Fan J, Ranu R S
Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins 80523, USA.
DNA Seq. 1997;7(5):285-8. doi: 10.3109/10425179709034047.
The delta Taq DNA polymerase is a new, genetically modified version of standard Taq DNA polymerase which lacks the 5'-->3'-exonuclease activity. The present study was designed to investigate the use of delta Taq DNA polymerase for direct cycle sequencing. Results show that delta Taq DNA polymerase can be used for direct cycle sequencing of the PCR amplified DNA, either from an asymmetrically amplified template (by PCR), double stranded DNA template, PCR amplified DNA cloned into a plasmid vector or from a single stranded template. The primer to template ratio and number of cycles necessary for best sequence data have been determined. From these results we conclude that delta Taq DNA polymerase is a highly versatile enzyme which can be used for DNA sequence determinations by direct cycle sequencing.
δTaq DNA聚合酶是标准Taq DNA聚合酶的一种经过基因改造的新版本,它缺乏5'→3'外切核酸酶活性。本研究旨在探讨δTaq DNA聚合酶在直接循环测序中的应用。结果表明,δTaq DNA聚合酶可用于对PCR扩增的DNA进行直接循环测序,这些DNA可来自不对称扩增模板(通过PCR)、双链DNA模板、克隆到质粒载体中的PCR扩增DNA或单链模板。已经确定了获得最佳序列数据所需的引物与模板比例和循环次数。从这些结果我们得出结论,δTaq DNA聚合酶是一种高度通用的酶,可用于通过直接循环测序进行DNA序列测定。