Sera were coagulated MK-8669 nmr overnight at 4 °C, and the clear supernatant was used for Western blotting. For this, cultures in 2 mL of M17 media were grown to an OD546 nm of 0.6–0.8, followed by induction for 90 min with either 20 μM to 3 mM CuSO4, 20 μM AgNO3 or CdSO4, 200 μM each of ZnSO4, FeSO4, NiCl2, CoCl2, nitrosoglutathione or H2O2, and 100 μM of 4-nitroquinoline-1-oxide. Cell lysates were prepared by centrifuging the cultures and treating the cell pellets with 50 μL of 10 mg mL−1 lysozyme, 1 mM EDTA and 10 mM Tris-Cl, pH 8, for 30 min at 37 °C. 10 μL of 1 mg mL−1 DNaseI in 100 mM MgCl2 was added and incubation was continued for 10 min at 25 °C. Cell debris was removed by centrifugation for 5 min at 12 000 g.

Protein concentrations in the supernatants were determined using the BioRad protein assay and 50 μg of protein resolved by electrophoresis on 12% SDS polyacrylamide

gels. Western blots were prepared as described previously (Towbin et al., 1979), using a horseradish peroxidase-coupled goat anti-rat IgG secondary antibody (Santa Cruz). Bands were visualized by chemiluminescence using 100 mM Tris-Cl, pH 8.5, 1.25 mM 3-aminophtalhydrazide, 0.2 mM p-coumaric acid and 0.01% H2O2. Chemiluminescence signals were captured using a Fuji LAS-1000 imaging system (Fuji Photo Film, Tokyo, Japan). The following commercial crystallization screens were used to look for initial crystallization conditions: Screen I and II (Hampton RGFP966 clinical trial Research), JCSG (Jena Bioscience) and PACT (Qiagen GmbH, Hilden, Germany). Flat-bottomed multi-subwell plates (Greiner, Langenthal, Switzerland) were used to set up sitting drop vapor-diffusion experiments by mixing 1 μL of 10 mg mL−1 YahD solution with 1 μL of screening solution and incubating at 18 °C. Initial conditions that yielded crystals were optimized by hanging drop vapor diffusion crystallization. Needle-shaped crystals were grown by mixing 1.5 μL of protein solution with 1 μL of well solution containing 37.5% polyethylene glycol 3350 and 150 mM of Na-dl-malate, pH 7.0. Crystals Tenoxicam grew to 50 μm in the longest direction within 3 weeks. For data collection, crystals were flash-frozen in liquid nitrogen

without the addition of a cryoprotectant. The crystals belonged to the orthorhombic space group P212121, with unit cell dimensions of a=40.67 Å, b=79.07 Å and c=130.03 Å. X-ray diffraction data were collected from a single crystal at beam line BL 14.1 at BESSY, Berlin, at 100 K and 0.918 Å wavelength. The data were integrated, reduced and scaled using XDS (Kabsch, 1993), resulting in a final data set that was fully complete at 1.88 Å resolution. A search model was built using the ccp4 suite program chainsaw (Stein, 2008), using the atomic coordinates of one monomer of the structure of the Bacillus cereus carboxylesterase (PDB accession 2HLI), which shares 32% amino acid identity with YahD. The sequence alignment of YahD to the B.