Strains were grown in LB to an optical density at 600 nm (OD600) of 1.0. For the colony assay, the LB cultures were 10 times diluted with sterile deionized water and spotted on the MSgg agar (1.5% agar), and the seeded agar plates were incubated at 30 °C for different times. For the pellicle assay, 1.5 μL of the diluted culture was added to 1.5 mL LBMG medium contained within a well of a 24-well microtiter plate, and the microtiter plates were incubated at 30 °C for the indicated times.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.