Gibson C W, Daneo-Moore L, Higgins M L
J Bacteriol. 1983 Jul;155(1):351-6. doi: 10.1128/jb.155.1.351-356.1983.
Growth sites which are bounded by raised wall bands can be observed in electron micrographs of replicas of Streptococcus faecium. When mitomycin C was added to an exponential-phase culture doubling in mass every 64 min, DNA synthesis was inhibited, and eventually cell division stopped. The growth sites formed before and after inhibition of DNA synthesis enlarged until they contained about 0.25 micron3 of cell volume, at which point they ceased to increase in size. When these sites approached this 0.25-micron3 limit, new sites were initiated; this result had also been observed in untreated cells undergoing a large range of exponential-phase mass doubling times. Thus, regardless of whether chromosome replication is inhibited or uninhibited, sites have the same finite capacity to enlarge to about 0.25 micron3, and when this capacity is reached, new sites are initiated. Although initiation of new growth sites seems to be independent of normal chromosome replication, these results confirm previous studies showing that chromosome replication is necessary for the terminal events of growth site development which result in the division of a site into two separate poles. Two classes of models for the regulation of growth site initiation are discussed.
在粪链球菌复制品的电子显微照片中可以观察到由凸起的壁带界定的生长位点。当将丝裂霉素C添加到每64分钟质量翻倍的指数生长期培养物中时,DNA合成受到抑制,最终细胞分裂停止。在DNA合成抑制前后形成的生长位点会扩大,直到它们包含约0.25立方微米的细胞体积,此时它们停止增大尺寸。当这些位点接近这个0.25立方微米的极限时,新的位点开始形成;在经历大范围指数生长期质量翻倍时间的未处理细胞中也观察到了这一结果。因此,无论染色体复制是被抑制还是未被抑制,位点都具有相同的有限能力扩大到约0.25立方微米,当达到这个能力时,新的位点就会开始形成。虽然新生长位点的起始似乎独立于正常的染色体复制,但这些结果证实了先前的研究,表明染色体复制对于生长位点发育的终末事件是必要的,这些终末事件导致一个位点分裂成两个独立的极。讨论了两类生长位点起始调控的模型。