Attenuance (D600 nm) measurements were taken every 10 min from selective or non-selective NM minimal media subcultures grown with IPTG (100 µM) and continuous shaking for 18 h at 37 °C in a Synergy H1 microplate reader (BioTek). For subculturing, 96-well SensoPlate microplates with a clear, flat bottom (Greiner Bio-One) were used. Each 200 µl subculture was generated by dilution (1:100) from independent post-exponential rich media cultures; these 1 mL rich cultures were inoculated and grown in 96-well assay blocks as described above for GFP fluorescence assays.

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