Activity and stability of urease enzyme immobilized on Amberlite resin

IF 1 Q4 CHEMISTRY, MULTIDISCIPLINARY Ovidius University Annals of Chemistry Pub Date : 2019-10-30 DOI:10.20944/preprints201910.0348.v1
Jawad Kadhim Jawad Al-Shams, M. Hussein, H. Al-Hakeim
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引用次数: 3

Abstract

Abstract Immobilization of enzymes is a good field of study to extend the life of enzyme and reduce the cost of the chemical processes, such as separation processes. Urease is an important enzyme with medical and industrial applications. The aim of the present study is to prepare an immobilized urease on a strong cation exchange resin (Amberlite IR120 Na) and study its activity and stability. We monitored the release of Na ions in the collected fractions and searching for enzyme in the fractions as indicators of immobilization by ion exchange phenomenon. Sodium is determined by using atomic absorption spectroscopy technique, while the enzyme concentration was tested by Bradford’s method. Immobilized urease activity was evaluated by salicylate-hypochlorite method. The results indicated a complete immobilization of urease enzyme on the resin surface with reserving 92% of the activity of free enzyme. The immobilized urease enzyme on resin showed good stability and it has a 62% of its activity after 154 days of storage at room temperature. It is concluded that a new immobilized urease enzyme system is prepared with good enzyme activity and stability.
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安培石树脂固定化脲酶的活性与稳定性
摘要酶的固定化是一个很好的研究领域,可以延长酶的使用寿命,降低分离等化学过程的成本。脲酶是一种具有重要医学和工业应用价值的酶。在强阳离子交换树脂(Amberlite IR120 Na)上制备固定化脲酶,并研究其活性和稳定性。我们监测了所收集的馏分中Na离子的释放,并在馏分中寻找酶作为离子交换现象固定的指标。钠用原子吸收光谱法测定,酶浓度用布拉德福德法测定。用水杨酸-次氯酸盐法测定固定化脲酶活性。结果表明,脲酶完全固定在树脂表面,保留了92%的游离酶活性。树脂固定化脲酶表现出良好的稳定性,室温保存154 d后,酶活性保持62%。结果表明,制备了一种新的固定化脲酶体系,具有良好的酶活性和稳定性。
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来源期刊
Ovidius University Annals of Chemistry
Ovidius University Annals of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
自引率
11.10%
发文量
20
审稿时长
5 weeks
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