检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:张艳丽[1,2] 任柳 张宇宏 张伟[1] ZHANG Yanli;REN Liu;ZHANG Yuhong;ZHANG Wei(Biotechnology Research Institute,Chinese Academy of Agricultural Sciences,Beijing 100081,China;College of Food Science&Technology,Nanchang University,Nanchang 330047,China;College of Life Science and Technology,Harbin Normal University,Harbin 150025,China)
机构地区:[1]中国农业科学院生物技术研究所,北京100081 [2]南昌大学食品学院,南昌330047 [3]哈尔滨师范大学生命科学与技术学院,哈尔滨150025
出 处:《中国农业科技导报》2020年第8期56-63,共8页Journal of Agricultural Science and Technology
基 金:国家自然科学基金项目(31972601)。
摘 要:毕赤酵母是使用最广泛、最具有发展前景的异源蛋白表达系统之一。在毕赤酵母GS115中实现了来源于棉铃虫(Helicoverpa armigera)葡萄糖氧化酶基因hagox的异源表达。以棉铃虫hagox基因连接pPICZαA质粒构建重组表达载体,电击转化毕赤酵母GS115H菌株后得到含有hagox基因的重组酵母菌株。通过平板显色、酶活力测定和SDS-PAGE分析,重组酵母中HaGOX成功表达。HaGOX含606个氨基酸,理论分子量66.9 kD,预测等电点pH 4.78。经测试重组HaGOX的最适pH为6.0~7.0,最适温度为40℃,对6-脱氧-葡萄糖和D-葡萄糖具有高催化活力,以D-葡萄糖为底物的比活力为13.63 U·mg^-1,对其他吡喃糖和二糖没有催化活力。Pichia pastoris is one of the most widely used and most promising heterologous protein expression systems.In the study,Helicoverpa armigera glucose oxidase(hagox)gene was expressed in Pichia pastoris.The hagox gene was ligated into the pPICZαA plasmid to construct the Pichia pastoris recombinant expression vector.The Pichia pastoris recombinant strain containing hagox gene was constructed by electroporating the recombinant plasmid into Pichia pastoris GS115 H.Then,the expression of recombinant protein HaGOX was detected by plate coloring,enzyme activity determination and SDS-PAGE.HaGOX encoded 606 amino acids,theoretical molecular weight was 66.9 kD and isoelectric point was 4.78.The optimal pH and temperature were pH 6.0~7.0 and 40℃,respectively,and optimal substrate were 6-deoxy-glucose and D-glucose.The specific activity of the recombinant enzyme was determined to be 13.63 U·mg^-1 by using D-glucose as substrate,and there was no catalytic activity for other pyranose and disaccharide.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.3