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Does oxygen enhance the radiation-induced inactivation of penicillinase. Progress report, December 1, 1979-November 30, 1980

Technical Report ·
DOI:https://doi.org/10.2172/5414499· OSTI ID:5414499
The radiation-induced inactivation of penicillinase in dilute aqueous solutions buffered with phosphate was studied, by examining enzyme radiosensitivity in the presence of various gases (He, O/sub 2/, H/sub 2/, N/sub 2/O, N/sub 2/O + O/sub 2/). The introduction of either N/sub 2/O or O/sub 2/ was found to reduce the radiodamage. On the other hand H/sub 2/ or N/sub 2/O + O/sub 2/ gas-mixture enhanced the radiosensitivity. In the presence of formate and oxygen, no enzyme inactivation was detected. The results indicated that the specific damaging efficiency of H atoms is almost four-fold higher than that of OH radical; therefore in phosphate buffer, where more than half of the free radicals are H atoms, it is the H radicals that are responsible for the majority of the damage. The superoxide radicals appeared to be completely inactive and did not contribute toward enzyme inactivation. Oxygen was shown to affect the radiosensitivity in two ways. On one side, it protected by converting e/sup -//sub aq/ and H radicals into harmless O/sub 2//sup -/ radicals. On the other side it increased the inactivation by enhancing the damage brought about by OH radicals (OER = 2.8). In the present case the oxygen effect of protection exceeded that of sensitization, thus giving rise to a moderate overall protection effect.
Research Organization:
Hebrew Univ., Jerusalem (Israel)
Sponsoring Organization:
US Energy Research and Development Administration (ERDA)
DOE Contract Number:
AC02-76EV03221
OSTI ID:
5414499
Report Number(s):
DOE/EV/03221-62
Country of Publication:
United States
Language:
English