McLennan A G, Keir H M
Nucleic Acids Res. 1975 Feb;2(2):223-37. doi: 10.1093/nar/2.2.223.
Sedimentation analysis of glycerol-density gradients has shown that freshly purified DNA polymerases A and B (pol A and pol B) of Euglena gracilis have molecular weights of 185,000 (8.7S) and 240,000 (10.3S) respectively. They can aggregate in fresh preparations to give forms of higher molecular weight as shown by gel filtration through Sepharose 6B, but on ageing pol B progressively generates species with sedimentation coefficients of 7.4-7.7S, 6.3-6.5S, 4.8S and finally 3.0S. Pol A apparently behaves in a similar fashion though it is unstable. Exposure of pol A and pol B to high ionic strengths can also cause their breakdown to species with lower sedimentation coefficients. The mitochondrial DNA polymerase is distinct, having a molecular weight of 170,000. It is proposed that pol A and pol B are oligomers of the 3.0S subunit and possibly other dissimilar subunits, with pol B having additional factors conferring upon it its extra catalytic functions.
甘油密度梯度沉降分析表明,纤细裸藻新纯化的DNA聚合酶A和B(pol A和pol B)的分子量分别为185,000(8.7S)和240,000(10.3S)。如通过琼脂糖6B凝胶过滤所示,它们在新鲜制剂中会聚集形成更高分子量的形式,但随着时间推移,pol B会逐渐产生沉降系数为7.4 - 7.7S、6.3 - 6.5S、4.8S,最终为3.0S的物种。尽管pol A不稳定,但显然表现出类似的行为。将pol A和pol B暴露于高离子强度下也会导致它们分解为沉降系数较低的物种。线粒体DNA聚合酶不同,分子量为170,000。有人提出,pol A和pol B是3.0S亚基以及可能其他不同亚基的寡聚体,pol B具有赋予其额外催化功能的其他因子。