Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-04-30T22:09:09.284Z Has data issue: false hasContentIssue false

Mapping of the pneumococcus chromosome: differences between recipient strains varying in hex property and the location of the opt-r2 gene

Published online by Cambridge University Press:  14 April 2009

L. O. Butler
Affiliation:
Department of Medical Microbiology, St George's Hospital Medical School, Hyde Park Corner, London SW1
G. Nicholas
Affiliation:
Department of Medical Microbiology, St George's Hospital Medical School, Hyde Park Corner, London SW1
R. W. Grist
Affiliation:
Department of Medical Microbiology, St George's Hospital Medical School, Hyde Park Corner, London SW1
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Transformation studies in pneumococcus had shown that loci determining the resistance to erythromycin and streptomycin were unlinked when strain Cl3 was recipient but linked when strain SIII-I was recipient. This phenomenon also applies to other pairs of markers studied in these two recipients, no matter whether the transforming DNA was derived from strain Cl3 or strain SIII-I. Other differences between the two recipient strains were also revealed. Whereas competent cultures of strain Cl3 were composed of all competent cells, which was in agreement with previous reports of pneumococcal cultures, strain SIII-I normally gave a maximum average of 28% competent cells. Strain SIII-I was unstable, since on repeated sub-culturing the competence peak profile changed and the value of ‘fcq’ increased. These properties were reflected in the two hex strains 401 and R6x which were found to be similar to the ‘altered SIII-I’ strain. The results from the linkage studies have been applied to the chromosome map and have placed the opt-r2 gene in the str-r41-containing chromosome arm.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1979

References

REFERENCES

Avery, O. T., MacLeod, C. M. & McCarty, M. (1955) Studies on the chemical nature of the substance inducing pneumococcal types. Induction of transformation by a deoxyribonucleic acid fraction isolated from Pneumococcus type III. Journal of Experimental Biology 89, 137157.Google Scholar
Butler, L. O. (1965) A co-precipitation method for the preparation of transforming DNA from small samples of low density bacterial cultures. Journal of General Microbiology 39, 247252.Google Scholar
Butler, L. O. (1973) Bacterial Transformation (ed. Archer, L. J.), pp. 351367. London: Academic Press.Google Scholar
Butler, L. O. & Nicholas, G. (1973) Mapping of the pneumococcus chromosome. Linkage between the genes conferring resistances to erythromycin and tetracycline and its implication to the replication of the chromosome. Journal of General Microbiology 79, 3144.Google Scholar
Butler, L. O. & Smiley, M. B. (1970) Characterization by transformation of an ampicillin-resistant mutant of pneumococcus. Journal of General Microbiology 61, 189195.CrossRefGoogle ScholarPubMed
Butler, L. O. & Smiley, M. B. (1973) Mapping of the pneumococcus chromosome: application of the density-shift method. Journal of General Microbiology 76, 101113.CrossRefGoogle Scholar
Ephrussi-Taylor, H. (1951) Transformation allogenes du pneumocoque. Experimental Cell Research 2, 589607.CrossRefGoogle Scholar
Fazekas de St Groth, S. (1961) Evaluation of quantal neutralization tests. Nature 191, 891893.CrossRefGoogle Scholar
Goodgal, S. H. & Herriott, R. M. (1961) Studies on transformation of Hemophilus influenzas. I. Competence. Journal of General Physiology 44, 12011227.CrossRefGoogle ScholarPubMed
Lacks, S. (1970) Mutants of Diplococus pneumoniae that lack deoxyribonucleases and other activities possibly pertinent to genetic transformation. Journal of Bacteriology 101, 373383.Google Scholar
Nester, E. W. & Lederberg, J. (1961) Linkage of genetic units of Bacillus subtilis in DNA transformation. Proceedings of the National Academy of Science 47, 5255.CrossRefGoogle ScholarPubMed
Porter, R. D. & Guild, W. R. (1969) Number of transformable units per cell in Diplococcus pneumoniae. Journal of Bacteriology 97, 10331035.CrossRefGoogle ScholarPubMed
Ravin, A. W. (1966) Intergenic and intragenic recombination during DNA-induced transformation. The Physiology of Gene and Mutation Expression. Symposium of the Mutation Process, p. 139. Czechoslovak Academy of Science.Google Scholar
Ravin, A. W. & Chen, K. C. (1967) Heterospecific transformation of pneumococcus and streptococcus. III. Reduction of linkage. Genetics 57, 851864.CrossRefGoogle Scholar
Rotheim, M. B. & Ravin, A. W. (1964) Sites of breakage in the DNA molecule as determined by recombinational analysis of streptomycin-resistance mutations in pneumococcus. Proceedings of the National Academy of Science (U.S.A.) 52, 3038.CrossRefGoogle ScholarPubMed
Sicard, A. M. (1964) A new synthetic medium for Diplococcus pneumoniae and its use for the study of reciprocal transformation of the amiA locus. Genetics 50, 3144.CrossRefGoogle Scholar
Tiraby, G. & Sicard, A. M. (1973) Integration efficiency in DNA-induced transformation of Pneumococcus. II. Genetic studies of mutant integrating all the markers with a high efficiency. Genetics 75, 3548.CrossRefGoogle ScholarPubMed
Tiraby, G., Fox, M. S. & Bernheimer, H. (1975) Marker discrimination in deoxyribonucleic acid-mediated transformation of various Pneumococcus strains. Journal of Bacteriology 131, 608618.CrossRefGoogle Scholar
Tiraby, G., Claverys, J.-P. & Sicard, A. M. (1973) Integration efficiency in DNA-induced transformation of pneumococcus. I. A method of transformation in solid medium and its use for isolation of transformation-deficient and recombination-modified mutants. Genetics 75, 2333.CrossRefGoogle Scholar