Chromosomal transformation of Escherichia coli recD strains with linearized plasmids

Author:

Russell C B1,Thaler D S1,Dahlquist F W1

Affiliation:

1. Institute of Molecular Biology, University of Oregon, Eugene 97403.

Abstract

Wild-type Escherichia coli are resistant to genetic transformation by purified linear DNA, probably in part because of exonuclease activity. We demonstrate that E. coli containing a recD mutation could be easily transformed by linearized plasmids containing a selectable marker. The marker was transferred to the chromosome by homologous recombination, whereas plasmid markers not in the region of homology were lost.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference47 articles.

1. recD: the gene for an essential third subunit of exonuclease V;Amundsen S. K.;Proc. Natl. Acad. Sci. USA,1986

2. Arber W. L. Enquist B. Hohn N. E. Murray and K. Murray. 1983. Experimental methods for use with Lambda p. 433-466. In R. W. Hendrix J. W. Roberts F. W. Stahl and R. A. Weisberg (ed.) Lambda II. Cold Spring Harbor Laboratory Cold Spring Harbor N.Y.

3. Two-codon insertion mutagenesis of plasmid genes by using single-stranded hexameric oligonucleotides;Barany F.;Proc. Natl. Acad. Sci. USA,1985

4. Identification and characterization of recD, a gene affecting plasmid maintenance and recombination in Escherichia coli;Biek D. P.;J. Bacteriol.,1986

5. A new class of Escherichia coli recBC mutants: implications for the role of RecBC enzyme in homologous recombination;Chaudhury A. M.;Proc. Natl. Acad. Sci. USA,1984

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