Genetic Analysis of Conjugational Recombination in Escherichia coli K12 Strains Deficient in RecBCD Enzyme
- 1 September 1987
- journal article
- research article
- Published by Microbiology Society in Microbiology
- Vol. 133 (9) , 2531-2538
- https://doi.org/10.1099/00221287-133-9-2531
Abstract
Conjugational recombination in Escherichia coli was investigated by comparing the effects of recN, recO, ruv and lexA mutations on the formation of recombinants in crosses with strains lacking RecBCD enzyme. The results presented reveal that recN and ruv mutations do not abolish residual recombination in a recB mutant, and have only a rather modest effect on recombination in recBC sbcA strains; in these respects they are quite different from recF, recJ and recO mutations. The differences between these two groups of genes are discussed in relation to the molecular exchanges needed to produce viable recombinants.This publication has 4 references indexed in Scilit:
- RecBC enzyme nicking at chi sites during DNA unwinding: Location and orientation-dependence of the cuttingCell, 1985
- Genetic analysis of the recJ gene of Escherichia coli K-12Journal of Bacteriology, 1984
- Inducible expression of a gene specific to the RecF pathway for recombination in Escherichia coli K12Molecular Genetics and Genomics, 1983
- Genetic analysis of the RecE pathway of genetic recombination in Escherichia coli K-12Journal of Bacteriology, 1981