College of Food Science and Engineering, Ocean University of China, Qingdao, 266003, P. R. China.
Laboratory for Marine Drugs and Bioproducts, Qingdao National Laboratory for Marine Science and Technology, Qingdao, 266235, P. R. China.
Chembiochem. 2021 Mar 16;22(6):1005-1011. doi: 10.1002/cbic.202000738. Epub 2020 Nov 26.
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.
单链 (ss) DNA 的环状结构具有各种独特的性质,但由于其可用性较差,限制了它们的更广泛应用。本文报道了一种方便的一锅法,通过 T4 DNA 连接酶将易于获得的短 DNA 片段进行收敛环化,有效地合成这些环。本方法的关键是将所有的衔接寡核苷酸分成几组,并在适当的间隔时间内依次添加到含有所有短 DNA 片段的溶液中。与简单的一锅法(即在反应开始时同时添加所有衔接物)相比,目标 ssDNA 环的选择性和产率都得到了极大的提高。这种收敛方法特别适用于制备大尺寸的环,否则很难获得。从通过 DNA 合成仪制备的 6 个短 DNA 片段(71-82 nt)出发,以 35 mol%的产率和高选择性合成了 452-nt 大小的 ssDNA 环。通过用外切核酸酶处理粗产物,即可获得令人满意的纯 DNA 环。