Simúth J, Sternbach H, Zelinka J, Chomutov R M, Nedospasov A A
FEBS Lett. 1987 Jun 22;218(1):163-6. doi: 10.1016/0014-5793(87)81039-6.
RNA polymerase from Streptomyces aureofaciens has been purified by polyethyleneimine precipitation followed by chromatography first on DEAE-cellulose, then heparin-Sepharose and finally on an aminooxybutylcellulose matrix containing immobilised S. aureofaciens DNA. The enzyme is composed of three subunits of approximately 145, 136 and 44 kDa that are in a ratio of approx. 1:1:2. In many isolations two additional subunits of approximately 68 and 39 kDa and some minor protein bands of approximately 110, 85 and 61 kDa are also present. Thus, the structure of this enzyme is very similar to other bacterial RNA polymerases, exhibiting an alpha 2 beta beta' core and the additional proteins rho and sigma.
通过聚乙烯亚胺沉淀,然后依次在DEAE - 纤维素、肝素 - 琼脂糖上进行层析,最后在含有固定化金色链霉菌DNA的氨氧基丁基纤维素基质上进行层析,已纯化出金色链霉菌的RNA聚合酶。该酶由三个亚基组成,分子量分别约为145、136和44 kDa,比例约为1:1:2。在许多分离物中,还存在另外两个分子量约为68和39 kDa的亚基以及一些分子量约为110、85和61 kDa的次要蛋白条带。因此,这种酶的结构与其他细菌RNA聚合酶非常相似,呈现出α2ββ'核心以及额外的ρ和σ蛋白。