首页> 外国专利> PLASMID VECTOR pHYP WITH HIGH SEGREGATION STABILITY FOR EXPRESSION OF RECOMBINANT PROTEIN, BACTERIUM - PRODUCENT OF PRECURSOR OF RECOMBINANT PROTEIN AND METHOD TO PRODUCE RECOMBINANT PROTEIN

PLASMID VECTOR pHYP WITH HIGH SEGREGATION STABILITY FOR EXPRESSION OF RECOMBINANT PROTEIN, BACTERIUM - PRODUCENT OF PRECURSOR OF RECOMBINANT PROTEIN AND METHOD TO PRODUCE RECOMBINANT PROTEIN

机译:高分离稳定性质粒蛋白表达,细菌重组产物前体细菌产率及其产生重组蛋白的方法。

摘要

FIELD: biotechnologies.;SUBSTANCE: invention is a vector for production of a vector for expression in a bacterial cell of a precursor of a target recombinant protein, fused with an N-end peptide, containing a decahistidine cluster and a site of recognition with proteinase, substantially containing of a section of initiation of replication of pBR322 ori; a gene of a repressor of a lactose operon; a bacterial promotor; an area coding the N-end leader peptide, containing a decahistidine cluster and, not necessarily, a site of recognition with proteinase; a section of cloning (polylinker); a section of termination of transcription functioning in the bacterial cell; a fragment coding a non-genome pair toxin-antitoxin, at the same time the gene of antitoxin is oriented so that the direction of its transcription matches the direction of transcription of the target gene; the gene coding the bacterial marker of selection. The invention also relates to a vector for expression in a bacterial cell of a precursor of a target recombinant protein fused with an N-end peptide, a bacterium containing such vector and the method for production of the recombinant protein using the bacterium.;EFFECT: invention makes it possible to produce a new vector with high segregation stability for highly efficient expression of recombinant proteins with a leader N-end peptide fused in the frame, containing a decahistidine cluster and a site of recognition with proteinase.;9 cl, 12 dwg, 1 tbl, 4 ex
机译:技术领域:本发明是用于产生在细菌细胞中表达的靶重组蛋白的前体的载体,所述靶重组蛋白的前体与N端肽融合,其包含十氨基酸组和蛋白酶的识别位点,基本上包含pBR322 ori的复制起始部分;乳糖操纵子阻遏物的基因;细菌启动子;编码N端前导肽的区域,该区域含有十组氨酸簇,并且不一定具有蛋白酶的识别位点;克隆部分(多连接子);在细菌细胞中转录功能终止的部分;编码非基因组毒素-抗毒素对的片段,同时使抗毒素的基因定向,使其转录方向与靶基因的转录方向匹配;编码选择细菌标记的基因。本发明还涉及用于在细菌细胞中表达与N末端肽融合的靶重组蛋白的前体的载体,包含该载体的细菌以及使用该细菌生产重组蛋白的方法。本发明使得有可能产生具有高分离稳定性的新载体,用于高效表达重组蛋白,其中重组前导N末端肽融合在框架中,该前导N末端肽含有十组氨酸簇和被蛋白酶识别的位点。9cl,12 dwg ,1 tbl,4前

著录项

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