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大肠杆菌连接酶进行的平端和单链连接:对体外扩增方案的影响。

Blunt-end and single-strand ligations by Escherichia coli ligase: influence on an in vitro amplification scheme.

作者信息

Barringer K J, Orgel L, Wahl G, Gingeras T R

机构信息

Salk Institute Biotechnology/Industrial Associates, Inc., San Diego, CA 92138.

出版信息

Gene. 1990 Apr 30;89(1):117-22. doi: 10.1016/0378-1119(90)90213-b.

Abstract

A ligase-based, in vitro DNA amplification system (LAR) has been described by Wu and Wallace [Genomics 4 (1989) 560-569]. This strategy is based on the ability of a DNA ligase to join the 5' phosphate of one DNA molecule to the 3' hydroxyl of a second during a nick-closing reaction. Escherichia coli DNA ligase has been used in place of the T4 DNA ligase in our study in order to limit template-independent ligation activities, which lower the sensitivity of this amplification procedure. The results of this study indicate that E. coli ligase also joins blunt-ended DNA molecules and some single-stranded oligodeoxyribonucleotides, in the absence of a complementary template, with an efficiency which is sensitive to both the concentrations of DNA substrate and enzyme.

摘要

吴和华莱士描述了一种基于连接酶的体外DNA扩增系统(LAR)[《基因组学》4(1989年)560 - 569]。该策略基于DNA连接酶在切口封闭反应中将一个DNA分子的5'磷酸与第二个DNA分子的3'羟基连接的能力。在我们的研究中,使用了大肠杆菌DNA连接酶来代替T4 DNA连接酶,以限制与模板无关的连接活性,这种活性会降低该扩增程序的灵敏度。这项研究的结果表明,在没有互补模板的情况下,大肠杆菌连接酶也能连接平端DNA分子和一些单链寡脱氧核糖核苷酸,其效率对DNA底物和酶的浓度都很敏感。

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