Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Feb;177(3):586–595. doi: 10.1128/jb.177.3.586-595.1995

Characterization of genetic elements required for site-specific integration of Lactobacillus delbrueckii subsp. bulgaricus bacteriophage mv4 and construction of an integration-proficient vector for Lactobacillus plantarum.

L Dupont 1, B Boizet-Bonhoure 1, M Coddeville 1, F Auvray 1, P Ritzenthaler 1
PMCID: PMC176632  PMID: 7836291

Abstract

Temperate phage mv4 integrates its DNA into the chromosome of Lactobacillus delbrueckii subsp. bulgaricus strains via site-specific recombination. Nucleotide sequencing of a 2.2-kb attP-containing phage fragment revealed the presence of four open reading frames. The larger open reading frame, close to the attP site, encoded a 427-amino-acid polypeptide with similarity in its C-terminal domain to site-specific recombinases of the integrase family. Comparison of the sequences of attP, bacterial attachment site attB, and host-phage junctions attL and attR identified a 17-bp common core sequence, where strand exchange occurs during recombination. Analysis of the attB sequence indicated that the core region overlaps the 3' end of a tRNA(Ser) gene. Phage mv4 DNA integration into the tRNA(Ser) gene preserved an intact tRNA(Ser) gene at the attL site. An integration vector based on the mv4 attP site and int gene was constructed. This vector transforms a heterologous host, L. plantarum, through site-specific integration into the tRNA(Ser) gene of the genome and will be useful for development of an efficient integration system for a number of additional bacterial species in which an identical tRNA gene is present.

Full Text

The Full Text of this article is available as a PDF (628.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abremski K. E., Hoess R. H. Evidence for a second conserved arginine residue in the integrase family of recombination proteins. Protein Eng. 1992 Jan;5(1):87–91. doi: 10.1093/protein/5.1.87. [DOI] [PubMed] [Google Scholar]
  2. Argos P., Landy A., Abremski K., Egan J. B., Haggard-Ljungquist E., Hoess R. H., Kahn M. L., Kalionis B., Narayana S. V., Pierson L. S., 3rd The integrase family of site-specific recombinases: regional similarities and global diversity. EMBO J. 1986 Feb;5(2):433–440. doi: 10.1002/j.1460-2075.1986.tb04229.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ball C. A., Johnson R. C. Efficient excision of phage lambda from the Escherichia coli chromosome requires the Fis protein. J Bacteriol. 1991 Jul;173(13):4027–4031. doi: 10.1128/jb.173.13.4027-4031.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ball C. A., Johnson R. C. Multiple effects of Fis on integration and the control of lysogeny in phage lambda. J Bacteriol. 1991 Jul;173(13):4032–4038. doi: 10.1128/jb.173.13.4032-4038.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Boccard F., Smokvina T., Pernodet J. L., Friedmann A., Guérineau M. The integrated conjugative plasmid pSAM2 of Streptomyces ambofaciens is related to temperate bacteriophages. EMBO J. 1989 Mar;8(3):973–980. doi: 10.1002/j.1460-2075.1989.tb03460.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boizet B., Lahbib-Mansais Y., Dupont L., Ritzenthaler P., Mata M. Cloning, expression and sequence analysis of an endolysin-encoding gene of Lactobacillus bulgaricus bacteriophage mv1. Gene. 1990 Sep 28;94(1):61–67. doi: 10.1016/0378-1119(90)90468-7. [DOI] [PubMed] [Google Scholar]
  7. Brasch M. A., Pettis G. S., Lee S. C., Cohen S. N. Localization and nucleotide sequences of genes mediating site-specific recombination of the SLP1 element in Streptomyces lividans. J Bacteriol. 1993 May;175(10):3067–3074. doi: 10.1128/jb.175.10.3067-3074.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brown D. P., Idler K. B., Backer D. M., Donadio S., Katz L. Characterization of the genes and attachment sites for site-specific integration of plasmid pSE101 in Saccharopolyspora erythraea and Streptomyces lividans. Mol Gen Genet. 1994 Jan;242(2):185–193. doi: 10.1007/BF00391012. [DOI] [PubMed] [Google Scholar]
  9. Brown D. P., Idler K. B., Katz L. Characterization of the genetic elements required for site-specific integration of plasmid pSE211 in Saccharopolyspora erythraea. J Bacteriol. 1990 Apr;172(4):1877–1888. doi: 10.1128/jb.172.4.1877-1888.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Campbell A. M. Chromosomal insertion sites for phages and plasmids. J Bacteriol. 1992 Dec;174(23):7495–7499. doi: 10.1128/jb.174.23.7495-7499.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Christiansen B., Johnsen M. G., Stenby E., Vogensen F. K., Hammer K. Characterization of the lactococcal temperate phage TP901-1 and its site-specific integration. J Bacteriol. 1994 Feb;176(4):1069–1076. doi: 10.1128/jb.176.4.1069-1076.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cluzel P. J., Veaux M., Rousseau M., Accolas J. P. Evidence for temperate bacteriophages in two strains of Lactobacillus bulgaricus. J Dairy Res. 1987 Aug;54(3):397–405. doi: 10.1017/s0022029900025577. [DOI] [PubMed] [Google Scholar]
  13. Coleman D., Knights J., Russell R., Shanley D., Birkbeck T. H., Dougan G., Charles I. Insertional inactivation of the Staphylococcus aureus beta-toxin by bacteriophage phi 13 occurs by site- and orientation-specific integration of the phi 13 genome. Mol Microbiol. 1991 Apr;5(4):933–939. doi: 10.1111/j.1365-2958.1991.tb00768.x. [DOI] [PubMed] [Google Scholar]
  14. Craig N. L., Nash H. A. E. coli integration host factor binds to specific sites in DNA. Cell. 1984 Dec;39(3 Pt 2):707–716. doi: 10.1016/0092-8674(84)90478-1. [DOI] [PubMed] [Google Scholar]
  15. Han Y. W., Gumport R. I., Gardner J. F. Complementation of bacteriophage lambda integrase mutants: evidence for an intersubunit active site. EMBO J. 1993 Dec;12(12):4577–4584. doi: 10.1002/j.1460-2075.1993.tb06146.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hottinger H., Ohgi T., Zwahlen M. C., Dhamija S., Söll D. Allele-specific complementation of an Escherichia coli leuB mutation by a Lactobacillus bulgaricus tRNA gene. Gene. 1987;60(1):75–83. doi: 10.1016/0378-1119(87)90215-0. [DOI] [PubMed] [Google Scholar]
  17. Lahbib-Mansais Y., Mata M., Ritzenthaler P. Molecular taxonomy of Lactobacillus phages. Biochimie. 1988 Mar;70(3):429–435. doi: 10.1016/0300-9084(88)90217-9. [DOI] [PubMed] [Google Scholar]
  18. Landy A. Dynamic, structural, and regulatory aspects of lambda site-specific recombination. Annu Rev Biochem. 1989;58:913–949. doi: 10.1146/annurev.bi.58.070189.004405. [DOI] [PubMed] [Google Scholar]
  19. Le Bourgeois P., Lautier M., Mata M., Ritzenthaler P. New tools for the physical and genetic mapping of Lactococcus strains. Gene. 1992 Feb 1;111(1):109–114. doi: 10.1016/0378-1119(92)90610-2. [DOI] [PubMed] [Google Scholar]
  20. Lee C. Y., Iandolo J. J. Integration of staphylococcal phage L54a occurs by site-specific recombination: structural analysis of the attachment sites. Proc Natl Acad Sci U S A. 1986 Aug;83(15):5474–5478. doi: 10.1073/pnas.83.15.5474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Lee C. Y., Iandolo J. J. Structural analysis of staphylococcal bacteriophage phi 11 attachment sites. J Bacteriol. 1988 May;170(5):2409–2411. doi: 10.1128/jb.170.5.2409-2411.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lee M. H., Pascopella L., Jacobs W. R., Jr, Hatfull G. F. Site-specific integration of mycobacteriophage L5: integration-proficient vectors for Mycobacterium smegmatis, Mycobacterium tuberculosis, and bacille Calmette-Guérin. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3111–3115. doi: 10.1073/pnas.88.8.3111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Leer R. J., van Luijk N., Posno M., Pouwels P. H. Structural and functional analysis of two cryptic plasmids from Lactobacillus pentosus MD353 and Lactobacillus plantarum ATCC 8014. Mol Gen Genet. 1992 Aug;234(2):265–274. doi: 10.1007/BF00283847. [DOI] [PubMed] [Google Scholar]
  24. Leong J. M., Nunes-Düby S. E., Oser A. B., Lesser C. F., Youderian P., Susskind M. M., Landy A. Structural and regulatory divergence among site-specific recombination genes of lambdoid phage. J Mol Biol. 1986 Jun 20;189(4):603–616. doi: 10.1016/0022-2836(86)90491-2. [DOI] [PubMed] [Google Scholar]
  25. Leong J. M., Nunes-Düby S., Lesser C. F., Youderian P., Susskind M. M., Landy A. The phi 80 and P22 attachment sites. Primary structure and interaction with Escherichia coli integration host factor. J Biol Chem. 1985 Apr 10;260(7):4468–4477. [PubMed] [Google Scholar]
  26. Lillehaug D., Birkeland N. K. Characterization of genetic elements required for site-specific integration of the temperate lactococcal bacteriophage phi LC3 and construction of integration-negative phi LC3 mutants. J Bacteriol. 1993 Mar;175(6):1745–1755. doi: 10.1128/jb.175.6.1745-1755.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Martín C., Mazodier P., Mediola M. V., Gicquel B., Smokvina T., Thompson C. J., Davies J. Site-specific integration of the Streptomyces plasmid pSAM2 in Mycobacterium smegmatis. Mol Microbiol. 1991 Oct;5(10):2499–2502. doi: 10.1111/j.1365-2958.1991.tb02095.x. [DOI] [PubMed] [Google Scholar]
  28. Mata M., Trautwetter A., Luthaud G., Ritzenthaler P. Thirteen Virulent and Temperate Bacteriophages of Lactobacillus bulgaricus and Lactobacillus lactis Belong to a Single DNA Homology Group. Appl Environ Microbiol. 1986 Oct;52(4):812–818. doi: 10.1128/aem.52.4.812-818.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mazodier P., Thompson C., Boccard F. The chromosomal integration site of the Streptomyces element pSAM2 overlaps a putative tRNA gene conserved among actinomycetes. Mol Gen Genet. 1990 Jul;222(2-3):431–434. doi: 10.1007/BF00633850. [DOI] [PubMed] [Google Scholar]
  30. Mead D. A., Szczesna-Skorupa E., Kemper B. Single-stranded DNA 'blue' T7 promoter plasmids: a versatile tandem promoter system for cloning and protein engineering. Protein Eng. 1986 Oct-Nov;1(1):67–74. doi: 10.1093/protein/1.1.67. [DOI] [PubMed] [Google Scholar]
  31. Moitoso de Vargas L., Pargellis C. A., Hasan N. M., Bushman E. W., Landy A. Autonomous DNA binding domains of lambda integrase recognize two different sequence families. Cell. 1988 Sep 23;54(7):923–929. doi: 10.1016/0092-8674(88)90107-9. [DOI] [PubMed] [Google Scholar]
  32. Pargellis C. A., Nunes-Düby S. E., de Vargas L. M., Landy A. Suicide recombination substrates yield covalent lambda integrase-DNA complexes and lead to identification of the active site tyrosine. J Biol Chem. 1988 Jun 5;263(16):7678–7685. [PubMed] [Google Scholar]
  33. Parsons R. L., Evans B. R., Zheng L., Jayaram M. Functional analysis of Arg-308 mutants of Flp recombinase. Possible role of Arg-308 in coupling substrate binding to catalysis. J Biol Chem. 1990 Mar 15;265(8):4527–4533. [PubMed] [Google Scholar]
  34. Pierson L. S., 3rd, Kahn M. L. Integration of satellite bacteriophage P4 in Escherichia coli. DNA sequences of the phage and host regions involved in site-specific recombination. J Mol Biol. 1987 Aug 5;196(3):487–496. doi: 10.1016/0022-2836(87)90026-x. [DOI] [PubMed] [Google Scholar]
  35. Pouwels P. H., Leunissen J. A. Divergence in codon usage of Lactobacillus species. Nucleic Acids Res. 1994 Mar 25;22(6):929–936. doi: 10.1093/nar/22.6.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Poyart-Salmeron C., Trieu-Cuot P., Carlier C., Courvalin P. Molecular characterization of two proteins involved in the excision of the conjugative transposon Tn1545: homologies with other site-specific recombinases. EMBO J. 1989 Aug;8(8):2425–2433. doi: 10.1002/j.1460-2075.1989.tb08373.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Raya R. R., Fremaux C., De Antoni G. L., Klaenhammer T. R. Site-specific integration of the temperate bacteriophage phi adh into the Lactobacillus gasseri chromosome and molecular characterization of the phage (attP) and bacterial (attB) attachment sites. J Bacteriol. 1992 Sep;174(17):5584–5592. doi: 10.1128/jb.174.17.5584-5592.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Reiter W. D., Palm P., Yeats S. Transfer RNA genes frequently serve as integration sites for prokaryotic genetic elements. Nucleic Acids Res. 1989 Mar 11;17(5):1907–1914. doi: 10.1093/nar/17.5.1907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Segall A. M., Nash H. A. Synaptic intermediates in bacteriophage lambda site-specific recombination: integrase can align pairs of attachment sites. EMBO J. 1993 Dec;12(12):4567–4576. doi: 10.1002/j.1460-2075.1993.tb06145.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Stover C. K., de la Cruz V. F., Fuerst T. R., Burlein J. E., Benson L. A., Bennett L. T., Bansal G. P., Young J. F., Lee M. H., Hatfull G. F. New use of BCG for recombinant vaccines. Nature. 1991 Jun 6;351(6326):456–460. doi: 10.1038/351456a0. [DOI] [PubMed] [Google Scholar]
  42. Sun J., Inouye M., Inouye S. Association of a retroelement with a P4-like cryptic prophage (retronphage phi R73) integrated into the selenocystyl tRNA gene of Escherichia coli. J Bacteriol. 1991 Jul;173(13):4171–4181. doi: 10.1128/jb.173.13.4171-4181.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Thompson J. F., Moitoso de Vargas L., Koch C., Kahmann R., Landy A. Cellular factors couple recombination with growth phase: characterization of a new component in the lambda site-specific recombination pathway. Cell. 1987 Sep 11;50(6):901–908. doi: 10.1016/0092-8674(87)90516-2. [DOI] [PubMed] [Google Scholar]
  44. Vasala A., Dupont L., Baumann M., Ritzenthaler P., Alatossava T. Molecular comparison of the structural proteins encoding gene clusters of two related Lactobacillus delbrueckii bacteriophages. J Virol. 1993 Jun;67(6):3061–3068. doi: 10.1128/jvi.67.6.3061-3068.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Waldman A. S., Goodman S. D., Scocca J. J. Nucleotide sequences and properties of the sites involved in lysogenic insertion of the bacteriophage HP1c1 genome into the Haemophilus influenzae chromosome. J Bacteriol. 1987 Jan;169(1):238–246. doi: 10.1128/jb.169.1.238-246.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Ye Z. H., Buranen S. L., Lee C. Y. Sequence analysis and comparison of int and xis genes from staphylococcal bacteriophages L54a and phi 11. J Bacteriol. 1990 May;172(5):2568–2575. doi: 10.1128/jb.172.5.2568-2575.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Ye Z. H., Lee C. Y. Nucleotide sequence and genetic characterization of staphylococcal bacteriophage L54a int and xis genes. J Bacteriol. 1989 Aug;171(8):4146–4153. doi: 10.1128/jb.171.8.4146-4153.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Yu A., Bertani L. E., Haggård-Ljungquist E. Control of prophage integration and excision in bacteriophage P2: nucleotide sequences of the int gene and att sites. Gene. 1989 Aug 1;80(1):1–11. doi: 10.1016/0378-1119(89)90244-8. [DOI] [PubMed] [Google Scholar]
  49. Zwahlen M. C., Hottinger H. Nucleotide sequence of a Lactobacillus delbrueckii gene encoding a minor (UCG) tRNA(ser). Nucleic Acids Res. 1989 Feb 25;17(4):1772–1772. doi: 10.1093/nar/17.4.1772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. van de Guchte M., Daly C., Fitzgerald G. F., Arendt E. K. Identification of int and attP on the genome of lactococcal bacteriophage Tuc2009 and their use for site-specific plasmid integration in the chromosome of Tuc2009-resistant Lactococcus lactis MG1363. Appl Environ Microbiol. 1994 Jul;60(7):2324–2329. doi: 10.1128/aem.60.7.2324-2329.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES