Literature DB >> 2442785

Plasmid repopulation kinetics in Staphylococcus aureus.

S K Highlander, R P Novick.   

Abstract

We have analyzed the kinetic route by which the indirectly controlled Staphylococcus aureus plasmid, pT181, responds to and corrects fluctuations in copy number. The kinetics of copy number correction from low to steady-state levels (termed repopulation) were determined using two different methods of copy number reduction. Thermosensitive replication (Tsr) mutants of pT181 were grown at nonpermissive temperatures to lower copy number and then shifted to a permissive temperature to allow repopulation. After the downshift, both wild-type and copy mutant plasmids, with active inhibitors, exhibited a burst of exponential replication that resulted in a two- to threefold overshoot of normal steady-state copy numbers. This was followed by inhibition of replication and eventual reestablishment of the steady-state replication rate. Similar replication kinetics were observed when these plasmids were introduced into naive cells by high-frequency transduction. By contrast, a pT181 copy mutant with a nonfunctional inhibitor-target regulation did not overshoot its steady-state copy number, but instead repopulated asymptotically. These results suggest that at low copy numbers, pT181 and its derivatives replicate at near-maximal rates and overshoot prior to the establishment of an inhibitory concentration of repressor. The maximal replication rate is independent of the plasmid's cop genotype. As the copy number increases, inhibitor accumulates and eventually reduces the replication rate. In the absence of an active inhibitor, the steady-state copy number is established at a level that must be limited by some other invariant factor.

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Year:  1987        PMID: 2442785     DOI: 10.1016/0147-619x(87)90029-1

Source DB:  PubMed          Journal:  Plasmid        ISSN: 0147-619X            Impact factor:   3.466


  8 in total

Review 1.  The family of highly interrelated single-stranded deoxyribonucleic acid plasmids.

Authors:  A Gruss; S D Ehrlich
Journal:  Microbiol Rev       Date:  1989-06

2.  In vitro inhibitory activity of RepC/C*, the inactivated form of the pT181 plasmid initiation protein, RepC.

Authors:  R Jin; A Rasooly; R P Novick
Journal:  J Bacteriol       Date:  1997-01       Impact factor: 3.490

3.  Staphylococcus aureus chromosomal mutations that decrease efficiency of Rep utilization in replication of pT181 and related plasmids.

Authors:  S Iordanescu; J Bargonetti
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

4.  An enhancer of DNA replication.

Authors:  M L Gennaro; R P Novick
Journal:  J Bacteriol       Date:  1988-12       Impact factor: 3.490

5.  The inactivated plasmid inititator protein RepC/RepC* may have a regulatory role.

Authors:  A Rasooly; R S Rasooly
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

6.  Lactobacillus hilgardii plasmid pLAB1000 consists of two functional cassettes commonly found in other gram-positive organisms.

Authors:  K Josson; P Soetaert; F Michiels; H Joos; J Mahillon
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490

7.  Successful Establishment of Plasmids R1 and pMV158 in a New Host Requires the Relief of the Transcriptional Repression of Their Essential rep Genes.

Authors:  José Á Ruiz-Masó; Luis M Luengo; Inmaculada Moreno-Córdoba; Ramón Díaz-Orejas; Gloria Del Solar
Journal:  Front Microbiol       Date:  2017-12-01       Impact factor: 5.640

8.  Crosstalk between vertical and horizontal gene transfer: plasmid replication control by a conjugative relaxase.

Authors:  Fabián Lorenzo-Díaz; Cris Fernández-López; Rudi Lurz; Alicia Bravo; Manuel Espinosa
Journal:  Nucleic Acids Res       Date:  2017-07-27       Impact factor: 16.971

  8 in total

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