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. 1979 Jan;137(1):635-43.
doi: 10.1128/jb.137.1.635-643.1979.

Plasmid copy number control: isolation and characterization of high-copy-number mutants of plasmid pE194

Plasmid copy number control: isolation and characterization of high-copy-number mutants of plasmid pE194

B Weisblum et al. J Bacteriol. 1979 Jan.

Abstract

A plasmid, pE194, obtained from Staphylococcus aureus confers resistance to macrolide, lincosamide, and streptogramin type B ("MLS") antibiotics. For full expression, the resistance phenotype requires a period of induction by subinhibitory concentrations of erythromycin. A copy number in the range of 10 to 25 copies per cell is maintained during cultivation at 32 degrees C. It is possible to transfer pE194 to Bacillus subtilis by transformation. In B. subtilis, the plasmid is maintained at a copy number of approximately 10 per cell at 37 degrees C, and resistance is inducible. Tylosin, a macrolide antibiotic which resembles erythromycin structurally and to which erythromycin induces resistance, lacks inducing activity. Two types of plasmid mutants were obtained and characterized after selection on medium containing 10 microgram of tylosin per ml. One mutant class appeared to express resistance constitutively and maintained a copy number indistinguishable from that of the parent plasmid. The other mutant type had a 5- to 10-fold-elevated plasmid copy number (i.e., 50 to 100 copies per cell) and expressed resistance inducibly. Both classes of tylosin-resistant mutants were shown to be due to alterations in the plasmid and not to modifications of the host genome.

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References

    1. Arch Roum Pathol Exp Microbiol. 1976 Jan-Jun;35(1-2):111-8 - PubMed
    1. J Mol Biol. 1976 May 5;103(1):199-208 - PubMed
    1. Ann Inst Pasteur (Paris). 1956 Jun;90(6):787-90 - PubMed
    1. Eur J Biochem. 1976 Jan 2;61(1):101-17 - PubMed
    1. Eur J Biochem. 1976 Jan 2;61(1):119-38 - PubMed

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