Nelson John R, Cai Yuyang Christine, Giesler Theresa L, Farchaus Joseph W, Sundaram Shanmuuga T, Ortiz-Rivera Maria, Hosta Lou P, Hewitt Peter L, Mamone J Anthony, Palaniappan C, Fuller Carl W
Genomics Reagents Department, Amersham Biosciences, Piscataway, NJ 08855, USA.
Biotechniques. 2002 Jun;Suppl:44-7.
We have developed a novel, isothermal DNA amplification strategy that employs phi29 DNA polymerase and rolling circle amplification to generate high-quality templates for DNA sequencing reactions. The TempliPhi DNA amplification kits take advantage of the fact that cloned DNA is typically obtained in circular vectors, which are readily replicated in vitro using phi29 DNA polymerase by a rolling circle mechanism. This single subunit, proofreading DNA polymerase has excellent processivity and strand displacement properties for generation of multiple, tandem double-stranded copies of the circular DNA, generating as much as 10(7)-fold amplification. Large amounts of product (1-3 microg) can be obtained in as little as 4 hours. Input DNA can be as little as 0.01 ng of purified plasmid DNA, a single bacterial colony, or a 1 microL of a saturated overnight culture. Additionally, the presence of an associated proof reading function within the phi29 DNA polymerase ensures high-fidelity amplification. Once completed, the product DNA can be used directly in sequencing reactions. Additionally, the properties of phi29 DNA polymerase and its use in applications such as amplification ofhuman genomic DNA for genotyping studies is discussed.
我们开发了一种新颖的等温DNA扩增策略,该策略利用phi29 DNA聚合酶和滚环扩增来生成用于DNA测序反应的高质量模板。TempliPhi DNA扩增试剂盒利用了这样一个事实,即克隆的DNA通常是在环状载体中获得的,这些环状载体很容易在体外使用phi29 DNA聚合酶通过滚环机制进行复制。这种单亚基的校对DNA聚合酶具有出色的持续合成能力和链置换特性,可生成环状DNA的多个串联双链拷贝,实现高达10^7倍的扩增。只需4小时就能获得大量产物(1 - 3微克)。输入的DNA可以少至0.01纳克纯化的质粒DNA、单个细菌菌落或1微升饱和过夜培养物。此外,phi29 DNA聚合酶中相关校对功能的存在确保了高保真扩增。一旦完成,产物DNA可直接用于测序反应。此外,还讨论了phi29 DNA聚合酶的特性及其在诸如用于基因分型研究的人类基因组DNA扩增等应用中的用途。