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基因卫士:一种专为生物安全设计的模块化质粒系统。

GeneGuard: A modular plasmid system designed for biosafety.

作者信息

Wright Oliver, Delmans Mihails, Stan Guy-Bart, Ellis Tom

机构信息

†Centre for Synthetic Biology and Innovation, Imperial College London, London SW7 2AZ, United Kingdom.

‡Department of Bioengineering, Imperial College London, London SW7 2AZ, United Kingdom.

出版信息

ACS Synth Biol. 2015 Mar 20;4(3):307-16. doi: 10.1021/sb500234s. Epub 2014 May 22.

DOI:10.1021/sb500234s
PMID:24847673
Abstract

Synthetic biology applications in biosensing, bioremediation, and biomining envision the use of engineered microbes beyond a contained laboratory. Deployment of such microbes in the environment raises concerns of unchecked cellular proliferation or unwanted spread of synthetic genes. While antibiotic-resistant plasmids are the most utilized vectors for introducing synthetic genes into bacteria, they are also inherently insecure, acting naturally to propagate DNA from one cell to another. To introduce security into bacterial synthetic biology, we here took on the task of completely reformatting plasmids to be dependent on their intended host strain and inherently disadvantageous for others. Using conditional origins of replication, rich-media compatible auxotrophies, and toxin-antitoxin pairs we constructed a mutually dependent host-plasmid platform, called GeneGuard. In this, replication initiators for the R6K or ColE2-P9 origins are provided in trans by a specified host, whose essential thyA or dapA gene is translocated from a genomic to a plasmid location. This reciprocal arrangement is stable for at least 100 generations without antibiotic selection and is compatible for use in LB medium and soil. Toxin genes ζ or Kid are also employed in an auxiliary manner to make the vector disadvantageous for strains not expressing their antitoxins. These devices, in isolation and in concert, severely reduce unintentional plasmid propagation in E. coli and B. subtilis and do not disrupt the intended E. coli host's growth dynamics. Our GeneGuard system comprises several versions of modular cargo-ready vectors, along with their requisite genomic integration cassettes, and is demonstrated here as an efficient vector for heavy-metal biosensors.

摘要

合成生物学在生物传感、生物修复和生物采矿中的应用设想将工程微生物用于实验室之外。在环境中部署此类微生物引发了对细胞不受控制的增殖或合成基因意外传播的担忧。虽然抗性质粒是将合成基因导入细菌时最常用的载体,但它们本质上也不安全,会自然地将DNA从一个细胞传播到另一个细胞。为了给细菌合成生物学引入安全性,我们在此承担了一项任务,即对质粒进行完全重新设计,使其依赖于预期的宿主菌株,而对其他菌株具有固有劣势。我们利用条件复制起点、富培养基兼容的营养缺陷型以及毒素-抗毒素对构建了一个相互依赖的宿主-质粒平台,称为GeneGuard。在这个平台中,R6K或ColE2-P9起点的复制起始因子由特定宿主反式提供,该宿主的必需thyA或dapA基因从基因组位置转移到质粒位置。这种相互安排在没有抗生素选择的情况下至少稳定100代,并且可在LB培养基和土壤中使用。毒素基因ζ或Kid也以辅助方式使用,以使载体对不表达其抗毒素的菌株不利。这些装置单独或协同作用,可大幅减少大肠杆菌和枯草芽孢杆菌中质粒的意外传播,且不会干扰预期的大肠杆菌宿主的生长动态。我们的GeneGuard系统包括几个版本的模块化载货就绪载体及其必需的基因组整合盒,并在此展示为一种用于重金属生物传感器的高效载体。

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