Literature DB >> 2832827

Computer simulation of DNA ligation: determination of initial DNA concentrations favouring the formation of recombinant molecules.

F Dardel1.   

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 (asymmetric or symmetric, 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.

Mesh:

Substances:

Year:  1988        PMID: 2832827      PMCID: PMC338170          DOI: 10.1093/nar/16.5.1767

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  10 in total

1.  Ligation of EcoRI endonuclease-generated DNA fragments into linear and circular structures.

Authors:  A Dugaiczyk; H W Boyer; H M Goodman
Journal:  J Mol Biol       Date:  1975-07-25       Impact factor: 5.469

2.  Topological distributions and the torsional rigidity of DNA. A Monte Carlo study of DNA circles.

Authors:  S D Levene; D M Crothers
Journal:  J Mol Biol       Date:  1986-05-05       Impact factor: 5.469

3.  Ring closure probabilities for DNA fragments by Monte Carlo simulation.

Authors:  S D Levene; D M Crothers
Journal:  J Mol Biol       Date:  1986-05-05       Impact factor: 5.469

4.  Rapid purification of DNA fragments by high-performance size-exclusion chromatography.

Authors:  J M Schmitter; Y Mechulam; G Fayat; M Anselme
Journal:  J Chromatogr       Date:  1986-06-13

5.  Enzymatic breakage and joining of deoxyribonucleic acid. VI. Further purification and properties of polynucleotide ligase from Escherichia coli infected with bacteriophage T4.

Authors:  B Weiss; A Jacquemin-Sablon; T R Live; G C Fareed; C C Richardson
Journal:  J Biol Chem       Date:  1968-09-10       Impact factor: 5.157

6.  The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.

Authors:  J Vieira; J Messing
Journal:  Gene       Date:  1982-10       Impact factor: 3.688

7.  New M13 vectors for cloning.

Authors:  J Messing
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

8.  Regulation of inter- and intramolecular ligation with T4 DNA ligase in the presence of polyethylene glycol.

Authors:  K Hayashi; M Nakazawa; Y Ishizaki; N Hiraoka; A Obayashi
Journal:  Nucleic Acids Res       Date:  1986-10-10       Impact factor: 16.971

9.  Control of phenylalanyl-tRNA synthetase genetic expression. Site-directed mutagenesis of the pheS, T operon regulatory region in vitro.

Authors:  J F Mayaux; G Fayat; M Panvert; M Springer; M Grunberg-Manago; S Blanquet
Journal:  J Mol Biol       Date:  1985-07-05       Impact factor: 5.469

10.  Studies on transformation of Escherichia coli with plasmids.

Authors:  D Hanahan
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

  10 in total
  5 in total

1.  Monitoring of naphthalene catabolism by bioluminescence with nah-lux transcriptional fusions.

Authors:  R S Burlage; G S Sayler; F Larimer
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

2.  Kinetic analysis for optimization of DNA ligation reactions.

Authors:  D Revie; D W Smith; T W Yee
Journal:  Nucleic Acids Res       Date:  1988-11-11       Impact factor: 16.971

3.  Fast purification of a functional elongator tRNAmet expressed from a synthetic gene in vivo.

Authors:  T Meinnel; Y Mechulam; G Fayat
Journal:  Nucleic Acids Res       Date:  1988-08-25       Impact factor: 16.971

Review 4.  Design of Experiments As a Tool for Optimization in Recombinant Protein Biotechnology: From Constructs to Crystals.

Authors:  Christos Papaneophytou
Journal:  Mol Biotechnol       Date:  2019-12       Impact factor: 2.695

5.  An infinitely expandable cloning strategy plus repeat-proof PCR for working with multiple shRNA.

Authors:  Glen John McIntyre; Jennifer Lynne Groneman; Anna Tran; Tanya Lynn Applegate
Journal:  PLoS One       Date:  2008-11-27       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.