Gragerov A I, Chenchik A A, Aivasashvilli V A, Beabealashvilli R Sh, Nikiforov V G
Mol Gen Genet. 1984;195(3):511-5. doi: 10.1007/BF00341455.
Methylation protection experiments with four promoters (P1 and P2 of the pBR322 plasmid, lacUV5 and lambda P0) have shown that the RNA polymerases from Escherichia coli and Pseudomonas putida, while differing in the primary structure of the subunits involved in DNA binding, display identical patterns of DNA contacts. Nor do these enzymes differ in covalent cross-linking patterns with a partially apurinized promoter. We conclude that the two RNA polymerases have very similar structures of DNA binding centers. The evolutionary conservation of this structure may account for the fact that diverse RNA polymerases often recognize and efficiently use promoters of distant bacterial species.
对四个启动子(pBR322 质粒的 P1 和 P2、lacUV5 和 λ P0)进行的甲基化保护实验表明,大肠杆菌和恶臭假单胞菌的 RNA 聚合酶虽然参与 DNA 结合的亚基一级结构不同,但显示出相同的 DNA 接触模式。这些酶在与部分脱嘌呤启动子的共价交联模式上也没有差异。我们得出结论,这两种 RNA 聚合酶具有非常相似的 DNA 结合中心结构。这种结构的进化保守性可能解释了这样一个事实,即多种 RNA 聚合酶常常能识别并有效利用远缘细菌物种的启动子。