Gharizadeh Baback, Ohlin Andreas, Mölling Paula, Bäckman Anders, Amini Bahram, Olcén Per, Nyrén Pål
Department of Biotechnology, Stockholm Center for Physics, Astronomy and Biotechnology, Royal Institute of Technology (KTH), Roslagstullbacken 21, SE-106 91, Stockholm, Sweden.
Mol Cell Probes. 2003 Aug;17(4):203-10. doi: 10.1016/s0890-8508(03)00054-9.
Pyrosequencing technology is a bioluminometric DNA sequencing method that employs a cascade of four enzymes to deliver sequence signals. To date this technology has been limited to the sequencing of short stretches of DNA. As an improvement to this technique, we have introduced a bacterial group-specific, multiple sequencing primer approach that circumvents sequencing of less informative semi-conservative regions of the 16S rRNA gene. This new approach is suitable for challenging templates, improving sequence data quality, avoiding sequencing of non-specific amplification products, lessening sequencing time, and moreover, this strategy should open the way for many new applications in the future. The group-specific, multiple sequencing primers can be applied in the Sanger dideoxy sequencing method as well. In addition, we have improved the chemistry of the Pyrosequencing system enabling sequencing of longer stretches of DNA, which allows numerous new applications.
焦磷酸测序技术是一种生物发光DNA测序方法,它利用四种酶的级联反应来传递序列信号。到目前为止,这项技术仅限于对短片段DNA进行测序。作为对该技术的改进,我们引入了一种细菌群体特异性的多重测序引物方法,该方法避免了对16S rRNA基因信息较少的半保守区域进行测序。这种新方法适用于具有挑战性的模板,可提高序列数据质量,避免对非特异性扩增产物进行测序,减少测序时间,此外,该策略应为未来的许多新应用开辟道路。群体特异性的多重测序引物也可应用于桑格双脱氧测序法。此外,我们改进了焦磷酸测序系统的化学性质,使其能够对更长片段的DNA进行测序,这使得许多新应用成为可能。