Abstract
Temperate bacteriophages of Bacillus subtilis were characterized according to host range and digestion of the bacteriophage genome by endonuclease EcoRI. The three bacteriophages, φ3T, SPO2, and φ105, were all heteroimmune, and the DNA digests showed dissimilar patterns by agarose-ethidium bromide gel electrophoresis.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Birdsell D. C., Hathaway G. M., Rutberg L. Characterization of Temperate Bacillus Bacteriophage phi105. J Virol. 1969 Sep;4(3):264–270. doi: 10.1128/jvi.4.3.264-270.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boice L. B. Evidence that Bacillus subtilis bacteriophage SP02 is temperate and heteroimmune to bacteriophage phi-105. J Virol. 1969 Jul;4(1):47–49. doi: 10.1128/jvi.4.1.47-49.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boice L., Eiserling F. A., Romig W. R. Structure of bacillus subtilis phage SPO2 and its DNA: similarity of Bacillus subtilis phages SPO2, phi 1O5 and SPP1. Biochem Biophys Res Commun. 1969 Feb 21;34(4):398–403. doi: 10.1016/0006-291x(69)90395-7. [DOI] [PubMed] [Google Scholar]
- Chow L. T., Boice L., Davidson N. Map of the partial sequence homology between DNA molecules of Bacillus subtilis bacteriophages SPO2 and phi105. J Mol Biol. 1972 Jul 28;68(3):391–400. doi: 10.1016/0022-2836(72)90093-9. [DOI] [PubMed] [Google Scholar]
- 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]
- Edgell M. H., Hutchison C. A., 3rd, Sclair M. Specific endonuclease R fragments of bacteriophage phiX174 deoxyribonucleic acid. J Virol. 1972 Apr;9(4):574–582. doi: 10.1128/jvi.9.4.574-582.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gromkova R., Goodgal S. H. Action of haemophilus endodeoxyribonuclease on biologically active deoxyribonucleic acid. J Bacteriol. 1972 Mar;109(3):987–992. doi: 10.1128/jb.109.3.987-992.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hedgpeth J., Goodman H. M., Boyer H. W. DNA nucleotide sequence restricted by the RI endonuclease. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3448–3452. doi: 10.1073/pnas.69.11.3448. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Kelly T. J., Jr, Smith H. O. A restriction enzyme from Hemophilus influenzae. II. J Mol Biol. 1970 Jul 28;51(2):393–409. doi: 10.1016/0022-2836(70)90150-6. [DOI] [PubMed] [Google Scholar]
- Mertz J. E., Davis R. W. Cleavage of DNA by R 1 restriction endonuclease generates cohesive ends. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3370–3374. doi: 10.1073/pnas.69.11.3370. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Middleton J. H., Edgell M. H., Hutchison C. A., 3rd Specific fragments of phi X174 deoxyribonucleic acid produced by a restriction enzyme from Haemophilus aegyptius, endonuclease Z. J Virol. 1972 Jul;10(1):42–50. doi: 10.1128/jvi.10.1.42-50.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morrow J. F., Berg P. Cleavage of Simian virus 40 DNA at a unique site by a bacterial restriction enzyme. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3365–3369. doi: 10.1073/pnas.69.11.3365. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mulder C., Delius H. Specificity of the break produced by restricting endonuclease R 1 in Simian virus 40 DNA, as revealed by partial denaturation mapping. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3215–3219. doi: 10.1073/pnas.69.11.3215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rettenmier C. W., Hemphill H. E. Abortive infection of lysogenic Bacillus subtilis 168(SPO2) by bacteriophage phi 1. J Virol. 1974 Apr;13(4):870–880. doi: 10.1128/jvi.13.4.870-880.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- 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]
- Rutberg L. Mapping of a temperate bacteriophage active on Bacillus subtilis. J Virol. 1969 Jan;3(1):38–44. doi: 10.1128/jvi.3.1.38-44.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sharp P. A., Sugden B., Sambrook J. Detection of two restriction endonuclease activities in Haemophilus parainfluenzae using analytical agarose--ethidium bromide electrophoresis. Biochemistry. 1973 Jul 31;12(16):3055–3063. doi: 10.1021/bi00740a018. [DOI] [PubMed] [Google Scholar]
- Smith H. O., Wilcox K. W. A restriction enzyme from Hemophilus influenzae. I. Purification and general properties. J Mol Biol. 1970 Jul 28;51(2):379–391. doi: 10.1016/0022-2836(70)90149-x. [DOI] [PubMed] [Google Scholar]
- Yasbin R. E., Ganesan A. T., Young F. E. Bacteriophage interference in Bacillus subtilis 168. J Virol. 1974 Apr;13(4):916–921. doi: 10.1128/jvi.13.4.916-921.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yasbin R. E., Wilson G. A., Young F. E. Transformation and transfection in lysogenic strains of Bacillus subtilis 168. J Bacteriol. 1973 Feb;113(2):540–548. doi: 10.1128/jb.113.2.540-548.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]