Smith S S, Braun R
Eur J Biochem. 1978 Jan 2;82(1):309-20. doi: 10.1111/j.1432-1033.1978.tb12025.x.
The DNA-dependent RNA polymerase II or B from the lower eukaryote Physarum polycephalum has been purified to apparent homogeneity by a new method employing poly(ethylene imine) precipitation and elution, and heparin-Sepharose affinity chromatography. The method is readily scaled up or down and affords a purification of over 5000-fold with a yield of 35-45%. The procedure is easy to perform and can be carried out in less than three days even on a large scale. Furthermore, it gives enzyme of higher purity and in at least 10-fold greater yield than previously published procedures for its purification from this organism. These improvements have allowed the detection of a series of subforms of the enzyme. The combination of precipitation using poly(ethylene imine) with chromatography on heparin-Sepharose may prove useful in the preparation of other proteins which interact with nucleic acids.
通过一种采用聚乙烯亚胺沉淀和洗脱以及肝素-琼脂糖亲和层析的新方法,已将来自低等真核生物多头绒泡菌的依赖DNA的RNA聚合酶II或B纯化至表观均一。该方法易于放大或缩小,可实现超过5000倍的纯化,产率为35 - 45%。该程序易于操作,即使大规模操作也可在不到三天内完成。此外,与先前报道的从该生物体中纯化该酶的方法相比,它能提供纯度更高且产量至少高出10倍的酶。这些改进使得能够检测到该酶的一系列亚形式。使用聚乙烯亚胺沉淀与肝素-琼脂糖层析相结合的方法可能在制备其他与核酸相互作用的蛋白质方面证明是有用的。