Levrier Antoine, Karpathakis Ioannis, Nash Bruce, Bowden Steven D, Lindner Ariel B, Noireaux Vincent
School of Physics and Astronomy, University of Minnesota, Minneapolis, MN, 55455, USA.
Université Paris Cité, INSERM U1284, Center for Research and Interdisciplinarity, F-75006, Paris, France.
Nat Commun. 2024 Mar 12;15(1):2223. doi: 10.1038/s41467-024-46585-1.
Bacteriophages constitute an invaluable biological reservoir for biotechnology and medicine. The ability to exploit such vast resources is hampered by the lack of methods to rapidly engineer, assemble, package genomes, and select phages. Cell-free transcription-translation (TXTL) offers experimental settings to address such a limitation. Here, we describe PHage Engineering by In vitro Gene Expression and Selection (PHEIGES) using T7 phage genome and Escherichia coli TXTL. Phage genomes are assembled in vitro from PCR-amplified fragments and directly expressed in batch TXTL reactions to produce up to 10 PFU/ml engineered phages within one day. We further demonstrate a significant genotype-phenotype linkage of phage assembly in bulk TXTL. This enables rapid selection of phages with altered rough lipopolysaccharides specificity from phage genomes incorporating tail fiber mutant libraries. We establish the scalability of PHEIGES by one pot assembly of such mutants with fluorescent gene integration and 10% length-reduced genome.
噬菌体是生物技术和医学领域宝贵的生物资源库。然而,由于缺乏快速工程化、组装、包装基因组以及筛选噬菌体的方法,开发利用这些丰富资源的能力受到了限制。无细胞转录-翻译(TXTL)技术为解决这一限制提供了实验平台。在此,我们描述了利用T7噬菌体基因组和大肠杆菌TXTL进行的体外基因表达与筛选噬菌体工程(PHEIGES)。噬菌体基因组通过PCR扩增片段在体外组装,并直接在批量TXTL反应中表达,从而在一天内产生高达10 PFU/ml的工程噬菌体。我们进一步证明了在批量TXTL中噬菌体组装存在显著的基因型-表型联系。这使得我们能够从包含尾丝突变体文库的噬菌体基因组中快速筛选出具有改变的粗糙脂多糖特异性的噬菌体。我们通过将此类突变体与荧光基因整合以及10%长度缩短的基因组进行一锅组装,确立了PHEIGES的可扩展性。