3-酮基嘌呤还原酶(TSC10)基因表达载体的构建及其在毕赤酵母中的表达  

Construction of 3-keto Purine Reductase (TSC10) Gene Expression Vector and Its Expression in Pichia Pastoris

作　　者：郑丽娜 刘美辰[1] 王思明[1] 白雪媛[1] 赵雨[1] 赵大庆[1] 王佳雯[1] ZHENG Li-na;LIU Mei-chen;WANG Si-ming;BAI Xue-yuan;ZHAO Yu;ZHAO Da-qing;WANG Jia-wen(Traditional Chinese Medicine and Biotechnology Research and Development Center,Changchun University of Chinese Medicine,Changchun 130117,China)

机构地区：[1]长春中医药大学中医药与生物工程研究开发中心,长春130117

出　　处：《科学技术与工程》2018年第10期31-34,共4页Science Technology and Engineering

基　　金：吉林省中药组学工程实验室建设项目(2014N155)资助

摘　　要：TSC10基因所编码的3-酮基嘌呤还原酶是酵母中神经酰胺合成的重要因子。设计了一种从酵母中提取神经酰胺经济、便捷、高效的方法:(1)利用构建含有TSC10基因的毕赤酵母GS115表达载体p PIC3.5K-TSC10;(2)电转化法将该表达质粒转化到GS115感受态细胞中;(3)用G418筛选以及PCR鉴定;(4)使用qRT-PCR和SDS-PAGE进行检测。结果经过G418筛选以及PCR鉴定后确定获得了包含TSC10基因的毕赤酵母转化子,经过qRT-PCR和SDS-PAGE进行检测后发现TSC10基因在20个阳性菌株中均可以稳定、高效表达。成功构建了3-酮基嘌呤还原酶高表达的毕赤酵母菌株,并为后续获得高收率神经酰胺奠定了基础。The 3-keto purine reductase encoded by TSC10 gene is an important factor in the synthesis of ceramide in yeast.The economical,convenient and efficient method was designed for extracting ceramide from yeast.①Using the expression vector pPIC3.5K-TSC10 containing the TSC10 gene of Pichia pastoris GS115.②The expression plasmid was transformed into GS115 competent cells by electroporation.③Screened with G418 and identified by PCR.④Detection was performed using qRT-PCR and SDS-PAGE.After purification by G418 and PCR identification,the Pichia pastoris transformants containing TSC10 gene were identified and analyzed by qRT-PCR and SDS-PAGE.The TSC10 gene was stable and highly expressed in 20 positive strains.This method successfully constructed the highly expressed Pichia pastoris of 3-ketopurine reductase and laid the foundation for the subsequent high yield of ceramide.

关 键 词：3-酮基嘌呤还原酶 毕赤酵母 基因表达 

分 类 号：Q78[生物学—分子生物学]