Gärtner C, Waldstein E A, Hagen U
Biochim Biophys Acta. 1980 Apr 30;607(2):247-55. doi: 10.1016/0005-2787(80)90077-5.
Gamma-irradiation of Escherichia coli cells made permeable to deoxynucleoside triphosphates (dNTP) by toluene induces a repair-type DNA synthesis. As previous studies have shown ATP stimulates this DNA synthesis; we studied the mechanism of the ATP effect by analyzing the kinetics of nucleotide incorporation at various dNTP concentrations. The V values of the DNA repair synthesis rise with increasing dose (0-50 Gy); nonirradiated cells showed a negligible nucleotide incorporation. The apparent Michaelis constant KM for dNTP in the assay was 83-143 microM and the value was much higher than for a DNA polymerase reaction in vitro. ATP stimulated the DNA synthesis with concomitant decrease of KM yet unchanged V values. Similar results were obtained with a rec BC strain. We propose that the ATP effect is due to a greater affinity of dNTPs to the DNA polymerase, possibly by a stabilisation of the structural integrity of the complex DNA with repair enzymes. Activation of exonucleases by ATP could be excluded. Addition of NAD to the reaction mixture inhibits the DNA synthesis possibly by activation of ligase which closes the nicks in the DNA strand.
用甲苯使大肠杆菌细胞对脱氧核苷三磷酸(dNTP)具有通透性后,进行γ射线照射可诱导修复型DNA合成。如先前研究所示,ATP可刺激这种DNA合成;我们通过分析在不同dNTP浓度下核苷酸掺入的动力学来研究ATP作用的机制。DNA修复合成的V值随剂量增加(0 - 50 Gy)而升高;未照射的细胞显示核苷酸掺入可忽略不计。测定中dNTP的表观米氏常数KM为83 - 143微摩尔,该值远高于体外DNA聚合酶反应的值。ATP刺激DNA合成,同时KM降低而V值不变。用rec BC菌株也得到了类似结果。我们提出,ATP的作用是由于dNTP对DNA聚合酶具有更高的亲和力,可能是通过稳定具有修复酶的复合DNA的结构完整性。可以排除ATP对外切核酸酶的激活作用。向反应混合物中添加NAD可能通过激活连接酶来封闭DNA链中的缺口从而抑制DNA合成。