Southeast Dairy Foods Research Center, Department of Food Science, North Carolina State University, Raleigh, North Carolina 27695.
Appl Environ Microbiol. 1993 Jan;59(1):208-12. doi: 10.1128/aem.59.1.208-212.1993.
Monoclonal antibodies were used to monitor the accumulation of the major capsid protein of the lactococcal small isometric bacteriophage u136 (P335 species) over the course of a one-step growth curve. A sandwich enzyme-linked immunosorbent assay was then used to distinguish two abortive phage resistance mechanisms, Hsp and Prf. Capsid protein production of u136 was almost totally inhibited by the Hsp-induced abortive mechanism, supporting previous data that this mechanism blocks phage DNA replication. Prf-induced abortive infection only partially (50%) inhibited capsid protein production, suggesting that this mechanism targets some other point, perhaps within transcription or translation processes. The results confirmed that Hsp and Prf act at different targets in the phage lytic cycle. Use of monoclonal antibodies also demonstrated that production of the major capsid protein is a nonlimiting step in the lytic cycle of lactococcal phage u136.
单克隆抗体被用于监测乳球菌小型等面体噬菌体 u136(P335 种)主要衣壳蛋白在一步生长曲线过程中的积累。然后,夹心酶联免疫吸附测定法被用于区分两种流产噬菌体抗性机制,Hsp 和 Prf。Hsp 诱导的流产机制几乎完全抑制了 u136 的衣壳蛋白产生,这支持了先前的数据,即该机制阻断噬菌体 DNA 复制。Prf 诱导的流产感染仅部分(50%)抑制衣壳蛋白产生,表明该机制针对其他某些点,可能在转录或翻译过程中。结果证实 Hsp 和 Prf 在噬菌体裂解周期中作用于不同的靶标。单克隆抗体的使用还表明,主要衣壳蛋白的产生是乳球菌噬菌体 u136 裂解周期中的非限速步骤。