0, 100 mM NaCl, containing a gradient

of 0–60 mM imidazole). Eluted fractions were collected and loaded on SDS-PAGE to determine the purity of eluted proteins. MM-102 For C-His-Rv0489, after washing with 4 column volumes of lysis buffer, elution was done with elution buffer II (20 mM Tris–HCl pH 7.0, 100 mM NaCl, 150 mM of imidazole). The fractions with highest amount of recombinant C-His-Rv0489, determined by SDS PAGE were pooled and diluted to the imidazole concentration of 15 mM. The pooled fractions were then applied a second time to the cobalt charged resin column pre-equilibrated with wash buffer. The process of purification was Rho inhibitor repeated as the first column application to obtain pure C-His-Rv0489. Purified C-His-Rv2135c and C-His-Rv0489 were concentrated using Amicon–Ultra 4 centrifugal filter unit (Merck find more Millipore USA) and stored in 20 mM Tris–HCl pH 7.0 containing 50% glycerol. Enzyme assays Phosphoglycerate mutase activity: Phosphoglycerate mutase activities of C-His-Rv2135c and C-HisRv0489 in the 3-PGA to 2-PGA (forward) direction were monitored using an assay coupled to the oxidation of NADH as earlier described [64]. The assay was done in 500 μl of reaction mixture, containing 30 mM Tris–HCl pH 7.0, 20 mM KCl, 5 mM MgSO4, 1 mM ADP, 0.15 mM NADH, 0.2 mM 2,3-bisphophoglyceric acid, 2.5 U enolase (Sigma), 2.5 U pyruvate kinase (Sigma), 2.5 U lactate dehydrogenase (Sigma) [64] with ten concentrations of 3-phosphoglyceric

acid (Sigma) (0.019, 0.039, 0.078, 0.156, 0.312, 0.625, 1.25, 2.5, 5 and 10 mM). Changes in absorbance at 340 nm using spectrophotometer

(Thermo Electron Corporation, USA) were used in monitoring Non-specific serine/threonine protein kinase the oxidation of NADH. The values of absorbance of test solutions were corrected by the absorbance of the solution without enzymes. The assays were carried out in triplicate. Acid phosphatase assay: The phosphatase activity was measured by monitoring the release of p-nitrophenol from p-nitrophenyl phosphate (pNPP) at a range of pH (3.0-7.5) as earlier described [64]. 25 mM sodium citrate buffer was used at pH 3.0-6.2 while 25 mM Tris–HCl was used at pH 7.0 and 7.5. The reaction, carried out at 37°C was started by the addition of the enzymes to the pre-warmed reaction buffer with eight concentrations of pNPP (New England Biolabs, USA) (0.78, 1.56, 3.125, 6.25, 12.5, 25, 50 and 100 Mm) in a total volume of 200 μl. The mixture was incubated for 60 min, and stopped with the addition of 600 μl of 1 N NaOH. Potato acid phosphatase (Sigma) was used as a positive control at pH 4.8 with 25 mM sodium citrate buffer. The amounts of released p-nitrophenol were estimated from the change in absorbance at 405 nm, corrected by the absorbance of the solution without the enzymes incubated at 37°C for the same period of time. All assays were carried out in triplicate. Malachite green assay: The activities of C-His-Rv2135c with other substrates were investigated.