Amplification of the tetracycline resistance determinant of pAMalpha1 in Enterococcus faecalis requires a site-specific recombination event involving relaxase

J Bacteriol. 2002 Sep;184(18):5187-93. doi: 10.1128/JB.184.18.5187-5193.2002.

Abstract

The small multicopy plasmid pAMalpha1 (9.75 kb) encoding tetracycline resistance in Enterococcus faecalis is known to generate tandem repeats of a 4.1-kb segment carrying tet(L) when cells are grown extensively in the presence of tetracycline. Here we show that the initial (rate-limiting) step involves a site-specific recombination event involving plasmid-encoded relaxase activity acting at two recombination sequences (RS1 and RS2) that flank the tet determinant. We also present the complete nucleotide sequence of pAMalpha1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Base Sequence
  • Conjugation, Genetic
  • Enterococcus faecalis / drug effects
  • Enterococcus faecalis / genetics*
  • Gene Amplification
  • Gene Deletion
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed*
  • Plasmids / genetics*
  • Recombination, Genetic*
  • Sequence Analysis, DNA
  • Tetracycline / pharmacology
  • Tetracycline Resistance / genetics*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Mob protein, Bacteria
  • MobB protein, bacteria
  • RepB protein, Bacteria
  • Trans-Activators
  • Tetracycline

Associated data

  • GENBANK/AF503772