Urease, one of the highly efficient known enzymes, catalyzes the hydrolysis of urea into ammonia and carbon dioxide. The present study aimed to extract urease from pea seeds (Pisum Sativum L).
The enzyme was then purified in three consequence steps: acetone precipitation, DEAE-cellulose ion-exchange chromatography, and gel filtration chromatography (Sephacryl S-200 column).
Results:
The purification fold was 12.85 with a yield of 40%. The molecular weight of the isolated urease was estimated by chromatography to be 269,000 Daltons.
Maximum urease activity (190 U/g) was achieved at the optimum conditions of 40[degree sign]C and pH of 7.5 after 5 min of incubation. The kinetic parameters,Km and Vmax, were estimated by Lineweaver-Burk fits and found to be 500 mM and 333.3 U/g, respectively.
The thermodynamic constants of activation, DeltaH, Ea, and DeltaS, were determined using Arrhenius plot and found to be 21.20 kJ/mol, 23.7 kJ/mol, and 1.18 kJ/mol/K, respectively.
Conclusions:
Urease was purified from germinating Pisum Sativum L. seeds.
The purification fold, yield, and molecular weight were determined. The effects of pH, concentration of enzyme, temperature, concentration of substrate, and storage period on urease activity were examined.
This may provide an insight on the various aspects of the property of the enzyme. The significance of extracting urease from different sources could play a good role in understanding the metabolism of urea in plants.
Author: Mohamed E EL-HefnawyMohamed SakranAli I IsmailEman Fahmy Aboelfetoh
Credits/Source: BMC Biochemistry 2014, 15:15
Published on: 2014-07-28
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