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. 2006 Oct;174(2):575-84.
doi: 10.1534/genetics.106.060889. Epub 2006 Aug 3.

Repair of DNA damage induced by bile salts in Salmonella enterica

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VSports在线直播 - Repair of DNA damage induced by bile salts in Salmonella enterica

Ana I Prieto et al. Genetics. 2006 Oct.

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Figures

F<sc>igure</sc> 1.—
Figure 1.—
Plate tests of SOS induction by bile salts. Each plate was seeded with >107 cells (which form a lawn after growth). A small amount of bile salt powder was placed in the center of the plate. Plates were incubated overnight at 37°. The plates at the top correspond to strain SV4851 (recA+/pGE108); the bottom plates correspond to SV4870 (recA1/pGE108).
F<sc>igure</sc> 2.—
Figure 2.—
Induction of genes in the oxyR and soxRS regulons by sodium deoxycholate. The strains shown, from left to right, are SV5158 (dps∷lacZ), SV5157 (katG∷lacZ), SV5159 (nfo∷lacZ), and SV5154 (fumC∷lacZ). Open bars show β-galactosidase activities of the fusions in LB. Solid bars show β-galactosidase activities of the fusions after exposure to 5% sodium deoxycholate. The data shown are means and standard deviations of four independent experiments.
F<sc>igure</sc> 3.—
Figure 3.—
Model for repair of bile-induced damage in S. enterica. Primary lesions (perhaps oxidized cytosines) are repaired by Dam-directed mismatch repair and by base excision repair. Either process generates single-stranded DNA that can induce the SOS response. Direct SOS induction can also occur if primary lesions impair DNA replication. Furthermore, single-strand breaks generated by DNA repair can give rise to double-strand breaks during DNA replication. Upon SOS induction, translesion DNA replication by the DinB polymerase may help to overcome DNA replication blockage. In turn, RecBCD may rescue arrested replication forks by either recombinational repair or degradation of double-strand ends.

References

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