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多层基因保障机制将微生物的生长限制在特定环境中。

Multilayered genetic safeguards limit growth of microorganisms to defined environments.

作者信息

Gallagher Ryan R, Patel Jaymin R, Interiano Alexander L, Rovner Alexis J, Isaacs Farren J

机构信息

Department of Molecular, Cellular & Developmental Biology, Yale University, New Haven, CT 06520, USA Systems Biology Institute, Yale University, West Haven, CT 06516, USA.

Department of Molecular, Cellular & Developmental Biology, Yale University, New Haven, CT 06520, USA.

出版信息

Nucleic Acids Res. 2015 Feb 18;43(3):1945-54. doi: 10.1093/nar/gku1378. Epub 2015 Jan 7.

Abstract

Genetically modified organisms (GMOs) are commonly used to produce valuable compounds in closed industrial systems. However, their emerging applications in open clinical or environmental settings require enhanced safety and security measures. Intrinsic biocontainment, the creation of bacterial hosts unable to survive in natural environments, remains a major unsolved biosafety problem. We developed a new biocontainment strategy containing overlapping 'safeguards'-engineered riboregulators that tightly control expression of essential genes, and an engineered addiction module based on nucleases that cleaves the host genome-to restrict viability of Escherichia coli cells to media containing exogenously supplied synthetic small molecules. These multilayered safeguards maintain robust growth in permissive conditions, eliminate persistence and limit escape frequencies to <1.3 × 10(-12). The staged approach to safeguard implementation revealed mechanisms of escape and enabled strategies to overcome them. Our safeguarding strategy is modular and employs conserved mechanisms that could be extended to clinically or industrially relevant organisms and undomesticated species.

摘要

转基因生物(GMOs)通常用于在封闭的工业系统中生产有价值的化合物。然而,它们在开放的临床或环境环境中的新兴应用需要加强安全保障措施。内在生物遏制,即创造无法在自然环境中生存的细菌宿主,仍然是一个主要未解决的生物安全问题。我们开发了一种新的生物遏制策略,其中包含重叠的“保障措施”——经过工程改造的核糖调节器,可严格控制必需基因的表达,以及基于核酸酶的工程化成瘾模块,该核酸酶可切割宿主基因组,从而将大肠杆菌细胞的活力限制在含有外源供应的合成小分子的培养基中。这些多层保障措施在允许的条件下保持强劲生长,消除持久性并将逃逸频率限制在<1.3×10(-12)。保障措施实施的分阶段方法揭示了逃逸机制,并启用了克服这些机制的策略。我们的保障策略是模块化的,并采用了保守机制,可扩展到临床或工业相关生物以及未驯化物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc3e/4330353/a834d3b2ac5b/gku1378fig1.jpg

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