Mullinix K P, Strain G C, Bogorad L
Proc Natl Acad Sci U S A. 1973 Aug;70(8):2386-90. doi: 10.1073/pnas.70.8.2386.
Nuclear DNA-dependent RNA polymerase II has been purified from leaves of Zea mays by a new procedure that improves enzyme stability and thus permits more manipulation during purification. The purification procedure includes a heating step, gel filtration on Sepharose 6B and 4B, and chromatography on DEAE- and DNA-celluloses. This method of purification yields an enzyme that exhibits maximal activity when denatured DNA is used as a template. Electrophoresis of highly purified enzyme on polyacrylamide gels containing sodium dodecyl sulfate indicates that maize RNA polymerase IIa is composed of several polypeptide subunits. The most highly purified preparations contain polypeptides with molecular weights of 200,000, 160,000, 35,000, 25,000, 20,000, and 17,000.
已通过一种新方法从玉米叶片中纯化出核DNA依赖性RNA聚合酶II,该方法提高了酶的稳定性,从而在纯化过程中允许更多操作。纯化程序包括加热步骤、在琼脂糖6B和4B上进行凝胶过滤以及在DEAE-纤维素和DNA-纤维素上进行色谱分离。这种纯化方法产生的一种酶,当使用变性DNA作为模板时表现出最大活性。在含有十二烷基硫酸钠的聚丙烯酰胺凝胶上对高度纯化的酶进行电泳表明,玉米RNA聚合酶IIa由几个多肽亚基组成。纯化程度最高的制剂含有分子量分别为200,000、160,000、35,000、25,000、20,000和17,000的多肽。