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The assayed strains were cultured overnight at 28 °C in rich NYG medium with the addition of different concentrations of IPTG or arabinose, washed twice with 10 mM MgCl2, and diluted to an OD600 nm = 0.4. Three microliters of the diluted cultures were then used to inoculate rich NYG medium plates containing 0.15% agar. The diameters of the swimming zones were measured after incubation of the plates at 28 °C for 24 h.
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