Literature DB >> 6765584

Partitioning of plasmid R1 in Escherichia coli. I. Kinetics of loss of plasmid derivatives deleted of the par region.

K Nordström, S Molin, H Aagaard-Hansen.   

Abstract

The stability of inheritance of plasmid R1drd-19 was tested. The copy number of the plasmid was determined in two different ways: As the ratio between covalently closed circular DNA and chromosomal DNA, and by quantitative determination of single-cell resistance to ampicillin. In the latter case, strains carrying the R1 ampicillin transposon Tn3 on prophage lambda was used as standard. The values were transformed to copy number per cell by using the Cooper-Helmstetter model for chromosome replication as well as by determination of chromosomal DNA per cell by the diphenylamine method. The copy number was found to be five to six per cell (or about four per newborn cell). Nevertheless, plasmid R1drd-19 was found to be completely stably inherited. This stability was shown not to be due to retransfer of the plasmid by the R1 conjugation system, since transfer-negative derivatives of the plasmid were also completely stably inherited. Smaller derivatives of plasmid R1drd-19 were found to be lost at a frequency of about 1.5% per cell generation. The copy-number control was not affected in these miniplasmids, since their copy numbers were the same as that of the full size plasmid. Quantitatively, the instability of the miniplasmids was in accord with random partitioning. It is, therefore, suggested that the plasmid R1drd-19 carries genetic information for partitioning (par) of plasmid copies at cell division, and that the par mechanism is distinct from the copy number control (cop) system. Finally, the par gene maps on the resistance transfer part of the plasmid, but far away from the origin of replication and the so-called basic replicon; this is in accord with the approximate location of the repB gene (Yoshikawa, 1974, J. Bacteriol., 118, 1123-1131).

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Year:  1980        PMID: 6765584     DOI: 10.1016/0147-619x(80)90011-6

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


  64 in total

1.  The active partition gene incC of IncP plasmids is required for stable maintenance in a broad range of hosts.

Authors:  Azeem Siddique; David H Figurski
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

2.  Phenotypic plasticity in bacterial plasmids.

Authors:  Paul E Turner
Journal:  Genetics       Date:  2004-05       Impact factor: 4.562

Review 3.  The ParMRC system: molecular mechanisms of plasmid segregation by actin-like filaments.

Authors:  Jeanne Salje; Pananghat Gayathri; Jan Löwe
Journal:  Nat Rev Microbiol       Date:  2010-10       Impact factor: 60.633

4.  Chromosome partitioning in Escherichia coli: novel mutants producing anucleate cells.

Authors:  S Hiraga; H Niki; T Ogura; C Ichinose; H Mori; B Ezaki; A Jaffé
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

5.  Bacterial actin: architecture of the ParMRC plasmid DNA partitioning complex.

Authors:  Jeanne Salje; Jan Löwe
Journal:  EMBO J       Date:  2008-07-24       Impact factor: 11.598

6.  Identification and sequence of the basic replication region of a broad-host-range plasmid isolated from Thiobacillus ferrooxidans.

Authors:  R A Dorrington; D E Rawlings
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

7.  A DNA segment conferring stable maintenance on R6K gamma-origin core replicons.

Authors:  F Wu; I Levchenko; M Filutowicz
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

8.  Analysis of Agrobacterium tumefaciens plasmid pTiC58 replication region with a novel high-copy-number derivative.

Authors:  D R Gallie; M Hagiya; C I Kado
Journal:  J Bacteriol       Date:  1985-03       Impact factor: 3.490

9.  Characterization of the replication and stability regions of Agrobacterium tumefaciens plasmid pTAR.

Authors:  D R Gallie; D Zaitlin; K L Perry; C I Kado
Journal:  J Bacteriol       Date:  1984-03       Impact factor: 3.490

Review 10.  Production of recombinant proteins in E. coli by the heat inducible expression system based on the phage lambda pL and/or pR promoters.

Authors:  Norma A Valdez-Cruz; Luis Caspeta; Néstor O Pérez; Octavio T Ramírez; Mauricio A Trujillo-Roldán
Journal:  Microb Cell Fact       Date:  2010-03-19       Impact factor: 5.328

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