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. 1965 Apr;89(4):1068–1074. doi: 10.1128/jb.89.4.1068-1074.1965

Mechanism of Action of Nalidixic Acid on Escherichia coli II. Inhibition of Deoxyribonucleic Acid Synthesis

William A Goss 1, William H Deitz 1, Thomas M Cook 1
PMCID: PMC277597  PMID: 14276097

Abstract

Goss, William A. (Sterling-Winthrop Research Institute, Rensselaer, N.Y.), William H. Deitz, and Thomas M. Cook. Mechanism of action of nalidixic acid on Escherichia coli. II. Inhibition of deoxyribonucleic acid synthesis. J. Bacteriol. 89:1068–1074. 1965.—Nalidixic acid was shown to inhibit specifically the synthesis of deoxyribonucleic acid (DNA) in Escherichia coli. Slight effects on protein and ribonucleic acid (RNA) synthesis were observed only at higher levels of drug or after prolonged incubation. The inhibition of DNA synthesis in E. coli 15TAU, as measured by incorporation of C14-labeled thymine, was observed after exposure to nalidixic acid for 10 min. Inhibition of the incorporation of C14-labeled uracil into RNA and C14-labeled l-arginine into protein (21 and 28% inhibition, respectively) was observed only after 60 min of exposure. When cultures of E. coli 15TAU were exposed to 3.0 μg/ml of nalidixic acid (slightly greater than the minimal growth inhibitory concentration), the incorporation of C14-labeled thymidine was inhibited 30 to 40% after 90 min. Nalidixic acid at 10 μg/ml, a lethal concentration, inhibited thymidine incorporation 72% during this period. Nalidixic acid at 1.0 μg/ml had no apparent effect on the incorporation of C14-labeled adenine or C14-labeled uracil into RNA of cultures of E. coli 198, a wild-type strain. However, incorporation of both bases into DNA was strongly inhibited after 60 min of exposure (66 and 69%, respectively). Nalidixic acid inhibited DNA replication during a single round of synthesis. In contrast with “thymineless death,” nalidixic acid was not lethal to E. coli 15TAU during restricted RNA and protein synthesis (i.e., in a medium containing thymine but lacking arginine and uracil). We have shown also that this chemotherapeutic agent has little effect on the synthesis of protein or RNA required to initiate DNA replication. After 75 min of inhibition, the capacity of E. coli 15TAU to synthesize DNA in a medium containing thymine, arginine, and uracil may be restored by a simple filtration and washing process, indicating that the drug is not firmly bound. These studies leave little doubt that a primary action of nalidixic acid is the inhibition of the synthesis of DNA in E. coli.

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Selected References

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

  1. BARNER H. D., COHEN S. S. The isolation and properties of amino acid requiring mutants of a thymineless bacterium. J Bacteriol. 1957 Sep;74(3):350–355. doi: 10.1128/jb.74.3.350-355.1957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. GALLANT J., SUSKIND S. R. Relationship between thymineless death and ultraviolet inactivation in Escherichia coli. J Bacteriol. 1961 Aug;82:187–194. doi: 10.1128/jb.82.2.187-194.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. GOSS W. A., DEITZ W. H., COOK T. M. MECHANISM OF ACTION OF NALIDIXIC ACID ON ESCHERICHIA COLI. J Bacteriol. 1964 Oct;88:1112–1118. doi: 10.1128/jb.88.4.1112-1118.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. KANAZIR D., BARNER H. D., FLAKS J. G., COHEN S. S. Some physiological and genetic properties of a strain of Escherichia coli requiring thymine, arginine and uracil. Biochim Biophys Acta. 1959 Aug;34:341–353. doi: 10.1016/0006-3002(59)90287-2. [DOI] [PubMed] [Google Scholar]
  5. MAALOE O., HANAWALT P. C. Thymine deficiency and the normal DNA replication cycle. I. J Mol Biol. 1961 Apr;3:144–155. doi: 10.1016/s0022-2836(61)80041-7. [DOI] [PubMed] [Google Scholar]
  6. MAALOE O. The control of normal DNA replication in bacteria. Cold Spring Harb Symp Quant Biol. 1961;26:45–52. doi: 10.1101/sqb.1961.026.01.010. [DOI] [PubMed] [Google Scholar]
  7. NAKADA D. Involvement of newly-formed protein in the syntheses of deoxyibonucleic acid. Biochim Biophys Acta. 1960 Nov 4;44:241–244. doi: 10.1016/0006-3002(60)91559-6. [DOI] [PubMed] [Google Scholar]
  8. ROODYN D. B., MANDEL H. G. A simple membrane fractionation method for determining the distribution of radioactivity in chemical fractions of Bacillus cereus. Biochim Biophys Acta. 1960 Jun 17;41:80–88. doi: 10.1016/0006-3002(60)90371-1. [DOI] [PubMed] [Google Scholar]

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