    2.5.1.47 | cell harvesting are resuspended in 50 mM Tris buffer, pH 8.0, containing 10 mM EDTA, 15 mM beta-mercaptoethanol, 0.05 mM N-p-tosyl-L-lysine chloromethylketone, leupeptin, aprotinin, pepstatin, lysozyme and pyridoxal 5'-phosphate, centrifuged, supernatant loaded on a DE52 anion exchange column, washed with 50 mM Tris buffer, pH 8.0, with 10 mM EDTA, and 15 mM beta-mercaptoethanol, elution with NaCl gradient in buffer, active fractions are pooled, concentrated and applied to a GSTrap 4B column, washed with PBS buffer, pH 7.4, containing 140 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, and 1.8 mM KH2PO4, elution with 50 mM Tris, pH 8.0, with 20 mM reduced glutathione and thrombin, dialyzed with 15 mM potassium phosphate, pH 7.2, applied on a DE 52 column, separation of enzyme from GST-tag and thrombin with a gradient of 15-300 mM potassium phosphate buffer, pH 7.2 |
| 2.5.1.47 | cells are harvested by centrifugation, washed with sterile water, again harvested by centrifugation, suspended in 20 mM potassium phosphate buffer, pH 7.4, containing 0.5 M NaCl, lysed with lysozyme at room temperature, one-step affinity chromatography with nickel metal-affinity resin columns, dialyzed against 20 mM potassium phosphate buffer, pH 7.5, 5% glycerol, and 5 mM 2-mercaptoethanol |
