Cells were continuously mixed with a magnetic stirrer. Fluorescence was monitored every 30 s using excitation/emission wavelengths of 575/615 nm with 5-nm slit widths. Results are shown without ERK inhibitor clinical trial subtraction of background fluorescence. Purified Nhe components were incubated 1 : 1 (v/v) with double-strength DDM (0.4 mM) or phosphate buffer, both at pH 7.2 for 15 min at 37 °C before mixing 1 : 1 (v/v) with an aqueous solution of 50 μM (2× final) 1-anilinonaphthalene-8-sulphonic acid (ANS; Fluka Chemicals). Once solutions had reached room temperature, samples were excited at 380 nm

and emission scans were read between 400 and 650 nm with 7-nm slit widths at 500 nm min−1. The Epacadostat cuvette was held at 25 °C. Scans are shown after subtraction of PBS and DDM. Tryptophan fluorescence was carried out as described previously (Lindbäck et al., 2010) using an excitation wavelength of 295 nm to selectively excite tryptophan. A Superdex 200 10/300 GL (Amersham Biosciences) column was loaded with the purified Nhe components in 50 mM Tris buffer pH 8 with 10 mM NaCl at a flow rate of 0.4 mL min−1 over 80 min at RT. Equal volumes (125 μL) of the Nhe proteins were mixed with DDM (3 mM) for 45 min at 37 °C prior to loading on to the column. Samples passed through a UV detector set at 220 nm. Samples were withdrawn at different times

for Western immunoblots against NheB. Dialysis membranes with molecular weight cut-off (MWCO) of 12–14 000 and 50 000 (Spectrum Laboratories Casein kinase 1 Inc., CA) were soaked and rinsed in 0.25 M phosphate buffer pH 6.8 with 10 mM NaCl. The NheB component alone (5 μg protein) with and without 2 mM DDM (105 μL total volume) was dialysed against 500 mL of buffer for 48 h at 4 °C with four buffer changes. An aliquot (20 μL) of each sample was examined

on Western blots. Purified NheB (2 μg) protein pre-incubated with and without DDM (3 mM) at 37 °C for 40 min was added to wells containing monolayer of Vero cells and incubated for 40 min at 37 °C. The monolayers were washed five times with physiological sodium chloride (37 °C) and then suspended in 50 μL 2× SDS–PAGE sample buffer. Twenty microlitres of each sample was applied to 12% SDS–PAGE and transferred to nitrocellulose membranes by Western immunoblotting. We used fluorescence of propidium to monitor for plasma membrane permeability. A 1 : 80 dilution of a 5-h culture supernatant of toxigenic B. cereus NVH 75/95 induced propidium uptake in both Vero cells and HT29 epithelial cell suspensions. Figure 1a shows the fluorescence of propidium in a suspension of Vero cells, which increased after a lag of approximately 300 s following exposure to NVH 75/95. The dependence on all three Nhe components was confirmed using the culture supernatant of a naturally occurring strain of B.