Watkins D K
Int J Radiat Biol Relat Stud Phys Chem Med. 1980 Sep;38(3):247-56. doi: 10.1080/09553008014551611.
DNA--membrane complexes from three strains of E. coli were irradiated and changes in the rates of DNA synthesis were observed. Doses from 1--10 krad to complexes from W3110 and pol A1 strains gave up to a 100 per cent increase in DNA synthesis; under the same conditions, no change was observed in Bs-1. The degree of stimulation did not depend on the presence of oxygen during irradiation, and a post-irradiation incubation was necessary to achieve activation. The properties of all three complexes were similar when unirradiated. Irradiation of intact organisms under conditions which produced marked, oxygen-dependent inhibition of the Bs-1 complex had no significant effect on those from W3110 and Pol A1. Enhanced DNA synthesis is concluded to be due wholly to repair of preexisting DNA. It is further postulated that DNA synthesis in untreated complexes (E. coli B's, W3110 and Pol A1) is mainly of the repair-type and does not necessarily take place at the site of DNA--membrane attachment.
对来自三株大肠杆菌的DNA-膜复合物进行辐照,并观察DNA合成速率的变化。对W3110和pol A1菌株的复合物施加1至10千拉德的剂量,可使DNA合成增加高达100%;在相同条件下,Bs-1菌株未观察到变化。刺激程度不取决于辐照期间氧气的存在,且辐照后孵育对于实现激活是必要的。未辐照时,所有三种复合物的性质相似。在对Bs-1复合物产生显著的、依赖氧气的抑制作用的条件下,对完整生物体进行辐照,对W3110和Pol A1菌株的复合物没有显著影响。得出结论,DNA合成增强完全是由于对预先存在的DNA进行修复。进一步推测,未处理的复合物(大肠杆菌Bs、W3110和Pol A1)中的DNA合成主要是修复型的,不一定发生在DNA-膜附着位点。