Cooper S, Schwimmer M, Scanlon S
J Bacteriol. 1978 Apr;134(1):60-5. doi: 10.1128/jb.134.1.60-65.1978.
The pattern of segregation of DNA in Escherichia coli B/rK was analyzed by using the Methocel technique for forming chains of cells and the membrane binding elution method. Strain B/rK was shown to have a relatively high degree of nonrandom segregation and was used in a critical experiment to test the proposal that only one DNA strand acts nonrandomly during segregation. Thymidine-labeled cells were bound to a nitrocellulose membrane, and newly dividing cells were eluted from the membrane for six generations. The segregation of DNA in the eluted cells as well as in the cells bound to the membrane was examined by the Methocel technique. No difference in segregation was found between the two populations of cells, a result which indicates that the two strands are equivalent in segregation and that the pattern of segregation is not the result of a permanent binding of any strand to a pole of a cell.
通过使用甲种纤维素技术形成细胞链以及膜结合洗脱法,对大肠杆菌B/rK中DNA的分离模式进行了分析。结果表明,B/rK菌株具有相对较高程度的非随机分离,并被用于一项关键实验,以检验关于在分离过程中只有一条DNA链进行非随机作用的提议。用胸苷标记的细胞被固定在硝酸纤维素膜上,新分裂的细胞从膜上洗脱六代。通过甲种纤维素技术检查洗脱细胞以及固定在膜上的细胞中DNA的分离情况。在这两个细胞群体之间未发现分离差异,这一结果表明两条链在分离过程中是等效的,并且分离模式不是任何一条链与细胞一极永久结合的结果。