Reeve J N, Cornett J B
J Virol. 1975 Jun;15(6):1308-16. doi: 10.1128/JVI.15.6.1308-1316.1975.
SPO1 bacteriophage injects its DNA into minicells produced by Bacillus subtilis CU403 divIVB1. The injected DNA is partially degraded to small trichloracetic acid-precipitable material and trichloroacetic acid-soluble material. The injected DNA is not replicated; however, it serves as a template for RNA and protein synthesis. The RNA produced specifically hybridizes to SPO1 DNA, and the amount of RNA hybridized can be reduced by competition with RNA isolated at all stages of the phage cycle from infected nucleate cells of the B. subtilis CU403 divIVB1. An unrelated phage, SPP1, also induces phage-specific RNA in infected minicells. Translation occurs in SPO1-infected minicells resulting in at least eight proteins which have been separated by gel electrophoresis, and two of these proteins have mobilities similar to proteins found only in infected B. subtilis CU403 divIVB1 nucleate cells. A large proportion of the polypeptide material synthesized in infected minicells is very small and heterogeneous in size.
SPO1噬菌体将其DNA注入枯草芽孢杆菌CU403 divIVB1产生的微细胞中。注入的DNA会部分降解为可被三氯乙酸沉淀的物质和可溶于三氯乙酸的物质。注入的DNA不会复制;然而,它可作为RNA和蛋白质合成的模板。产生的RNA能与SPO1 DNA特异性杂交,并且通过与从枯草芽孢杆菌CU403 divIVB1受感染的有核细胞的噬菌体周期各个阶段分离得到的RNA竞争,杂交的RNA量可以减少。一种不相关的噬菌体SPP1也会在受感染的微细胞中诱导产生噬菌体特异性RNA。在SPO1感染的微细胞中会发生翻译,产生至少八种已通过凝胶电泳分离的蛋白质,其中两种蛋白质的迁移率与仅在受感染的枯草芽孢杆菌CU403 divIVB1有核细胞中发现的蛋白质相似。在受感染的微细胞中合成的大部分多肽物质非常小且大小不均一。