Ferretti L, Sgaramella V
Nucleic Acids Res. 1981 Aug 11;9(15):3695-705. doi: 10.1093/nar/9.15.3695.
Specific, complete and reversible inhibition of the joining of blunt ended DNA duplexes catalyzed by the T4 DNA ligase can be obtained by using ATP, the enzyme cofactor, at concentrations of 5 mM and higher. On cohesive DNA ends, 5 mM ATP, which completely inhibits blunt end ligation, brings about only a limited (8%) reduction in the level of joining obtainable under optimal ATP concentration (0,5 mM or lower). A similar but less drastic uncoupling of the two kinds of joining can be achieved at lower ATP concentration (2,5 mM) using 1 mM Mg++. The joining of DNA blunt ends can also be inhibited almost completely by 10 mM spermidine, without noticeable effect on the joining of cohesive termini.
通过使用浓度为5 mM及更高的酶辅因子ATP,可以实现对T4 DNA连接酶催化的平端DNA双链体连接的特异性、完全且可逆的抑制。对于粘性DNA末端,5 mM的ATP可完全抑制平端连接,而在最佳ATP浓度(0.5 mM或更低)下可实现的连接水平仅有限降低(8%)。在较低的ATP浓度(2.5 mM)下,使用1 mM的Mg++可实现两种连接的类似但不太显著的解偶联。10 mM的亚精胺也几乎可以完全抑制DNA平端的连接,而对粘性末端的连接没有明显影响。