Yamaguchi Yukihiro, Nimbari Sachiko, Obata Hiroko, Ookawara Tomomi, Eguchi Hironobu, Kurotsu Toshitsugu, Suzuki Keiichiro
Department of Biochemistry, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan.
Yakugaku Zasshi. 2002 Jul;122(7):495-8. doi: 10.1248/yakushi.122.495.
The direct sequencing of PCR products, a bacterial colony (plasmid DNA), or a phage plaque (lambda DNA) is a very powerful technique in several molecular biological applications. Recently, we reported the successful application of this direct sequencing methodology, called recyclesequencing. Occasionally, however, our sequencing efforts failed due to the presence of agarose gel containing Luria-Bertani (LB) medium. Consequently, we pursued a semiquantitative investigation of the inhibitory effects of agarose and LB medium on the direct sequencing reaction. We found that LB medium concentrations greater than 26.7% inhibited the sequencing reaction. Furthermore, agarose concentrations greater than 0.20% in a reaction mixture also inhibited the sequencing reaction.
对聚合酶链反应(PCR)产物、细菌菌落(质粒DNA)或噬菌体噬菌斑(λDNA)进行直接测序,在多个分子生物学应用中是一项非常强大的技术。最近,我们报道了这种称为循环测序的直接测序方法的成功应用。然而,偶尔我们的测序工作会因含有Luria-Bertani(LB)培养基的琼脂糖凝胶的存在而失败。因此,我们对琼脂糖和LB培养基对直接测序反应的抑制作用进行了半定量研究。我们发现,LB培养基浓度大于26.7%会抑制测序反应。此外,反应混合物中琼脂糖浓度大于0.20%也会抑制测序反应。