Nesvera J, Klaus S, Stokrová J, Hochmannová J
J Basic Microbiol. 1987;27(1):63-7. doi: 10.1002/jobm.3620270109.
The specific binding of Escherichia coli RNA polymerase molecules to the DNA of plasmid pNH602, a deletion derivative of R6K having an increased copy number, was detected by electron microscopy. Seven strong RNApol binding sites were found on pNH602 DNA linearized with BamHI or EcoRI restriction endonuclease. All of these specific sites occur in genetically defined regions of the pNH602 molecule. Two of them correspond with the recently reported transcription initiation sites within a region essential for plasmid R6K replication.
通过电子显微镜检测了大肠杆菌RNA聚合酶分子与质粒pNH602(R6K的缺失衍生物,拷贝数增加)的DNA的特异性结合。在用BamHI或EcoRI限制性内切酶线性化的pNH602 DNA上发现了七个强RNApol结合位点。所有这些特定位点都出现在pNH602分子的基因定义区域中。其中两个与最近报道的质粒R6K复制必需区域内的转录起始位点相对应。