The protocol of the animal experiment was reviewed and approved by the Ethics Committee on Animal Experiments at the Faculty of Medical Sciences, Kyushu University. This was carried out by counting this website the numbers of colony formers. In the case of HBO treatment, appropriate numbers (ca. 10 to 107 per plate) of bacterial cells were spread on yeast extract agar plates, which were exposed to HBO (see above) and incubated overnight in ambient air. For UV killing, approximately 106 bacteria suspended in 5 mL of PBS were irradiated in a shallow dish under a 10 W germicidal lamp (Toshiba, Tokyo, Japan) at a distance

of 35 cm for various lengths of time. For killing by chemicals, similar bacterial suspensions were incubated with various concentrations of each test substance at 37°C for 30 mins. The bacterial suspensions thus treated were diluted appropriately

with PBS and plated on yeast extract agar plates, which were incubated overnight. Cells in 50 mL of a log-phase culture in yeast extract broth (turbidity 600 nm ≈ 0.2) were placed under HBO at 3 atm or in ambient air for 2 hrs in shallow vessels. The cells were collected by centrifugation, washed twice with PBS, and resuspended in 1 mL PBS. The cell suspension was sonicated on ice for 2 mins using a sonicator (Sonifier 250, Branson, Danbury, CT, USA) set at 50% duty cycle and 10% output control. After removal of cell debris by centrifugation, the protein concentration of LY2606368 mouse the supernatant was determined using a Pierce BCA protein assay kit (Thermo Scientific, Waltham, MA, USA) with BSA as standard, and adjusted to 1 mg/mL with PBS. Catalase activity was determined by measuring the amount of remaining H2O2 with titanium sulfate as previously described (12), one unit of activity being defined as the amount capable of decomposing 1.0 μmol of H2O2 per min. The activity of NADH peroxidase was assayed as previously described (13), one unit of activity being defined as the amount required for oxidizing 1.0 nmol of NADH per min. SOD

activity was assayed by the NBT reduction method as previously described (14,15), one unit of activity being defined as the amount Cyclin-dependent kinase 3 required to cut the rate of reduction of NBT by 50%. O2 and N2 gases were purchased from Fukuoka Sanso (Fukuoka, Japan). Hydrogen peroxide (H2O2), mitomycin C, methyl methane sulfonate, xanthine oxidase and NADH were obtained from Sigma-Aldrich (St. Louis, MO, USA). Titanium (IV) sulfate solution (5%) was from Nakarai Tesque (Kyoto, Japan). Xanthine was from Katayama Chemical (Osaka, Japan) and NBT from Boehringer Mannheim (Mannheim, Germany). All other chemicals used were of reagent grade. A Genesys 10UV spectrophotometer (Thermo Electron, Kyoto, Japan) was used for determination of turbidity and absorbance. The light path was 1 cm in length. All experiments were repeated at least three times and the results expressed as mean ± standard deviation.