Inselburg J
J Bacteriol. 1971 Feb;105(2):620-8. doi: 10.1128/jb.105.2.620-628.1971.
The deoxyribonucleic acid (DNA) of resistance (R) factor 222 carried by Escherichia coli strain P678-54 was found in the normally chromosomeless progeny (minicells) of that strain. The entry of the R222 DNA into minicells appears to be via segregation at the time of their formation from normal cells. The R222 DNA can replicate in minicells although the extent of its replication appears to be limited. An analysis of the R222 DNA structure indicates that it exists in minicells as double-stranded linear, open circular, and twisted circular monomers (molecular weight, about 6.2 x 10(7) daltons). The monomers visualized by electron microscopy are 31.0 +/- 0.5 mum in length. An examination of the effect of acridine orange on the replication of R222 and colicin E1 DNA indicates the dye intereferes with plasmid DNA replication.
在大肠杆菌菌株P678 - 54携带的抗性(R)因子222的脱氧核糖核酸(DNA),在该菌株正常无染色体的后代(微小细胞)中被发现。R222 DNA进入微小细胞似乎是在它们从正常细胞形成时通过分离实现的。R222 DNA能够在微小细胞中复制,尽管其复制程度似乎有限。对R222 DNA结构的分析表明,它在微小细胞中以双链线性、开环和扭曲环状单体形式存在(分子量约为6.2×10⁷道尔顿)。通过电子显微镜观察到的单体长度为31.0±0.5微米。对吖啶橙对R222和大肠杆菌素E1 DNA复制影响的研究表明,该染料会干扰质粒DNA的复制。