Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Apr;62(4):1452–1453. doi: 10.1128/aem.62.4.1452-1453.1996

An origin of DNA replication from Lactococcus lactis bacteriophage c2.

N R Waterfield 1, M W Lubbers 1, K M Polzin 1, R W Le Page 1, A W Jarvis 1
PMCID: PMC167916  PMID: 8919811

Abstract

An origin of DNA relication was identified in the intergenic region between the early and late gene regions of prolate lactococcal phage c2. A DNA fragment containing this origin, designated ori, was shown to direct DNA replication in Lactococcus lactis but not in Escherichia coli. A comparison of ori with the corresponding regions of other prolate phages revealed strict conservation of the nucleotide sequence in one half of this intergenic region. This conserved region alone would not support DNA replication. No open reading frames were identified in the ori fragment, suggesting that host factors alone are sufficient to initiate DNA replication at ori. A novel class of lactococcal vectors and E. coli-L. lactis shuttle vectors based on ori have been constructed.

Full Text

The Full Text of this article is available as a PDF (168.3 KB).

Selected References

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

  1. Beresford T. P., Ward L. J., Jarvis A. W. Temporally Regulated Transcriptional Expression of the Genomes of Lactococcal Bacteriophages c2 and sk1. Appl Environ Microbiol. 1993 Nov;59(11):3708–3712. doi: 10.1128/aem.59.11.3708-3712.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Firshein W. Role of the DNA/membrane complex in prokaryotic DNA replication. Annu Rev Microbiol. 1989;43:89–120. doi: 10.1146/annurev.mi.43.100189.000513. [DOI] [PubMed] [Google Scholar]
  3. Jarvis A. W., Fitzgerald G. F., Mata M., Mercenier A., Neve H., Powell I. B., Ronda C., Saxelin M., Teuber M. Species and type phages of lactococcal bacteriophages. Intervirology. 1991;32(1):2–9. doi: 10.1159/000150179. [DOI] [PubMed] [Google Scholar]
  4. Lubbers M. W., Waterfield N. R., Beresford T. P., Le Page R. W., Jarvis A. W. Sequencing and analysis of the prolate-headed lactococcal bacteriophage c2 genome and identification of the structural genes. Appl Environ Microbiol. 1995 Dec;61(12):4348–4356. doi: 10.1128/aem.61.12.4348-4356.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Macrina F. L., Evans R. P., Tobian J. A., Hartley D. L., Clewell D. B., Jones K. R. Novel shuttle plasmid vehicles for Escherichia-Streptococcus transgeneric cloning. Gene. 1983 Nov;25(1):145–150. doi: 10.1016/0378-1119(83)90176-2. [DOI] [PubMed] [Google Scholar]
  6. Mojumdar M., Khan S. A. Characterization of the tetracycline resistance gene of plasmid pT181 of Staphylococcus aureus. J Bacteriol. 1988 Dec;170(12):5522–5528. doi: 10.1128/jb.170.12.5522-5528.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Platteeuw C., Simons G., de Vos W. M. Use of the Escherichia coli beta-glucuronidase (gusA) gene as a reporter gene for analyzing promoters in lactic acid bacteria. Appl Environ Microbiol. 1994 Feb;60(2):587–593. doi: 10.1128/aem.60.2.587-593.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Powell I. B., Tulloch D. L., Hillier A. J., Davidson B. E. Phage DNA synthesis and host DNA degradation in the life cycle of Lactococcus lactis bacteriophage c6A. J Gen Microbiol. 1992 May;138(5):945–950. doi: 10.1099/00221287-138-5-945. [DOI] [PubMed] [Google Scholar]
  9. Schouler C., Bouet C., Ritzenthaler P., Drouet X., Mata M. Characterization of Lactococcus lactis phage antigens. Appl Environ Microbiol. 1992 Aug;58(8):2479–2484. doi: 10.1128/aem.58.8.2479-2484.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Schouler C., Ehrlich S. D., Chopin M. C. Sequence and organization of the lactococcal prolate-headed bIL67 phage genome. Microbiology. 1994 Nov;140(Pt 11):3061–3069. doi: 10.1099/13500872-140-11-3061. [DOI] [PubMed] [Google Scholar]
  11. Summers D. K., Sherratt D. J. Multimerization of high copy number plasmids causes instability: CoIE1 encodes a determinant essential for plasmid monomerization and stability. Cell. 1984 Apr;36(4):1097–1103. doi: 10.1016/0092-8674(84)90060-6. [DOI] [PubMed] [Google Scholar]
  12. Wells J. M., Wilson P. W., Le Page R. W. Improved cloning vectors and transformation procedure for Lactococcus lactis. J Appl Bacteriol. 1993 Jun;74(6):629–636. doi: 10.1111/j.1365-2672.1993.tb05195.x. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES