Paterson M C, Boyle J M, Setlow R B
J Bacteriol. 1971 Jul;107(1):61-7. doi: 10.1128/jb.107.1.61-67.1971.
Escherichia coli K-12, polAl(-) is a mutant strain whose extracts are deficient in Kornberg deoxyribonucleic acid (DNA) polymerase activity. We have compared the mutant and parental strains on the basis of a number of responses to ultraviolet (UV) and X-irradiation. For both types of radiation, the mutant is more sensitive by approximately the same factor as measured by reduction in colony formation, depression of DNA synthesis, and enhancement of DNA degradation. The rate of repair of X-ray-induced single-strand breaks in the mutant is also slower, as is the repair of breaks after excision repair of UV damage. On the other hand, the mutant has a significant capability to reactivate UV-irradiated lambda phage, although it is almost totally deficient in the ability to carry out UV reactivation. The data indicate that the polAl mutation leaves the cells with some ability to perform excision and strand-rejoining repair but that an exonuclease, whose identity remains obscure, is the agent responsible for the extensive breakdown of the DNA in polAl(-) cells after irradiation.
大肠杆菌K - 12,polA1( - )是一种突变菌株,其提取物缺乏 Kornberg 脱氧核糖核酸(DNA)聚合酶活性。我们基于对紫外线(UV)和X射线照射的多种反应,对突变菌株和亲本菌株进行了比较。对于这两种类型的辐射,通过菌落形成减少、DNA合成抑制和DNA降解增强来衡量,突变体的敏感性大约高相同倍数。突变体中X射线诱导的单链断裂的修复速率也较慢,紫外线损伤切除修复后的断裂修复也是如此。另一方面,突变体具有显著的能力重新激活紫外线照射的λ噬菌体,尽管它几乎完全缺乏进行紫外线复活的能力。数据表明,polA1突变使细胞具有一定的切除和链重新连接修复能力,但一种核酸外切酶(其身份仍然不明)是辐射后polA1( - )细胞中DNA广泛降解的原因。