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Aberrant immunity behaviour of hybrid λimm 21 phages containing the DNA of ColE1-type plasmids

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Summary

Hybrid λ and λimm 21 bacteriophages carrying various ColE1-type plasmids have been constructed in vitro. The λimm 21/plasmid recombinants display aberrant immunity behaviour, giving clear plaques under conditions where the parental phages give turbid ones and being able to grow on homoimmune lysogens. λimm λ/plasmid recombinants show no such unusual behaviour. Studies with hybrids of a λimm 21 cITS phage carrying pMB9 DNA showed the operation of the plasmid's replication system to be the basic cause of the aberrant immunity behaviour. The plasmid replication system could act as a complete alternative to the phage system during vegetative phage growth. The probable reason that λimm 21 phages show such altered phenotypes when carrying a functional plasmid replication origin, whereas λimm λ and λimm 434 (Mukai et al., 1978) phages do not, is the relative ease of titration of the phage 21 repressor to allow transcription from p R 21. Various uses are considered for the altered phenotypic behaviour of λimm 21/ColE1-type plasmid hybrids.

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References

  • Appleyard, R.K.: Segregation of new lysogenic types during growth of a doubly lysogenic strain derived from Escherichia coli K12. Genetics 39, 440–452 (1954)

    Google Scholar 

  • Bazaral, M., Helinski, D.R.: Circular DNA forms of colicinogenic factors E1, E2 and E3 from Escherichia coli. J. Mol. Biol. 36, 185–194 (1968)

    Google Scholar 

  • Benton, W.D., Davis, R.W.: Screening λgt recombinant clones by hybridization to single plaques in situ. Science 196, 180–182 (1977)

    Google Scholar 

  • Blattner, F.R., Williams, B.G., Blechl, A.E., Denniston-Thompson, K., Faber, H.E., Furlong, L.-A., Grunwald, D.J., Kiefer, D.O., Moore, D.D., Schum J.W., Sheldon, E.L., Smithies, O.: Charon phages: safer derivatives of bacteriophage lambda for DNA cloning. Science 196, 161–169 (1977)

    Google Scholar 

  • Borck, K., Beggs, J.D., Brammar, W.J., Hopkins, A.S., Murray N.E.: The construction in vitro of transducing derivatives of phage lambda. Mol. Gen. Genet. 146, 199–207 (1976)

    Google Scholar 

  • Cabello, F., Timmis, K., Cohen, S.N.: Replication control in a composite plasmid constructed by in vitro linkage of two distinct replicons. Nature 259, 285–290 (1976)

    Google Scholar 

  • Clarke, L., Carbon, J.: Functional expression of cloned yeast DNA in Escherichia coli: Specific complementation of argino-succinate lyase (arg H) mutations. J. Mol. Biol. 120, 517–532 (1978)

    Google Scholar 

  • Couturier, M., Dambly, C.: Activation séquentielle des fonctions tardives chez les bactériophages tempérés Compt. Rend. Acad. Sci. Paris 270, 428–430 (1970)

    Google Scholar 

  • Dove, W.F., Inokuchi, H., Stevens, W.F.: Replication control in phage lambda. In: The bacteriophage lambda (A.D. Hershey, ed.). pp. 747–771. New York, Cold Spring Harbor Laboratories 1971

    Google Scholar 

  • Enquist, L.W., Skalka, A.: Replication of bacteriophage λDNA dependent on the function of host and viral genes. I. Interaction of red, gam and rec. J. Mol. Biol. 75, 185–212 (1973)

    Google Scholar 

  • Franklin, N.C.: The N operon of lambda: extent and regulation as observed in fusions to the tryptophan operon of Escherichia coli. In: The bacteriophage lambda (A.D. Hershey, ed.) pp. 621–638. New York: Cold Spring Harbor Laboratories 1971

    Google Scholar 

  • Friedman, D.I., Ponce-Campos, R.: Differential effect of phage regulator functions on transcription from various promoters. J. Mol. Biol. 98, 537–549 (1975)

    Google Scholar 

  • Gall, J.G., Pardue, M.L.: Nucleic acid hybridizations in cytological preparations. Methods Enzymol. 21D, 470–480 (1971)

    Google Scholar 

  • Geider, K.: Molecular aspects of DNA replication in Escherichia coli systems. Curr. Top. Microbiol. Immunol. 74, 55–112 (1976)

    Google Scholar 

  • Georgopoulos, C.P., Herskowitz, I.: Escherichia coli mutants blocked in lambda DNA synthesis. In: The bacteriophage lambda (A.D. Hershey, ed.), pp. 553–564. New York: Cold Spring Harbor Laboratories 1971

    Google Scholar 

  • Goebel, W., Schrempf, H.: Replication of plasmid DNA in temperature-sensitive DNA replication mutants of Escherichia coli. Biochim. Biophys. Acta 262 32–41 (1972)

    Google Scholar 

  • Greenstein, M., Skalka, A.: Replication of bacteriophage lambda DNA: in vivo studies of the interaction between the viral gamma protein and the host recBC DNAase. J. Mol. Biol. 97, 543–559 (1975)

    Google Scholar 

  • Heffron, F., Bedinger, P., Champoux, J.J., Falkow, S.: Deletions affecting the transposition of an antibiotic resistance gene. Proc. Natl. Acad. Sci. U.S.A. 74, 702–706 (1977)

    Google Scholar 

  • Henderson, D., Weil, J.: Recombination-deficient deletions in phage lambda and their interaction with chi mutations. Genetics 79, 143–174 (1975)

    Google Scholar 

  • Jacob, F., Wollman, E.L.: Étude génétique d'un bactériophage tempéré d'Escherichia coli. I. Le système génétique du bactériophage λ. Ann. Inst. Pasteur Lille 87, 653–673 (1954)

    Google Scholar 

  • Kahn, M., Helinski, D.R.: Construction of a novel plasmid-phage hybrid: use of the hybrid to demonstrate ColE1 replication in vivo in the absence of a ColE1 specified protein. Proc. Natl. Acad. Sci. U.S.A. 75, 2200–2204 (1978)

    Google Scholar 

  • Katz, L., Kingsbury, D.T., Helinski, D.R.: Stimulation by cyclic adenosine monophosphate of plasmid DNA replication and catabolite repression of the plasmid DNA-protein relaxation complex. J. Bacteriol. 114, 577–591 (1973)

    Google Scholar 

  • Lederberg, E.M., Cohen, S.N.: Transformation of Salmonella typhimurium by plasmid deoxyribonucleic acid. J. Bacteriol 119, 1072–1074 (1974)

    Google Scholar 

  • Lennox, E.S.: Transduction of linked characters of the host of bacteriophage P1. Virology 1, 190–206 (1955)

    Google Scholar 

  • Mukai, T., Ohkubo, H., Shimada, K., Takagi, Y.: Isolation and characterisation of a plaque-forming lambda bacteriophage carrying a ColE1 plasmid. J. Bacteriol. 135, 171–177 (1978)

    Google Scholar 

  • Murray, N.E., Brammar, W.J., Murray K: Lambdoid phages that simplify recovery of in vitro recombinants. Mol. Gen. Genet. 150, 53–61 (1977)

    Google Scholar 

  • Murray, N.E., Manduca de Ritis, P., Foster, L.A.:DNA targets for the Escherichia coli K restriction system analysed genetically in recombinants between phages phi80 and lambda. Mol. Gen. Genet. 120, 261–281 (1973)

    Google Scholar 

  • Old, R., Murray, K., Roizes, G.: Recognition sequence of restriction endonuclease III from Haemophilus influenzae. J. Mol. Biol. 92, 331–339 (1975)

    Google Scholar 

  • Parkinson, J.S.: Genetics of the left arm of the chromosome of bacteriophage lambda. Genetics 59, 311–325 (1968)

    Google Scholar 

  • Perlman, D.: Frequency of replication from alternative origins in the composite R plasmid NR1. J. Bacteriol. 133, 729–736 (1978)

    Google Scholar 

  • Ptashne, M.: Repressor and its action. In: The bacteriophage lambda (A.D. Hershey, ed.), pp. 221–238. New York: Cold Spring Harbor Laboratories 1971

    Google Scholar 

  • Ptashne, M., Hopkins, N.: The operators controlled by the λ phage repressor. Proc. Natl. Acad.Sci. U.S.A. 60, 1282–1287 (1968)

    Google Scholar 

  • Rownd, R.H.: Plasmid replication. In: DNA synthesis present and future. NATO Advanced Institute Series, Series A, Life Sciences (Molineux, J. and Kohiyama, M., eds.) Vol. 17, pp. 751–772. New York and London: Plenum Press 1977

    Google Scholar 

  • Sakaki, Y., Karu, A.E., Linn, S., Echols, H.: Purification and properties of the γ-protein specified by bacteriophage λ: an inhibitor of the host recBC recombination enzyme. Proc. Natl. Acad. Sci. U.S.A. 70, 2215–2219 (1973)

    Google Scholar 

  • Sly, W.S., Rabideau, K.: The mechanism of λc17cI virulence. J. Mol. Biol. 42, 385–400 (1969)

    Google Scholar 

  • Smith, H.O., Nathans, D.: Nomenclature for restriction enzymes. J. Mol. Biol. 81, 419–423 (1973)

    Google Scholar 

  • Stahl, F.W., Crasemann, J.N., Stahl, M.M.: Rec-mediated recombinational hot spot activity in phage lambda. III. Chi mutations are site-mutations stimulating rec-mediated recombination. J. Mol. Biol. 94, 203–212 (1975)

    Google Scholar 

  • Staudenbauer, W.L., Lanka, E., Schuster, H.: Replication of small plasmids in extracts of E. coli. Mol. Gen. Genet. 162, 243–249 (1978)

    Google Scholar 

  • Timmis, K., Cabello, F., Cohen, S.N.: Utilization of two distinct modes of replication by a hybrid plasmid constructed in vitro from separate replicons. Proc. Natl. Acad. Sci. U.S.A. 71, 4556–4560 (1974)

    Google Scholar 

  • Warren, G., Sherratt, D.: Incompatibility and transforming efficiency of ColE1 and related plasmids. Mol. Gen. Genet. 161, 39–47 (1978)

    Google Scholar 

  • Weil, J., Signer, E.R.: Recombination in bacteriophage λ. II. Site specific recombination promoted by the integration system. J. Mol. Biol. 34, 273–279 (1968)

    Google Scholar 

  • Yanofsky, C., Ito, J.: Nonsense condons and polarity in the tryptophan operon. J. Mol. Biol. 21, 313–344 (1966)

    Google Scholar 

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Communicated by B.A. Bridges

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Windass, J.D., Brammar, W.J. Aberrant immunity behaviour of hybrid λimm 21 phages containing the DNA of ColE1-type plasmids. Molec. Gen. Genet. 172, 329–337 (1979). https://doi.org/10.1007/BF00271733

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