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Mitochondrial mutations affecting resistance to erythromycin and mikamycin in Paramecium aurelia: provisional results with a new method

Published online by Cambridge University Press:  14 April 2009

Clara Queiroz
Affiliation:
Institute of Animal Genetics, Edinburgh
G. H. Beale
Affiliation:
Institute of Animal Genetics, Edinburgh

Summary

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A new method for obtaining mitochondrial mutants of Paramecium aurelia is described. Sensitive organisms were first placed in medium containing a low concentration (0·02 mg/ml) of erythromycin (ERY), insufficient to prevent fission. The paramecia were then transferred through a graded series of increasing ERY concentrations, with a period of growth at each concentration. A high yield of ERY-resistant mutants was obtained.

Continuous growth in 0·02 mg/ml ERY also resulted in the accumulation of a spectrum of mutants resistant to various concentrations of ERY. Many of these mutants are also resistant to mikamycin. On returning the resistant paramecia to media lacking ERY, some clones remained resistant whilst others reverted to sensitivity.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1974

References

REFERENCES

Adoutte, A. & Beisson, J. (1970). Cytoplasmic inheritance of erythromycin resistant mutations in Paramecium aurelia. Molecular and General Genetics 108, 7077.CrossRefGoogle ScholarPubMed
Adoutte, A. & Beisson, J. (1972). Evolution of mixed populations of genetically different mitochondria in Paramecium aurelia. Nature, London 235, 393396.CrossRefGoogle ScholarPubMed
Beale, G. H. (1969). A note on the inheritance of erythromycin resistance in Paramecium aurelia. Genetical Research, Cambridge 14, 341342.CrossRefGoogle ScholarPubMed
Beale, G. H. (1973). Genetic studies on mitochondrially inherited mikamycin-resistance in Paramecium aurelia. Molecular and General Genetics 127, 241248.CrossRefGoogle ScholarPubMed
Beale, G. H., Knowles, J. K. C. & Tait, A. (1972). Mitochondrial genetics in Paramecium. Nature, London 235, 396397.Google Scholar
Birky, C. W. (1973). On the origin of mitochondrial mutants: Evidence for intracellular selection of mitochondria in the origin of antibiotic resistant cells in yeast. Genetics 74, 421432.Google Scholar
Coen, D., Deutsch, J., Netter, P., Petrochilo, E. & Slonimsky, P. (1970). Mitochondrial genetics. I. Methodology and phenomenology. In Control of Organdie Development (ed. Miller, P.L.), pp. 449496. Cambridge University Press.Google Scholar
Knowles, J. K. C. (1972). Observations on two mitochondrial phenotypes in single paramecium cells. Experimental Cell Research 70, 223226.Google Scholar
Linnane, A. W., Saunders, G. W., Gingold, E. B. & Lukins, H. B. (1968). Biogenesis of mitochondria. 5. Cytoplasmic inheritance of erythromycin resistance in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the U.S.A. 59, 19031910.Google Scholar
Thomas, D. Y. & Wilkie, D. (1968). Inhibition of mitochondrial synthesis in yeast by erythromycin: cytoplasmic and nuclear factors controlling resistance. Genetical Research, Cambridge 11, 3341.CrossRefGoogle ScholarPubMed