Kitayama S, Matsuyama A
Biochim Biophys Acta. 1977 Mar 2;475(1):23-31. doi: 10.1016/0005-2787(77)90335-5.
DNA polymerase activities in Micrococcus radiodurans were separated into two fractions after purification more than 2000 fold. They differ in pH optimum and residual activities in the absence of a full deoxyribonucleoside triphosphates complement. NAD partly inhibited one of the activities. Both activities were eluted as a single peak on gel filtration and sedimented at the same rate on glycerol gradient centrifugation. Molecular weight 140000 was calculated from Stokes radius and sedimentation constant. Deoxyribonuclease activity was detected on one of the polymerase activities which preferentially degraded double-stranded DNA. Priming activity of nicked DNA was reduced by gamma-irradiation. These results have been related to the possible rolls in repair synthesis in vivo or DNA synthesis in permeable cells of M. radiodurans.
在对耐辐射微球菌中的DNA聚合酶活性进行了超过2000倍的纯化后,将其分为两个组分。它们在最适pH值以及在缺乏完整的脱氧核糖核苷三磷酸互补物时的残余活性方面存在差异。NAD部分抑制了其中一种活性。在凝胶过滤中,两种活性均以单峰形式洗脱,并且在甘油梯度离心中以相同速率沉降。根据斯托克斯半径和沉降常数计算出分子量为140000。在其中一种聚合酶活性中检测到了脱氧核糖核酸酶活性,该活性优先降解双链DNA。切口DNA的引发活性因γ射线照射而降低。这些结果与耐辐射微球菌在体内修复合成或可渗透细胞中DNA合成中可能发挥的作用有关。