Salhi S, Elie C, Forterre P, de Recondo A M, Rossignol J M
Biologie Moléculaire de la Réplication, UPR 2-CNRS, IRSC, Villejuif, France.
J Mol Biol. 1989 Oct 20;209(4):635-44.
The activity of a homogeneous DNA polymerase from the thermophilic archaebacterium, Sulfolobus acidocaldarius, on a singly primed, single-stranded recombinant phage M13 DNA has been examined. At the optimal temperature (70 to 75 degrees C) this template is efficiently replicated in ten minutes using a ratio of enzyme molecule to primed-template of 0.8. Analysis of DNA products during the course of polymerization shows that species of quite homogeneous size are observed and that the number of primers extended by the enzyme is constant, whatever the enzyme molecule to primed template ratio is in the range 1/50 to 2, indicating that the 100 x 10(3) Mr DNA polymerase from S. acidocaldarius is randomly recycled on the template molecules. At non-optimal temperature (60 degrees C and 80 degrees C) the distribution of products observed indicated the presence of arrest sequences; some have been shown to be reversible. One of these pausing signals detected at 80 degrees C has been further analysed, and has been found to be DNA sequence-dependent.
对嗜热古细菌嗜酸热硫化叶菌(Sulfolobus acidocaldarius)的一种同源DNA聚合酶在单引物单链重组噬菌体M13 DNA上的活性进行了检测。在最佳温度(70至75摄氏度)下,使用酶分子与引物模板的比例为0.8,该模板在十分钟内即可有效复制。聚合过程中对DNA产物的分析表明,观察到的产物大小相当均匀,并且无论酶分子与引物模板的比例在1/50至2的范围内如何,被该酶延伸的引物数量都是恒定的,这表明嗜酸热硫化叶菌的100×10³ Mr DNA聚合酶在模板分子上随机循环利用。在非最佳温度(60摄氏度和80摄氏度)下观察到的产物分布表明存在终止序列;其中一些已被证明是可逆的。对在80摄氏度下检测到的其中一个暂停信号进行了进一步分析,发现它依赖于DNA序列。