DNA低聚物的酶促生产

Ashaa Preyadharishini Shunmugam, B. Hogberg, Jayavel
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引用次数: 0

摘要

如果DNA纳米技术要成为治疗、诊断或生命科学研究的一种可行技术,那么主要是单链DNA的组成材料就必须廉价、大量和高质量地生产。先前的实验表明,克隆模板的生产是通过一个高度可扩展的酶促过程中被称为MOSIC(单克隆化学计量法)的相对化学计量比完美控制的。为了评估酶促生产寡核苷酸的技术是否在DNA纳米技术中有更多的应用,本项目利用辅助噬菌体制备了一个编码晶体模板的假基因。该方法使单链DNA的生产具有产率高、成本低、易于扩展的特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enzymatic production Of DNA oligos
If DNA nanotechnology is to become a viable technology for therapeutics, diagnostics or life science research, the component materials mostly single stranded DNA will have to be produced cheaply, abundantly and with very high quality. Prior experiments demonstrated the production of clonal template through perfectly controlled relative stoichiometric ratios in a highly scalable enzymatic process called the MOSIC method (Monoclonal StoichiometrIC). To assess whether the technique for the production of oligos enzymatically could be useful in more applications in DNA nanotechnology, a pseudogene coding a crystal template was produced using helper phages in this project. This method enables the production of such single stranded DNA with high yield, low cost and easily scalable method.
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