Benzinger R, Enquist L W, Skalka A
J Virol. 1975 Apr;15(4):861-71. doi: 10.1128/JVI.15.4.861-871.1975.
The in vivo activity of the recBC nuclease was assayed by transfection of isogenic rec+ and rec minus spheroplasts with bacteriophage DNA of various origin and structure. The results indicate that the recBC nuclease can limit transfection at several stages during the production of an infective center; such limitations depend primarily on whether the DNA is in, or assumes, a nuclease-sensitive structure. The first stage of limitation can occur when a nuclease-sensitive transfecting molecule enters the spheroplast. Other potential limitation points occur during replication and maturation of the bacteriophage DNA. The initial stage can be bypassed by using recBC nuclease-resistant molecules such as circular forms. Through analysis of results with other DNA structures, we found that in vivo the effects of the double-strand exonucleolytic activity of the recBC nuclease predominated. The effects of the single-strand nuclease activities seem to be modified from those observed for the purified enzyme in vitro (Karu et al., 1974). Inside the cell, the single-strand exonuclease activity is very weak and the single-strand endonuclease activity is abolished almost completely.
通过用各种来源和结构的噬菌体DNA转染同基因的rec⁺和rec⁻原生质球来测定recBC核酸酶的体内活性。结果表明,recBC核酸酶可在产生感染中心的几个阶段限制转染;这种限制主要取决于DNA是否处于或呈现核酸酶敏感结构。当核酸酶敏感的转染分子进入原生质球时,可能会出现第一个限制阶段。噬菌体DNA复制和成熟过程中还会出现其他潜在的限制点。使用如环状形式的recBC核酸酶抗性分子可以绕过初始阶段。通过对其他DNA结构结果的分析,我们发现在体内recBC核酸酶的双链外切核酸酶活性起主要作用。单链核酸酶活性的影响似乎与体外纯化酶所观察到的有所不同(卡鲁等人,1974年)。在细胞内,单链外切核酸酶活性非常弱,单链内切核酸酶活性几乎完全丧失。