Inouye M
J Bacteriol. 1971 May;106(2):539-42. doi: 10.1128/jb.106.2.539-542.1971.
A defective recA gene, which is involved in recombination, is shown in this article to permit limited cell division, when deoxyribonucleic acid (DNA) synthesis is blocked. Thymidine starvation or nalidixic acid blocked DNA synthesis, and stopped cell division of a rec(+)thy(-) strain of Escherichia coli. However, with the same treatments, a recAthy(-) strain could continue to divide for at least 5 hr, and cell numbers increased 2.5- to 4-fold. After several hours of thymidine starvation, the culture contained very long cells (snakes) and small (normal-sized) cells. The short cells contained very little, if any, DNA. Cells of all ages divided in the absence of thymidine. Specific differences in membrane proteins were observed between thymidine-starved rec(+) and recA cells, as expected from previous experiments in which these proteins were associated with cell division and DNA synthesis. It is proposed that septum formation is controlled negatively by the recA(+) gene.
本文显示,参与重组的recA基因存在缺陷时,在脱氧核糖核酸(DNA)合成受阻的情况下仍允许有限的细胞分裂。胸苷饥饿或萘啶酸会阻断DNA合成,并使大肠杆菌rec(+)thy(-)菌株的细胞分裂停止。然而,采用相同处理时,recAthy(-)菌株可继续分裂至少5小时,细胞数量增加2.5至4倍。胸苷饥饿数小时后,培养物中含有非常长的细胞(蛇形细胞)和小的(正常大小)细胞。短细胞几乎不含DNA(如果含有的话)。所有年龄段的细胞在无胸苷的情况下都会分裂。正如之前实验所预期的那样,在胸苷饥饿的rec(+)细胞和recA细胞之间观察到了膜蛋白的特异性差异,在这些实验中,这些蛋白与细胞分裂和DNA合成相关。有人提出,recA(+)基因对隔膜形成起负调控作用。