Stuy J H
J Bacteriol. 1980 Dec;144(3):1003-8. doi: 10.1128/jb.144.3.1003-1008.1980.
Whole phages HP1 and HP3, vegetative-phage deoxyribonucleic acid (DNA), and single and tandem double prophage DNA were exposed to ultraviolet radiation and then assayed on a wild-type (DNA repair-proficient) Haemophilus influenzae Rd strain and on a repair-deficient uvr-1 strain. Host cell reactivation (DNA repair) was observed for whole-phage and vegetative-phage DNA but not for single and double prophage DNA. Competent (phage-resistant) Haemophilus parainfluenzae cells were normally transfected with H. influenzae-grown phage DNA and with tandem double prophage DNA but not at all with single prophage DNA. CaCl2-treated H. influenzae suspensions could be transfected with vegetative phage DNA and with double prophage DNA but not with single prophage DNA. These observations support the hypothesis that transfection with single prophage DNA occurs through prophage DNA single-strand insertion into the recipient chromosome (at the bacterial att site) followed by DNA replication and then prophage induction.
将完整噬菌体 HP1 和 HP3、营养期噬菌体脱氧核糖核酸(DNA)以及单拷贝和串联双拷贝原噬菌体 DNA 暴露于紫外线辐射下,然后在野生型(DNA 修复功能正常)的流感嗜血杆菌 Rd 菌株和修复缺陷型 uvr - 1 菌株上进行检测。观察到完整噬菌体和营养期噬菌体 DNA 存在宿主细胞复活(DNA 修复)现象,而单拷贝和双拷贝原噬菌体 DNA 则未出现。感受态(抗噬菌体)副流感嗜血杆菌细胞通常能用在流感嗜血杆菌中培养的噬菌体 DNA 和串联双拷贝原噬菌体 DNA 进行转染,但完全不能用单拷贝原噬菌体 DNA 进行转染。经氯化钙处理的流感嗜血杆菌悬浮液能用营养期噬菌体 DNA 和双拷贝原噬菌体 DNA 进行转染,但不能用单拷贝原噬菌体 DNA 进行转染。这些观察结果支持这样一种假说,即单拷贝原噬菌体 DNA 的转染是通过原噬菌体 DNA 单链插入受体染色体(在细菌附着位点),随后进行 DNA 复制,然后诱导原噬菌体形成。