterial propulsion. In particular, we directly measure the force required to hold the bacterium in the optical trap and determine the propulsion matrix, which relates the translational and angular velocity of the flagellum to the torques and forces propelling the bacterium. From the propulsion matrix, dynamical properties such as torques, swimming speed, and power can be obtained by measuring the angular velocity of the motor. We find significant heterogeneities among different individuals even though all bacteria started from a single colony. The propulsive efficiency, defined as the ratio of the propulsive power output to the rotary power input provided by the motors, is found to be approximately 2%, which is consistent with the efficiency predicted theoretically for a rigid helical coil.