Storch Marko, Casini Arturo, Mackrow Ben, Fleming Toni, Trewhitt Harry, Ellis Tom, Baldwin Geoff S
‡Dr. Reddy's Chirotech Centre, Milton Road, Cambridge, CB4 0PE, U.K.
ACS Synth Biol. 2015 Jul 17;4(7):781-7. doi: 10.1021/sb500356d. Epub 2015 Apr 16.
The ability to quickly and reliably assemble DNA constructs is one of the key enabling technologies for synthetic biology. Here we define a new Biopart Assembly Standard for Idempotent Cloning (BASIC), which exploits the principle of orthogonal linker based DNA assembly to define a new physical standard for DNA parts. Further, we demonstrate a new robust method for assembly, based on type IIs restriction enzyme cleavage and ligation of oligonucleotides with single stranded overhangs that determine the assembly order. It allows for efficient, parallel assembly with great accuracy: 4 part assemblies achieved 93% accuracy with single antibiotic selection and 99.7% accuracy with double antibiotic selection, while 7 part assemblies achieved 90% accuracy with double antibiotic selection. The linkers themselves may also be used as composable parts for RBS tuning or the creation of fusion proteins. The standard has one forbidden restriction site and provides for an idempotent, single tier organization, allowing all parts and composite constructs to be maintained in the same format. This makes the BASIC standard conceptually simple at both the design and experimental levels.
快速且可靠地组装DNA构建体的能力是合成生物学的关键支撑技术之一。在此,我们定义了一种用于幂等克隆的新型生物部件组装标准(BASIC),该标准利用基于正交接头的DNA组装原理来定义DNA部件的新物理标准。此外,我们展示了一种新的稳健组装方法,该方法基于IIs型限制性内切酶切割以及与确定组装顺序的单链突出端寡核苷酸的连接。它能够实现高效、并行组装且具有很高的准确性:4部件组装在单抗生素筛选下准确率达到93%,在双抗生素筛选下准确率达到99.7%,而7部件组装在双抗生素筛选下准确率达到90%。接头本身也可用作核糖体结合位点(RBS)调控或融合蛋白创建的可组合部件。该标准有一个禁止的限制性位点,并提供幂等的单层组织架构,允许所有部件和复合构建体以相同格式保存。这使得BASIC标准在设计和实验层面在概念上都很简单。