Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1974 Dec;14(6):1476–1481. doi: 10.1128/jvi.14.6.1476-1481.1974

Induction of Prophage SPO2 in Bacillus subtilis: Prophage Excision in the Absence of Bacterial or Bacteriophage DNA Synthesis

Fré Arwert 1, Lars Rutberg 1
PMCID: PMC355678  PMID: 4214949

Abstract

Bacillus subtilis lysogenic for SPO2 wild type was induced under conditions preventing synthesis of both bacterial and phage DNA. The infectivity of phage DNA in transfection is strongly decreased under these conditions, whereas the activity of single phage genes as measured by marker rescue with superinfecting phage is unaffected. DNA from induced cells was sedimented in neutral sucrose gradients. After induction, phage DNA was detected at a position in the gradients, which was different from the bulk of the bacterial DNA, corresponding to linear double-stranded DNA of about 25 × 106 daltons. Similar results were obtained with bacteria lysogenic for a SPO2 prophage carrying a DNA-negative mutation. No separation of phage and bacterial DNA activity was detected when chloramphenicol was present during the induction period. These experiments show that prophage SPO2 can excise from the bacterial chromosome without previous replication.

Full text

PDF
1476

Selected References

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

  1. Anagnostopoulos C., Spizizen J. REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS. J Bacteriol. 1961 May;81(5):741–746. doi: 10.1128/jb.81.5.741-746.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Armentrout R. W., Rutberg L. Heat induction of prophage phi 105 in Bacillus subtilis: replication of the bacterial and bacteriophage genomes. J Virol. 1971 Oct;8(4):455–468. doi: 10.1128/jvi.8.4.455-468.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Armentrout R. W., Rutberg L. Mapping of prophage and mature deoxyribonucleic acid from temperate Bacillus bacteriophage phi 105 by marker rescue. J Virol. 1970 Dec;6(6):760–767. doi: 10.1128/jvi.6.6.760-767.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Arwert F., Rutberg L. Induction of prophage SPO2 in Bacillus subtilis by 6-(para)-hydroxyphenylazouracil. J Virol. 1974 Dec;14(6):1470–1475. doi: 10.1128/jvi.14.6.1470-1475.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Arwert F., Venema G. Transformation in Bacillus subtilis. Fate of newly introduced transforming DNA. Mol Gen Genet. 1973;123(2):185–198. doi: 10.1007/BF00267334. [DOI] [PubMed] [Google Scholar]
  6. Bron S., Venema G. Ultraviolet inactivation and excision-repair in Bacillus subtilis. I. Construction and characterization of a transformable eightfold auxotrophic strain and two ultraviolet-sensitive derivatives. Mutat Res. 1972 May;15(1):1–10. doi: 10.1016/0027-5107(72)90086-3. [DOI] [PubMed] [Google Scholar]
  7. Brown N. C. 6-(p-hydroxyphenylazo)-uracil: a selective inhibitor of host DNA replication in phage-infected Bacillus subtilis. Proc Natl Acad Sci U S A. 1970 Nov;67(3):1454–1461. doi: 10.1073/pnas.67.3.1454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chow L. T., Davidson N. Electron microscope study of the structures of the Bacillus subtilis prophages, SPO2 and phi105. J Mol Biol. 1973 Apr 5;75(2):257–264. doi: 10.1016/0022-2836(73)90019-3. [DOI] [PubMed] [Google Scholar]
  9. Gottesman M. E., Yarmolinsky M. B. The integration and excision of the bacteriophage lambda genome. Cold Spring Harb Symp Quant Biol. 1968;33:735–747. doi: 10.1101/sqb.1968.033.01.084. [DOI] [PubMed] [Google Scholar]
  10. Inselburg J. W., Eremenko-Volpe T., Greenwald L., Meadow W. L., Marmur J. Physical and genetic mapping of the SPO2 prophage on the chromosome of Bacillus subtilis 168. J Virol. 1969 Jun;3(6):627–628. doi: 10.1128/jvi.3.6.627-628.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Menninger J. R., Wright M., Menninger L., Meselson M. Attachment and detachment of bacteriophage lambda DNA in lysogenization and induction. J Mol Biol. 1968 Mar 28;32(3):631–637. doi: 10.1016/0022-2836(68)90347-1. [DOI] [PubMed] [Google Scholar]
  12. Okubo S., Romig W. R. Impaired transformability of Bacillus subtilis mutant sensitive to mitomycin C and ultraviolet radiation. J Mol Biol. 1966 Feb;15(2):440–454. doi: 10.1016/s0022-2836(66)80120-1. [DOI] [PubMed] [Google Scholar]
  13. Romig W. R. Infectivity of Bacillus subtilis bacteriophage deoxyribonucleic acids extracted from mature particles and from lysogenic hosts. Bacteriol Rev. 1968 Dec;32(4 Pt 1):349–357. [PMC free article] [PubMed] [Google Scholar]
  14. Rothman J. L. Transduction studies on the relation between prophage and host chromosome. J Mol Biol. 1965 Jul;12(3):892–912. doi: 10.1016/s0022-2836(65)80336-9. [DOI] [PubMed] [Google Scholar]
  15. Rutberg L., Armentrout R. W. Deoxyribonucleic acid polymerase activity in a deoxyribonucleic acid polymerase I-deficient mutant of Bacillus subtilis infected with temperature bacteriophage SPO2. J Virol. 1972 Oct;10(4):658–660. doi: 10.1128/jvi.10.4.658-660.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Rutberg L., Armentrout R. W., Jonasson J. Unrelatedness of temperate Bacillus subtilis bacteriophages SP02 and phi105. J Virol. 1972 May;9(5):732–737. doi: 10.1128/jvi.9.5.732-737.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Rutberg L. Heat induction of prophage phi 105 in Bacillus subtilis: bacteriophage-induced bidirectional replication of the bacterial chromosome. J Virol. 1973 Jul;12(1):9–12. doi: 10.1128/jvi.12.1.9-12.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Spizizen J., Reilly B. E., Evans A. H. Microbial transformation and transfection. Annu Rev Microbiol. 1966;20:371–400. doi: 10.1146/annurev.mi.20.100166.002103. [DOI] [PubMed] [Google Scholar]
  19. Trautner T. A., Spatz H. C. Transfection in B. subtilis. Curr Top Microbiol Immunol. 1973;62:61–88. doi: 10.1007/978-3-642-65772-6_3. [DOI] [PubMed] [Google Scholar]
  20. Yasunaka K., Tsukamoto H., Okubo S., Horiuchi T. Isolation and properties of suppressor-sensitive mutants of Bacillus subtilis bacteriophage SP02. J Virol. 1970 Jun;5(6):819–821. doi: 10.1128/jvi.5.6.819-821.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES