Resistance of Deinococcus radiodurans to mutagenesis is facilitated by pentose phosphate pathway in the mutS1 mutant background

Curr Microbiol. 2008 Jul;57(1):66-71. doi: 10.1007/s00284-008-9154-4. Epub 2008 Apr 4.

Abstract

MutS1 is a key protein involved in mismatch repair system for ensuring fidelity of replication and recombination in Deinococcus radiodurans. The zwf gene encodes glucose-6-phosphate dehydrogenase (G6PD) in the pentose phosphate (PP) pathway, which provides adequate metabolites as precursors of DNA repair. In this study, mutS1 and zwf were disrupted by homologous recombination. The zwf mutant (Deltazwf) and the zwf/mutS1 double mutant (Deltazwf/mutS1) were sensitive to ultraviolet (UV) light, H(2)O(2), and DNA cross-linking agent mitomycin C (MMC), whereas the mutS1 mutant (DeltamutS1) showed resistance to UV light, H(2)O(2) and MMC as the wild-type strain. Inactivation of mutS1 resulted in a 3.3-fold increase in frequency of spontaneous rifampicin-resistant mutagenesis and a 4.9-fold increment in integration efficiency of a donor point-mutation marker during bacterial transformation. Although inactivation of zwf had no obvious effect compared with the wild-type strain, dual disruption of zwf and mutS1 resulted in a 4.7-fold increase in mutation frequency and a 7.4-fold increase in integration efficiency. These results suggest that inactivation of the PP pathway decreases the resistance of D. radiodurans cells to DNA damaging agents and increases mutation frequency and integration efficiency in the mutS1 mutant background.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • DNA Damage
  • DNA Mismatch Repair
  • DNA, Bacterial / genetics
  • Deinococcus / drug effects*
  • Deinococcus / genetics
  • Deinococcus / metabolism
  • Deinococcus / radiation effects*
  • Glucosephosphate Dehydrogenase / genetics
  • Glucosephosphate Dehydrogenase / metabolism
  • Mitomycin / pharmacology
  • MutS DNA Mismatch-Binding Protein / genetics
  • MutS DNA Mismatch-Binding Protein / metabolism*
  • Mutagenesis*
  • Mutagens / pharmacology
  • Mutation
  • Pentose Phosphate Pathway*
  • Transformation, Bacterial
  • Ultraviolet Rays

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Mutagens
  • Mitomycin
  • Glucosephosphate Dehydrogenase
  • MutS DNA Mismatch-Binding Protein