Kirkwood T B, Burdett I D
Laboratory of Computing, National Institute for Medical Research, London, England.
J Theor Biol. 1988 Feb 7;130(3):255-73. doi: 10.1016/s0022-5193(88)80029-8.
Knowledge of the growth patterns of micro-organisms is required to understand how cell growth and division are controlled and co-ordinated in relation to mechanisms of wall assembly and chromosome duplication. Direct observation, e.g. by time-lapse studies, is usually limited in accuracy by the small size of the cells. Indirect methods have therefore been developed which give estimates of the growth patterns of cells, based on the analysis of distributions of cell size in populations in balanced exponential growth. Previously, we have compared such methods (Burdett & Kirkwood, 1983) and concluded that the most powerful approach is that proposed by Collins & Richmond (1962), in which growth rate is calculated as a function of cell size using size distributions of extant, separating and new-born cells. A limitation of this method has been, however, that it gives only an estimate for the average growth rate of cells at a given size, irrespective of the state of progress of individual cells through the cell cycle. In this paper, we describe an extension to the standard Collins-Richmond procedure which provides separate estimates for the growth pattern of cells in distinct stages of the cell cycle, and we illustrate the method in relation to growth of mononucleate, binucleate and septate cells of Bacillus subtilis. It is demonstrated that this three-stage analysis is clearly superior to the standard method, in that it provides more detailed and probably more realistic information. We also demonstrate how to assess the precision and accuracy of the estimated growth pattern. Generalization of the method to any number of stages and to multiple as well as binary fission is described.
要理解细胞生长和分裂如何与细胞壁组装及染色体复制机制相关联并受到控制和协调,就需要了解微生物的生长模式。直接观察,例如通过延时研究,通常会因细胞尺寸小而在准确性上受到限制。因此,人们开发了间接方法,这些方法基于对处于平衡指数生长状态的群体中细胞大小分布的分析,来估计细胞的生长模式。此前,我们已对这些方法进行了比较(Burdett和Kirkwood,1983年),并得出结论,最有效的方法是Collins和Richmond(1962年)提出的方法,该方法根据现存、正在分离和新生细胞的大小分布,将生长速率计算为细胞大小的函数。然而,该方法的一个局限性在于,它只能给出给定大小细胞平均生长速率的估计值,而不考虑单个细胞在细胞周期中的进展状态。在本文中,我们描述了对标准Collins-Richmond程序的扩展,该扩展为细胞周期不同阶段的细胞生长模式提供了单独的估计值,并且我们以枯草芽孢杆菌单核、双核和分隔细胞的生长为例说明了该方法。结果表明,这种三阶段分析明显优于标准方法,因为它提供了更详细且可能更符合实际的信息。我们还展示了如何评估估计生长模式的精度和准确性。本文描述了将该方法推广到任意数量阶段以及多分裂和二分裂的情况。