Pogliano J, Osborne N, Sharp M D, Abanes-De Mello A, Perez A, Sun Y L, Pogliano K
Department of Biology, University of California, San Diego 92093-0349, USA.
Mol Microbiol. 1999 Feb;31(4):1149-59. doi: 10.1046/j.1365-2958.1999.01255.x.
At the onset of sporulation in Bacillus subtilis, two potential division sites are assembled at each pole, one of which will be used to synthesize the asymmetrically positioned sporulation septum. Using the vital stain FM 4-64 to label the plasma membrane of living cells, we examined the fate of these potential division sites in wild-type cells and found that, immediately after the formation of the sporulation septum, a partial septum was frequently synthesized within the mother cell at the second potential division site. Using time-lapse deconvolution microscopy, we were able to watch these partial septa first appear and then disappear during sporulation. Septal dissolution was dependent on sigma E activity and was partially inhibited in mutants lacking the sigma E-controlled proteins SpoIID, SpoIIM and SpoIIP, which may play a role in mediating the degradation of septal peptidoglycan. Our results support a model in which sigma E inhibits division at the second potential division site by two distinct mechanisms: inhibition of septal biogenesis and the degradation of partial septa formed before sigma E activation.
在枯草芽孢杆菌芽孢形成开始时,每个极会组装两个潜在的分裂位点,其中一个将用于合成不对称定位的芽孢形成隔膜。我们使用活体染料FM 4 - 64标记活细胞的质膜,研究了野生型细胞中这些潜在分裂位点的命运,发现芽孢形成隔膜形成后不久,母细胞内的第二个潜在分裂位点经常会合成一个部分隔膜。通过延时去卷积显微镜,我们能够观察到这些部分隔膜在芽孢形成过程中先出现然后消失。隔膜溶解依赖于σE活性,在缺乏σE控制的蛋白质SpoIID、SpoIIM和SpoIIP的突变体中受到部分抑制,这些蛋白质可能在介导隔膜肽聚糖的降解中发挥作用。我们的结果支持了一个模型,即σE通过两种不同机制抑制第二个潜在分裂位点的分裂:抑制隔膜生物合成以及降解在σE激活之前形成的部分隔膜。