Hydrodynamics converts chiral flagellar rotation into contactless actuation of microdiscs

Abstract

Motile bacteria are a wonder of nature's engineering: microscopic engines that transduce biochemical energy into the work they require to explore their environment. This added energy turns the surrounding fluid into a bath that departs from an equilibrium one. Bacterial baths agitate suspended spheres more vividly than thermal fluctuations and can power microscopic ratchets. A salient requirement to extract work from bacterial baths was the asymmetric shape of the ratchets, designed to rectify the interactions with bacteria. In contrast with past results, here we show that swimming E. coli power the persistent rotation of discs, in absence of asymmetry. Combining state-of-the art nanoprinting, quantitative measurements of the dynamics of individual bacteria, and hydrodynamic modeling, we elucidate the mechanism and show that the counter-rotation of the flagella and the bacterium body lead to a torque dipole and traction onto the disc, and subsequent rotation. Remarkably, the mechanism is independent of the direction or orientation of navigation of bacteria under the disc, hence additive and contactless. Resulting from the interplay of the torque dipole of flagellated bacteria with simple geometric confinement, this hydrodynamic mechanism bridges scales, leveraging the chirality of bacteria nanomotors towards the manipulation of objects at least ten thousand times larger. The study lays the groundwork for novel bio-hybrid micromachines that harness living microorganisms for controlled motion at the microscale. Our findings provide further fundamental insights into bacterial hydrodynamics and open avenues for the development of autonomous, self-powered microdiscs for the study of chiral fluids.