Department of Gastroenterology, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan, Hubei, 430071, China.
Department of Burn and Plastic Surgery, Shenzhen Institute of Translational Medicine, Health Science Center, Shenzhen Second People's Hospital, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong, 518035, China.
Nat Commun. 2022 Aug 2;13(1):4491. doi: 10.1038/s41467-022-31934-9.
Phages are regarded as powerful antagonists of bacteria, especially in industrial fermentation processes involving bacteria. While bacteria have developed various defense mechanisms, most of which are effective against a narrow range of phages and consequently exert limited protection from phage infection. Here, we report a strategy for developing phage-resistant Escherichia coli strains through the simultaneous genomic integration of a DNA phosphorothioation-based Ssp defense module and mutations of components essential for the phage life cycle. The engineered E. coli strains show strong resistance against diverse phages tested without affecting cell growth. Additionally, the resultant engineered phage-resistant strains maintain the capabilities of producing example recombinant proteins, D-amino acid oxidase and coronavirus-encoded nonstructural protein nsp8, even under high levels of phage cocktail challenge. The strategy reported here will be useful for developing engineered E. coli strains with improved phage resistance for various industrial fermentation processes for producing recombinant proteins and chemicals of interest.
噬菌体被视为细菌的强大拮抗剂,尤其是在涉及细菌的工业发酵过程中。尽管细菌已经发展出多种防御机制,但其中大多数机制对狭窄范围的噬菌体有效,因此对噬菌体感染的保护作用有限。在这里,我们报告了一种通过同时基因组整合基于 DNA 硫代磷酸化的 Ssp 防御模块和噬菌体生命周期必需成分的突变来开发抗噬菌体大肠杆菌菌株的策略。工程大肠杆菌菌株表现出对多种测试噬菌体的强抗性,而不影响细胞生长。此外,即使在高浓度噬菌体鸡尾酒的挑战下,所得的工程抗噬菌体菌株仍保持产生重组蛋白、D-氨基酸氧化酶和冠状病毒编码的非结构蛋白 nsp8 的能力。这里报道的策略将有助于开发具有改进的抗噬菌体能力的工程大肠杆菌菌株,用于各种工业发酵过程,以生产感兴趣的重组蛋白和化学品。