Soriano L, Smith J, Croisille Y, Dastugue B
Nucleic Acids Res. 1974 Sep;1(9):1085-97. doi: 10.1093/nar/1.9.1085.
R-DNA polymerase, D-DNA polymerase, DNase and RNase H activities in mitochondria from chick embryonic brain were studied by ion-exchange chromatography. Two main fractions were separated according to their chromatographic behaviour: a fraction M Ib which is eluted with the washing buffer from two successive DEAE-cellulose columns and a fraction M IV which is eluted at 400 mM KC1 from a phosphocellulose column. Although the two fractions contain both the DNA polymerase and the degrading activities, all the specific activities are higher in fraction M IV than in fraction M Ib. Heat inactivation experiments have shown that R-DNA polymerase is inactivated in both fractions, whereas RNase H and DNase are not affected. Thus, degrading activities and R-DNA polymerase activity seem to be catalyzed by different molecular entities. However the fact that in most cases these activities co-chromatograph suggests that the corresponding molecules form rather stable complexes.
通过离子交换色谱法研究了鸡胚脑线粒体中的R-DNA聚合酶、D-DNA聚合酶、DNA酶和RNase H活性。根据它们的色谱行为分离出两个主要部分:一个部分M Ib,用洗涤缓冲液从两个连续的DEAE-纤维素柱上洗脱下来;另一个部分M IV,从磷酸纤维素柱上在400 mM KCl浓度下洗脱下来。尽管这两个部分都含有DNA聚合酶和降解活性,但M IV部分的所有比活性都高于M Ib部分。热失活实验表明,R-DNA聚合酶在两个部分中都被灭活,而RNase H和DNA酶不受影响。因此,降解活性和R-DNA聚合酶活性似乎由不同的分子实体催化。然而,在大多数情况下这些活性共色谱的事实表明相应的分子形成了相当稳定的复合物。