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Convergent DNA synthesis: a non-enzymatic dimerization approach to circular oligodeoxynucleotides.

机译:聚合DNA合成:环状寡聚脱氧核苷酸的非酶二聚化方法。

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摘要

We report a novel convergent approach to the construction of circular DNA oligonucleotides from two smaller linear precursors. Circular DNAs 34-74 nucleotides (nt) in size are constructed non-enzymatically in a single step from two half-length oligomers. A DNA template is used to assemble the constituent parts into a triple helical complex which brings the four reactive ends together for chemical ligation with BrCN/imidazole/Ni2+. A homodimerization reaction strategy is successfully used on a small scale to construct circles 42, 58 and 74 nt in size. In addition, a heterodimerization strategy is successfully used in two cases to construct circular 34mers from different 16mer and 18mer precursors. Measurement of preparative yields for one biologically active 34mer circle shows that the dimerization strategy gives a yield higher than that from conventional cyclization and nearly as high as that for a normally synthesized linear DNA, establishing that there is not necessarily a yield penalty for circle construction. Six additional preparative circle constructions, giving conversions of approximately 33-85% from precursors to circular product, are also described. Convergent strategies allow the construction of medium and large size DNA molecules in higher yields than can be achieved by standard linear synthesis alone.
机译:我们报告了一种新颖的收敛方法,用于从两个较小的线性前体构建环状DNA寡核苷酸。环状DNA 34-74个核苷酸(nt)的大小由两个半长的寡聚体一步一步地非酶促地构建。使用DNA模板将组成部分组装成三重螺旋复合物,该复合物将四个反应性末端连接在一起,以便与BrCN /咪唑/ Ni2 +化学连接。均二聚化反应策略已成功用于小规模构建大小为42、58和74 nt的圆。另外,在两种情况下成功使用异二聚化策略从不同的16mer和18mer前体构建环状34mer。对一个具有生物活性的34mer环的制备产率的测量结果表明,二聚化策略产生的产率高于常规环化反应的产率,几乎与正常合成的线性DNA的产率相同,这表明对环的构建未必会有产率损失。还描述了六种其他的制备圆结构,从前体到圆形产品的转化率约为33-85%。收敛策略允许以比仅通过标准线性合成所能获得的更高的产率构建中型和大型DNA分子。

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