Associate toxin–antitoxin with CRISPR-Cas to harness (ATTACH) engineered microbes
Zhao Huiwei, Zhou Tao, Zhang Ming, Wang Chengqiang, Wang Rui, Shu Xian, Cheng Feiyue, Xue Qiong, Liu Chao, Xu Jing, Cao Xinyue, Du Jun, Wang Liangliang, Liu Hongwei, Li Ming
Journal:NUCLEIC ACIDS RESEARCH
IF:15
DOI:10.1093/nar/gkag213
PMID:41816914
Published:2026-03-12
research field:合成生物学基因线路生物 containment 技术微生物工程
Abstract
Robust biocontainment is essential for the safe use of engineered microbes, but existing strategies suffer from genetic instability and/or laborious construction. Here, we present ATTACH, a kill switch that associates toxin–antitoxin with CRISPR-Cas to harness engineered microbes. Our approach employs a CRISPR-repressed toxin–antitoxin (CreTA) module to make microbes addicted to the type I-F Cas effector proteins, and places both the Cas3 nuclease and the chromosome-targeting guide RNA under inducible promoters, thereby improving the genetic stability and stringency of the CRISPR-based suicidal program. Additionally, we have developed a single-plasmid, antibiotic-independent ATTACH device, which shows robust, stringent containment of a microbial chassis in murine gut, and negligible impacts on culture growth or lycopene production during batch fermentation. Our data highlight the potential of CreTA to stabilize CRISPR-based kill switches, advancing their development into more portable and reliable biocontainment tools for engineered microbes.
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