玉米蛋白磷酸酶2C基因(ZmPP2C2)的原核表达和蛋白纯化

Lixia Liu, Xiaoli Hu
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引用次数: 0

摘要

将玉米蛋白磷酸酶2C基因编码区(ZmPP2C2)亚克隆到表达载体pET30a-c(+)中,导入大肠杆菌BL21 (DE3)进行表达。SDS-PAGE分析显示,ZmPP2C2在37°C、1mM IPTG下表达4 h。超声提取实验表明,该重组蛋白在裂解缓冲液中含量较少,在包涵体中含量最多。收集包涵体,用尿素裂解缓冲液溶解。用Ni-NTA柱经300 mM咪唑洗脱纯化六组氨酸标记的ZmPP2C2融合蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prokaryotic expression, protein purification of a protein phosphatase 2C gene (ZmPP2C2) from maize
The coding region of the protein phosphatase 2C gene (ZmPP2C2) from Zea mays (maize) was sub-cloned into expression vector, pET30a-c(+), and introduced into E. coli BL21 (DE3) for expression. SDS-PAGE analysis indicated ZmPP2C2 was great expressed at 37°C for 4 h with 1mM IPTG. Ultrasonic extraction experiment showed this recombinant protein was little in lysis buffer solution, but most in inclusion body. Inclusion body was collected and dissolved by lysis buffer solution with carbamide. The hexahistidine-tagged ZmPP2C2 fusion protein was purified by Ni-NTA column by 300 mM imidazole elution.
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