首页> 美国卫生研究院文献>Journal of Virology >Assembly of bacteriophage phi X174: identification of a virion capsid precursor and proposal of a model for the functions of bacteriophage gene products during morphogenesis.
【2h】

Assembly of bacteriophage phi X174: identification of a virion capsid precursor and proposal of a model for the functions of bacteriophage gene products during morphogenesis.

机译:噬菌体phi X174的组装:病毒体衣壳前体的鉴定和在形态发生过程中噬菌体基因产物功能模型的建议。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A capsomeric structure sedimenting with an S value of 108 in sucrose gradients was isolated from Escherichia coli infected with bacteriophage phi X174. The 108S material contained viral proteins F, G, H, and D, and the relative amounts of these proteins in the 108S material were similar to those in the infectious 132S particle, which has previously been described as a possible intermediate in the assembly of 114S phage particles. Electron micrographs indicated that the size and shape of the 108S material resemble those of the 132S particle. The 108S material contained no DNA, and its formation occurred independently of DNA synthesis. The 108S material accumulated in infected cells when viral DNA replication was prevented either by mutation in phage genes A or C or by removal of thymidine from a culture infected with wild-type phage or with a lysis gene E mutant. Upon restoration of thymidine to cells infected with the lysis gene E mutant and then starved of thymidine, the accumulated 108S material was converted to 132S particles and to 114S phage particles, implying that the 108S material is a precursor of phage particles. A model that proposes possible functions for the products of phi X174 genes A, B, C, D, F, and G during viral replication and phage maturation is described.
机译:从感染了噬菌体phi X174的大肠杆菌中分离出沉淀在蔗糖梯度中的S值为108的帽状结构。 108S材料包含病毒蛋白F,G,H和D,并且108S材料中这些蛋白的相对含量类似于传染性132S颗粒中的含量,之前已将其描述为114S装配中的可能中间体。噬菌体颗粒。电子显微照片表明,108S材料的尺寸和形状类似于132S颗粒的尺寸和形状。 108S材料不含DNA,其形成与DNA合成无关。当通过噬菌体基因A或C突变或通过从感染了野生型噬菌体或裂解基因E突变体的培养物中去除胸腺嘧啶脱氧核苷来阻止病毒DNA复制时,108S物质会积聚在感染细胞中。在将胸苷恢复到被裂解基因E突变体感染的细胞中,然后使胸苷饥饿后,所积累的108S物质被转化为132S颗粒和114S噬菌体颗粒,这意味着108S材料是噬菌体颗粒的前体。描述了一个模型,该模型提出了在病毒复制和噬菌体成熟过程中phi X174基因A,B,C,D,F和G的产物的可能功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号