Department of Biosystems, Laboratory of Gene Technology, KULeuven, Kasteelpark Arenberg 21 Box 2462, Leuven, 3001, Belgium.
Laboratory of Applied Biotechnology, Department of Biotechnology, Ghent University, Valentin Vaerwyckweg 1, Gent, 9000, Belgium.
Microb Biotechnol. 2022 Jan;15(1):370-386. doi: 10.1111/1751-7915.13922. Epub 2021 Oct 14.
To meet the needs of synthetic biologists, DNA assembly methods have transformed from simple 'cut-and-paste' procedures to highly advanced, standardised assembly techniques. Implementing these standardised DNA assembly methods in biotechnological research conducted in non-model hosts, including Pseudomonas putida and Pseudomonas aeruginosa, could greatly benefit reproducibility and predictability of experimental results. SEVAtile is a Type IIs-based assembly approach, which enables the rapid and standardised assembly of genetic parts - or tiles - to create genetic circuits in the established SEVA-vector backbone. Contrary to existing DNA assembly methods, SEVAtile is an easy and straightforward method, which is compatible with any vector, both SEVA- and non-SEVA. To prove the efficiency of the SEVAtile method, a three-vector system was successfully generated to independently co-express three different proteins in P. putida and P. aeruginosa. More specifically, one of the vectors, pBGDes, enables genomic integration of assembled circuits in the Tn7 landing site, while self-replicatory vectors pSTDesX and pSTDesR enable inducible expression from the XylS/Pm and RhaRS/PrhaB expression systems, respectively. Together, we hope these vector systems will support research in both the microbial SynBio and Pseudomonas field.
为了满足合成生物学家的需求,DNA 组装方法已经从简单的“切和粘贴”程序转变为高度先进、标准化的组装技术。在非模式宿主(包括 Pseudomonas putida 和 Pseudomonas aeruginosa)中进行生物技术研究时,实施这些标准化的 DNA 组装方法,可以极大地提高实验结果的可重复性和可预测性。SEVAtile 是一种基于 Type IIS 的组装方法,它能够快速、标准化地将遗传元件(或瓷砖)组装到已建立的 SEVA 载体骨架中,以创建遗传回路。与现有的 DNA 组装方法不同,SEVAtile 是一种简单直接的方法,与任何载体(包括 SEVA 和非 SEVA)都兼容。为了证明 SEVAtile 方法的效率,成功生成了一个三载体系统,可在 P. putida 和 P. aeruginosa 中独立共表达三种不同的蛋白质。具体来说,其中一个载体 pBGDes 可使组装的回路在 Tn7 着陆位点进行基因组整合,而自复制载体 pSTDesX 和 pSTDesR 可分别从 XylS/Pm 和 RhaRS/PrhaB 表达系统诱导表达。我们希望这些载体系统能够支持微生物合成生物学和 Pseudomonas 领域的研究。