Table 3.
Frequencies of mutations to Lac+ in E. coli CC101~CC106 strains with overexpressed dinB gene after incubation with hydrogen peroxide.
| Strain | Base substitution | Plasmid | Mutants/108 viable cells | Increase in mutation frequency (b − a) | Fold increase in mutation frequency (b/a) | |
|---|---|---|---|---|---|---|
| No H2O2 a | 10 mM H2O2 b | |||||
| CC101 | A:T→C:G | pDinB | 1.9 | 4.2 | 2.3 | 2.2 |
| pDinB003 | 1.5 | 1.8 | 0.3 | 1.2 | ||
| CC105 | A:T→T:A | pDinB | 3.6 | 4.4 | 0.8 | 1.2 |
| pDinB003 | 1.5 | 3.4 | 1.9 | 2.3 | ||
| CC106 | A:T→G:C | pDinB | 1.1 | 11.6 | 10.5 | 10.5 |
| pDinB003 | 0.8 | 1.8 | 1.0 | 2.3 | ||
E. coli CC101, CC105, and CC106 transformed with a plasmid wild-type plasmid (pDinB) and a mutant Pol IV (pDinB003) in stationary phase were incubated at 37°C with 1 mM of IPTG for 5 hr, followed by the treatment 10 mM H2O2 for 1 hr. The mutant Pol IV (DinB003) was generated by site-specific mutagenesis replacing aspartic acid in position 103 with aspargine [4]. The mutation frequency was expressed as number of mutants/108 viable cells.