Lee H L, Cohn G, Cosowsky L, McGowan R, Blamire J
Microbios. 1985;43(176S):277-95.
In order to interfere specifically with either the host of phage DNA metabolism and separate the effects of new phage DNA synthesis from the effects of host cell breakdown and PIL-DNA formation, UV irradiation of either the host, A. nidulans, or intact phage AS-1, prior to infection was utilized. Several conclusions were reached. First, a photoreactivation system was present in UV-irradiated A. nidulans. Second, the complete burst size of AS-1 was severely affected by UV irradiation of cells and/or phage; third, UV treatment of cells infected with healthy phage caused an early release of phage at 12 h instead of 16 h post-infection; however, healthy cells infected with UV-irradiated phage caused a delayed release of phage as 20 h.
为了特异性干扰宿主或噬菌体DNA代谢,并将新噬菌体DNA合成的影响与宿主细胞裂解和PIL-DNA形成的影响区分开来,在感染前对宿主构巢曲霉或完整噬菌体AS-1进行紫外线照射。得出了几个结论。第一,紫外线照射的构巢曲霉中存在光复活系统。第二,细胞和/或噬菌体的紫外线照射严重影响AS-1的完整爆发量;第三,用健康噬菌体感染的细胞经紫外线处理后,在感染后12小时而不是16小时导致噬菌体提前释放;然而,用紫外线照射的噬菌体感染健康细胞会导致噬菌体延迟释放,时间为20小时。