Abstract
Properties of the viral R plasmid Rphi6P are described. As a temperate bacteriophage, it plaques on the facultative phototroph Rhodopseudomonas sphaeroides. Under aerobic conditions the phage had a latent period of 180 min, a burst time of 200 min, and a burst size of 15 to 20 particles per infective center. The encapsidated viral genome occurred as a supercoiled, circular DNA duplex with a mean contour length of 16.5 +/- 10 micron. Percent guanine plus cytosine, as calculated from thermal denaturation profiles, was 63.5. Mitomycin C-induced loss of the prophage suggested an extrachromosomal location in the host cell. Use of this curing agent enabled the isolation of a plasmid-free strain of R. sphaeroides. Biophysical analysis of the plasmid-free strain lysogenized with Rphi6P confirmed that the prophage occurred as a plasmid in the host cell.
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- Adhya S., Cleary P., Campbell A. A deletion analysis of prophage lambda and adjacent genetic regions. Proc Natl Acad Sci U S A. 1968 Nov;61(3):956–962. doi: 10.1073/pnas.61.3.956. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen S. N. Transposable genetic elements and plasmid evolution. Nature. 1976 Oct 28;263(5580):731–738. doi: 10.1038/263731a0. [DOI] [PubMed] [Google Scholar]
- Espejo R. T., Canelo E. S. Properties and characterization of the host bacterium of bacteriophage PM2. J Bacteriol. 1968 May;95(5):1887–1891. doi: 10.1128/jb.95.5.1887-1891.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Espejo R. T., Canelo E. S. Properties of bacteriophage PM2: a lipid-containing bacterial virus. Virology. 1968 Apr;34(4):738–747. doi: 10.1016/0042-6822(68)90094-9. [DOI] [PubMed] [Google Scholar]
- Espejo R. T., Canelo E. S., Sinsheimer R. L. DNA of bacteriophage PM2: a closed circular double-stranded molecule. Proc Natl Acad Sci U S A. 1969 Aug;63(4):1164–1168. doi: 10.1073/pnas.63.4.1164. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fenner F. Classification and nomenclature of viruses. Second report of the International Committee on Taxonomy of Viruses. Intervirology. 1976;7(1-2):1–115. doi: 10.1159/000149938. [DOI] [PubMed] [Google Scholar]
- Freifelder D., Baran N., Folkmanis A., Freifelder D. L. Circular dimers of a lambda DNA in infected, nonlysogenic Escherichia coli. Virology. 1977 Sep;81(2):183–191. doi: 10.1016/0042-6822(77)90136-2. [DOI] [PubMed] [Google Scholar]
- Gibson K. D., Niederman R. A. Characterization of two circular satellite species of deoxyribonucleic acid in Rhodopseudomonas spheroides. Arch Biochem Biophys. 1970 Dec;141(2):694–704. doi: 10.1016/0003-9861(70)90190-6. [DOI] [PubMed] [Google Scholar]
- Goebel W., Helinski D. R. Generation of higher multiple circular DNA forms in bacteria. Proc Natl Acad Sci U S A. 1968 Dec;61(4):1406–1413. doi: 10.1073/pnas.61.4.1406. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gottesman M. E., Yarmolinsky M. B. Integration-negative mutants of bacteriophage lambda. J Mol Biol. 1968 Feb 14;31(3):487–505. doi: 10.1016/0022-2836(68)90423-3. [DOI] [PubMed] [Google Scholar]
- Guerry P., LeBlanc D. J., Falkow S. General method for the isolation of plasmid deoxyribonucleic acid. J Bacteriol. 1973 Nov;116(2):1064–1066. doi: 10.1128/jb.116.2.1064-1066.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heffron F., Sublett R., Hedges R. W., Jacob A., Falkow S. Origin of the TEM-beta-lactamase gene found on plasmids. J Bacteriol. 1975 Apr;122(1):250–256. doi: 10.1128/jb.122.1.250-256.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ikeda H., Tomizawa J. Prophage P1, and extrachromosomal replication unit. Cold Spring Harb Symp Quant Biol. 1968;33:791–798. doi: 10.1101/sqb.1968.033.01.091. [DOI] [PubMed] [Google Scholar]
- KONDO E., MITSUHASHI S. DRUG RESISTANCE OF ENTERIC BACTERIA. IV. ACTIVE TRANSDUCING BACTERIOPHAGE P1 CM PRODUCED BY THE COMBINATION OF R FACTOR WITH BACTERIOPHAGE P1. J Bacteriol. 1964 Nov;88:1266–1276. doi: 10.1128/jb.88.5.1266-1276.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lang D. Molecular weights of coliphages and coliphage DNA. 3. Contour length and molecular weight of DNA from bacteriophages T4, T5 and T7, and from bovine papilloma virus. J Mol Biol. 1970 Dec 28;54(3):557–565. doi: 10.1016/0022-2836(70)90126-9. [DOI] [PubMed] [Google Scholar]
- Miller R. V., Pemberton J. M., Richards K. E. F116, D3 and G101: temperate bacteriophages of Pseudomonas aeruginosa. Virology. 1974 Jun;59(2):566–569. doi: 10.1016/0042-6822(74)90466-8. [DOI] [PubMed] [Google Scholar]
- Mise K., Arber W. Plaque-forming transducing bacteriophage P1 derivatives and their behaviour in lysogenic conditions. Virology. 1976 Jan;69(1):191–205. doi: 10.1016/0042-6822(76)90206-3. [DOI] [PubMed] [Google Scholar]
- Mural R. J., Friedman D. I. Isolation and characterization of a temperate bacteriophage specific for Rhodopseudomonas spheroides. J Virol. 1974 Nov;14(5):1288–1292. doi: 10.1128/jvi.14.5.1288-1292.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Palchaudhuri S., Chakrabarty A. Isolation of plasmid deoxyribonucleic acid from Pseudomonas putida. J Bacteriol. 1976 Apr;126(1):410–416. doi: 10.1128/jb.126.1.410-416.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pemberton J. M., Clark A. J. Detection and characterization of plasmids in Pseudomonas aeruginosa strain PAO. J Bacteriol. 1973 Apr;114(1):424–433. doi: 10.1128/jb.114.1.424-433.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pemberton J. M. Size of the chromosome of Pseudomonas aeruginosa PAO. J Bacteriol. 1974 Sep;119(3):748–752. doi: 10.1128/jb.119.3.748-752.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pemberton J. M., Tucker W. T. Naturally occurring viral R plasmid with a circular supercoiled genome in the extracellular state. Nature. 1977 Mar 3;266(5597):50–51. doi: 10.1038/266050a0. [DOI] [PubMed] [Google Scholar]
- Richmond M. H. Extrachromosomal elements and the spread of antibiotic resistance in bacteria. Biochem J. 1969 Jun;113(2):225–234. doi: 10.1042/bj1130225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosner J. L. Formation, induction, and curing of bacteriophage P1 lysogens. Virology. 1972 Jun;48(3):679–689. doi: 10.1016/0042-6822(72)90152-3. [DOI] [PubMed] [Google Scholar]
- Saunders V. A., Saunders J. R., Bennett P. M. Extrachromosomal deoxyribonucleic acid in wild-type and photosynthetically incompetent strains of Rhodopseudomonas spheroides. J Bacteriol. 1976 Mar;125(3):1180–1187. doi: 10.1128/jb.125.3.1180-1187.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sistrom W. R. Transfer of chromosomal genes mediated by plasmid r68.45 in Rhodopseudomonas sphaeroides. J Bacteriol. 1977 Aug;131(2):526–532. doi: 10.1128/jb.131.2.526-532.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takano T., Ikeda S. Phage P1 carrying kanamycin resistance gene of R factor. Virology. 1976 Mar;70(1):198–200. doi: 10.1016/0042-6822(76)90252-x. [DOI] [PubMed] [Google Scholar]
- Walker D. H., Jr, Walker J. T. Genetic studies of coliphage P1. II. Relatedness to P7. J Virol. 1976 Jul;19(1):271–274. doi: 10.1128/jvi.19.1.271-274.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yun T., Vapnek D. Electron microscopic analysis of bacteriophages P1, P1Cm, and P7. Determination of genome sizes, sequence homology, and location of antibiotic-resistance determinants. Virology. 1977 Mar;77(1):376–385. doi: 10.1016/0042-6822(77)90434-2. [DOI] [PubMed] [Google Scholar]
- Zabrovitz S., Segev N., Cohen G. Growth of bacteriophage P1 in recombination-deficient hosts of Escherichia coli. Virology. 1977 Jul 15;80(2):233–248. doi: 10.1016/s0042-6822(77)80001-9. [DOI] [PubMed] [Google Scholar]