Hochmannová J, Nesvera J, Stokrová J
Folia Microbiol (Praha). 1985;30(5):407-13. doi: 10.1007/BF02928749.
A stable deletion derivative pNH602 was obtained when the recently described higher-copy-number point mutant pNH601 of plasmid R6K was introduced to a minicells-producing strain of Escherichia coli. The size of plasmid pNH602 is 18.8 Mg/mol as determined by electron microscopy. The 7.2 Mg/mol fragment of R6K genome missing in pNH602 carries the Smr-determinant and the region finO and, according to the results of restriction analysis, it includes one EcoRI site. With its radioisotopically determined 33 copies of pNH602 per E. coli K-12 chromosome (npc), representing a 23% increase of the point mutant pNH601 and 150% enhancement of R6K npc, plasmid pNH602 differs from another closely related R6K deletion derivative pAS3 of the same size which exhibits only 20 npc. Both pNH602 and pAS3 plasmids are conjugative.
当最近描述的质粒R6K的高拷贝数点突变体pNH601被导入产微小细胞的大肠杆菌菌株时,获得了稳定的缺失衍生物pNH602。通过电子显微镜测定,质粒pNH602的大小为18.8 Mg/mol。pNH602中缺失的R6K基因组的7.2 Mg/mol片段携带Smr决定簇和finO区域,根据限制性分析结果,它包含一个EcoRI位点。通过放射性同位素测定,每大肠杆菌K-12染色体(npc)有33个pNH602拷贝,这比点突变体pNH601增加了23%,比R6K的npc增加了150%,质粒pNH602与另一个大小相同的密切相关的R6K缺失衍生物pAS3不同,后者仅表现出20个npc。pNH602和pAS3质粒都是接合型的。