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Physical and genetical analysis of bacteriophage T4 generalized transduction

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Summary

This report describes a comparison of the efficiency of transduction of genes in E. coli by the generalized transducing bacteriophages T4GT7 and P1CM. Both phages are capable of transducing many genetic markers in E. coli although the frequency of transduction for particular genes varies over a wide range. The frequency of transduction for most genes depends on which transducing phage is used as well as on the donor and recipient bacterial strains. Analysis of T4GT7 phage lysates by cesium chloride density gradient centrifugation shows that transducing phage particles contain primarily bacterial DNA and carry little, if any, phage DNA. In this regard transducing phages P1CM and T4GT7 are similar; both phages package either bacterial or phage DNA but not both DNAs into the same particle.

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References

  • Chelala CA, Margolin P (1974) Effects of deletions on co-transduction linkage in Salmonella typhimurium. Mol Gen Genet 131:97–112

    Google Scholar 

  • Drexler H (1970) Transduction by bactriophage T1. Proc Natl Acad Sci USA 66:1083–1088

    Google Scholar 

  • Ikeda H, Tomizawa JI (1965) Transducing fragments in generalized transduction by phage P1. J Mol Biol 14:85–109

    Google Scholar 

  • Jackson EN, Laski F, Andres C (1982) Bacteriophage P22 mutants that alter the specificity of DNA packaging. J Mol Biol 154:551–564

    Google Scholar 

  • Koerner JF, Snustad DP (1979) Shut-off of host macromolecular synthesis after T-even bacteriophage infection. Microbiol Rev 43:199–223

    Google Scholar 

  • Kondo E, Mitsuhashi S (1964) Drug resistance of enteric bacteria. IV. Active transducing bacteriophage P1CM produced by the combination of R-factor with bacteriophages P1. J Bacteriol 88:1266–1276

    Google Scholar 

  • Laski F, Jackson EN (1982) Maturation cleavage of bacteriophage P22 DNA in the absence of DNA packaging. J Mol Biol 154:565–579

    Google Scholar 

  • Lennox ES (1955) Transduction of linked genetic characters of the host by bacteriophage P1. Virology 1:190–206

    Google Scholar 

  • Luria SE, Adams JN, Ting RC (1960) Tranduction of lactose utilizing ability among strains of E. coli and S. dysenteriae and the properties of the transducing phage particles. Virology 12:348–390

    Google Scholar 

  • Masters M (1977a) The frequency of P1 transduction of the genes of Escherichia coli as a function of chromosomal position: Preferential transduction of the origin of replication. Mol Gen Genet 155:197–202

    Google Scholar 

  • Masters M (1977b) P1 transduction frequencies: A clue to chromosome structure? In: Molineux I, Kohijama M (eds) DNA synthesis. Plenum, New York, p 431

    Google Scholar 

  • Miller J (1972) In: Experiments in Molecular Genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor NY

    Google Scholar 

  • Morton D, Kutter EM, Guttman BS (1978) Synthesis of T4 DNA and bacteriophage in the absence of dCMP hydroxymethylase. J Virol 28:262–269

    Google Scholar 

  • Newman BJ, Masters M (1980) The variation in frequency with which markers are transduced by phage P1 is primarily a result of discrimination during recombination. Mol Gen Genet 180:585–589

    Google Scholar 

  • Ramsey N, Ritchie DA (1983) Uncoupling of initiation site cleavage from subsequent headful cleavages in bacteriophage T1 DNA packaging. Nature (London) 301:264–266

    Google Scholar 

  • Schmieger H (1970) The molecular structure of the transducing particles of Salmonella phage P22. Mol Gen Genet 109:323–337

    Google Scholar 

  • Schmieger H (1972) Phage P22 mutants with increased or decreased transduction abilities. Mol Gen Genet 119:75–88

    Google Scholar 

  • Schmieger H, Buck U (1975) Apperance of transducing particles and the fate of host DNA after infection of Salmonella typhimurium with P22-mutants with increased transducing ability (HT-mutants)

  • Snustad DP, Bursch CJH, Hefeneider SH (1976) Mutants of bacteriophage T4 deficient in the ability to induce nuclear disruption. J Virol 18:268–288

    Google Scholar 

  • Streisinger G, Emrich J, Stahl MM (1967) Chromosome structure in phage T4, terminal redundancy and length determination. Proc Natl Acad Sci USA 57:292–295

    Google Scholar 

  • Susskind MM, Botstein D (1978) Molecular genetics of bacteriophage P22. Mirobiol Rev 42:385–413

    Google Scholar 

  • Tye BK, Huberman JA, Botstein DJ (1974) Non-random permutation of phage P22 DNA. J Mol Biol 85:501–532

    Google Scholar 

  • Weaver HR, Snustad DP, Jorgenson SE, Koerner JG (1970) Isolation of T4 mutants defective in the ability to degrade host deoxyribonucleic acid. J Virol 5:700–705

    Google Scholar 

  • Wilson GG, Young KKY, Edlin GJ, Konigsberg W (1979) High frequency generalized transduction by bacteriophage T4. Nature (London) 280:80–82

    Google Scholar 

  • Young KKY, Edlin GJ, Wilson GG (1982) Genetic analysis of bacteriophage T4 transducing bacteriophages. J Virol 41:345–347

    Google Scholar 

  • Zinder ND, Lederberg J (1952) Genetic exchange in Salmonella. J Bacteriol 64:679–699

    Google Scholar 

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Communicated by G. O'Donovan

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Young, K.K.Y., Edlin, G. Physical and genetical analysis of bacteriophage T4 generalized transduction. Molec Gen Genet 192, 241–246 (1983). https://doi.org/10.1007/BF00327673

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  • DOI: https://doi.org/10.1007/BF00327673

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