Extraction, precipitation and characterization of urease from Vicia faba L.

Dalal S. Bedan
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引用次数: 5

Abstract

This study aimed to extract urease enzyme from available plant source which was broad beans (Vicia faba L.) using aqueous solution in a ratio1:3(w:v) .The crude extract appeared enzyme activity 33.3 U/ml. Results of this study revealed the possibility to precipitate urease enzyme after extraction using different precipitation methods consisted of Acetone precipitation; Alcohol precipitation and Ammonium sulfate precipitation, these ways of urease precipitation gave enzyme activities 74.8; 43.6 and 82.2 U/ml respectively .The enzyme precipitation using 60% saturation ratio of Ammonium sulfate gave the maximum activity of urease precipitation among other precipitation methods. Enzyme characterization appeared the optimum pH of urease activity was 8.0 and gave enzyme activity 93.8U/ml, while the optimum pH of urease stability was 6.0; the enzyme maintains its activity. On the other side the optimum temperature of precipitated urease activity was 50°C and the enzyme activity reached 99.3U/ml while the optimal temperature of urease stability was 40°C ,the precipitated urease maintain 100% of activity. The effect of other factors on urease action were studied also, these are consisted of the storage time of enzyme ,urease maintain its activity for 8days and the activity begun to decline after that time; the effect of time reusability was also revealed that the enzyme could be used for six times and maintain its activity. The influence of different mineral salts on precipitated urease were also recorded ;these salts were CuSO4 , MgSO4, MgCl2,KCl,CaCl2and FeSo4, results appeared that magnesium and calcium salts were activator for the precipitated urease while copper ,potassium and ferrous salts were inhibitor of the precipitated urease. Urea concentration as an enzyme substrate were also examined and results appeared the optimal substrate concentration was 30mM; enzyme activity reached to125.2U/ml.
蚕豆中脲酶的提取、沉淀及特性研究。
以蚕豆为原料,以蚕豆为原料,以1:3(w:v)的比例提取脲酶,粗提物酶活性为33.3 U/ml。本研究结果表明,不同的提取方法均可沉淀脲酶:丙酮沉淀法;醇沉法和硫酸铵沉淀法所得脲酶活性为74.8;结果表明,硫酸铵饱和比为60%时脲酶沉淀活性最高。酶学表征表明,脲酶活性的最佳pH为8.0,酶活性为93.8U/ml,脲酶稳定性的最佳pH为6.0;酶保持其活性。另一方面,沉淀脲酶活性的最佳温度为50℃,酶活性达到99.3U/ml;脲酶稳定性的最佳温度为40℃,沉淀脲酶保持100%的活性。同时研究了其他因素对脲酶作用的影响,即酶的贮存时间,脲酶的活性维持在8d, 8d后活性开始下降;结果表明,该酶可重复使用6次并保持其活性。记录了不同矿物盐对沉淀脲酶的影响,即CuSO4、MgSO4、MgCl2、KCl、cacl2和FeSo4,结果表明,镁和钙盐是沉淀脲酶的活化剂,而铜、钾和亚铁盐是沉淀脲酶的抑制剂。对尿素作为酶底物的浓度进行了考察,结果表明,最适底物浓度为30mM;酶活性达到125.2 2u /ml。
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