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The magA gene where the code it does the protein which is joined to

机译:magA基因,在该基因上编码与之连接的蛋白质

摘要

PURPOSE: To obtain a new gene coding for a protein bound to an organic membrane covering magnetic fine particles produced in a specific magnetic bacterium and providing protein-bound magnetic fine particles useful in the medical or fermentation fields. etc., without requiring the practice of treatment such as immobilization. ;CONSTITUTION: This new isolated and purified magA gene codes for a protein bound to an organic membrane covering magnetic fine particles produced in a microbial cell of a magnetic bacterium AMB-1 and comprises a DNA sequence represented by the formula. The magnetic fine particles having the organic membrane, covering the surfaces thereof and bound to an enzyme, an antibody or other useful proteins useful in the medical or fermentation fields can be obtained simply by culturing transformed magnetic bacterium. separating the magnetic fine particles produced in the microbial cell without requiring the practice of treatment such as immobilization. The magA gene is obtained by transducing a transposon Tn5 which is a metastatic gene having a medicine- resistant factor into the magnetic bacterium AMB-1, then preparing a variant strain deficient in the productivity of the magnetic fine particles and cloning the gene.;COPYRIGHT: (C)1996,JPO
机译:目的:获得编码与有机膜结合的蛋白质的新基因,该有机膜覆盖特定磁性细菌中产生的磁性细颗粒,并提供在医学或发酵领域有用的与蛋白质结合的磁性细颗粒。等等,而无需诸如固定的治疗方法。 ;组成:这个新的分离和纯化的magA基因编码与覆盖在磁性细菌AMB-1的微生物细胞中产生的磁性细颗粒的有机膜结合的蛋白质,并包含由下式表示的DNA序列。可以通过培养转化的磁性细菌简单地获得具有有机膜的磁性细颗粒,该磁性细颗粒覆盖其表面并且与酶,抗体或在医学或发酵领域中有用的其他有用的蛋白质结合。分离微生物细胞中产生的磁性细颗粒,而无需进行诸如固定化的处理。 magA基因的获得是通过将转座子Tn5(具有耐药性的转移基因)转导到磁性细菌AMB-1中,然后制备变异体菌株来实现的,该变异株缺乏磁性细颗粒的生产力并克隆该基因。 :(C)1996,日本特许厅

著录项

  • 公开/公告号JP3625544B2

    专利类型

  • 公开/公告日2005-03-02

    原文格式PDF

  • 申请/专利权人 TDK株式会社;松永 是;

    申请/专利号JP19950263487

  • 发明设计人 松永 是;

    申请日1995-09-18

  • 分类号C12N15/09;C07K17/02;C12N1/21;C12P21/02;

  • 国家 JP

  • 入库时间 2022-08-21 22:26:29

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