Witte A, Wanner G, Sulzner M, Lubitz W
Institute of Microbiology and Genetics, University of Vienna, Austria.
Arch Microbiol. 1992;157(4):381-8. doi: 10.1007/BF00248685.
Expression of cloned gene E of bacteriophage PhiX174 induces lysis by formation of a transmembrane tunnel structure in the cell envelope of Escherichia coli. Ultrastructural studies of the location of the lysis tunnel indicate that it is preferentially located at the septum or at polar regions of the cell. Furthermore, the diameter and shape of individual tunnel structures vary greatly indicating that its structure is not rigid. Apparently, the contours of individual lysis tunnels are determined by enlarged meshes in the peptidoglycan net and the force produced at its orifice, by the outflow of cytoplasmic content. Once the tunnel is formed the driving force for the lysis process is the osmotic pressure difference between cytoplasm and medium. During the lysis process areas of the cytoplasmic membrane which are not tightly attached to the envelope are extended inward by the negative pressure produced during lysis. After cell lysis external medium can diffuse through the lysis tunnel filling the inner cell space of the still rigid bacterial ghosts.
噬菌体PhiX174的克隆基因E的表达通过在大肠杆菌细胞膜中形成跨膜通道结构诱导细胞裂解。对裂解通道位置的超微结构研究表明,它优先位于细胞的隔膜或极性区域。此外,单个通道结构的直径和形状差异很大,表明其结构并非刚性。显然,单个裂解通道的轮廓由肽聚糖网中扩大的网孔以及细胞质内容物流出在其孔口产生的力决定。一旦通道形成,裂解过程的驱动力就是细胞质与培养基之间的渗透压差异。在裂解过程中,未紧密附着于细胞膜的细胞质膜区域会因裂解过程中产生的负压而向内延伸。细胞裂解后,外部培养基可通过裂解通道扩散,填充仍然刚性的细菌空壳的内部细胞空间。