Skip to main content
Log in

Integration of bacteriophages λ and ⊘80 in wild-type Escherichia coli at secondary attachment sites

II. Genetic structure and mechanism of polylysogen formation for λ, ⊘80 and the λatt80 hybrid

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

The frequency of occurrence and the genetic structure of polylysogens were studied for phages λ, ⊘80 and λatt80. In the case of λ, frequency of polylysogenization is high (0.20 to 0.41) with a tandem integration of prophages at the primary att site (attλ). With ⊘80 and λatt80, this frequency is about 10 times lower, and usually one prophage becomes integrated at the primary att site (att80-I) while another (sometimes two others) integrates at one of the secondary sites. At least four secondary att80 sites have been found in wild-type Escherichia coli Footnote 1, two of which (near the his and tolC loci) are preferred. The frequency of secondary integration of ⊘80 and λatt80 does not differ significantly in the wild-type host and in that deleted for the primary att site (0.041 and 0.045, respectively, among surviving cells at an MOI of 10).

Homoimmune superinfection has revealed a constitutive cI-independent expression of the ⊘80 int gene in the prophage state. The only ⊘80 tandem detected proved to be unstable. With the ⊘80int - mutant, we observed stabilization of ⊘80 tandems; as a consequence, their frequency of occurrence during coinfection with ⊘80int + was up to the λ level and no nontandem insertions were found. A model is proposed for the ⊘80 and λatt80 nontandem integration.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Notes

  1. By the \ldwild type\rd we mean strains with the primary att site

Abbreviations

TP:

transducing phage(s)

PFU:

plaque-forming units

PC:

pink λ clear-resistant colonies on EMBO plates

MOI:

multiplicity of infection

O :

origin of Hfr transfer

References

  • Arber W (1960) Polylysogeny for bacteriophage lambda. Virology 11:250–272

    Google Scholar 

  • Bachmann BJ, Low KB, Taylor AL (1976) Recalibrated linkage map of Escherichia coli K-12. Bacteriol Rev 40:116–150

    Google Scholar 

  • Bachmann BJ, Low B (1980) Linkage map of Escherichia coli K-12. Edition 6. Microbiol Rev 44:1–56

    Google Scholar 

  • Bertani G (1962) Multiple lysogeny from a single infection. Virology 18:131–139

    Google Scholar 

  • Bertani LE (1971) Stabilization of P2 tandem double lysogens by int mutations in the prophage. Virology 46:426–436

    Google Scholar 

  • Bertani G, Six E (1958) Inheritance of prophage P2 in bacterial crosses. Virology 6:357–381

    Google Scholar 

  • Campbell A, Zissler J (1966) The steric effect in lysogenization by bacteriophage lambda. Virology 28:659–662

    Google Scholar 

  • Freifelder D, Kirschner I (1971) The formation of homoimmune double lysogens of phage λ and segregation of single lysogens from them. Virology 44:633–637

    Google Scholar 

  • Gottesman M, Weisberg R (1971) Prophage integration and excision. In: Hershey AD (ed) The Bacteriophage Lambda. Cold Spring Harbor Lab, Cold Spring Harbor, New York, pp 113–139

    Google Scholar 

  • Gottesman ME, Yarmolinsky MB (1969) The integration and excision of the bacteriophage lambda genome. Cold Spring Harbor Symp Quant Biol 33:735–747

    Google Scholar 

  • Harris JD, Helling JS, Martinez II, Calendar R, Isaksson LA (1978) Temperature-sensitive Escherichia coli mutant producing a temperature-sensitive σ subunit of DNA dependent RNA polymerase. Proc Natl Acad Sci USA 75:6177–6181

    Google Scholar 

  • Ilyina TS, Zvorykina NM, Nechaeva EV, Svarchevsky AN, Rybchin VN (1977) Preferable secondary attachment site of prophage ⊘80 on the chromosome of Escherichia coli K-12. Genetika (Moskva) 13:1809–1820

    Google Scholar 

  • Kholodii GYa, Mindlin SZ (1984) Integration of bacteriophages λ and ⊘80 in wild-type Escherichia coli at secondary attachment sites. I. Formation of secondary lysogens. Mol Gen Genet 197:104–108

    Google Scholar 

  • Luria SE, Fraser DK, Adams JN, Burrous JW (1958) Lysogenization, transduction and genetic recombination in bacteria. Cold Spring Harbor Symp Quant Biol 23:71–82

    Google Scholar 

  • Mousset S, Thomas K (1969) Ter, a function which generates the ends of the mature λ chromosome. Nature 221:242–244

    Google Scholar 

  • Rybchin VN (1984) Genetics of bacteriophage ⊘80—a review. Gene 27:3–11

    Google Scholar 

  • Shimada K, Campbell A (1974) Int-constitutive mutants of bacteriophage lambda. Proc Natl Acad Sci USA 71:237–241

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by D. Goldfarb

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kholodii, G.Y., Mindlin, S.Z. Integration of bacteriophages λ and ⊘80 in wild-type Escherichia coli at secondary attachment sites. Mol Gen Genet 198, 491–496 (1985). https://doi.org/10.1007/BF00332945

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00332945

Keywords

Navigation