首页 | 本学科首页   官方微博 | 高级检索  
     检索      

纤维素酶嵌合体EGX-Gluc1C的构建与表达
引用本文:陈玲玲,徐进平.纤维素酶嵌合体EGX-Gluc1C的构建与表达[J].安徽农业科学,2018,46(1):102-104.
作者姓名:陈玲玲  徐进平
作者单位:武汉大学生命科学学院病毒学国家重点实验室,湖北武汉,430072;武汉大学生命科学学院病毒学国家重点实验室,湖北武汉,430072
摘    要:目的]设计和构建一种由β-糖苷水解酶Gluc1C和多功能纤维素酶EGX融合而成的纤维素酶嵌合体EGX-Gluc1C。方法]首先构建了嵌合体的质粒,采用GST标准纯化方法,分别获得重组蛋白Gluc1C、EGX、纤维素酶嵌合体EGX-Gluc1C,并且制备了抗Gluc1C的血清。结果]通过GST纯化的3个蛋白纯度达90%,可以进行后续的酶活检测;通过Western blot验证,发现抗Gluc1C的血清效价很高(稀释比例达1∶5 000)。结论]该研究可为纤维素酶的工业化应用提供一定理论依据。

关 键 词:纤维素酶  EGX  Gluc1C  抗体  纤维素酶嵌合体

Construction and Expression of the Chimera Cellulase EGX-Gluc1C
CHEN Ling-ling,XU Jin-ping.Construction and Expression of the Chimera Cellulase EGX-Gluc1C[J].Journal of Anhui Agricultural Sciences,2018,46(1):102-104.
Authors:CHEN Ling-ling  XU Jin-ping
Abstract:Objective] To design and construct chimera cellulase EGX-Gluc1C originated from the fusion of β-glucosidase Gluc1 C and a cullulase EGX.Method] First,we generated the plasmid inserting chimera cellulase.Then,we purified the recombinant Gluc1C,EGX and EGX-Gluc1C according to the standard GST purification manual.We also generated the anti-Gluc1C serum from the rabbit.Result]The coomassie staining results demonstrated that the purity of these proteins was 90%,which was sufficient for enzyme catalytic assay.Through verification of western blot,the anti-Gluc1 C serum produced from rabbit was of high quality and the dilution ratio can be 1:5 000.Conclusion] The study provided a theoretical basis for the industrial application of cellulase.
Keywords:
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号