DNA聚合酶
聚合酶
聚合酶
多重位移放大
PCR的应用
生物
重组酶聚合酶扩增
热启动PCR
DNA聚合酶Ⅱ
分子生物学
DNA钳
DNA聚合酶Ⅰ
核酸
环介导等温扩增
DNA
聚合酶链反应
计算生物学
生物化学
多重聚合酶链反应
水热
基因
逆转录酶
DNA提取
作者
Igor P. Oscorbin,М. Л. Филипенко
标识
DOI:10.1016/j.csbj.2023.09.008
摘要
DNA polymerases are a superfamily of enzymes synthesizing DNA using DNA as a template. They are essential for nucleic acid metabolism and for DNA replication and repair. Modern biotechnology and molecular diagnostics rely heavily on DNA polymerases in analyzing nucleic acids. Among a variety of discovered DNA polymerases, Bst polymerase, a large fragment of DNA polymerase I from Geobacillus stearothermophilus, is one of the most commonly used but is not as well studied as Taq polymerase. The ability of Bst polymerase to displace an upstream DNA strand during synthesis, coupled with its moderate thermal stability, has provided the basis for several isothermal DNA amplification methods, including LAMP, WGA, RCA, and many others. Bst polymerase is one of the key components defining the robustness and analytical characteristics of diagnostic test systems based on isothermal amplification. Here, we present an overview of the biochemical and structural features of Bst polymerase and provide information on its mutated analogs.
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