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无细胞提取物中的纯化及DNA合成:DNA聚合酶II的特性

Purification and DNA synthesis in cell-free extracts: properties of DNA polymerase II.

作者信息

Kornberg T, Gefter M L

出版信息

Proc Natl Acad Sci U S A. 1971 Apr;68(4):761-4. doi: 10.1073/pnas.68.4.761.

Abstract

The major DNA-synthesizing enzyme present in Pol A(1) (-)Escherichia coli (DNA polymerase II) has been purified to homogeneity as judged by polyacrylamide gel electrophoresis. The enzyme requires all four deoxynucleoside triphosphates, Mg(++), NH(4) (+), and native DNA for maximal activity. The enzyme activity is sensitive to sulfhydryl reagents and is insensitive to anti-DNA polymerase I antiserum. A second DNA-synthesizing enzyme, present in low amounts, has been identified in Pol A(1) (-) extracts. The relationship of this enzyme to DNA polymerases I and II is discussed.

摘要

通过聚丙烯酰胺凝胶电泳判断,存在于Pol A(1) (-)大肠杆菌中的主要DNA合成酶(DNA聚合酶II)已被纯化至同质。该酶需要所有四种脱氧核苷三磷酸、Mg(++)、NH(4) (+)和天然DNA才能达到最大活性。该酶活性对巯基试剂敏感,对抗DNA聚合酶I抗血清不敏感。在Pol A(1) (-)提取物中已鉴定出第二种含量较低的DNA合成酶。讨论了这种酶与DNA聚合酶I和II的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e51/389037/1d5ce8700c88/pnas00079-0071-a.jpg

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