Higgins M L, Gibson C W, Daneo-Moore L
Ann Inst Pasteur Microbiol (1985). 1985 Jan-Feb;136A(1):59-62. doi: 10.1016/s0769-2609(85)80022-3.
Three-dimensional reconstruction methods were applied to electron micrographs of Streptococcus faecium to study the initiation of cell wall growth sites during a nutritional shift-up experiment. Upon lowering the mass doubling time from 76 to 33 min by the addition of excess glutamate, the formation of new cell wall growth sites was studied in relation to other growth parameters (autolytic capacity, cell number, mass, RNA, DNA and peptidoglycan). The findings from these studies, to be described below, support a model in which new sites are introduced when cells grow to a relatively constant, growth-rate-independent size, while the rate at which sites form and grow increases with growth rate. In this model, chromosome synthesis does not regulate the formation of new sites of cell wall growth, but existing sites cannot be completed until rounds of chromosome synthesis are completed.
应用三维重建方法对粪肠球菌的电子显微照片进行研究,以探讨营养转换实验期间细胞壁生长位点的起始情况。通过添加过量谷氨酸将质量倍增时间从76分钟降至33分钟后,研究了新细胞壁生长位点的形成与其他生长参数(自溶能力、细胞数量、质量、RNA、DNA和肽聚糖)之间的关系。以下将描述这些研究的结果,这些结果支持了一个模型,即当细胞生长到相对恒定的、与生长速率无关的大小时会引入新的位点,而位点形成和生长的速率则随生长速率增加。在这个模型中,染色体合成并不调节新的细胞壁生长位点的形成,但在多轮染色体合成完成之前,现有的位点无法完成。