The chemical stock solutions were diluted using a 2-fold serial dilution method.56 Then, 10 μL of the diluted/undiluted stock solution was placed in a 96-well plate with 190 μL of fresh BHI-diluted L. monocytogenes EGDe overnight culture (1:1000 dilution). The plate was incubated in a microplate reader (BioTek Instruments, Inc., Winooski, VT) at 37 °C with 0.05 linear agitation. The absorbance at 600 nm (OD600) was monitored by the microplate reader every hour for 24 h. The lowest chemical concentration among the groups that showed no increase of OD600 over 24 h was determined as MIC.
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