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Journal of Bacteriology, March 2002, p. 1801-1805, Vol. 184, No. 6
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.6.1801-1805.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Ulrich Szewzyk,1 and Elisabeth Grohmann1*
Fachgebiet Ökologie der Mikroorganismen, Institut für Technischen Umweltschutz, Technische Universität Berlin, D-10587 Berlin, Germany,1 Centro de Investigaciones Biológicas, CSIC, E-28006 Madrid, Spain2
Received 16 August 2001/ Accepted 10 December 2001
The tra genes orf1 to orf11 of pIP501 were shown to be transcribed as a single operon of 11.3 kb in Enterococcus faecalis by reverse transcription-PCR. The transcriptional start site of the tra mRNA was mapped at 110 bp upstream from the predicted TTG start codon of the first gene of the operon, the traA relaxase. The TraA protein (660 amino acids) and a C-terminally truncated version of the TraA protein (293 amino acids) were purified as fusions with glutathione S-transferase. oriT cleavage activity of both TraA proteins was demonstrated in vitro on supercoiled plasmid pVA2241 DNA containing oriTpIP501. The activity of the DNA relaxase TraA is strictly dependent on the presence of Mg2+ or Mn2+ and is highest at temperatures of between 42 and 45°C.
Present address: PROIMI-Universidad Nacional de Tucumán, Tucumán, Argentina.
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