In the present study, serum GOT(Glutamic Oxalacetic Transaminase) was purified, the purified enzyme showed the maximum activity at 37ºC and pH 7.5. During purification of serum GOT ion exchange chromatography lead to four separate forms (termed I, II, III and IV). GOT II with the highest specific activity was pure after chromatography on Sephacryl S300. . S.GOT levels were investigated in serum samples from patient with pulmonary tuberculosis .The S.GOT levels were determined at and 37ć .The study revealed that the serum GOT activity was higher in patient of tuberculous pulmonary than in control subjects.The mean serum GOT activity in the patients group was(90±8 IU/L) as compared to control group (27±0.65IU/L) showing a highly significant (p<0.001)difference .The study was concentrated to comprehensive measurement of the rate reaction kinetics(Km,Vmax,Hill coefficient),the first order forward rate constant k1 and half life t1/2 of the enzyme reaction in both normal and tuberculosis serum to evaluate any change In the number and structure of the active site then the rate of enzyme –substrate binding.
The Study of Serum GOT(Glutamic Oxalacetic Transaminase) Activity and Some kinetic Parameters in Patient with Pulmonary Tuberculosis
:Glutamic Oxalacetic Transaminase.Tuberculosis
Publication Date
Sat Dec 30 2023
Journal Name
Basrah Journal Of Surgery
Publication Date
Fri Jan 01 2021
Journal Name
Annals Of Tropical Medicine & Public Health
Newly developed method for determination of methyldopa drug using ammonium ceric
(IV) nitrate by continuous flow injection analysis via homemade NAG-ADF-300-2
analyser
Continuous flow injection analysis
Methyldopa
Photometer
turbidmetric
A new, simple, sensitive and fast developed method was used for the determination of methyldopa in pure and pharmaceutical formulations by using continuous flow injection analysis. This method is based on formation a burgundy color complex between methyldopa andammonium ceric (IV) nitrate in aqueous medium using long distance chasing photometer NAG-ADF-300-2. The linear range for calibration graph was 0.05-8.3 mmol/L for cell A and 0.1-8.5 mmol/L for cell B, and LOD 952.8000 ng /200 µL for cell A and 3.3348 µg /200 µL for cell B respectively with correlation coefficient (r) 0.9994 for cell A and 0.9991 for cell B, RSD % was lower than 1 % for n=8. The results were compared with classical method UV-Spectrophotometric at λ max=280 n
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Publication Date
Wed Jul 05 2017
Journal Name
Chemical Engineering Communications
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