Stock Center, Yale University, CT, USA) and Pseudomonas fluorescens ATCC 13525 (P. fluorescens, American Type Culture
Collection, VA, USA) and Gram-positive Listeria innocua CECT 910 (L. innocua, Spanish Type Culture Collection,
Spain) and Staphylococcus epidermidis ATCC 35984
(S. epidermidis, American Type Culture Collection,
VA, USA) were used in this study. The bacteria were grown for 16–18
h in Tryptic Soy Agar (TSA) and subcultured every week up to five
passages. In each assay, bacteria were harvested from TSA plates,
inoculated into 10 mL of Tryptic Soy Broth (TSB, Oxoid, Basingstoke,
UK), and incubated for 16–18 h at the optimum growth temperature
(30 °C for P. fluorescens and 37 °C for
the remaining bacteria), at 180 rpm. Then, the cultures were diluted
in TSB to an optical density of 0.1 at 600 nm (OD600) and
grown up to the exponential phase, at the previously described conditions.
The final bacterial concentration was set to OD600 = 0.15
(P. fluorescens) or OD600 = 0.1 (remaining
bacteria).