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- W2036733441 abstract "The endogenous tonB gene of Escherichia coli was used as a target for spontaneous deletion mutations which were isolated from ruvAB−, recG−, and ruvC− cells. The rates of tonB mutation were essentially the same in ruv+, ruvAB−, recG−, and ruvC− cells. We analyzed tonB mutants by sequencing. In the ruv+, recG−, and ruvC− strains, the spectra were different from those obtained from the ruvAB− cells, where deletions dominated followed by IS insertions, base substitutions, and frameshifts, in that order. We then analyzed the tonB-trp large deletion, due to simultaneous mutations of the trp operon, and found that the frequency in ruvAB− was higher than those in ruv+, recG−, and ruvC− cells. To characterize deletion formation further, we analyzed all the tonB mutants from one colicin plate. Seven deletions were identified at five sites from the 45 tonB mutants of ruv+ cells and 24 deletions at 11 sites from the 43 tonB mutants of ruvAB− cells. Thus, the ruvAB− strain is a deletion mutator. We discuss the role of RuvAB in avoiding deletions." @default.
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- W2036733441 date "2004-10-01" @default.
- W2036733441 modified "2023-10-16" @default.
- W2036733441 title "Role of the RuvAB protein in avoiding spontaneous formation of deletion mutations in the Escherichia coli K-12 endogenous tonB gene" @default.
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- W2036733441 doi "https://doi.org/10.1016/j.bbrc.2004.08.078" @default.
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