Bacterial motion is strongly affected by the presence of a surface. One of the hallmarks of swimming near a surface is a defined curvature of bacterial trajectories, underlining the importance of counter rotations of the cell body and flagellum for locomotion of the microorganism. We find that there is another mode of bacterial motion on solid surfaces, i.e., self trapping due to fluid flows created by a rotating flagellum perpendicular to the surface. For a rod-like bacterium, such as Escherichia coli, this creates a peculiar situation in that the bacterium appears to swim along a minor axis of the cell body and is pressed against the surface. Although a full hydrodynamic theory is still lacking to explain the self-trapping phenomenon, the effect is intriguing and can be exploited to study a variety of biophysical phenomena of swimming bacteria. In particular, we showed that self-trapped E. coli cells display a chemotaxis response that is identical to the classical rotation assay in which antibodies are used to physically ''glue'' a flagellum to the surface.

We describe a new method for accurately and reproducibly delivering a minute amount of a chemical to a small target in an aqueous environment. Our method is based on a micropipette with a check valve at its tip that can be opened and closed on demand. We demonstrate that this device can produce a flux of 10−12 l in a short pulse lasting less than 100 ms. The finite width of the pulse is due to molecular dispersion of the chemical, in this case, fluorescein. The chemical distribution near the micropipette tip is measured and compared with the results of a numerical integration assuming stokeslet flow. Our technique is of general utility and has applications in microbiology and neuroscience when a precise control of the spatiotemporal chemical distribution around a specimen is desired.

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