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首页> 外文期刊>Nature methods >Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC
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Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC

机译:利用SLIC在体外利用同源重组产生重组DNA

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摘要

We describe a new cloning method, sequence and ligation independent cloning (SLIC), which allows the assembly of multiple DNA fragments in a single reaction using in vitro homologous recombination and single-strand annealing. SLIC mimics in vivo homologous recombination by relying on exonuclease-generated ssDNA overhangs in insert and vector fragments, and the assembly of these fragments by recombination in vitro. SLIC inserts can also be prepared by incomplete PCR (iPCR) or mixed PCR. SLIC allows efficient and reproducible assembly of recombinant DNA with as many as 5 and 10 fragments simultaneously. SLIC circumvents the sequence requirements of traditional methods and functions much more efficiently at very low DNA concentrations when combined with RecA to catalyze homologous recombination. This flexibility allows much greater versatility in the generation of recombinant DNA for the purposes of synthetic biology.
机译:我们描述了一种新的克隆方法,序列和连接独立克隆(SLIC),它允许使用体外同源重组和单链退火在单个反应中组装多个DNA片段。 SLIC通过依赖核酸外切酶在插入片段和载体片段中产生的ssDNA突出端模拟体内同源重组,并通过体外重组组装这些片段。 SLIC插入片段也可以通过不完全PCR(iPCR)或混合PCR制备。 SLIC允许高效,可重复地组装重组DNA,同时具有多达5和10个片段。 SLIC规避了传统方法的序列要求,并且在与RecA结合以催化同源重组时,在非常低的DNA浓度下能更有效地发挥作用。为了合成生物学的目的,这种灵活性使重组DNA的产生具有更大的通用性。

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