Center for Phage Technology, Department of Biochemistry and Biophysics, Texas A&M University, 2128 TAMU, College Station, TX, 77843-2128, USA,
J Microbiol. 2014 Mar;52(3):243-58. doi: 10.1007/s12275-014-4087-z. Epub 2014 Mar 1.
The lysis of bacterial hosts by double-strand DNA bacteriophages, once thought to reflect merely the accumulation of sufficient lysozyme activity during the infection cycle, has been revealed to recently been revealed to be a carefully regulated and temporally scheduled process. For phages of Gramnegative hosts, there are three steps, corresponding to subversion of each of the three layers of the cell envelope: inner membrane, peptidoglycan, and outer membrane. The pathway is controlled at the level of the cytoplasmic membrane. In canonical lysis, a phage encoded protein, the holin, accumulates harmlessly in the cytoplasmic membrane until triggering at an allele-specific time to form micron-scale holes. This allows the soluble endolysin to escape from the cytoplasm to degrade the peptidoglycan. Recently a parallel pathway has been elucidated in which a different type of holin, the pinholin, which, instead of triggering to form large holes, triggers to form small, heptameric channels that serve to depolarize the membrane. Pinholins are associated with SAR endolysins, which accumulate in the periplasm as inactive, membrane-tethered enzymes. Pinholin triggering collapses the proton motive force, allowing the SAR endolysins to refold to an active form and attack the peptidoglycan. Surprisingly, a third step, the disruption of the outer membrane is also required. This is usually achieved by a spanin complex, consisting of a small outer membrane lipoprotein and an integral cytoplasmic membrane protein, designated as o-spanin and i-spanin, respectively. Without spanin function, lysis is blocked and progeny virions are trapped in dead spherical cells, suggesting that the outer membrane has considerable tensile strength. In addition to two-component spanins, there are some single-component spanins, or u-spanins, that have an N-terminal outer-membrane lipoprotein signal and a C-terminal transmembrane domain. A possible mechanism for spanin function to disrupt the outer membrane is to catalyze fusion of the inner and outer membranes.
双链 DNA 噬菌体裂解细菌宿主的过程,曾被认为仅仅反映了在感染周期中溶菌酶活性的积累,最近被揭示是一个精心调控和时间安排的过程。对于革兰氏阴性宿主的噬菌体,有三个步骤,分别对应于细胞包膜的三层结构的颠覆:内膜、肽聚糖和外膜。该途径在细胞质膜水平上受到控制。在典型的裂解中,噬菌体编码的一种蛋白,即溶菌素,在细胞质膜中无害地积累,直到在特定的等位基因时间触发,形成微米级别的孔。这使得可溶性溶菌酶能够从细胞质中逃逸出来,降解肽聚糖。最近,人们阐明了一个平行的途径,其中一种不同类型的溶菌素,即穿孔溶菌素,而不是触发形成大孔,而是触发形成小的七聚体通道,使膜去极化。穿孔溶菌素与 SAR 溶菌素相关联,SAR 溶菌素作为无活性的、膜结合的酶积累在周质中。穿孔溶菌素的触发导致质子动力势崩溃,允许 SAR 溶菌素折叠成活性形式并攻击肽聚糖。令人惊讶的是,还需要第三个步骤,即破坏外膜。这通常是通过一个 spanin 复合物来实现的,该复合物由一个小的外膜脂蛋白和一个完整的细胞质膜蛋白组成,分别命名为 o-spanin 和 i-spanin。如果没有 spanin 功能,裂解就会受阻,子代病毒颗粒会被困在死亡的球形细胞中,这表明外膜具有相当大的拉伸强度。除了二组分的 spanin 外,还有一些单组分的 spanin,或 u-spanin,它们具有 N 端的外膜脂蛋白信号和 C 端的跨膜结构域。spanin 功能破坏外膜的可能机制是催化内膜和外膜的融合。