首页> 外国专利> Cloned factor C cDNA of the Singapore Horseshoe Crab, Carcinoscorpius rotundicauda and purification of Factor C proenzyme

Cloned factor C cDNA of the Singapore Horseshoe Crab, Carcinoscorpius rotundicauda and purification of Factor C proenzyme

机译:新加坡Horse蟹的C因子cDNA的克隆及C因子原酶的纯化

摘要

Full-length and deletion subclones of cDNAs for Factor C of Carcinoscorpius rotundicauda are provided. These cDNAs have been cloned into &lgr;gt 22 and pGEM 11Zf(+). Further manipulations of the 5' and 3' ends of these cDNAs have been carried out, and these cDNAs have been further subcloned into other expression vectors such as pGEMEX-1, pET 3b, and the yeast shuttle vectors YEpsec 1 and pEMBLyex 4, and pPIC 9 and pHIL D2. Also provided are host cells transformed with expression vectors containing DNA molecules encoding proteins having Factor C-like enzymatic activity, methods of producing such proteins, methods for purifying Factor C zymogens, and methods for protecting Factor C zymogens from autoactivation by Gram negative bacterial endotoxin while the proenzyme is being purified and/or processed from amoebocyte lysates or from recombinant clones, or during storage or subsequent handling. This protection is afforded by the addition of 5-30% Me.sub.2 SO, which reversibly inhibits the Factor C zymogen.
机译:提供了轮状Carcinoscorpius undundicauda的C因子cDNA的全长和缺失亚克隆。这些cDNA已被克隆到≥22和pGEM 11Zf(+)中。已经对这些cDNA的5'和3'末端进行了进一步的操作,并将这些cDNA进一步亚克隆至其他表达载体,例如pGEMEX-1,pET 3b和酵母穿梭载体YEpsec 1和pEMBLyex 4,以及pPIC 9和pHIL D2。还提供了用表达载体转化的宿主细胞,该表达载体含有编码具有因子C样酶活性的蛋白质的DNA分子的DNA分子,产生这种蛋白质的方法,纯化因子C酶原的方法以及保护因子C酶原免于被革兰氏阴性细菌内毒素自激活的方法。从变形细胞,重组克隆,或在储存或后续处理过程中纯化和/或加工该酶。通过添加5-30%Me.sub.2 SO可逆地抑制因子C酶原,从而提供了这种保护。

著录项

  • 公开/公告号US5712144A

    专利类型

  • 公开/公告日1998-01-27

    原文格式PDF

  • 申请/专利权人 NATIONAL UNIVERSITY OF SINGAPORE;

    申请/专利号US19950460521

  • 发明设计人 JEAK LING DING;BOW HO;

    申请日1995-06-02

  • 分类号C12N9/50;

  • 国家 US

  • 入库时间 2022-08-22 02:40:20

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