Escherichia coli K-12 cell suspensions in buffer were exposed to ozone
at a concentration of 600 ppm. Measurements were made of cell viabili
ty, glyceraldehyde-3-phosphate dehydrogenase, malate dehydrogenase, la
ctate dehydrogenase, glutathione disulfide reductase, nonprotein sulfh
ydryl and total sulfhydryl compounds. Cell viability was not affected
when E. coli K-12 was exposed to ozone for less than 10 minutes. The m
ost sensitive parameter was glyceraldehyde-3-phosphate dehydrogenase f
ollowed by nonprotein sulfhydryl and total sulfhydryl compounds. Effec
ts on malate dehydrogenase, lactate dehydrogenase and glutathione disu
lfide reductase were negligible. Cell survival and induction of lipid
oxidation were also determined using two strains of E. coli K-12 (rec
A, deficient in DNA repair and wild-type). The extent of membrane lipi
d oxidation correlated with cell viability in a dose-dependent manner
and the survival curves of both strains showed similar sensitivity to
ozone. The data suggest that the sulfhydryl group in the membrane is t
he primary target of ozone attack. Rec A DNA repair system does not ap
pear to play a role in ozone resistance. Copyright (C) 1997 Elsevier S
cience Ireland Ltd.