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一种低温表达型T载体及其应用
引用本文:何燕斌,齐亚坤,黄霖霆,周蓉,邵蔚蓝.一种低温表达型T载体及其应用[J].生物工程学报,2015,31(12):1773-1783.
作者姓名:何燕斌  齐亚坤  黄霖霆  周蓉  邵蔚蓝
作者单位:1 南京师范大学 生命科学学院,江苏 南京 210046,1 南京师范大学 生命科学学院,江苏 南京 210046,1 南京师范大学 生命科学学院,江苏 南京 210046,1 南京师范大学 生命科学学院,江苏 南京 210046,2 江苏大学 环境与安全工程学院,江苏 镇江 212000
基金项目:国家自然科学基金 (No. 31170017) 资助。
摘    要:在现代生物学和生物技术研究中,通过基因重组表达获得目标蛋白已成为常规技术。因其培养简单、操作方便、遗传背景清楚、克隆表达技术成熟,大肠杆菌表达系统通常是人们表达重组蛋白的首选。但是在常规温度下进行基因的重组表达,动、植物和常温微生物的基因产物多数在数小时内变性沉淀;还有一些重组蛋白对宿主具有细胞毒性,难以得到重组表达。因此,我们构建了1种新型T载体——pEXC-T;它结合TA克隆技术和低温诱导表达功能,具有表达水平高、操作方便、目标蛋白得到分子伴侣保护和低温保存等特点。采用构建和优化的pEXC载体,P1抗原蛋白、溶血素PLO两种不稳定性蛋白在pEXC中都实现了高效的可溶性表达。低温表达系统p EXC的建立和发展为蛋白质的结构与功能的研究,以及抗原和药用蛋白的制备提供了便利的途径。

关 键 词:大肠杆菌,表达系统,低温诱导,可溶性蛋白
收稿时间:2015/1/20 0:00:00

An expression T-vector and its application at low temperatures
Yanbin He,Yakun Qi,Linting Huang,Rong Zhou and Weilan Shao.An expression T-vector and its application at low temperatures[J].Chinese Journal of Biotechnology,2015,31(12):1773-1783.
Authors:Yanbin He  Yakun Qi  Linting Huang  Rong Zhou and Weilan Shao
Institution:1 Department of Life Sciences, Nanjing Normal University, Nanjing 210046, Jiangsu, China,1 Department of Life Sciences, Nanjing Normal University, Nanjing 210046, Jiangsu, China,1 Department of Life Sciences, Nanjing Normal University, Nanjing 210046, Jiangsu, China,1 Department of Life Sciences, Nanjing Normal University, Nanjing 210046, Jiangsu, China and 2 School of Environment and Safety Engineering, Jiangsu University, Zhejiang 212000, Jiangsu, China
Abstract:In modern biology and biotechnology research, recombinant gene expression has been the most popular method to obtain the target protein. In recent years, many foreign genes have been efficiently expressed in Escherichia coli. However, proteins encoded by animal, plant or mesophilic microbial genes often lose activities or become denatured within a few hours at regular growth temperatures for E. coli; some other target proteins are toxic to host cells and therefore difficult to be over-expressed. The new T-vector, pEXC-T, was constructed by combining TA cloning and cold-shock inducting to obtain high expression levels with low costs. This paper reports the construction of pEXC-T and optimization of induction techniques for gene expression. Two instable proteins were tested and successfully expressed in soluble form by using pEXC vector. The development of pEXC-T offers a convenient technique for the preparations of recombinant proteins to be used in structure/function studies, or as diagnostic markers and medicinal proteins.
Keywords:Escherichia coli  expression system  cold-shock induction  soluble protein
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