Abstract
A bioassay method for the polyene antibiotics nystatin and amphotericin B is proposed based on the measurement of the efflux of rubidium ions from a rubidium-loaded yeast culture challenged with the antibiotics. For this purpose a major proportion of the intracellular K+ ions in a Saccharomyces cerevisiae culture has been substituted by Rb+ ions. The rubidium leakage is measured by atomic absorption spectrophotometry, and a straight-line, dose-response correlation has been obtained for both antibiotics.
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Selected References
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- Borst-Pauwels G. W., Schnetkamp P., van Well P. Activation of Rb + and Na + uptake into yeast by monovalent cations. Biochim Biophys Acta. 1973 Jan 2;291(1):274–279. doi: 10.1016/0005-2736(73)90419-7. [DOI] [PubMed] [Google Scholar]
- Borst-Pauwels G. W., Wolters G. H., Henricks J. J. The interaction of 2,4-dinitrophenol with anaerobic Rb+ transport across the yeast cell membrane. Biochim Biophys Acta. 1971 Feb 2;225(2):269–276. doi: 10.1016/0005-2736(71)90220-3. [DOI] [PubMed] [Google Scholar]
- Clements-Jewery S. Nystatin-induced potassium efflux from Saccharomyces cerevisiae measured by flame photometry: a potential bioassay approach. Antimicrob Agents Chemother. 1976 Apr;9(4):585–586. doi: 10.1128/aac.9.4.585. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gale E. F. The release of potassium ions from Candida albicans in the presence of polyene antibiotics. J Gen Microbiol. 1974 Feb;80(2):451–465. doi: 10.1099/00221287-80-2-451. [DOI] [PubMed] [Google Scholar]
- Hammond S. M., Kliger B. N. Mode of action of the polyene antibiotic candicidin: binding factors in the wall of Candida albicans. Antimicrob Agents Chemother. 1976 Apr;9(4):561–568. doi: 10.1128/aac.9.4.561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hammond S. M., Lambert P. A., Kliger B. N. The mode of action of polyene antibiotics; induced potassium leakage in Candida albicans. J Gen Microbiol. 1974 Apr;81(2):325–330. doi: 10.1099/00221287-81-2-325. [DOI] [PubMed] [Google Scholar]
- KINSKY S. C. Alterations in the permeability of Neurospora crassa due to polyene antibiotics. J Bacteriol. 1961 Dec;82:889–897. doi: 10.1128/jb.82.6.889-897.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LAMPEN J. O., ARNOW P. M., BOROWSKA Z., LASKIN A. I. Location and role of sterol at nystatin-binding sites. J Bacteriol. 1962 Dec;84:1152–1160. doi: 10.1128/jb.84.6.1152-1160.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MARINI F., ARNOW P., LAMPEN J. O. The effect of monovalent cations on the inhibition of yeast metabolism by nystatin. J Gen Microbiol. 1961 Jan;24:51–62. doi: 10.1099/00221287-24-1-51. [DOI] [PubMed] [Google Scholar]
- SUTTON D. D., ARNOW P. M., LAMPEN J. O. Effect of high concentrations of nystatin upon glycolysis and cellular permeability in yeast. Proc Soc Exp Biol Med. 1961 Oct;108:170–175. doi: 10.3181/00379727-108-26882. [DOI] [PubMed] [Google Scholar]
- Venables P., Russell A. D. Nystatin-induced changes in Saccharomyces cerevisiae. Antimicrob Agents Chemother. 1975 Feb;7(2):121–127. doi: 10.1128/aac.7.2.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Venables P., Russell A. D. Some effects of nystatin on Saccharomyces cerevisiae. Microbios. 1972 Dec;6(24):239–246. [PubMed] [Google Scholar]
- Zygmunt W. A. Intracellular Loss of Potassium in Candida albicans After Exposure to Polyene Antifungal Antibiotics. Appl Microbiol. 1966 Nov;14(6):953–956. doi: 10.1128/am.14.6.953-956.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
