Fersht A R, Shi J P, Tsui W C
J Mol Biol. 1983 Apr 25;165(4):655-67. doi: 10.1016/s0022-2836(83)80272-1.
A simple kinetic analysis of the values of kcat and KM for base insertion and misinsertion during DNA replication is presented and applied to the problem of base misinsertion by DNA polymerase I of Escherichia coli. The role of minor tautomeric forms of deoxynucleoside triphosphates (dNTPs) in purine x pyrimidine mismatching has been examined and it has been shown that the misinsertion frequency via this route should be close to the tautomerization constant in solution and is independent of any effect of the polymerase on the tautomerization of a dNTP when bound. Kinetic data on purine x pyrimidine mismatching indicate that the dNTP in a polymerase-DNA-mismatched-dNTP complex is predominantly in the major tautomeric form. The mutagenic effect of Mn2+ in DNA replication is shown to be mediated by decreasing the values of kcat/KM for the insertion of correct dNTPs, whilst the values of this rate constant for misinsertion are relatively unaffected or increased.
本文对DNA复制过程中碱基插入和错配的kcat和KM值进行了简单的动力学分析,并将其应用于大肠杆菌DNA聚合酶I的碱基错配问题。研究了脱氧核苷三磷酸(dNTP)的次要互变异构形式在嘌呤x嘧啶错配中的作用,结果表明,通过该途径的错配频率应接近溶液中的互变异构常数,且与聚合酶对结合时dNTP互变异构的任何影响无关。嘌呤x嘧啶错配的动力学数据表明,聚合酶-DNA-错配-dNTP复合物中的dNTP主要处于主要互变异构形式。结果表明,Mn2+在DNA复制中的诱变作用是通过降低正确dNTP插入的kcat/KM值来介导的,而错配的该速率常数的值相对不受影响或增加。