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1.
Braz. j. med. biol. res ; 42(11): 1015-1019, Nov. 2009. ilus, tab
Article in English | LILACS | ID: lil-529107

ABSTRACT

Pretreatment of Escherichia coli cultures with the iron chelator 2,2’-dipyridyl (1 mM) protects against the lethal effects of low concentrations of hydrogen peroxide (<15 mM). However, at H2O2 concentrations equal to or greater than 15 mM, dipyridyl pretreatment increases lethality and mutagenesis, which is attributed to the formation of different types of DNA lesions. We show here that pretreatment with dipyridyl (1 mM) prior to challenge with high H2O2 concentrations (≥15 mM) induced mainly G:C→A:T transitions (more than 100X with 15 mM and more than 250X with 20 mM over the spontaneous mutagenesis rate) in E. coli. In contrast, high H2O2 concentrations in the absence of dipyridyl preferentially induced A:T→T:A transversions (more than 1800X and more than 300X over spontaneous mutagenesis for 15 and 20 mM, respectively). We also show that in the fpg nth double mutant, the rpoB gene mutation (RifS-RifR) induced by 20 mM H2O2 alone (20X higher) was increased in 20 mM H2O2 and dipyridyl-treated cultures (110X higher), suggesting additional and/or different lesions in cells treated with H2O2 under iron deprivation. It is suggested that, upon iron deprivation, cytosine may be the main damaged base and the origin of the pre-mutagenic lesions induced by H2O2.


Subject(s)
Chelating Agents/pharmacology , DNA Damage , DNA, Bacterial/drug effects , Escherichia coli/drug effects , Hydrogen Peroxide/pharmacology , /pharmacology , Cytosine , Escherichia coli/genetics , Metalloproteins , Mutagenicity Tests
2.
Braz. j. med. biol. res ; 27(11): 2551-5, Nov. 1994. graf
Article in English | LILACS | ID: lil-153974

ABSTRACT

The iron chelator o-phenanthroline enhances the lethal effect of H2O2 about four hundred times in Escherichia coli when both substances are added simultaneously to the culture mediu. If o-phenanthroline is added for increasing periods of time prior to the addition of H2O2, there is a shift from this lethal interaction to protection by the chelator about seven hundred times. It is known that the Fe2+ -o-phenanthroline(I) and Fe2+ -o-phenanthroline(II) complexes are formed quickly whereas the final and more stable Fe2+ -o-phenanthroline(III) complex is formed slowly, Moreover, the mono and bis complexes react with H2O2 to produce OH., whereas the tris complex is stable towards H2O2. Therefore, the lethal effect could be explained by the kinetics of reaction of o-phenanthroline with intracellular Fe2+, i.e., the mono and bis complexes are more reactive than intracellular Fe2+


Subject(s)
Escherichia coli/drug effects , Hydrogen Peroxide/pharmacology , Phenanthrolines/pharmacology , 2,2'-Dipyridyl/pharmacology , DNA/drug effects , Escherichia coli/growth & development , Hydroxyl Radical/pharmacology , Iron Chelating Agents/pharmacology , Time Factors
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