ABSTRACT
Killing of bacterial spores by H(2)O(2) at elevated but sublethal temperatures and neutral pH occurred without lysis. However, with prolonged exposure or higher concentrations of the agent, secondary lytic processes caused major damage successively to the coat, cortex, and protoplast, as evidenced by electron and phase contrast microscopy. These processes were also reflected in changes in differential scanning calorimetric profiles for H(2)O(2)-treated spores. Endothermic transitions in the profiles occurred at lower temperatures than usual as a result of H(2)O(2) damage. Thus, H(2)O(2) sensitized the cells to heat damage. Longer exposure to H(2)O(2) resulted in total disappearance of the transitions, indicative of major disruptions of cell structure. Spores but not vegetative cells were protected against the lethal action of H(2)O(2) by the transition metal cations Cu, Cu, Co, Co, Fe, Fe, Mn, Ti, and Ti. The metal chelator EDTA was also somewhat protective, while o-phenanthroline, citrate, deferoxamine, and ethanehydroxydiphosphonate were only marginally so. Superoxide dismutase and a variety of other free-radical scavengers were not protective. In contrast, reducing agents such as sulfhydryl compounds and ascorbate at concentrations of 20 to 50 mM were highly protective. Decoating or demineralization of the spores had only minor effects. The marked dependence of H(2)O(2) sporicidal activity on moderately elevated temperature and the known low reactivity of H(2)O(2) itself suggest that radicals are involved in its killing action. However, the protective effects of a variety of oxidized or reduced transition metal ions indicate that H(2)O(2) killing of spores is markedly different from that of vegetative cells.
