[2个DNA依赖性DNA聚合酶的分离和部分纯化]。

Mikrobiologicheskii zhurnal Pub Date : 1991-09-01
S V Bezuglyĭ, V V Babichev, I G Skripal', L P Malinovskaia
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引用次数: 0

摘要

通过DEAE-cellulose DE-52和Green a -sepharose色谱柱的连续层析,从Acholeplasma laidlawii PG-8细胞(Acholeplasmataceae属的典型代表)的有限生物量中分离并部分纯化了两种形式的dna依赖性dna聚合酶。用NaCl浓度为0.1 M的离子交换柱洗脱第一种形式的dna聚合酶,用NaCl浓度为0.6 M和0.4 M的离子交换柱洗脱第二种形式的dna聚合酶。这两种酶的活性都能够实现DNA合成。dna聚合酶的生产条件为分离浓缩的高活性酶提供了便利条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The isolation and partial purification of 2 DNA-dependent DNA polymerases from Acholeplasma laidlawii PG-8].

Two forms of DNA-dependent DNA-polymerase have been isolated and partially purified from the limited amount of biomass of cells Acholeplasma laidlawii PG-8, a typical representative of genus Acholeplasmataceae, as a result of successive chromatography on the columns with DEAE-cellulose DE-52 and Green A-sepharose. The first form of DNA-polymerase is eluted from the ion-exchange column with NaCl concentration of 0.1 M from the column with Green A-sepharose of 0.27 M, while the second form-with NaCl concentrations of 0.6 and 0.4 M, respectively. The both enzymatic activities are able to implement DNA synthesis. The conditions of DNA-polymerase production proved to be rather convenient for isolation of the concentrated and highly active enzymes.

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