Mapping of Cleavage Sites for Restriction Endonucleases in λdv Plasmids
- 1 September 1975
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 57 (2), 595-606
- https://doi.org/10.1111/j.1432-1033.1975.tb02335.x
Abstract
Restriction nucleases from Escherichia coli carrying the resistance transfer factor RI, from Hemophilus influenzae, Hemophilus parainfluenzae, and Bacillus subtilis were used for the generation of specific DNA fragments from lambdadv plasmids. Cleavage maps were established for various plasmids containing different but overlapping parts of bacteriophage lambdaDNA by analysis of digestion patterns obtained in polyacrylamide gel electrophoresis. The correlation between the plasmid cleavage maps and the genetic map of lambda was based upon the location of the EcoRI cleavage site at 81.3% of lambda fractional length and the position of promoters PL and PR on the plasmid DNA fragments.Keywords
This publication has 22 references indexed in Scilit:
- Studies on the cleavage of bacteriophage lambda DNA with EcoRI restriction endonucleaseJournal of Molecular Biology, 1975
- The role of recombination in the formation of circular oligomers of the λdv1 plasmidJournal of Molecular Biology, 1974
- Electron microscope study of the structures of λdv DNAsJournal of Molecular Biology, 1974
- Genetic evidence for two types of gene arrangements in new λdv plasmid mutantsJournal of Molecular Biology, 1974
- Separation and analysis of promoter sites in bacteriophage lambda DNA by specific endonucleasesJournal of Molecular Biology, 1974
- Control Elements in the DNA of BacteriophageCold Spring Harbor Symposia on Quantitative Biology, 1974
- A Suggested nomenclature for bacterial host modification and restriction systems and their enzymesJournal of Molecular Biology, 1973
- Mapping the DNA Fragments produced by Cleavage of λ DNA with Endonuclease RINature, 1973
- A restriction enzyme from Hemophilus influenzae: II. Base sequence of the recognition siteJournal of Molecular Biology, 1970
- dv: An Autonomously Replicating DNA FragmentCold Spring Harbor Symposia on Quantitative Biology, 1968