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在肝素琼脂糖-4B柱色谱上纯化Eco R1核酸内切酶。

Purification of Eco R1 endonuclease on heparin Sepharose-4B column chromatography.

作者信息

Pai S H, Chuang J Z, Kou M C, Hsu T T

出版信息

Proc Natl Sci Counc Repub China B. 1984 Jan;8(1):41-5.

PMID:6099579
Abstract

Restriction endonucleases play a very important role in genetic engineering and DNA mapping. Among hundreds of restriction endonucleases, the Eco R1 enzyme is the most useful and widely investigated enzyme. After sonication and ultracentrifugation, crude extracts of E. coli RY 13 were purified by employing the polyethyleneimine precipitate, ammonium sulfate precipitate and heparin Sepharose-4B affinity column chromatography. The Eco R1 enzyme were purified at about 42 folds and the specific activity was about 100,000 U/mg of protein. The whole purification procedure was finished within two days. The recovery was about 42%. The enzyme was sufficiently concentrated for direct specific DNA hydrolysis.

摘要

限制性内切酶在基因工程和DNA图谱分析中起着非常重要的作用。在数百种限制性内切酶中,Eco R1酶是最有用且研究最广泛的酶。对大肠杆菌RY 13的粗提物进行超声处理和超速离心后,通过聚乙烯亚胺沉淀、硫酸铵沉淀和肝素琼脂糖-4B亲和柱层析进行纯化。Eco R1酶被纯化了约42倍,比活性约为100,000 U/mg蛋白质。整个纯化过程在两天内完成。回收率约为42%。该酶已充分浓缩,可直接用于特异性DNA水解。

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Heparin inhibits EcoRI endonuclease cleavage of DNA at certain EcoRI sites.
Nucleic Acids Res. 1990 Jun 11;18(11):3255-60. doi: 10.1093/nar/18.11.3255.

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