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Transposon-Directed Mutagenesis and Chromosome Mobilization in Acinetobacter calcoaceticus EBF65/65

Published online by Cambridge University Press:  14 April 2009

K. J. Towner
Affiliation:
Department of Microbiology and PHLS Laboratory, University Hospital, Queen's Medical Centre, Nottingham NG7 2UH

Summary

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RP4::Mu was used to insert Tn3171 into the Acinetobacter calcoaceticus EBF65/65 chromosome. Insertions occurred at a frequency of approximately 10−7 per recipient cell. Auxotrophic mutations resulted from 28% of the Tn3171 insertions examined, with a possible ‘hot-spot’ for insertion in a gene for arginine biosynthesis. The frequency of subsequent precise excision of Tn3171 from the chromosome was less than 10−10. When attempts were made using RP4 derivatives to mobilize the chromosome from a strain containing an arg::Tn3171 insertion, it was found that the enhanced transfer frequency of the adjacent region of the chromosome was dependent on the original Tn3171 insertion, but was independent of the presence of Tn3171 on the mobilizing plasmid.

Type
Short Paper
Copyright
Copyright © Cambridge University Press 1983

References

REFERENCES

Harayama, S., Tsuda, M. & Iino, T.(1980). High frequency mobilization of the chromosome of Escherichia coli by a mutant of plasmid RP4 temperature-sensitive for maintenance. Molecular and General Genetics 180, 4756.CrossRefGoogle ScholarPubMed
Hinchliffe, E., Nugent, M. E. & Vivian, A. (1980). Naturally occurring plasmids in Acinetobacter calcoaceticus: pAV2, a plasmid which influences the fertility of the sex factor pAVl. Journal of General Microbiology 121, 411418.Google Scholar
Holloway, B. W. (1979). Plasmids that mobilize bacterial chromosome. Plasmid 2, 119.CrossRefGoogle ScholarPubMed
Lichtenstein, C. & Brenner, S. (1982). Unique insertion site of Tn7 in the E. coli chromosome. Nature 297, 601603.CrossRefGoogle ScholarPubMed
Sherratt, D. (1981). In vivo genetic manipulation in bacteria. In Genetics as a Tool in Microbiology (ed. Glover, S. W. and Hopwood, D. A.), p. 43. Cambridge University Press.Google Scholar
Towner, K. J. (1978). Chromosome mapping in Acinetobacter calcoaceticus. Journal of General Microbiology 104, 175180.CrossRefGoogle ScholarPubMed
Towner, K. J. (1980). Behaviour of bacteriophage Mu in Acinetobacter calcoaceticus EBF65/65. Journal of General Microbiology 121, 425431.Google ScholarPubMed
Towner, K. J. (1981): A clinical isolate of Escherichia coli owing its trimethoprim resistance to a chromosomally-located trimethoprim transposon. Journal of Antimicrobial Chemotherapy 7, 157162.CrossRefGoogle ScholarPubMed
Towner, K. J. & Vivian, A. (1976 a). RP4-mediated chromosome mobilization in Acinetobacter calcoaceticus. Journal of General Microbiology 93, 355360.CrossRefGoogle Scholar
Towner, K. J. & Vivian, A. (1976 b). RP4 fertility variants in Acinetobacter calcoaceticus. Genetical Research 28, 301306.CrossRefGoogle ScholarPubMed
Towner, K. J. & Vivian, A. (1977). Plasmids capable of transfer and chromosome mobilization in Acinetobacter calcoaceticus. Journal of General Microbiology 101, 167171.CrossRefGoogle Scholar