Literature DB >> 9603880

DNA synthesis and viability of a mutT derivative of Escherichia coli WP2 under conditions of amino acid starvation and relation to stationary-phase (adaptive) mutation.

B A Bridges1, S Ereira.   

Abstract

Escherichia coli WP2 bacteria with an ochre amino acid auxotrophy show no evidence of growth during the first few days after plating at densities above 10(8) on plates lacking the required amino acid. They lose viability for some days, and then a subpopulation recovers and there is cell turnover. At very low plating densities (around 10(2) per plate), almost every cell will eventually form a small but visible colony. At intermediate plating densities (10(6) to 10(7) per plate), there is an immediate increase in the number of viable bacteria. The results are consistent with a model that assumes that growth is dependent on trace amounts of tryptophan or a tryptophan-complementing substance and that death is due to extracellular toxic species in the medium, including active oxygen species. Mutations in mutT bacteria under these conditions result from incorporation of 7,8-dihydro-8-oxo-dGTP into DNA and thus largely reflect DNA synthesis associated with the increase in the number of viable cells at the initial density used (10(7) per plate). We show that the increase in cell number and much of this DNA synthesis can be eliminated by the presence of 10(8) scavenger bacteria and by removal of early-arising mutant colonies that release the required amino acid. The synthesis that remains is equivalent to less than a quarter of a genome per day and is marginally reduced, if at all, in a polA derivative. We cannot exclude the possibility that this residual DNA synthesis is peculiar to mutT bacteria due to transcriptional leakiness, although there is no evidence that this is a major problem in this strain. If such DNA synthesis also occurs in wild-type bacteria, it may well be important for adaptive mutation since use of a more refined agar in selective plates both eliminated the initial increase in cell number seen at low density (10(7) per plate) and reduced the rate of appearance of mutants at plating densities above 10(8) per plate.

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Year:  1998        PMID: 9603880      PMCID: PMC107257     

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  22 in total

1.  Mutants of Escherichia coli requiring methionine or vitamin B12.

Authors:  B D DAVIS; E S MINGIOLI
Journal:  J Bacteriol       Date:  1950-07       Impact factor: 3.490

2.  mutY 'directs' mutation?

Authors:  B A Bridges
Journal:  Nature       Date:  1995-06-29       Impact factor: 49.962

Review 3.  DNA turnover and mutation in resting cells.

Authors:  B A Bridges
Journal:  Bioessays       Date:  1997-04       Impact factor: 4.345

4.  The origin of mutants.

Authors:  J Cairns; J Overbaugh; S Miller
Journal:  Nature       Date:  1988-09-08       Impact factor: 49.962

5.  Reversion of the tyrosine ochre strain Escherichia coli WU3610 under starvation conditions depends on a new gene tas.

Authors:  A R Timms; B A Bridges
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

6.  DNA turnover in buffer-held Escherichia coli and its effect on repair of UV damage.

Authors:  M S Tang; T C Wang; M H Patrick
Journal:  Photochem Photobiol       Date:  1979-03       Impact factor: 3.421

7.  Radiation-sensitive mutants of T4D. I. T4y: a new radiation-sensitive mutant; effect of the mutation on radiation survival, growth and recombination.

Authors:  J M Boyle; N Symonds
Journal:  Mutat Res       Date:  1969 Nov-Dec       Impact factor: 2.433

8.  Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence.

Authors:  B G Hall
Journal:  Genetics       Date:  1988-12       Impact factor: 4.562

Review 9.  Adaptive mutation: the uses of adversity.

Authors:  P L Foster
Journal:  Annu Rev Microbiol       Date:  1993       Impact factor: 15.500

10.  Functional cooperation of MutT, MutM and MutY proteins in preventing mutations caused by spontaneous oxidation of guanine nucleotide in Escherichia coli.

Authors:  T Tajiri; H Maki; M Sekiguchi
Journal:  Mutat Res       Date:  1995-05       Impact factor: 2.433

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  5 in total

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Authors:  P L Foster
Journal:  Annu Rev Genet       Date:  1999       Impact factor: 16.830

2.  Mutations arise independently of transcription in non-dividing bacteria.

Authors:  D Barionovi; P Ghelardini; G Di Lallo; L Paolozzi
Journal:  Mol Genet Genomics       Date:  2003-05-24       Impact factor: 3.291

3.  Effect of endogenous carotenoids on "adaptive" mutation in Escherichia coli FC40.

Authors:  B A Bridges; P L Foster; A R Timms
Journal:  Mutat Res       Date:  2001-01-25       Impact factor: 2.433

4.  Defects in the error prevention oxidized guanine system potentiate stationary-phase mutagenesis in Bacillus subtilis.

Authors:  Luz E Vidales; Lluvia C Cárdenas; Eduardo Robleto; Ronald E Yasbin; Mario Pedraza-Reyes
Journal:  J Bacteriol       Date:  2008-11-14       Impact factor: 3.490

5.  Occurrence of leu+ revertants under starvation cultures in Escherichia coli is growth-dependent.

Authors:  Jianling Jin; Peiji Gao; Yumin Mao
Journal:  BMC Genet       Date:  2002-04-25       Impact factor: 2.797

  5 in total

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