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Stepwise Strategy for One‐Pot Synthesis of Single‐Stranded DNA Rings from Multiple Short Fragments
Author(s) -
Sui Zhe,
An Ran,
Komiyama Makoto,
Liang Xingguo
Publication year - 2021
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.202000738
Subject(s) - dna , dna ligase , oligonucleotide , chemistry , combinatorial chemistry , selectivity , ring (chemistry) , stereochemistry , biochemistry , organic chemistry , catalysis
Cyclic rings of single‐stranded (ss) DNA have various unique properties, but wider applications have been hampered by their poor availability. This paper reports a convenient one‐pot method in which these rings are efficiently synthesized by using T4 DNA ligase through convergent cyclization of easily available short DNA fragments. The key to the present method is to separate all the splint oligonucleotides into several sets, and add each set sequentially at an appropriate interval to the solutions containing all the short DNA fragments. Compared with simple one‐pot strategies involving simultaneous addition of all the splints at the beginning of the reaction, both the selectivity and the yields of target ssDNA rings are greatly improved. This convergent method is especially useful for preparing large‐sized rings that are otherwise hard to obtain. By starting from six short DNA fragments (71–82 nt), prepared by a DNA synthesizer, a ssDNA ring of 452‐nt size was synthesized in 35 mol % yield and in high selectivity. Satisfactorily pure DNA rings were obtainable simply by treating the crude products with exonuclease.