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Updated: May 23, 2026

A Microfluidic Device for Quantifying Bacterial Chemotaxis in Stable Concentration Gradients
Published on: April 19, 2010
Local chemotactic response of Escherichia coli in fluid and near surfaces
Adam Gargasson1, Julien Bouvard1, Carine Douarche1
1Université Paris-Saclay, CNRS, FAST, 91405 Orsay, France. harold.auradou@universite-paris-saclay.fr.
Abstract:
Bacteria can adjust their swimming behaviour in response to chemical variations, a phenomenon known as chemotaxis. This process is characterised by a drift velocity that depends non-linearly on the concentration of chemical species and its "local" gradient. To study this process more effectively, we optimised a 3-channel microfluidic device to generate a stable, linear concentration profile of chemoattractants. This setup allows us to monitor the response of Escherichia coli to casamino acids or α-methyl-DL-aspartic acid at the individual level. By analysing the movement of a population of individuals both in fluid and on surfaces, we achieve faster, more accurate quantification of the population's chemotactic response. In the fluid, the chemotactic response is described by the equation vc = χ(c)∇c, with χ(c) = χ0/[(1 + c/c-)(1 + c/c+)] the chemotactic susceptibility. For c- ≪ c ≪ c+, i.e. when bacteria perform chemotaxis, the bacterial chemotactic velocity is proportional to the concentration gradient divided by the concentration and vc ∝ ∇c/c = ∇(log c). However, on surfaces, the chemotactic flux is inhibited.
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