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噬菌体PM2温度敏感突变体的特性:膜突变体

Characterization of temperature-sensitive mutants of bacteriophage PM2: membrane mutants.

作者信息

Brewer G J

出版信息

Mol Gen Genet. 1978 Nov 16;167(1):65-74. doi: 10.1007/BF00270322.

Abstract

In an effort to understand the genetic regulation of membrane morphogenesis, twenty-nine temperature-sensitive mutants of the membrane-containing bacteriophage PM2 were isolated. Characterization at restrictive temperature revealed groups showing no lysis (Groups I--IV), partial lysis (Groups V--VIII), and full lysis (groups IX--XII) of the host Pseudomonas BAL-31. When the cell lysis data are considered in conjunction with data on stimulation of viral DNA synthesis, at least six mutant groups are defined. Analysis by gel electrophoresis of the pattern of viral proteins synthesized under restrictive conditions further divides the mutants into twelve groups. Temperature shift experiments delineate early, intermediate and late mutants. Complementation data support some of these groupings. The observed low levels of complementation and recombination are discussed in terms of gene product/genome restriction, bound to the membrane at the site of infection. It is of particular interest to membrane morphogenesis that under restrictive conditions late mutants in Groups II, III and IV make empty-appearing vesicles inside the cell that are the size of virus membranes as seen in thin sections of cells in the electron microscope. Mutants ts 1 (Group II) and ts 12 (Group III) show defects in their ability to incorporate into membranes viral structural proteins sp 13 and sp 6.6. The possibility is discussed that either of these proteins control the size and shape of the viral membrane.

摘要

为了了解膜形态发生的遗传调控,分离出了29个含膜噬菌体PM2的温度敏感突变体。在限制温度下进行表征时,发现这些突变体可分为几组:宿主假单胞菌BAL - 31不发生裂解的组(第I - IV组)、部分裂解的组(第V - VIII组)和完全裂解的组(第IX - XII组)。当将细胞裂解数据与病毒DNA合成刺激数据结合考虑时,至少可定义六个突变体组。通过凝胶电泳分析在限制条件下合成的病毒蛋白模式,可进一步将这些突变体分为十二组。温度转换实验确定了早期、中期和晚期突变体。互补数据支持了其中一些分组。根据基因产物/基因组限制,即在感染位点与膜结合的情况,对观察到的低水平互补和重组进行了讨论。对于膜形态发生特别有趣的是,在限制条件下,第II、III和IV组的晚期突变体在细胞内形成了外观为空泡的囊泡,其大小与电子显微镜下细胞超薄切片中所见的病毒膜大小相同。突变体ts 1(第II组)和ts 12(第III组)在将病毒结构蛋白sp 13和sp 6.6整合到膜中的能力上存在缺陷。文中讨论了这两种蛋白质中的任何一种控制病毒膜大小和形状的可能性。

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