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Cationic reverse micellar based purification of recombinant glutaminase free L-asparaginase II of Bacillus subtilis WB800N from fermentation media

机译:基于发酵培养基的枯草芽孢杆菌WB800n的重组谷氨酰胺酶自由L-天冬酰胺酶II的阳离子反向胶束纯化

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摘要

Reverse micellar extraction (RME), a liquid-liquid based separation is a versatile tool for protein purification. A statistical approach was employed for the purification of recombinant glutaminase free anti-cancerous enzyme viz., L-asparaginase II to evaluate the effects of RME in current study. The cationic system (CTAB/iso-octane/hexanol/butanol) was used in RME to optimize both forward and backward protein extraction efficiency. By adapting Taguchi's orthogonal array (OA), maximum forward extraction efficiency (FEE) of 86.98% with 84.82% enzyme activity recovery and 1.04 times purification fold achieved with the optimized parameters. Under the optimal levels, the back extraction efficiency (BEE) was observed to be 96.97% with 93.07% enzyme activity recovery and 1.38 times purification fold. Further, mass transfer kinetic studies of RME indicated the mass transfer coefficients of forward and backward extraction to be 0.049 min(-1) and 0.036 min(-1) respectively.
机译:反向胶束萃取(RME),基于液液的分离是蛋白质纯化的通用工具。 用于纯化重组谷氨酰胺酶游离抗癌酶Ziz的统计方法。,L-天冬酰胺酶II,以评估RME在目前研究中的作用。 在RME中使用阳离子系统(CTAB / ISO-辛烷/己醇/丁醇),以优化前向后蛋白质提取效率。 通过调整Taguchi的正交阵列(OA),86.98%的最大前进提取效率(费用)84.82%的酶活性回收率和通过优化参数实现1.04倍净化折叠。 在最佳水平下,观察到后萃取效率(蜂)为96.97%,酶活性回收率为93.07%,净化折叠1.38倍。 此外,RME的传质动力学研究表明向前和向后提取的质量转移系数分别为0.049分钟(-1)和0.036分钟(-1)。

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