Cell morphological changes were analyzed by an inverted light microscope BGJ398 mouse (Leica DMIL; Leica Microsystems S.p.A, Milan, Italy). Cell viability was determined by the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay. The absorbance was read at 490 nm using an enzyme-linked immunosorbent assay plate reader. Plu1961/Plu1962-treated CF-203 cells or untreated CF-203 cells were seeded in 6-well microtiter plate containing Insect-Xpress culture medium with a coverslip in the bottom and incubated for 12 h. Then the coverslip was turned upside down on a glass slide containing 0.25 μg mL−1 Mitotrack Red, incubated at the

room temperature for 20 min. Cells were then incubated in PBS containing 0.5% Triton X-100 at room temperature for 10 min. After being washed with PBS, cells were incubated at room temperature for 1 h with PBS containing 2% BSA. Then the coverslip was turned upside down on a glass slide containing 5 μg mL−1 Mouse anti-α-Tubulin-Alexa 488 and incubated at room temperature for 1 h. After washing four

times, cells were then incubated at room temperature for 20 min in 5 μg mL−1 4′,6-diamino-2-phenylindole dihydrochloride (DAPI).After washing extensively with PBS, a fluorescence quencher was added to seal the tablet. Confocal images were acquired using Zeiss LSM 510 META (Germany) and processed with lsm image browser software and adobe photoshop (CS2). The confocal fluorescence microscopy was performed three times on different days. Cell viability and nuclear morphology were assessed by the http://www.selleckchem.com/ALK.html Hoechst 33342 and propidium iodide co-staining method (Yuan et al., 2002). The Apoptosis and Necrosis Assay Kit (Beyotime Institute of Biotechnology, Hai men, China) was used according to the manufacturer’s instructions. CF-203 cells treated with different concentrations of Plu1961/Plu1962 binary toxin and treated with PBS (negative controls) were collected after

24 h. Cells were homogenized by freezing and thawing several times and mixed in DNA extraction buffer (10 mmol mL−1 Janus kinase (JAK) Tris-HCl, 150 mmol mL−1 NaCl, 10 mmol mL−1 EDTA-NaOH, 0.1% SDS, pH 8.0) on ice. Homogenized cells were treated with 20 mg mL−1 RNase for 30 min at 37 °C. Subsequently, 100 mg mL−1 of proteinase K was added, and cells were incubated at 50 °C for 60 min. DNA samples were extracted using a standard phenol–chloroform extraction method and analyzed by 2% agarose gel. To evaluate the biological activity of Plu1961/Plu1962, their encoding genes were cloned and expressed in BL21 (DE3). The theoretical molecular weight (MW) of 342-amino acid protein Plu1961 is 39 kDa, while theoretical MW of Plu1962 which consists of 412 amino acids is 46.5 kDa. After inducing with 1 mmol L−1 IPTG, prominent bands of c. 39 and 46.5 kDa were found in the supernatants of induced cultures of BL21 (plu1961) and BL21 (plu1962), respectively (Fig.