SL. pNASR were treated with 100 μM DETA/NO and further cultured at 37 °C. Aliquots were collected after 0–8 h in culture, with the resulting bacterial pellets resuspended in PBS. Rluc8 activity was measured by determining bioluminescence intensities in the presence of coelenterazine, as described above. The switch events were also analyzed by PCR using fimS and rluc8 primers.
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