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J. Bacteriol., Jul 1995, 3641-3646, Vol 177, No. 13
KR Kumaresan, SS Springhorn and SA Lacks
Both the lethal and the mutagenic actions of N-methyl-N'-nitro-N-
nitrosoguanidine (MNNG) on cells of Streptococcus pneumoniae were greatly
potentiated by a component of yeast extract added to the cellular
environment. This component was found to be an oxidation product of
glutathione, glutathione disulfide (GSSG). At low concentrations in the
medium, both GSSG and glutathione potentiated MNNG action, but at high
concentrations, glutathione (and other sulfhydryl compounds) abolished the
effect. Point mutations in a cellular gene conferred resistance to the
potentiating effect, and they blocked uptake of either GSSG or glutathione
into the cells as well. This gene apparently encodes a component of the
system for glutathione transport in S. pneumoniae. The mechanism by which
GSSG, an apparently innocuous substance in the environment, renders low
levels of MNNG genotoxic and cytotoxic thus depends on its transport into
the cell, where it is reduced by glutathione reductase and then activates
intracellular MNNG. Also, it was observed that mutants of S. pneumoniae
defective in DNA mismatch repair are more resistant to MNNG than are
wild-type cells by a factor of 2.5.
Copyright © 1995, American Society for Microbiology
Lethal and mutagenic actions of N-methyl-N'-nitro-N-nitrosoguanidine potentiated by oxidized glutathione, a seemingly harmless substance in the cellular environment
Biology Department, Brookhaven National Laboratory, Upton, New York 11973, USA.
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