The chromosomal 3',5"-aminoglycoside phosphotransferase in Streptococcus pneumoniae is closely related to its plasmid-coded homologs in Streptococcus faecalis and Staphylococcus aureus

J Bacteriol. 1983 Dec;156(3):1373-7. doi: 10.1128/jb.156.3.1373-1377.1983.

Abstract

The apparently chromosomally encoded 3',5"-aminoglycoside phosphotransferase (type III), from the high-level aminoglycoside-resistant Streptococcus pneumoniae BM4200, was compared with homologous enzymes coded for by the plasmids pJH1 and pSH2, originally isolated from Streptococcus faecalis and Staphylococcus aureus, respectively, and also found in a wild strain of S. aureus, BM4600. The enzymes appeared to be indistinguishable, and we conclude that the gene encoding 3',5"-aminoglycoside phosphotransferase (type III) can cross generic barriers within gram-positive cocci.

MeSH terms

  • Enterococcus faecalis / enzymology*
  • Enterococcus faecalis / genetics
  • Genes, Bacterial
  • Isoelectric Point
  • Kanamycin Kinase
  • Molecular Weight
  • Phosphotransferases / genetics*
  • Phosphotransferases / metabolism
  • Plasmids*
  • Staphylococcus aureus / enzymology*
  • Staphylococcus aureus / genetics
  • Streptococcus pneumoniae / enzymology*
  • Streptococcus pneumoniae / genetics
  • Substrate Specificity

Substances

  • Phosphotransferases
  • Kanamycin Kinase