Rees P J, Fry B A
J Gen Virol. 1983 Jan;64 (Pt 1):191-8. doi: 10.1099/0022-1317-64-1-191.
Rapidly sedimenting complexes (RSCs) of replicating phage K DNA, isolated by rate zonal centrifugation in sucrose gradients, contain bacterial membrane lipids and protein. During the first half of the latent period the number of DNA molecules in a RSC increased from 1 to about 27. Digestion by Pronase caused the complexes to dissociate and release virion lengths of DNA which sedimented slowly like free mature DNA. RSCs treated with SDS disintegrated and released tangled DNA molecules, each about one virion length in size, but these structures retained their fast sedimentation characteristic. Chloramphenicol (CM) at 100 micrograms/ml did not completely inhibit complex formation or DNA replication, indicating that pre-existing host proteins were involved in these processes. CM reduced DNA replication by 50 to 80%. It is concluded that phage K DNA replicates attached to the cytoplasmic membrane of the host.
通过蔗糖梯度速率区带离心分离得到的正在复制的噬菌体K DNA的快速沉降复合物(RSCs)含有细菌膜脂和蛋白质。在潜伏期的前半段,一个RSC中的DNA分子数量从1增加到约27个。链霉蛋白酶消化导致复合物解离并释放出病毒粒子长度的DNA,这些DNA像游离的成熟DNA一样沉降缓慢。用SDS处理的RSCs解体并释放出缠结的DNA分子,每个分子大小约为一个病毒粒子长度,但这些结构保留了它们快速沉降的特性。100微克/毫升的氯霉素(CM)并没有完全抑制复合物的形成或DNA复制,这表明先前存在的宿主蛋白参与了这些过程。CM使DNA复制减少了50%至80%。结论是噬菌体K DNA在附着于宿主细胞质膜的情况下进行复制。