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Method for highly expressing recombinant protein of engineering bacteria and use thereof

机译:高表达工程菌重组蛋白的方法及其应用

摘要

Provided are methods for highly expressing 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:提供了高表达工程细菌的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,并且该方法适用于大规模生产通过工程技术表达的重组蛋白质大肠杆菌细菌

著录项

  • 公开/公告号IL232759A

    专利类型

  • 公开/公告日2017-11-30

    原文格式PDF

  • 申请/专利权人 PROTEIN DESIGN LAB LTD.;XIAOQING QIU;

    申请/专利号IL20140232759

  • 发明设计人 XIAOQING QIU;

    申请日2014-05-22

  • 分类号C12N;

  • 国家 IL

  • 入库时间 2022-08-21 12:52:28

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