Computer simulation of DNA ligation: determination of initial DNA concentrations favouring the formation of recombinant molecules
Open Access
- 1 January 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 16 (5) , 1767-1778
- https://doi.org/10.1093/nar/16.5.1767
Abstract
A computer program was used to simulate the dynamic process of a ligation of DNA fragments. More specifically, the influence of the initial DNA fragments lengths and concentrations on the relative abundance of the various end-products was systematically investigated. Depending on the nature of the DNA extremities (assymetric or symetric, dephosphorylated or not), sets of initial conditions could be found that optimized the yield of active recombinant molecules. These results can be directly used to increase the efficiency of the ligation step, in particular for the construction of cDNA or genomic libraries.Keywords
This publication has 10 references indexed in Scilit:
- Studies on transformation of Escherichia coli with plasmidsPublished by Elsevier ,2006
- Topological distributions and the torsional rigidity of DNAJournal of Molecular Biology, 1986
- Ring closure probabilities for DNA fragments by Monte Carlo simulationJournal of Molecular Biology, 1986
- Regulation of inter- and intramolecular ligation with T4 DNA ligase in the presence of polyethylene glycolNucleic Acids Research, 1986
- Rapid purification of DNA fragments by high-performance size-exclusion chromatographyJournal of Chromatography B: Biomedical Sciences and Applications, 1986
- Control of phenylalanyl-tRNA synthetase genetic expressionJournal of Molecular Biology, 1985
- [2] New M13 vectors for cloningPublished by Elsevier ,1983
- The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primersGene, 1982
- Ligation of EcoRI endonuclease-generated DNA fragments into linear and circular structuresJournal of Molecular Biology, 1975
- Enzymatic breakage and joining of deoxyribonucleic acid. VI. Further purification and properties of polynucleotide ligase from Escherichia coli infected with bacteriophage T4.1968