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PMID: 7494470 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Comparison of ccd of F, parDE of RP4, and parD of R1 using a novel conditional replication control system of plasmid R1.

Molecular microbiology ·Vol. 17 ·No. 2 ·1995-07-00 ·Pages 211-20

Jensen RB, Grohmann E, Schwab H, Díaz-Orejas R, Gerdes K

Abstract

A number of plasmid-encoded gene systems are thought to stabilize plasmids by killing plasmid-free cells (also termed post-segregational killing or plasmid addiction). Here we analyse the mechanisms of plasmid stabilization by ccd of F, parDE of RP4 and parD of R1, and compare them to hok/sok of R1. To induce synchronous plasmid loss we constructed a novel plasmid replication-arrest system, which possesses the advantage that plasmid replication can be completely arrested by the addition of IPTG, a non-metabolizable inducer. Using isogenic plasmid constructions we have found, for the first time, consistent correlation between the effect on steady-state loss rates and the effect on cell proliferation in the plasmid replication-arrest assay for all three systems. The parDE system had the most pronounced effect both on plasmid stabilization and on plasmid retention after replication arrest. In contrast, ccd and parD both exhibited weaker effects than anticipated from previously published results. Thus, our results indicate that the function and efficiencies of some of the systems should be reconsidered. Our results are consistent with the previously postulated hypothesis that ccd and parDE act by killing plasmid-free segregants, whereas parD seems to act by inhibiting cell division of plasmid-free segregants.

MeSH Terms
Bacterial Proteins/genetics,physiology Bacterial Toxins/genetics Base Sequence DNA Replication DNA Topoisomerase IV DNA-Binding Proteins Escherichia coli/genetics,growth & development Escherichia coli Proteins F Factor/genetics Genes, Bacterial/physiology Genes, Lethal/physiology Genetic Vectors/genetics Isopropyl Thiogalactoside Molecular Sequence Data R Factors/genetics,metabolism
Chemicals
Bacterial Proteins Bacterial Toxins DNA-Binding Proteins Escherichia coli Proteins Hok protein, E coli ParD protein, E coli ParD protein, Plasmid R1 parD protein, Bacteria Isopropyl Thiogalactoside DNA Topoisomerase IV
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Jensen R B
Department of Molecular Biology, Odense University, Denmark.
Grohmann E
Schwab H
Díaz-Orejas R
Gerdes K
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1995-07-00
Pages
211-20
Language
English
Region
England
NLM ID
8712028
Subset
IM
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