[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.%[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.
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