Endonuclease V protects Escherichia coli against specific mutations caused by nitrous acid

1999 ◽  
Vol 435 (3) ◽  
pp. 245-254 ◽  
Author(s):  
Karen A Schouten ◽  
Bernard Weiss
2009 ◽  
Vol 191 (17) ◽  
pp. 5369-5376 ◽  
Author(s):  
Young-Man Kwon ◽  
Bernard Weiss

ABSTRACT When Escherichia coli K-12 is grown anaerobically in medium containing tryptophan and sodium nitrate, it produces red compounds. The reaction requires functional genes for trytophanase (tnaA), a tryptophan permease (tnaB), and a nitrate reductase (narG), as well as a natural drop in the pH of the culture. Mass spectrometry revealed that the purified chromophores had mass/charge ratios that closely match those for indole red, indoxyl red, and an indole trimer. These compounds are known products of chemical reactions between indole and nitrous acid. They are derived from an initial reaction of 3-nitrosoindole with indole. Apparently, nitrite that is produced from the metabolic reduction of nitrate is converted in the acid medium to nitrous acid, which leads to the nitrosation of the indole that is generated by tryptophanase. An nfi (endonuclease V) mutant and a recA mutant were selectively killed during the period of chromophore production, and a uvrA strain displayed reduced growth. These effects depended on the addition of nitrate to the medium and on tryptophanase activity in the cells. Unexpectedly, the killing of a tnaA + nfi mutant was not accompanied by marked increases in mutation frequencies for several traits tested. The vulnerability of three DNA repair mutants indicates that a nitrosoindole or a derivative of a nitrosoindole produces lethal DNA damage.


2006 ◽  
Vol 188 (18) ◽  
pp. 6553-6560 ◽  
Author(s):  
Brian Budke ◽  
Andrei Kuzminov

ABSTRACT Endonuclease V, encoded by the nfi gene, initiates removal of the base analogs hypoxanthine and xanthine from DNA, acting to prevent mutagenesis from purine base deamination within the DNA. On the other hand, the RdgB nucleotide hydrolase in Escherichia coli is proposed to prevent hypoxanthine and xanthine incorporation into DNA by intercepting the noncanonical DNA precursors dITP and dXTP. Because many base analogs are mutagenic when incorporated into DNA, it is intuitive to think of RdgB as acting to prevent similar mutagenesis from deaminated purines in the DNA precursor pools. To test this idea, we used a set of Claire Cupples' strains to detect changes in spontaneous mutagenesis spectra, as well as in nitrous acid-induced mutagenesis spectra, in wild-type cells and in rdgB single, nfi single, and rdgB nfi double mutants. We found neither a significant increase in spontaneous mutagenesis in rdgB and nfi single mutants or the double mutant nor any changes in nitrous acid-induced mutagenesis for rdgB mutant strains. We conclude that incorporation of deaminated purines into DNA is nonmutagenic.


2006 ◽  
Vol 188 (3) ◽  
pp. 829-833 ◽  
Author(s):  
Bernard Weiss

ABSTRACT In Escherichia coli, nitrosative mutagenesis may occur during nitrate or nitrite respiration. The endogenous nitrosating agent N2O3 (dinitrogen trioxide, nitrous anhydride) may be formed either by the condensation of nitrous acid or by the autooxidation of nitric oxide, both of which are metabolic by-products. The purpose of this study was to determine which of these two agents is more responsible for endogenous nitrosative mutagenesis. An nfi (endonuclease V) mutant was grown anaerobically with nitrate or nitrite, conditions under which it has a high frequency of A:T-to-G:C transition mutations because of a defect in the repair of hypoxanthine (nitrosatively deaminated adenine) in DNA. These mutations could be greatly reduced by two means: (i) introduction of an nirB mutation, which affects the inducible cytoplasmic nitrite reductase, the major source of nitric oxide during nitrate or nitrite metabolism, or (ii) flushing the anaerobic culture with argon (which should purge it of nitric oxide) before it was exposed to air. The results suggest that nitrosative mutagenesis occurs during a shift from nitrate/nitrite-dependent respiration under hypoxic conditions to aerobic respiration, when accumulated nitric oxide reacts with oxygen to form endogenous nitrosating agents such as N2O3. In contrast, mutagenesis of nongrowing cells by nitrous acid was unaffected by an nirB mutation, suggesting that this mutagenesis is mediated by N2O3 that is formed directly by the condensation of nitrous acid.


1959 ◽  
Vol 14 (8-9) ◽  
pp. 528-537 ◽  
Author(s):  
F. Kaudewitz

Cells of E. coli B incubated with NaNO2 undergo inactivation. In non-metabolizing cells the inactivation follows a two hit curve. In metabolizing cells the rate of inactivation is increased and the inactivation curve does not show two-hit kinetics. The rate of inactivation decreases with rising pH and decreasing NaNO2-concentration. Therefore nitrous acid appears to be the active substance.Nitrous acid proved to be a potent mutagen as shown by isolation of auxotrophic mutants. With an inactivation rate of 10-4 about 1.4 per cent of the surviving cells were auxotrophs. The probability that this increase in mutants may be due to selection during inactivation of auxotrophs present before exposure was excluded experimentally. In none of 559 auxotrophic colonies grown from single cells which had survived contact with nitrous acid wild-type sectors were found. For metabolizing and nonmetabolizing cells the increase of the percentage of auxotrophic mutants with increasing time of exposure to HNO2 followed a two-hit curve. In these experiments the percentage of induced mutants was independent of the different rate of inactivation caused by different states of metabolism and dependent only on the time of incubation with nitrous acid. The results are discussed as being in agreement with the assumption that in non-metabolizing cells nitrous acid acts directly on the cellular DNA leading to inactivation and mutation.


1997 ◽  
Vol 179 (2) ◽  
pp. 310-316 ◽  
Author(s):  
G Guo ◽  
Y Ding ◽  
B Weiss
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