Exponentially growing Saccharomyces cerevisiae cells are more sensitiv
e to oxidants such as hydrogen peroxide and superoxides than stationar
y phase cells. Using disruption mutations in the genes encoding the tw
o S. cerevisiae superoxide dismutases, we show that the principal mech
anism of toxicity of redox-cycling compounds, such as menadione and pl
umbagin, is via the production of superoxide anions. Using two-dimensi
onal polyacrylamide gel electrophoresis we have compared the pattern o
f protein expression in cells labelled with L-[S-35]methionine and str
essed with either H2O2 or menadione. Three groups of proteins were evi
dent: those whose levels are elevated by both H2O2 and menadione, and
those specifically induced by either H2O2 or menadione. Experiments wi
th promoter fusions demonstrated that one of the heat inducible forms
of HSP7O (SSA1) was inducible with H2O2. Furthermore, induction of the
yeast H2O2-responsive TRX2 promoter by menadione required the metabol
ism of menadione.