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CLONED DNA POLYMERASES FROM THERMOTOGA MARITIMA AND MUTANTS THEREOF

机译:滨海嗜热菌的克隆DNA聚合酶及其突变

摘要

The invention relates to a substantially pure thermostable DNA polymerase from Thermotoga (Tne and Tma) and mutants thereof. The Tne DNA polymerase has a molecular weight of about 100 kilodaltons and is more thermostable than Taq DNA polymerase. The mutant DNA polymerase has at least one mutation selected from the group consisting of (1) a first mutation that substantially reduces or eliminates 35 exonuclease activity of said DNA polymerase; (2) a second mutation that substantially reduces or eliminates 53 exonuclease activity of said DNA polymerase; (3) a third mutation in the O helix of said DNA polymerase resulting in said DNA polymerase becoming non-discriminating against dideoxynucleotides. The present invention also relates to the cloning and expression of the wild type or mutant DNA polymerases in E. coli, to DNA molecules containing the cloned gene, and to host cells which express said genes. The DNA polymerases of the invention may be used in well-known DNA sequencing and amplification reactions.
机译:本发明涉及得自Thermotoga的基本上纯的热稳定DNA聚合酶(Tne和Tma)及其突变体。 Tne DNA聚合酶的分子量约为100道尔顿,比Taq DNA聚合酶更热稳定。突变DNA聚合酶具有至少一个选自( 1 )第一突变的突变,该突变基本上降低或消除了所述DNA聚合酶的35种核酸外切酶活性。 ( 2 )第二个突变,该突变实质上降低或消除了所述DNA聚合酶的53个核酸外切酶活性; ( 3 )所述DNA聚合酶O螺旋的第三个突变,导致所述DNA聚合酶与双脱氧核苷酸无区别。本发明还涉及野生型或突变型DNA聚合酶在E中的克隆和表达。大肠杆菌,含有克隆基因的DNA分子以及表达所述基因的宿主细胞。本发明的DNA聚合酶可以用于众所周知的DNA测序和扩增反应中。

著录项

  • 公开/公告号US2003027296A1

    专利类型

  • 公开/公告日2003-02-06

    原文格式PDF

  • 申请/专利权人 CHATTERJEE DEB K.;

    申请/专利号US19990229173

  • 发明设计人 DEB K. CHATTERJEE;

    申请日1999-01-13

  • 分类号C12Q1/68;

  • 国家 US

  • 入库时间 2022-08-22 00:06:46

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