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T4 DNA连接酶对四种碱基突出端连接保真度的全面分析及其在DNA组装中的应用

Comprehensive Profiling of Four Base Overhang Ligation Fidelity by T4 DNA Ligase and Application to DNA Assembly.

作者信息

Potapov Vladimir, Ong Jennifer L, Kucera Rebecca B, Langhorst Bradley W, Bilotti Katharina, Pryor John M, Cantor Eric J, Canton Barry, Knight Thomas F, Evans Thomas C, Lohman Gregory J S

机构信息

Research Department , New England Biolabs , Ipswich , Massachusetts 01938 , United States.

Applications and Product Development , New England Biolabs , Ipswich , Massachusetts 01938 , United States.

出版信息

ACS Synth Biol. 2018 Nov 16;7(11):2665-2674. doi: 10.1021/acssynbio.8b00333. Epub 2018 Oct 29.

Abstract

Synthetic biology relies on the manufacture of large and complex DNA constructs from libraries of genetic parts. Golden Gate and other Type IIS restriction enzyme-dependent DNA assembly methods enable rapid construction of genes and operons through one-pot, multifragment assembly, with the ordering of parts determined by the ligation of Watson-Crick base-paired overhangs. However, ligation of mismatched overhangs leads to erroneous assembly, and low-efficiency Watson Crick pairings can lead to truncated assemblies. Using sets of empirically vetted, high-accuracy junction pairs avoids this issue but limits the number of parts that can be joined in a single reaction. Here, we report the use of comprehensive end-joining ligation fidelity and bias data to predict high accuracy junction sets for Golden Gate assembly. The ligation profile accurately predicted junction fidelity in ten-fragment Golden Gate assembly reactions and enabled accurate and efficient assembly of a lac cassette from up to 24-fragments in a single reaction.

摘要

合成生物学依赖于从遗传元件库制造大型复杂的DNA构建体。金门和其他依赖II型S限制酶的DNA组装方法能够通过一锅多片段组装快速构建基因和操纵子,各元件的排序由沃森-克里克碱基配对的突出端连接决定。然而,错配突出端的连接会导致错误组装,低效的沃森-克里克配对会导致组装片段截短。使用经过实验验证的高精度连接对集合可避免此问题,但限制了单次反应中可连接的元件数量。在此,我们报告利用全面的末端连接连接保真度和偏差数据来预测用于金门组装的高精度连接对集合。连接图谱准确预测了十片段金门组装反应中的连接保真度,并能够在单次反应中从多达24个片段准确高效地组装出一个乳糖操纵子盒。

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