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PMID: 2644236 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Site-specific recombination at oriT of plasmid R1162 in the absence of conjugative transfer.

Journal of bacteriology ·Vol. 171 ·No. 2 ·1989-02-00 ·Pages 799-806

Meyer R

Abstract

R1162 is efficiently comobilized during conjugative transfer of the self-transmissible plasmid R751. Bacteriophage M13 derivatives that contain two directly repeated copies of oriT, the site on R1162 DNA required in cis for mobilization, were constructed. Phage DNA molecules underwent recombination during infection of Escherichia coli, with the product retaining a single functional copy of oriT. Recombination was strand specific and depended on R1162 gene products involved in mobilization, but did not require the self-transmissible plasmid vector. Two genes were identified, one essential for recombination and the other affecting the frequency of recombination. Recombination of bacteriophage DNA could form the basis of a simple model for some of the events occurring during conjugation without the complexity of a true mating system.

MeSH Terms
Amino Acid Sequence Base Sequence Cloning, Molecular Conjugation, Genetic DNA, Bacterial/genetics Drug Resistance, Microbial/genetics Escherichia coli/genetics Genes, Bacterial Molecular Sequence Data Plasmids Recombination, Genetic
Chemicals
DNA, Bacterial
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Meyer R
Department of Microbiology, University of Texas, Austin 78712.
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21 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1989-02-00
Pages
799-806
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC209667
Subset
IM
Grants
NIGMS NIH HHS · GM-37462 · United States
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