Characterization of contaminating DNA in Taq polymerase which occurs during amplification with a primer set for Legionella 5S ribosomal RNA

Mol Cell Probes. 1994 Feb;8(1):11-4. doi: 10.1006/mcpr.1994.1002.

Abstract

An amplification product that occurred in negative controls of a PCR using a primer system for Legionella 55 ribosomal RNA was characterized by direct sequencing. The amplification product did not hybridize to a Legionella specific oligonucleotide. It was derived from bacterial DNA contaminating Taq DNA polymerase, a phenomenon that was previously reported for amplification reactions with universal primer sets for bacterial 16S rRNA. The sequence of the 5S ribosomal fragment had close homology to the 5S-rRNA of the species Pseudomonas fluorescens, Pseudomonas aeruginosa, Alcaligenes faecalis, and Azotobacter vinelandii. These findings confirm that the DNA contaminations in Taq DNA polymerase belong to other species than Thermus aquaticus or Escherichia coli.

MeSH terms

  • Base Sequence
  • DNA Probes
  • DNA, Bacterial / analysis
  • DNA, Bacterial / genetics*
  • DNA-Directed DNA Polymerase / genetics*
  • Escherichia coli / genetics
  • Legionella / genetics*
  • Molecular Sequence Data
  • Nucleic Acid Amplification Techniques*
  • Polymerase Chain Reaction
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas fluorescens / genetics
  • RNA, Bacterial / analysis
  • RNA, Bacterial / genetics*
  • RNA, Ribosomal, 5S / analysis
  • RNA, Ribosomal, 5S / genetics*
  • Sequence Homology, Nucleic Acid
  • Taq Polymerase

Substances

  • DNA Probes
  • DNA, Bacterial
  • RNA, Bacterial
  • RNA, Ribosomal, 5S
  • Taq Polymerase
  • DNA-Directed DNA Polymerase

Associated data

  • GENBANK/X01555
  • GENBANK/X01556
  • GENBANK/X01557
  • GENBANK/X01590
  • GENBANK/X05081
  • GENBANK/X05517