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Accumulation in gram-postive and gram-negative bacteria as a mechanism of resistance to erythromycin

J Bacteriol. 1968 Mar;95(3):1111-7. doi: 10.1128/jb.95.3.1111-1117.1968.

Abstract

Erythromycin was recovered in high yield after incubation with gram-negative bacteria. The cell-free protein-synthesizing preparation from gram-negative bacteria is equally as susceptible to the antibiotic as is that from gram-positive bacteria. Thus, neither destruction of erythromycin nor the absence of the step susceptible to the antibiotic plays an important role in the resistance mechanism of gram-negative bacteria. A 100-fold difference in accumulation of erythromycin between gram-positive and gram-negative bacteria was observed. This alone explains the resistance of gram-negative bacteria to erythromycin. Furthermore, data showed that the inhibition of growth is closely related to the accumulation of erythromycin. The concentration of intracellular erythromycin in gram-positive bacteria was found to be 44- to 90-fold greater than that of the extracellular medium. However, the antibiotic did not accumulate on the cell walls, nor was the accumulation energy-dependent. It is proposed that it takes place by the binding of erythromycin to the bacterial ribosomes, forming a very stable complex. The dissociation constants of erythromycin-Staphylococcus aureus complex and erythromycin-Bacillus subtilis complex were determined to be 1.1 x 10(-7) and 3.4 x 11(-7)m, respectively.

MeSH terms

  • Azides / pharmacology
  • Bacillus subtilis / drug effects*
  • Carbon Isotopes
  • Cell Wall / metabolism
  • Cyanides / pharmacology
  • Dinitrophenols / pharmacology
  • Drug Resistance, Microbial*
  • Erythromycin / metabolism
  • Erythromycin / pharmacology*
  • Escherichia coli / drug effects*
  • Hot Temperature
  • Peptide Biosynthesis
  • Proteus / drug effects*
  • Ribosomes / metabolism
  • Staphylococcus / drug effects*

Substances

  • Azides
  • Carbon Isotopes
  • Cyanides
  • Dinitrophenols
  • Erythromycin