Effect of the CopB auxiliary replication control system on stability of maintenance of Par(+) plasmid R1

J Bacteriol. 2004 Jan;186(1):207-11. doi: 10.1128/JB.186.1.207-211.2004.

Abstract

Plasmid R1 is a low-copy-number plasmid that is present at a level of about four or five copies per average cell. The copy number is controlled posttranscriptionally at the level of synthesis of the rate-limiting initiator protein RepA. In addition to this, R1 has an auxiliary system that derepresses a second promoter at low copy numbers, leading to increased repA mRNA synthesis. This promoter is normally switched off by a constitutively synthesized plasmid-encoded repressor protein, CopB; in cells with low copy numbers, the concentration of CopB is low and the promoter is derepressed. Here we show that the rate of loss of a Par(+) derivative of the basic replicon of R1 increased about sevenfold when the cells contained a high concentration of the CopB protein formed from a compatible plasmid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Helicases*
  • DNA Replication*
  • DNA-Binding Proteins*
  • Escherichia coli / genetics
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Gene Dosage
  • Gene Expression Regulation, Bacterial*
  • Plasmids / genetics*
  • Promoter Regions, Genetic
  • Proteins / genetics
  • Proteins / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Trans-Activators*

Substances

  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • Proteins
  • Repressor Proteins
  • Trans-Activators
  • replication initiator protein
  • DNA Helicases