首页> 外国专利> RECOMBINANT DNA FOR PRODUCING HUMAN PROLACTIN, PRODUCTION OF STRAIN AND HUMAN PROLACTIN

RECOMBINANT DNA FOR PRODUCING HUMAN PROLACTIN, PRODUCTION OF STRAIN AND HUMAN PROLACTIN

机译:用于生产人催乳素,菌株和人催乳素的重组DNA

摘要

PURPOSE:To produce a large amount of human prolactin (HP) by transducing DNA integrated with a promoter, Shine-Dalgano sequence and translation initiation codon at the upper stream of gene to code HP into Escherichia coli. CONSTITUTION:A promoter (preferably tryptophan base, lactose base, tack base, Pierre base, etc.), Shine-Dalgano sequence (SD sequence) and translation initiation codon are integrated in this order to the upper stream of a gene to code HP polypeptide to give recombinant DNA for producing HP. In the operation, the promoter has 16-18 pairs of base pairs existing between positions -10 to -35 from the transfer initiation point of mRNA and the SD sequence and the translation initiation codon. The recombination, for example, is carried out by making pL100 from plasmid phPRL9 and PUC19. The recombinant DNA is transduced into Escherichia coli, which is transformed and the bacterium is cultivated to produce HP.
机译:目的:通过转导整合有启动子,Shine-Dalgano序列和基因上游翻译起始密码子的DNA来生产大量人类催乳激素(HP),以将HP编码到大肠杆菌中。组成:启动子(最好是色氨酸碱基,乳糖碱基,粘性碱基,Pierre碱基等),Shine-Dalgano序列(SD序列)和翻译起始密码子按此顺序整合到基因的上游以编码HP多肽产生用于生产HP的重组DNA。在该操作中,启动子具有从mRNA的转移起始点和SD序列以及翻译起始密码子之间的位置-10至-35之间存在的16-18对碱基对。重组例如通过由质粒phPRL9和PUC19制备pL100来进行。重组DNA被转导到大肠杆菌中,该大肠杆菌被转化并且该细菌被培养以产生HP。

著录项

  • 公开/公告号JPH02445A

    专利类型

  • 公开/公告日1990-01-05

    原文格式PDF

  • 申请/专利权人 SHIKISHIMA BOSEKI KK;

    申请/专利号JP19880315317

  • 申请日1988-12-14

  • 分类号C12N1/21;C12N15/00;C12N15/16;C12P21/02;C12R1/19;

  • 国家 JP

  • 入库时间 2022-08-22 06:20:24

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