The substrate consisted of 0.2M D,L \u2013 aspartic acid and 0.002M solution of alpha keto glutarate in 0.05 M Phosphate buffer (pH7.4). The experimental and control tubes 0.5 ml of substrate was added and the reaction was started by addition of 0.1 ml of liver homogenate (1 in 50 dilutions). The mixture was incubated (370C) for 60 minutes and the reaction was stopped by addition of 0.5 ml of 0.001 M 2,4-dinitrophenyl hydrazine (DNPH).In the control tube the enzyme source was added after the addition of DNPH solution. The tubes were kept at room temperature for 20 minutes with occasional shaking. Then 5 ml of 0.4N NaOH was added and mixed thoroughly. After 10 minutes OD was recorded at 540nm.
The LDH activity was assayed by the method of Wroblewski and LaDue (1955). The total 3 ml reaction mixture comprised 2.7 ml of 0.1 M phosphate buffer (pH 7.5), 0.1ml of NADH solution (2 mg NADH dissolved in 1ml of phosphste buffer sol.), 0.1 ml of the tissue homogenate, and 0.1 ml of 0.2 M sodium pyruvate. The was started after the addition of substrate (sodium pyruvate). The OD was recorded at 340 nm, every 30 seconds. The enzymic activity was expressed as units/mg protein/min, at 250C, where 1 unit was equal to\u2206 0.01 OD/min.
NADH sol. (2.0 mg NADH dissolved in 1ml of phosphste buffer sol.), 0.1 ml of the tissue homogenate, and 0.1 ml of oxaloacetate sol. (2 mg oxaloacetate dissolved in 2ml of chilled G.D.W). The OD was recorded at 340 nm at 30 seconds intervals, for 3minutes. Distilled water was used as the blank. The MDH activity was expressed as units/mg protein/min, at 250C, where 1 unit was equal to\u2206 0.01 OD/min.
The enzyme was assyed by the method of Hestrin (1949), modified by Augustinsson (1957). The AchE assay system (2.1ml) comprises 1.0 ml of 4mM acetyl Choline (pH 4.0) substrate buffer mixture (1:9) and 1.0 ml of M/15 phosphate buffer (Ph-7.2). Before adding the substrate 1.0 ml of the buffer solution was taken and 0.1 ml of the homogenate (10%) was added. The contents of the tubes were equilibrated (37oC) for two minutes. The substrate (acetylcholine) was added and incubated (37oC, 30 minutes). Adding 2.0 ml of the alkaline hydroxylamine solution terminated the reaction and the contents were mixed well. The enzyme source was then added to the control tubes. Colour was developed by adding 1.0 ml of 10% ferric chloride solution and 1ml of 1:2 HCl solution to each contents were filtered and the OD was recorded at 540 nm against the reagent blank set to zero density.
The protein estimation was assayed by the method of Lowry, 1951. The assay system consisted of two steps, Preparation of sample and Estimation of protein. In the preparation ml sample was taken then added 1 ml 10% T.C.A. Then the contents were centrifuged (5000 rpm for 20 minutes). The supernatant was discarded and dissolved the residue with addition of 0.5 ml 0.1(N) NaOH. After dissolving 0.1 ml sample was taken for protein estimation and added 5 ml Alkaline CuSO4. 0.5 ml of Folinn reagent (1N) was added after waiting 10 minutes. Then the mixture was incubated at room temperature in dark place for 30 minutes and OD was recorded at 660 nm. In the Blank and standard the procedure was same except 0.1 ml BSA (10mg/50ml) was taken in standard instead 0.1 sample.
The enzyme was assayed by the method of Lowry et. al., 1954. The total volume of the assay system was 2 ml. The experimental tubes contained 0.2 ml bicarbonate buffer, MgCl2 0.1 ml, enzyme 0.1 ml, Distilled water 0.5 ml and 0.1 ml substrate (pnpp). The mixture was incubated 370C for 15 minutes. Adding 1 ml NaOH terminated the reaction.
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