Abstract
When Escherichia coli is infected with bacteriophage φR, parental deoxyribonucleic acid (the single- or double-stranded DNA containing the isotopic label of the infecting phage) becomes firmly attached to a cellular structure and can be isolated as a rapidly sedimenting component as described earlier for φX174. If this component is centrifuged to equilibrium, two peaks of infective DNA are observed at densities of 1.30 and 1.15 g/ml. At low multiplicities of infection, 32P-labeled parental DNA is found associated with only the cellular components in the dense band; as the multiplicities of infection are increased, the dense band becomes saturated and parental DNA molecules are then found at the light density as well. Actively replicating host DNA is found only in the dense band, whereas progeny DNA, which does not replicate semiconservatively, can become associated with cellular components in the light band. This fractionation of cellular components on the basis of their buoyant density separates primary sites of DNA replication associated with the dense band from nonfunctional binding sites in the light band.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Burton A. J., Yagi S. Intracellular development of bacteriophage phiR. I. Host modification of the replicative process. J Mol Biol. 1968 Jun 28;34(3):481–496. doi: 10.1016/0022-2836(68)90174-5. [DOI] [PubMed] [Google Scholar]
- Burton A., Sinsheimer R. L. The process of infection with bacteriophage phi-X174 VII. Ultracentrifugal analysis of the replicative form. J Mol Biol. 1965 Dec;14(2):327–347. doi: 10.1016/s0022-2836(65)80185-1. [DOI] [PubMed] [Google Scholar]
- Denhardt D. T., Sinsheimer R. L. The process of infection with bacteriophage phi-X174. 3. Phage maturation and lysis after synchronized infection. J Mol Biol. 1965 Jul;12(3):641–646. doi: 10.1016/s0022-2836(65)80318-7. [DOI] [PubMed] [Google Scholar]
- Denhardt D. T., Sinsheimer R. L. The process of infection with bacteriophage phi-X174. IV. Replication of the viral DNA in a synchronized infection. J Mol Biol. 1965 Jul;12(3):647–662. doi: 10.1016/s0022-2836(65)80319-9. [DOI] [PubMed] [Google Scholar]
- GUTHRIE G. D., SINSHEIMER R. L. Observations on the infection of bacterial protoplasts with the deoxyribonucleic acid of bacteriophage phi X174. Biochim Biophys Acta. 1963 Jun 25;72:290–297. [PubMed] [Google Scholar]
- Godson G. N., Sinsheimer R. L. Use of Brij lysis as a general method to prepare polyribosomes from Escherichia coli. Biochim Biophys Acta. 1967 Dec 19;149(2):489–495. doi: 10.1016/0005-2787(67)90176-1. [DOI] [PubMed] [Google Scholar]
- Knippers R., Salivar W. O., Newbold J. E., Sinsheimer R. L. The process of infection with bacteriophage phiX174. XXVI. Transfer of the parental DNA of bacteriophage phiX174 into progeny bacteriophage particles. J Mol Biol. 1969 Feb 14;39(3):641–654. doi: 10.1016/0022-2836(69)90150-8. [DOI] [PubMed] [Google Scholar]
- Knippers R., Sinsheimer R. L. Process of infection with bacteriophage phiX174. XX. Attachment of the parental DNA of bacteriophage phiX174 to a fast-sedimenting cell component. J Mol Biol. 1968 May 28;34(1):17–29. doi: 10.1016/0022-2836(68)90231-3. [DOI] [PubMed] [Google Scholar]
- Levine A. J., Sinsheimer R. L. The process of infection with bacteriophage phiX174. XXV. Studies with bacteriophage phiX174 mutants blocked in progeny replicative form DNA synthesis. J Mol Biol. 1969 Feb 14;39(3):619–639. doi: 10.1016/0022-2836(69)90149-1. [DOI] [PubMed] [Google Scholar]
- Roth T. F., Hayashi M. Allomorphic forms of bacteriophage phiX-174 replicative DNA. Science. 1966 Nov 4;154(3749):658–660. doi: 10.1126/science.154.3749.658. [DOI] [PubMed] [Google Scholar]
- SINSHEIMER R. L., STARMAN B., NAGLER C., GUTHRIE S. The process of infection with bacteriophage phi-XI74. I. Evidence for a "replicative form". J Mol Biol. 1962 Mar;4:142–160. doi: 10.1016/s0022-2836(62)80047-3. [DOI] [PubMed] [Google Scholar]
- Salivar W. O., Sinsheimer R. L. Intracellular location and number of replicating parental DNA molecules of bacteriophages lambda and phi-X174. J Mol Biol. 1969 Apr 14;41(1):39–65. doi: 10.1016/0022-2836(69)90124-7. [DOI] [PubMed] [Google Scholar]
- Smith D. W., Hanawalt P. C. Properties of the growing point region in the bacterial chromosome. Biochim Biophys Acta. 1967 Dec 19;149(2):519–531. doi: 10.1016/0005-2787(67)90180-3. [DOI] [PubMed] [Google Scholar]
- Stone A. B. Some factors which influence the replication of the replicative form of bacteriophage OX174. Biochem Biophys Res Commun. 1967 Feb 8;26(3):247–254. doi: 10.1016/0006-291x(67)90113-1. [DOI] [PubMed] [Google Scholar]
- YARUS M., SINSHEIMER R. L. THE U.V.-RESISTANCE OF DOUBLE-STRANDED PHIX174 DNA. J Mol Biol. 1964 Apr;8:614–615. doi: 10.1016/s0022-2836(64)80018-8. [DOI] [PubMed] [Google Scholar]
- Yarus M. J., Sinsheimer R. L. The process of infection with bacteriophage phiX174. 8. Evidence for an essential bacterial "site". J Virol. 1967 Feb;1(1):135–144. doi: 10.1128/jvi.1.1.135-144.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
