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Transduction of multi-copy plasmid pBR322 by bacteriophage Mu

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Summary

The temperate bacteriophage Mu transduces the 4363 bp multi-copy plasmid pBR322 at frequencies similar to those of chromosomal markers. Plasmid transducing particles contain DNA molecules of Mu DNA length. Plasmid DNA is transduced as a head-to-tail oligomer that becomes circularized in the recipient cell. The rec system of the donor strain participates in oligomer formation and the rec system of the recipient strain is required for oligomer circularization. Possible mechanisms that may explain the origin of plasmid transducing particles are discussed.

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References

  • Allet B, Bukhari AI (1975) Analysis of Mu and λ-Mu hybrid DNAs by specific endonucleases. J Mol Biol 92:529–540

    Google Scholar 

  • Bolivar F, Rodriquez R, Greene PJ, Betlach M, Heyneker HL, Boyer HW, Crosa J, Falkow S (1977) Construction and characterization of new cloning vehicles. Gene 2:95–113

    Google Scholar 

  • Bukhari AI, Ljungquist E (1977) Bacteriophage Mu: Methods for cultivation and use. In: Bukhari AI, Shapiro JA, Adhya SL (eds) DNA insertion elements, plasmids and episomes. Cold Spring Harbor Press, New York, pp 749–756

    Google Scholar 

  • Bukhari AI, Taylor AL (1975) Influence of insertions on packaging of host sequences covalently linked to bacteriophage Mu DNA. Proc Natl Acad Sci USA 72:4399–4403

    Google Scholar 

  • Bukhari AI, Froshauer S, Botchan M (1976) Ends of bacteriophage Mu DNA. Nature 264:580–583

    Google Scholar 

  • Canosi U, Lüder G, Trautner TA (1982) SPP1-mediated plasmid transduction. J Virol 44:431–436

    Google Scholar 

  • Clewell DB (1972) Nature of ColE1 plasmid replication in Escherichia coli in the presence of chloramphenicol. J Bacteriol 110:667–676

    Google Scholar 

  • Cohen SN, Chang ACY, Hsu L (1972) Nonchromosomal antibiotic resistance in bacteria: Genetic transformation of Escherichia coli by R-factor DNA. Proc Natl Acad Sci USA 69:2110–2114

    Google Scholar 

  • Couturier M, Van Vliet F (1974) Vegetative recombination in bacteriophage Mu-1. Virology 60:1–8

    Google Scholar 

  • Daniell E, Abelson J, Kim JS, Davidson N (1973) Heteroduplex structures of bacteriophage Mu DNA. Virology 51:237–239

    Google Scholar 

  • Daniell E, Kohne DE, Abelson J (1975) Characterization of the inhomogeneous DNA in virions of bacteriophage Mu by DNA reannealing kinetics. J Virol 15:739–743

    Google Scholar 

  • Doherty MJ, Morrison PT, Kolodner R (1983) Genetic recombination of bacterial plasmid DNA. Physical and genetical analysis of the products of plasmid recombination in Escherichia coli. J Mol Biol 167:539–560

    Google Scholar 

  • Faelen M, Toussaint A, Couturier M (1971) Mu-1 promoted integration of a λ-gal phage in the chromosome of Escherichia coli. Mol Gen Genet 113:367–370

    Google Scholar 

  • Feiss M, Siegele DA, Rudolph CF, Frackman S (1982) Cosmid DNA packaging in vivo. Gene 17:123–130

    Google Scholar 

  • Howe MM (1973) Transduction by bacteriophage Mu-1. Virology 55:103–117

    Google Scholar 

  • Hsu MT, Davidson N (1974) Electron microscope heteroduplex study of the heterogeneity of Mu phage and prophage DNA. Virology 58:229–239

    Google Scholar 

  • Iida S, Meyer J, Kenedy KE, Arber W (1982) A site-specific, conservative recombination system carried by bacteriophage P1. Mapping the recombinase gene cin and the crossover site cix for the inversion of the C segment. EMBO J 1:1445–1453

    Google Scholar 

  • Ish-Horowicz D, Burke JF (1981) Rapid and efficient cosmid cloning. Nucl Acids Res 9:2989–2998

    Google Scholar 

  • Peden KWC (1983) Revised sequence of the tetracycline resistance gene of pBR322. Gene 22:277–280

    Google Scholar 

  • Priess H, Kamp D, Kahmann R, Bräuer B, Delius H (1982) Nucleotide sequence of the immunity region of bacteriophage Mu. Mol Gen Genet 186:315–321

    Google Scholar 

  • Radloff R, Bauer W, Vinograd J (1967) A dye-buoyant-density method for detection and isolation of closed circular duplex DNA: The closed circular DNA in Hela cells. Proc Natl Acad Sci USA 57:1514–1521

    Google Scholar 

  • Rigby PWJ, Dieckmann M, Rhoses C, Berg P (1977) labelling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase III. Mol Gen Genet 149:131–134

    Google Scholar 

  • Schaus NA, Wright A (1980) Inhibition of the Escherichia coli exonuclease V by bacteriophage Mu. Virology 102:214–217

    Google Scholar 

  • Shimada K, Umene K, Nakamura T, Takagi Y (1978) Recombination in hybrid ColE1 DNAs as analysed by λ-mediated transduction. Cold Spring Harbor Symp Quant Biol 43:991–998

    Google Scholar 

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517

    Google Scholar 

  • Sutcliffe JG (1978) Complete nucleotide sequence of the Escherichia coli plasmid pBR322. Cold Spring Harbor Symp Quant Biol 43:77–90

    Google Scholar 

  • Takahashi H, Saito H (1982) Mechanism of pBR322 transduction mediated by cytosine-substituting T4 bacteriophage. Mol Gen Genet 186:497–500

    Google Scholar 

  • Teifel-Greding J (1984) Integrative suppression — a way to detect homologies between the Escherichia coli chromosome and cloned DNA fragments. FEMS Microbiol Lett, in press

  • Teifel J, Schmieger H (1979) The origin of the DNA in transducing particles of bacteriophage Mu. Density gradient analyses of intact phages. Mol Gen Genet 176:293–295

    Google Scholar 

  • Teifel J, Schmieger H (1981a) The origin of the DNA in transducing particles of bacteriophage Mu. Density gradient analyses of DNA. Mol Gen Genet 184:312–313

    Google Scholar 

  • Teifel J, Schmieger H (1981b) The influence of host DNA replication on the formation of infectious and transducing Mu particles. Mol Gen Genet 184:308–311

    Google Scholar 

  • To CA, Eisenstark A, Toreci H (1966) Structure of mutator phage Mu-1 of E. coli. J Ultrastruct Res 14:441–448

    Google Scholar 

  • Twigg AJ, Sherratt DJ (1980) Trans-complementable copy-number mutants of plasmid ColE1. Nature 283:216–218

    Google Scholar 

  • Umene K, Shimada K, Tagaki Y (1978) Packaging of ColE1 DNA having a Lambda phage cohesive end site. Mol Gen Genet 159:39–45

    Google Scholar 

  • Van Vliet F, Couturier M, De Lafonteyne J, Jedlicki E (1978) Mu-1 directed inhibition of DNA breakdown in E. coli recA cells. Mol Gen Genet 164:109–112

    Google Scholar 

  • Warren GJ, Clark AJ (1980) Sequence specific recombination of plasmid ColE1. Proc Natl Acad Sci USA 77:6724–6728

    Google Scholar 

  • Wijffelman CA, Westmaas GC, van de Putte P (1972) Vegetative recombination of bacteriophage Mu-1 in Escherichia coli. Mol Gen Genet 116:40–46

    Google Scholar 

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Communicated by H. Böhme

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Teifel-Greding, J. Transduction of multi-copy plasmid pBR322 by bacteriophage Mu. Mol Gen Genet 197, 169–174 (1984). https://doi.org/10.1007/BF00327938

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  • DOI: https://doi.org/10.1007/BF00327938

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