| Literature DB >> 9092646 |
R K Bruick1, M Koppitz, G F Joyce, L E Orgel.
Abstract
A rapid method for the synthesis of oligodeoxynucleotides (ODNs) terminated by 5'-amino-5'-deoxythymidine is described. A 3'-phosphorylated ODN (the donor) is incubated in aqueous solution with 5'-amino- 5'-deoxythymidine in the presence of N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC), extending the donor by one residue via a phosphoramidate bond. Template- directed ligation of the extended donor and an acceptor ODN, followed by acid hydrolysis, yields the acceptor ODN extended by a single 5'-amino-5'-deoxythymidine residue at its 5'terminus.Entities:
Keywords: NASA Discipline Exobiology; NASA Discipline Number 93-10; NASA Program NSCORT; Non-NASA Center
Mesh:
Substances:
Year: 1997 PMID: 9092646 PMCID: PMC146550 DOI: 10.1093/nar/25.6.1309
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971