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Manufacturing method null of the useful material which uses the microbe and the said microbe which possess the high manifestation vector and the said high manifestation vector

机译:使用具有高表达载体和所述高表达载体的微生物和所述微生物的有用材料的制造方法无效

摘要

PURPOSE: To provide a new high-expression vector useful for the production of an exogenote product. ;CONSTITUTION: A high-expression vector pHT having HWP promoter and a multicloning site of formula, e.g. pHT210. A plasmid having a DNA fragment produced by linking an α-amylase (BLA) gene of Bacillus licheniformis to the downstream of an MWP promoter region of Bacillus brevis 47 (FERM P-7224) is treated with a restriction enzyme, the HWP promoter region fragments extracted from the plasmid are linked together, a Bacillus brevis is transformed to obtain a plasmid containing HWP promoter in place of MWP promoter and the obtained plasmid is subjected to restriction enzyme treatment, ligase treatment and linker treatment to obtain a high-expression vector free from BLA gene.;COPYRIGHT: (C)1994,JPO&Japio
机译:目的:提供一种新的高表达载体,可用于生产外源基因产品。 ;组成:具有HWP启动子和下式的多克隆位点的高表达载体pHT,例如pHT210。用限制性内切酶处理一种质粒,该质粒具有将地衣芽孢杆菌的α-淀粉酶(BLA)基因连接至短芽孢杆菌47的MWP启动子区域(FERM P-7224)下游的DNA片段。将从质粒中提取的质粒连接在一起,转化短芽孢杆菌以获得含有HWP启动子代替MWP启动子的质粒,并对获得的质粒进行限制性内切酶处理,连接酶处理和接头处理,从而获得了一种不含HWP启动子的高表达载体。 BLA基因。;版权:(C)1994,JPO&Japio

著录项

  • 公开/公告号JP2727391B2

    专利类型

  • 公开/公告日1998-03-11

    原文格式PDF

  • 申请/专利权人 HIGETA SHOYU KK;UDAKA JUZO;

    申请/专利号JP19920216605

  • 发明设计人 EBISU SHOGO;UDAKA JUZO;TAKAGI HIROAKI;

    申请日1992-07-23

  • 分类号C12N15/09;C12N1/21;C12P21/02;

  • 国家 JP

  • 入库时间 2022-08-22 03:00:47

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