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Study of cycle of cell wall assembly in Streptococcus faecalis by three-dimensional reconstructions of thin sections of cells.

机译:粪便链球菌细胞壁组装的循环研究通过细胞薄片的三维重建。

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摘要

A new ultrastructural method was used to study rounds of envelope synthesis that occur in Streptococcus faecalis in "growth zones" found between pairs of naturally occurring surface markers. The technique consists of producing three-dimensional reconstructions of these growth zones from the mathematical rotation, about a central axis, of measurements taken from central, longitudinal thin sections of cells. A cycle of exponential-phase envelope growth was then simulated by arranging a series of these reconstructions in increasing order of the amount of peripheral wall surface area or the amount of cell volume that each was calculated to contain. Using this simulated cycle of growth, the geometry of a single growth zone during a round of synthesis was studied. Based on this analysis, a model was developed for the assembly of the cell wall of S. faecalis. The model states that new cell wall surface is synthesized by the regulated flow of essentially two channels of cell wall precursors into a single growth zone. One channel of precursors would be involved in the assembly of a bilayered cross wall that would proceed at a fairly constant rate until the cross wall closes. The second channel of precursors would be involved in the separation of the bilayered cross wall into two segments of peripheral wall. These precursors would intercalate into and thicken the separating layers of the cross wall. The flow of precursors through this channel would be progressively reduced through a cycle. These decreases, when coupled with internal hydrostatic pressure, apparently would result in the enlarging peripheral wall becoming increasingly more curved and would also promote cell division by reducing the total amount of cell wall that must be assembled in order for septation to occur.
机译:一种新的超微结构方法被用来研究在粪链球菌中在自然表面标记物对之间发现的“生长区”中发生的一系列包膜合成。该技术包括根据围绕中心轴的数学旋转,从细胞的中央,纵向薄层中获取的测量结果,对这些生长区进行三维重建。然后,通过按周壁表面积量或计算得出的每一个都包含的细胞体积的升序排列一系列这些重构,来模拟指数相包膜生长的周期。使用这种模拟的生长周期,研究了一轮合成过程中单个生长区的几何形状。基于该分析,开发了用于粪粪链球菌细胞壁组装的模型。该模型指出,新的细胞壁表面是通过基本两个细胞壁前体通道进入单个生长区的调节流合成的。前体的一个通道将参与双层横壁的组装,该组装将以相当恒定的速率进行,直到横壁关闭。前体的第二通道将涉及将双层横壁分离成周壁的两个部分。这些前体将插入并增加横壁的分隔层。通过该通道的前体流量将在一个周期内逐渐减少。当与内部静水压力相结合时,这些降低显然会导致扩大的周壁变得越来越弯曲,并且还将通过减少必须组装才能发生分离的细胞壁的总量来促进细胞分裂。

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