Tanniche Imen, Fisher Amanda K, Gillam Frank, Collakova Eva, Zhang Chenming, Bevan David R, Senger Ryan S
Department of Biological Systems Engineering, Virginia Tech, Blacksburg, Virginia, USA.
School of Plant & Environmental Sciences; Virginia Tech, Blacksburg, Virginia, USA.
Biotechnol Bioeng. 2022 Dec;119(12):3657-3667. doi: 10.1002/bit.28240. Epub 2022 Oct 8.
Lambda-polymerase chain reaction (λ-PCR) is a novel and open-source method for DNA assembly and cloning projects. λ-PCR uses overlap extension to ultimately assemble linear and circular DNA fragments, but it allows the single-stranded DNA (ssDNA) primers of the PCR extension to first exist as double-stranded DNA (dsDNA). Having dsDNA at this step is advantageous for the stability of large insertion products, to avoid inhibitory secondary structures during direct synthesis, and to reduce costs. Three variations of λ-PCR were created to convert an initial dsDNA product into an ssDNA "megaprimer" to be used in overlap extension: (i) complete digestion by λ-exonuclease, (ii) asymmetric PCR, and (iii) partial digestion by λ-exonuclease. Four case studies are presented that demonstrate the use of λ-PCR in simple gene cloning, simultaneous multipart assemblies, gene cloning not achievable with commercial kits, and the use of thermodynamic simulations to guide λ-PCR assembly strategies. High DNA assembly and cloning efficiencies have been achieved with λ-PCR for a fraction of the cost and time associated with conventional methods and some commercial kits.
λ聚合酶链反应(λ-PCR)是一种用于DNA组装和克隆项目的新型开源方法。λ-PCR利用重叠延伸最终组装线性和环状DNA片段,但它允许PCR延伸的单链DNA(ssDNA)引物首先以双链DNA(dsDNA)的形式存在。在此步骤拥有dsDNA有利于大插入产物的稳定性,避免直接合成过程中的抑制性二级结构,并降低成本。创建了三种λ-PCR变体,将初始dsDNA产物转化为用于重叠延伸的ssDNA“大引物”:(i)用λ外切核酸酶完全消化,(ii)不对称PCR,以及(iii)用λ外切核酸酶部分消化。本文展示了四个案例研究,证明了λ-PCR在简单基因克隆、同时多片段组装、商业试剂盒无法实现的基因克隆以及使用热力学模拟指导λ-PCR组装策略方面的应用。与传统方法和一些商业试剂盒相比,λ-PCR以一小部分成本和时间实现了高DNA组装和克隆效率。