Skip to main content
Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1972 Mar;1(3):259–262. doi: 10.1128/aac.1.3.259

Mode of Action of Primaquine: Preferential Inhibition of Protein Biosynthesis in Bacillus megaterium

John G Olenick 1, Fred E Hahn 1
PMCID: PMC444202  PMID: 4625625

Abstract

The growth of a strain of Bacillus megaterium was prevented by a minimal inhibitory concentration of primaquine of 52 μg/ml or 2 × 10−4m. When exponentially growing cultures received the drug at 6 × 10−4m, the rate of growth was drastically reduced and no further growth occurred after 15 min of exposure. At this concentration, primaquine was bactericidal, causing a 50% reduction in the viable population after one doubling time of 45 min. Supplying primaquine to cultures 30 min after adding radioactive-labeled phenylalanine, thymidine, uracil, or diaminopimelic acid produced an immediate and complete inhibition of protein biosynthesis but no inhibition of deoxyribonucleic acid biosynthesis for at least 15 min, and caused the formation of ribonucleic acid and cell wall polymer to proceed linearly at rates similar to those established prior to the addition of drug. This pattern of inhibition of macromolecular biosyntheses suggests that the major in vivo action of primaquine in B. megaterium is to block protein synthesis.

Full text

PDF
259

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aikawa M., Beaudoin R. L. Morphological effects of 8-aminoquinolines on the exoerythrocytic stages of Plasmodium fallax. Mil Med. 1969 Sep;134(10):986–999. [PubMed] [Google Scholar]
  2. BODMER W. F., GRETHER S. UPTAKE AND INCORPORATION OF THYMINE, THYMIDINE, URACIL, URIDINE, AND 5-FLUOROURACIL INTO THE NUCLEIC ACIDS OF BACILLUS SUBTILIS. J Bacteriol. 1965 Apr;89:1011–1014. doi: 10.1128/jb.89.4.1011-1014.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ciak J., Hahn F. E. Chloroquine: mode of action. Science. 1966 Jan 21;151(3708):347–349. doi: 10.1126/science.151.3708.347. [DOI] [PubMed] [Google Scholar]
  4. Grandgenett D. P., Stahly D. P. Repression of diaminopimelate decarboxylase by L-lysine in different Bacillus species. J Bacteriol. 1971 Mar;105(3):1211–1212. doi: 10.1128/jb.105.3.1211-1212.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Morris C. R., Andrew L. V., Whichard L. P., Holbrook D. J., Jr The binding of antimalarial aminoquinolines to nucleic acids and polynucleotides. Mol Pharmacol. 1970 May;6(3):240–250. [PubMed] [Google Scholar]
  6. Olenick J. G., Cook T. M., Hahn F. E. Bactericidal action of 2-hydroxy-3-(cyclohexylpropyl)-1,4-naphthoquinone on Bacillus megaterium. J Bacteriol. 1971 Aug;107(2):528–534. doi: 10.1128/jb.107.2.528-534.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES