Tomita H, Kai M, Kusama T, Aoki Y
Department of Radiological Health, Faculty of Medicine, University of Tokyo, Japan.
J Radiat Res. 1995 Mar;36(1):46-55. doi: 10.1269/jrr.36.46.
Plasmid pBR322 DNA (4363 base pairs) in aerobic aqueous solution was irradiated with 60Co gamma-radiation. The change of diffusion coefficients (D) of chemical species, rate constants (k) of radical-DNA interaction and solubilities of O2 in water cannot be ignored when a temperature varies more than a few tens of centigrade. It is important to examine the variation of the yields of DNA strand breaks as a function of temperature in order to analyze the mechanisms of DNA strand breaks from the chemical point of view. Hence, we observed the change of the yield of strand breaks with temperatures between -20 and 42 degrees C by agarose gel electrophoresis. We also observed the change of the yield of strand breaks with the concentration of OH scavenger (Tris) from 1 mmol dm-3 to 100 mmol dm-3 and summarized it with previous experiments. This summarization indicated that the order of the lifetime of OH radical in cellular environment is several nanosecond. This value is consistent with the measurement of the lifetime of 8.7 nanosecond for OH radical in mammalian cell (Roots, R. and Okada, S. (1975) Radiat. Res. 64, 306-320).
在有氧水溶液中,用⁶⁰Coγ射线辐照质粒pBR322 DNA(4363个碱基对)。当温度变化超过几十摄氏度时,化学物质的扩散系数(D)、自由基与DNA相互作用的速率常数(k)以及水中O₂的溶解度的变化都不能忽略。从化学角度分析DNA链断裂的机制时,研究DNA链断裂产率随温度的变化很重要。因此,我们通过琼脂糖凝胶电泳观察了在-20至42摄氏度之间温度变化时链断裂产率的变化。我们还观察了链断裂产率随OH清除剂(Tris)浓度从1 mmol dm⁻³到100 mmol dm⁻³的变化,并将其与之前的实验进行了总结。该总结表明,细胞环境中OH自由基的寿命顺序为几纳秒。这个值与哺乳动物细胞中OH自由基寿命为8.7纳秒的测量结果一致(Roots, R.和Okada, S.(1975年)《辐射研究》64, 306 - 320)。