Heidelbach M, Skladny H, Schairer H U
Zentrum für Molekulare Biologie, Universität Heidelberg, Germany.
J Bacteriol. 1992 Apr;174(8):2733-5. doi: 10.1128/jb.174.8.2733-2735.1992.
The DNA-dependent RNA polymerase (EC 2.7.7.6) of the myxobacterium Stigmatella aurantiaca has been purified. It shows three main polypeptide bands with apparent molecular weights of 146,000, 105,000, and 40,000 in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. beta and beta' subunits of the S. aurantiaca polymerase were shown to migrate in the 146,000-molecular-weight polypeptide band and the main sigma factor was shown to migrate in the 105,000-molecular-weight band by using heterologous antisera.
橙色粘球菌的DNA依赖性RNA聚合酶(EC 2.7.7.6)已被纯化。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中,它显示出三条主要的多肽带,表观分子量分别为146,000、105,000和40,000。通过使用异源抗血清,橙色粘球菌聚合酶的β和β'亚基在分子量为146,000的多肽带中迁移,主要的σ因子在分子量为105,000的带中迁移。