首页> 外国专利> METHOD FOR HIGHLY EXPRESSING RECOMBINANT PROTEIN OF ENGINEERING BACTERIA AND USE THEREOF

METHOD FOR HIGHLY EXPRESSING RECOMBINANT PROTEIN OF ENGINEERING BACTERIA AND USE THEREOF

机译:高效表达工程菌重组蛋白的方法及其应用

摘要

Provided are a method for highly expressing a recombinant protein of engineering bacteria and the use thereof. The method comprises the following steps: (1) engineering bacteria of Escherichia coli with pET system are transfected with recombinant mutated plasmid to obtain positive monoclonal colonies; (2) the positive monoclonal colonies are enriched to obtain a seed bacteria solution, and the seed bacteria solution is induced to enrichment and growth in a large amount; and (3) the bacteria supernatant containing the recombinant protein as the expression target is separated, and then the recombinant protein in the bacteria supernatant is extracted and purified. The method is characterized in that the engineering bacteria of Escherichia coli with pET system are E. coli B834 (DE3). The components of the mass enrichment medium and the protein purification steps are also optimized such that a significant improvement in the yield and purity of the protein is achieved and the method is suitable for applying to the large-scale production of recombinant protein expressed by the engineering bacteria of Escherichia coli.
机译:提供了一种高表达工程细菌重组蛋白的方法及其用途。该方法包括以下步骤:(1)用重组突变质粒转染pET系统工程大肠杆菌,获得阳性单克隆。 (2)富集阳性单克隆菌落以获得种子细菌溶液,并诱导种子细菌溶液大量富集和生长; (3)分离含有重组蛋白作为表达靶标的细菌上清液,然后提取纯化细菌上清液中的重组蛋白。该方法的特征在于,具有pET系统的大肠杆菌的工程菌是大肠杆菌B834(DE3)。还优化了质量富集培养基的成分和蛋白质纯化步骤,从而显着提高了蛋白质的产量和纯度,并且该方法适用于通过工程技术表达的重组蛋白质的大规模生产大肠杆菌。

著录项

  • 公开/公告号EA025689B1

    专利类型

  • 公开/公告日2017-01-30

    原文格式PDF

  • 申请/专利权人 PROTEIN DESIGN LAB LTD.;

    申请/专利号EA20140000607

  • 发明设计人 XIAOQING;

    申请日2012-11-23

  • 分类号C12N15/70;C12N1/20;C12N1/21;C12N15/67;C07K1/18;C12R1/19;

  • 国家 EA

  • 入库时间 2022-08-21 13:39:13

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号