Silver R P, Falkow S
J Bacteriol. 1970 Oct;104(1):331-9. doi: 10.1128/jb.104.1.331-339.1970.
The molecular nature of R-factor deoxyribonucleic acid (DNA) was examined in Escherichia coli by using a method for the specific labeling of the derepressed R factor, R1, in a female cell after conjugation. Sixty minutes after mating, the R factor was isolated as a single molecule with a molecular weight of 65 x 10(6) daltons. This single molecular species sedimented as either a covalently closed molecule or a "nicked" circle. When the single R-factor component was centrifuged in a CsCl density gradient, only a single homogeneous species with a buoyant density of 1.711 g/cm(3) was observed. R-factor DNA was also isolated directly from exponentially growing cells of E. coli as a covalently closed single molecular species comprising about 1% of the total cellular DNA. Previous studies in Proteus show that R1 factor DNA components of buoyant density 1.709, 1.711, and 1.716 g/cm(3) can be identified as distinct replicons. It is suggested that the single molecule of R1 observed in E. coli is most simply explained as a composite structure resulting from a recombinational assemblage of a 1.709 and 1.716 g/cm(3) replicon.
通过一种在接合后对雌性细胞中去阻遏的R因子R1进行特异性标记的方法,对大肠杆菌中R因子脱氧核糖核酸(DNA)的分子性质进行了研究。交配60分钟后,R因子被分离为一个分子量为65×10⁶道尔顿的单一分子。这种单一分子种类以共价闭合分子或“带切口”的环状形式沉降。当单一的R因子成分在氯化铯密度梯度中离心时,仅观察到一种浮力密度为1.711 g/cm³的单一均匀种类。R因子DNA也可直接从大肠杆菌指数生长的细胞中分离出来,作为一种共价闭合的单一分子种类,约占细胞总DNA的1%。先前对变形杆菌的研究表明,浮力密度为1.709、1.711和1.716 g/cm³的R1因子DNA成分可被鉴定为不同的复制子。有人提出,在大肠杆菌中观察到的R1单一分子最简单的解释是由1.709和1.716 g/cm³复制子的重组组合形成的复合结构。