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Isolation and characterization of deletion mutants affected in early genes of bacteriophage ϕ80

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Summary

When Escherichia coli cells that had been irradiated with ultraviolet light were infected with bacteriophage ϕ80, five major (pE, pB, pA, pC and pD) and two minor (pU and pV) proteins were found to be synthesized during early stages of infection. The genss coding for the five major proteins were mapped on the ϕ80 chromosome using various deletion mutants which lacked the capacity to synthesize some or all the major proteins. The size and positions of all the deletions were determined by gel electrophoresis of EcoRI digests of phage DNA and by electron microscopy of heteroduplexes between DNAs of the deletion and wild-type phage. The five major proteins designated pE(25K), pB(40K), pA(45K), pC(34K) and pD(31K) were shown to be encoded in this order presumably by a single operon that was located at 60.2–67.4% on the ϕ80 genome. These proteins were found to be involved in phage recombination. The absence of pE or pB resulted in a Red phenotype and the absence of three proteins (pE, pB and pA) resulted in a Fec phenotype. The exact positions of the genes for the minor proteins pU(29K) and pV(26K) have not been determined.

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References

  • Beck E, Sommer R, Auerswald EA, Kurz C, Zink B, Osterburg G, Schaller H, Sugimoto K, Sugisaki H, Okamoto T, Takanami M (1978) Nucleotide sequence of bacteriophage fd DNA. Nucl Acids Res 5:4495–4503

    Google Scholar 

  • Childs GJ, Ohtsubo H, Ohtsubo E, Sonnenberg F, Freundlich M (1977) Restriction endonuclease mapping of the Escherichia coli K12 chromosome in the vicinity of the ilv genes. J Mol Biol 117:175–193

    Google Scholar 

  • Davis RW, Simon M, Davidson N (1971) Electron microscope heteroduplex methods for mapping regions of base sequence homology in nucleic acids. In: Colowick SP, Kaplan NO (eds) Methods in enzymology, vol 21 D. Academic Press, New York, p 413–428

    Google Scholar 

  • Fiandt M, Hradecna Z, Lozeron HA, Szybalski W (1971) Electron micrographic mapping of deletions, insertions, inversions, and homologies in the DNAs of coliphages lambda and phi 80. In: Hershey AD (ed) The bacteriophage lambda. Cold Spring Harbor Laboratories, New York, p 329–354

    Google Scholar 

  • Gelfand DH, Hayashi M (1969) Electrophoretic characterization of ϕx-174 specific proteins. J Mol Biol 44:501–516

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Matsushiro A (1961) Isolation of UV-inducible temperate phage ϕ80. Biken J 4:133–135

    Google Scholar 

  • Matsushiro A, Sato K, Kida S (1964) Characteristics of the transducing elements of bacteriophage ϕ80. Virology 23:299–306

    Google Scholar 

  • Morita T, Matsushiro A (1981) Regulation of early gene expression of bacteriophage ϕ80: Transcriptional regulation by ϕ80 gene 30. (in preparation)

  • Oppenheim AB, Katzir N, Oppenheim A (1977) Regulation of protein synthesis in bacteriophage λ. Restoration of gene expression in λN strains by mutation in the cro gene. Virology 79:405–425

    Google Scholar 

  • Radding CM (1966) Regulation of exonuclease. I. Properties of exonuclease purified from lysogens of T11 and wild type. J Mol Biol 18:235–250

    Google Scholar 

  • Sato K, Nishimune Y, Numich R, Matsushiro A, Inokuchi H, Ozeki H (1968) Suppressor-sensitive mutants of coliphage ϕ80. Virology 34:637–649

    Google Scholar 

  • Signer E (1971) General recombination. In: Hershey AD (ed) The bacteriophage lambda. Cold Spring Harbor Laboratories, New York, p 139–174

    Google Scholar 

  • Signer E, Weil J (1968) Recombination in bacteriophage λ. I. Mutants deficient in general recombination. J Mol Biol 34:261–271

    Google Scholar 

  • Simon MN, Studier FW (1973) Physical mapping of the early region of bacteriophage T7 DNA. J Mol Biol 79:249–265

    Google Scholar 

  • Smith MG (1967) Isolation of high molecular weight DNA from normal and phage-infected Escherichia coli. In: Grossman L, Moldave K (eds) Methods in enzymology vol 12A. Academic Press, New York, p 545–550

    Google Scholar 

  • Yamagishi H, Inokuchi H, Ozeki H (1976a) Excision and duplication of su3+-transducing fragments carried by bacteriophage ϕ80. I. Novel structure of ϕ80 sus2psu3+ DNA molecule. J Virology 18:1016–1023

    Google Scholar 

  • Yamagishi H, Inokuchi H, Ozeki H (1976b) Excision and duplication of su3+-transducing fragments carried by bacteriophage ϕ80. II. Red- or rec-dependent excision and duplication. J Mol Biol 106:133–150

    Google Scholar 

  • Yamagishi H, Ozeki H (1972) Comparative study of thermal inactivation of phage ϕ80 and lambda. Virology 48:316–322

    Google Scholar 

  • Zissler J, Signer E, Schaefer F (1971) The role of recombination in growth of bacteriophage lambda. I. The gamma gene. In: Hershey AD (ed) The bacteriophage lambda. Cold Spring Harbor Laboratories, New York, p 455–468

    Google Scholar 

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Communicated by T. Yura

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Morita, T., Ichikawa, N., Yamaguchi, T. et al. Isolation and characterization of deletion mutants affected in early genes of bacteriophage ϕ80. Molec. Gen. Genet. 183, 144–151 (1981). https://doi.org/10.1007/BF00270153

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  • DOI: https://doi.org/10.1007/BF00270153

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