Nomura N, Ray D S
J Virol. 1980 Apr;34(1):162-7. doi: 10.1128/JVI.34.1.162-167.1980.
M13 replicative form II (RFII) DNA was prepared from Escherichia coli RS5052 (polAex1) cells in the late stage of infection, and the DNA sequence at the discontinuity was examined. The data presented here suggest that the single discontinuity in the late stage of infection RFII maps at the same position as the gene II protein nicking site on fd RFI which was determined in vitro (Meyer et al., Nature (London) 278:365-367, 1979) and has a 5' terminal nucleotide sequence identical to that at the nick produced by gene II protein in vitro. The discontinuity in the in vivo RFII appears to be a single break in the phosphodiester backbone, leaving a 3' OH terminus. RFII molecules containing a gap, i.e., missing nucleotides at the site of discontinuity, were not detected.
在感染后期从大肠杆菌RS5052(polAex1)细胞中制备M13复制型II(RFII)DNA,并检测了不连续处的DNA序列。此处呈现的数据表明,感染后期RFII中的单个不连续处与体外确定的fd RFI上基因II蛋白切口位点位于相同位置(Meyer等人,《自然》(伦敦)278:365 - 367,1979),并且其5'末端核苷酸序列与基因II蛋白在体外产生的切口处的序列相同。体内RFII中的不连续处似乎是磷酸二酯主链上的单个断裂,留下一个3' OH末端。未检测到在不连续位点含有缺口(即缺失核苷酸)的RFII分子。