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短小芽孢杆菌过氧化氢酶在聚乙二醇/硫酸钠双水相体系中的部分表征

Partial characterization of Bacillus pumilus catalase partitioned in poly(ethylene glycol)/sodium sulfate aqueous two-phase systems.

作者信息

Yuzugullu Karakus Yonca, Isik Semih

机构信息

a Department of Biology Faculty of Arts and Science , Kocaeli University , Kocaeli , Turkey.

b The Graduate School of Natural and Applied Sciences , Kocaeli University , Kocaeli , Turkey.

出版信息

Prep Biochem Biotechnol. 2019;49(4):391-399. doi: 10.1080/10826068.2019.1573197. Epub 2019 Feb 15.

Abstract

Aqueous two-phase partitioning system (ATPS) was used to extract and purify catalase from Bacillus pumilus. The system parameters for effective purification of catalase were optimized. The best catalase recovery (123%) with a 4.6-fold purification was obtained in the bottom phase of ATPS including the mixture of 15% (w/w) PEG4000, 10% (w/w) NaSO and 3% (w/w) NaCl at pH 5.0. The purified enzyme was characterized regarding its activity and stability. The highest enzyme activity was observed at pH 7.0 and 37 °C on hydrogen peroxide. The enzyme was quite stable at temperatures between 30 and 55 °C and a pH range of 7.0-9.0. The K and V values were determined from Lineweaver-Burk plot as 11 mM and 1667 µmole mlmin, respectively. Overall, it can be said that ATPS is a rapid, reasonable, straightforward and cost-effective process for catalase purification in comparison to the chromatographic methods.

摘要

采用双水相分配系统(ATPS)从短小芽孢杆菌中提取和纯化过氧化氢酶。对有效纯化过氧化氢酶的系统参数进行了优化。在pH 5.0的ATPS下层相中,使用15%(w/w)聚乙二醇4000、10%(w/w)硫酸钠和3%(w/w)氯化钠的混合物,获得了最佳的过氧化氢酶回收率(123%)和4.6倍的纯化倍数。对纯化后的酶进行了活性和稳定性表征。在pH 7.0和37°C条件下,该酶对过氧化氢的活性最高。该酶在30至55°C的温度和7.0至9.0的pH范围内相当稳定。通过Lineweaver-Burk图确定的米氏常数(Km)和最大反应速度(Vmax)值分别为11 mM和1667 μmol ml-1 min-1。总体而言,与色谱方法相比,可以说ATPS是一种快速、合理、直接且经济高效的过氧化氢酶纯化方法。

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