category
NAR
date
Mar 12, 2026
slug
status
Published
summary
创新性提出将毒素-抗毒素系统与CRISPR-Cas结合的自杀开关(ATTACH),通过CreTA模块实现微生物对Cas效应蛋白的依赖性,采用可诱导启动子调控Cas3和向导RNA,开发出单质粒、抗生素独立的生物 containment 装置,在肠道环境和发酵过程中均表现出优异的稳定性和安全性。
tags
基因编辑
合成生物学
核酸蛋白工具酶
type
Post

📄 原文题目

Associate toxin–antitoxin with CRISPR-Cas to harness (ATTACH) engineered microbes

🔗 原文链接

💡 AI 核心解读

创新性提出将毒素-抗毒素系统与CRISPR-Cas结合的自杀开关(ATTACH),通过CreTA模块实现微生物对Cas效应蛋白的依赖性,采用可诱导启动子调控Cas3和向导RNA,开发出单质粒、抗生素独立的生物 containment 装置,在肠道环境和发酵过程中均表现出优异的稳定性和安全性。

📝 英文原版摘要

<span class="paragraphSection"><div class="boxTitle">Abstract</div>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.</span>
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