Aarsman Mirjam E G, Piette André, Fraipont Claudine, Vinkenvleugel Thessa M F, Nguyen-Distèche Martine, den Blaauwen Tanneke
Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, 1098 SM Amsterdam, the Netherlands.
Mol Microbiol. 2005 Mar;55(6):1631-45. doi: 10.1111/j.1365-2958.2005.04502.x.
Cell division proteins FtsZ (FtsA, ZipA, ZapA), FtsE/X, FtsK, FtsQ, FtsL/B, FtsW, PBP3, FtsN and AmiC localize at mid cell in Escherichia coli in an interdependent order as listed. To investigate whether this reflects a time dependent maturation of the divisome, the average cell age at which FtsZ, FtsQ, FtsW, PBP3 and FtsN arrive at their destination was determined by immuno- and GFP-fluorescence microscopy of steady state grown cells at a variety of growth rates. Consistently, a time delay of 14-21 min, depending on the growth rate, between Z-ring formation and the mid cell recruitment of proteins down stream of FtsK was found. We suggest a two-step model for bacterial division in which the Z-ring is involved in the switch from cylindrical to polar peptidoglycan synthesis, whereas the much later localizing cell division proteins are responsible for the modification of the envelope shape into that of two new poles.
细胞分裂蛋白FtsZ(FtsA、ZipA、ZapA)、FtsE/X、FtsK、FtsQ、FtsL/B、FtsW、PBP3、FtsN和AmiC以所列的相互依赖顺序定位于大肠杆菌的细胞中部。为了研究这是否反映了分裂体的时间依赖性成熟,通过对处于各种生长速率的稳态生长细胞进行免疫荧光和GFP荧光显微镜观察,确定了FtsZ、FtsQ、FtsW、PBP3和FtsN到达其目的地时的平均细胞年龄。一致地,根据生长速率,在Z环形成与FtsK下游蛋白质的细胞中部募集之间发现了14 - 21分钟的时间延迟。我们提出了一个细菌分裂的两步模型,其中Z环参与从圆柱形到极性肽聚糖合成的转变,而定位时间晚得多的细胞分裂蛋白负责将包膜形状改变为两个新极的形状。