Philipps Universität Marburg, Synthetic Microbiology Center Marburg (SYNMIKRO), Marburg, 35043, Germany.
Nat Commun. 2022 Jun 14;13(1):3430. doi: 10.1038/s41467-022-30843-1.
CRISPR SWAPnDROP extends the limits of genome editing to large-scale in-vivo DNA transfer between bacterial species. Its modular platform approach facilitates species specific adaptation to confer genome editing in various species. In this study, we show the implementation of the CRISPR SWAPnDROP concept for the model organism Escherichia coli, the fast growing Vibrio natriegens and the plant pathogen Dickeya dadantii. We demonstrate the excision, transfer and integration of large chromosomal regions between E. coli, V. natriegens and D. dadantii without size-limiting intermediate DNA extraction. CRISPR SWAPnDROP also provides common genome editing approaches comprising scarless, marker-free, iterative and parallel insertions and deletions. The modular character facilitates DNA library applications, and recycling of standardized parts. Its multi-color scarless co-selection system significantly improves editing efficiency and provides visual quality controls throughout the assembly and editing process.
CRISPR SWAPnDROP 将基因组编辑的限制扩展到细菌物种之间的大规模体内 DNA 转移。其模块化平台方法促进了物种特异性适应,从而在各种物种中实现基因组编辑。在这项研究中,我们展示了 CRISPR SWAPnDROP 概念在模式生物大肠杆菌、快速生长的嗜盐菌和植物病原菌菊欧文氏菌中的实施。我们证明了在大肠杆菌、嗜盐菌和菊欧文氏菌之间切除、转移和整合大染色体区域,而没有大小限制的中间 DNA 提取。CRISPR SWAPnDROP 还提供了常见的基因组编辑方法,包括无疤痕、无标记、迭代和并行插入和缺失。模块化特征便于 DNA 文库应用和标准化部件的回收。其多色无疤痕共选择系统显著提高了编辑效率,并在整个组装和编辑过程中提供了可视化质量控制。