Strand Break Formation in Plasmid DNA Irradiated in Aqueous Solution: Effect of Medium Temperature and Hydroxyl Radical Scavenger Concentration.
Author(s) -
Hiroyuki Tomita,
Michiaki Kai,
Tomoko KUSAMA,
Yoshiro Aoki
Publication year - 1995
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.36.46
Subject(s) - scavenger , chemistry , hydroxyl radical , dna , aqueous solution , agarose , irradiation , yield (engineering) , agarose gel electrophoresis , radical , reaction rate constant , dna damage , photochemistry , biophysics , nuclear chemistry , analytical chemistry (journal) , kinetics , biochemistry , chromatography , organic chemistry , materials science , biology , metallurgy , physics , quantum mechanics , nuclear physics
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).
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