| Literature DB >> 15203333 |
Baback Gharizadeh1, Jonas Eriksson, Nader Nourizad, Tommy Nordström, Pål Nyrén.
Abstract
Pyrosequencing is a DNA sequencing technique based on the bioluminometric detection of inorganic pyrophosphate, which is released when nucleotides are incorporated into a target DNA. Since the technique is based on an enzymatic cascade, the choice of enzymes is a critical factor for efficient performance of the sequencing reaction. In this study we have analyzed the performance of an alternative DNA polymerase, Sequenase, on the sequencing performance of the Pyrosequencing technology. Compared to the Klenow fragment of DNA polymerase I, Sequenase could read through homopolymeric regions with more than five T bases. In addition, Sequenase reduces remarkably interference from primer-dimers and loop structures that give rise to false sequence signals. By using Sequenase, synchronized extensions and longer reads can be obtained on challenging templates, thereby opening new avenues for applications of Pyrosequencing technology.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15203333 DOI: 10.1016/j.ab.2004.03.018
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365