Boling M E, Setlow J K
J Virol. 1974 Nov;14(5):1056-62. doi: 10.1128/JVI.14.5.1056-1062.1974.
Rescue of wild-type markers from transfecting phage DNA in cómpetent Haemophilus influenzae cells by superinfection with temperature-sensitive phage (marker rescue) is approximately linearly dependent upon the concentration of transfecting DNA. The amount of marker rescue with a constant amount of transfecting DNA increases with increasing multiplicities of superinfecting phage up to about 4, and then decreases at higher multiplicities. Host restriction of transfecting DNA does not affect marker rescue. The frequency of wild-type recombinants from marker rescue is much greater than that from multiple infection with whole phages, and is comparable to that obtained with two mutant-transfecting DNAs. The amount of marker rescue decreases exponentially with time between entrance of the transfecting DNA and superinfection, and the rate of decrease is independent of map position of the rescued marker. Marker rescue is drastically reduced in the recombination-defective strains, rec1 and rec2.
通过用温度敏感噬菌体进行超感染,从感受态流感嗜血杆菌细胞中转染噬菌体DNA来拯救野生型标记(标记拯救),大致呈线性依赖于转染DNA的浓度。在转染DNA量恒定的情况下,标记拯救量随着超感染噬菌体的感染复数增加而增加,直至约4,然后在更高的感染复数下减少。转染DNA的宿主限制不影响标记拯救。标记拯救产生的野生型重组体频率远高于全噬菌体多次感染产生的频率,且与用两个突变转染DNA获得的频率相当。标记拯救量随着转染DNA进入与超感染之间的时间呈指数下降,且下降速率与被拯救标记的图谱位置无关。在重组缺陷菌株rec1和rec2中,标记拯救显著减少。