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. 1975 Jan;2(1):131–141. doi: 10.1093/nar/2.1.131

Studies on the structure of replicative intermediates in bacteriophage M13 single stranded DNA synthesis.

B E Kessler-Liebscher, W L Staudenbauer, P H Hofschneider
PMCID: PMC342817  PMID: 1129143

Abstract

Pulse-labeled replicative intermediates in M 13 single stranded DNA synthesis can be separated by dye-buoyant density centrifugation into two major fractions: Supercoiled molecules (RI I) containing viral strands of more than one genome length, and "relaxed" molecules (RI II) with labeled DNA chains shorter than unit length. It is postulated that RI II molecules might be formed in vivo by site-specific nicking of RF I molecules.

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Selected References

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

  1. Dressler D. The rolling circle for phiX DNA replication. II. Synthesis of single-stranded circles. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1934–1942. doi: 10.1073/pnas.67.4.1934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dürwald H., Hoffmann-Berling H. DNA synthesis in nucleotide-permeable Escherichia coli cells. II. Synthesis of replicative from DNA of phage phi X174. J Mol Biol. 1971 Jun 28;58(3):755–773. doi: 10.1016/0022-2836(71)90038-6. [DOI] [PubMed] [Google Scholar]
  3. Gilbert W., Dressler D. DNA replication: the rolling circle model. Cold Spring Harb Symp Quant Biol. 1968;33:473–484. doi: 10.1101/sqb.1968.033.01.055. [DOI] [PubMed] [Google Scholar]
  4. Henry T. J., Knippers R. Isolation and function of the gene A initiator of bacteriophage phi-chi 174, a highly specific DNA endonuclease. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1549–1553. doi: 10.1073/pnas.71.4.1549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hirt B. Selective extraction of polyoma DNA from infected mouse cell cultures. J Mol Biol. 1967 Jun 14;26(2):365–369. doi: 10.1016/0022-2836(67)90307-5. [DOI] [PubMed] [Google Scholar]
  6. Iyer V. N., Rupp W. D. Usefulness of benzoylated naphthoylated DEAE-cellulose to distinguish and fractionate double-stranded DNA bearing different extents of single-stranded regions. Biochim Biophys Acta. 1971 Jan 1;228(1):117–126. doi: 10.1016/0005-2787(71)90551-x. [DOI] [PubMed] [Google Scholar]
  7. Kluge F. Replicative intermediates in bacteriophage M13 single stranded DNA synthesis. Hoppe Seylers Z Physiol Chem. 1974 Apr;355(4):410–414. doi: 10.1515/bchm2.1974.355.1.410. [DOI] [PubMed] [Google Scholar]
  8. Lin N. S., Pratt D. Role of bacteriophage M13 gene 2 in viral DNA replication. J Mol Biol. 1972 Dec 14;72(1):37–49. doi: 10.1016/0022-2836(72)90066-6. [DOI] [PubMed] [Google Scholar]
  9. Ray D. S. Replication of bacteriophage M13. II. The role of replicative forms in single-strand synthesis. J Mol Biol. 1969 Aug 14;43(3):631–643. doi: 10.1016/0022-2836(69)90364-7. [DOI] [PubMed] [Google Scholar]
  10. Staudenbauer W. L., Hofschneider P. H. Membrane attachment of replicating parental DNA molecules of bacteriophage M13. Biochem Biophys Res Commun. 1971 Mar 19;42(6):1035–1041. doi: 10.1016/0006-291x(71)90008-8. [DOI] [PubMed] [Google Scholar]
  11. Staudenbauer W. L., Hofschneider P. H. Replication of bacteriophage M 13. Mechanism of single-strand DNA synthesis in an escherichia coli mutant thermosensitive in chromosomal DNA replication. Eur J Biochem. 1972 Nov 7;30(3):403–412. doi: 10.1111/j.1432-1033.1972.tb02111.x. [DOI] [PubMed] [Google Scholar]
  12. Staudenbauer W. L. Involvement of DNA polymerases I and III in the replication of bacteriophage M-13. Eur J Biochem. 1974 Nov 1;49(1):249–256. doi: 10.1111/j.1432-1033.1974.tb03829.x. [DOI] [PubMed] [Google Scholar]

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