大肠杆菌
底盘
微生物学
化学
生物
工程类
生物化学
基因
结构工程
作者
Aarón Pantoja‐Angles,Zahir Ali,Sherin Abdelrahman,Cynthia Olivia Baldelamar-Juárez,Shahid Chaudhary,M. A. Raji,Luis F. Rivera,Lingyun Zhao,Charlotte A. E. Hauser,Magdy M. Mahfouz
标识
DOI:10.1101/2025.08.30.673081
摘要
ABSTRACT Synthetic biology enables the integration of sophisticated genetic programs into microorganisms, transforming them into potent vehicles for therapeutic applications. Engineering strategies for microorganisms are rapidly evolving, offering promising solutions for cancer therapy, microbiome modulation, digestive health support, and beyond. Developing novel tools to engineer safe, nonpathogenic microbial platforms is essential for advancing clinical therapies. In this work, we present an innovative engineering approach for the probiotic Escherichia coli Nissle (EcN), aimed at creating a safe and efficient chassis for the bioproduction of therapeutics. The EcN endogenous pM1 and pM2 plasmids were cured and re-engineered to introduce a CRISPR-Cas12 chromosome shredding device and a therapeutic-producing genetic circuit, thereby generating a nonproliferative therapeutic-delivery system. Next, we build an AI-based bioinformatic pipeline to predict Anticancer-Cell-Penetrating Peptides (ACCPP) candidates. As a proof-of-concept, a selected ACCPP was produced in the engineered EcN chromosome-shredded (CS) chassis. This strategy yields a robust and controllable platform for the safe production and delivery of therapeutics, paving the way for the future development of microbial therapies and their clinical applications. GRAPHICAL ABSTRACT
科研通智能强力驱动
Strongly Powered by AbleSci AI