Research Department, New England Biolabs, Ipswich, Massachusetts 01938, United States.
ACS Synth Biol. 2022 Jun 17;11(6):2036-2042. doi: 10.1021/acssynbio.1c00525. Epub 2022 May 25.
Large DNA constructs (>10 kb) are invaluable tools for genetic engineering and the development of therapeutics. However, the manufacture of these constructs is laborious, often involving multiple hierarchical rounds of preparation. To address this problem, we sought to test whether Golden Gate assembly (GGA), an DNA assembly methodology, can be utilized to construct a large DNA target from many tractable pieces in a single reaction. While GGA is routinely used to generate constructs from 5 to 10 DNA parts in one step, we found that optimization permitted the assembly of >50 DNA fragments in a single round. We applied these insights to genome construction, successfully assembling the 40 kb T7 bacteriophage genome from up to 52 parts and recovering infectious phage particles after cellular transformation. The assembly protocols and design principles described here can be applied to rapidly engineer a wide variety of large and complex assembly targets.
大型 DNA 构建体(>10kb)是遗传工程和治疗药物开发的宝贵工具。然而,这些构建体的制造非常繁琐,通常涉及多个层次的准备工作。为了解决这个问题,我们试图测试 Golden Gate 组装(GGA)是否可用于在单个反应中使用许多易于处理的片段构建大型 DNA 靶标。虽然 GGA 通常用于在一步中从 5 到 10 个 DNA 部分生成构建体,但我们发现优化后允许在单个回合中组装超过 50 个 DNA 片段。我们将这些见解应用于基因组构建,成功地从多达 52 个部分组装了 40kb 的 T7 噬菌体基因组,并在细胞转化后回收了感染性噬菌体颗粒。这里描述的组装方案和设计原则可用于快速构建各种大型和复杂的组装靶标。