由非标准氨基酸介导的工程正交和专性细菌共生

IF 20.5 1区 生物学 Q1 MICROBIOLOGY
Amanda M. Forti, Michaela A. Jones, Defne N. Elbeyli, Neil D. Butler, Aditya M. Kunjapur
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引用次数: 0

摘要

微生物可以通过基因工程实现基于合成化学物质的内在生物控制。然而,对外源化学物质的依赖限制了所含微生物的生存环境。在这里,我们设计了一个正交专性共栖大肠杆菌,自主创造环境允许一个伙伴微生物的生存。我们设计了一个大肠杆菌菌株(生产者),通过异源表达从简单的碳源生物合成非标准氨基酸(nsAA)。我们设计了第二种大肠杆菌菌株(利用者),依靠相同的nsAA作为合成营养不良菌生长,14天的逃逸率为每个菌落形成单位2.8 × 10−9。共培养实验表明,利用菌依赖于产生菌,利用菌与非产生菌的大肠杆菌共接种约107个菌落形成单位时未发现逃逸现象。依赖性维持在一个简化的合成玉米根相关群落内。这项工作提供了生态学的见解,并提出了一种独立于外源化学物质的潜在生物控制策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Engineered orthogonal and obligate bacterial commensalism mediated by a non-standard amino acid

Engineered orthogonal and obligate bacterial commensalism mediated by a non-standard amino acid

Microorganisms can be genetically engineered for intrinsic biological containment based on synthetic chemical provision. However, reliance on an exogenous chemical limits the contexts where a contained microorganism could survive. Here we design an orthogonal obligate commensalism in Escherichia coli that autonomously creates environments permissive for survival of a partner microbe. We engineer one E. coli strain (the producer) to biosynthesize a non-standard amino acid (nsAA) from simple carbon sources through heterologous expression. We engineer a second E. coli strain (the utilizer) to rely on the same nsAA for growth as a synthetic auxotroph, with a 14-day escape rate of 2.8 × 10−9 escapees per colony-forming unit. Co-culture experiments show utilizer dependence on the producer, with no escape detected during co-inoculation of ~107 colony-forming units of utilizer and a non-producer E. coli strain. Dependence is maintained within a simplified synthetic maize root-associated community. This work provides ecological insights and presents a potential biocontainment strategy independent of an exogenous chemical.

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来源期刊
Nature Microbiology
Nature Microbiology Immunology and Microbiology-Microbiology
CiteScore
44.40
自引率
1.10%
发文量
226
期刊介绍: Nature Microbiology aims to cover a comprehensive range of topics related to microorganisms. This includes: Evolution: The journal is interested in exploring the evolutionary aspects of microorganisms. This may include research on their genetic diversity, adaptation, and speciation over time. Physiology and cell biology: Nature Microbiology seeks to understand the functions and characteristics of microorganisms at the cellular and physiological levels. This may involve studying their metabolism, growth patterns, and cellular processes. Interactions: The journal focuses on the interactions microorganisms have with each other, as well as their interactions with hosts or the environment. This encompasses investigations into microbial communities, symbiotic relationships, and microbial responses to different environments. Societal significance: Nature Microbiology recognizes the societal impact of microorganisms and welcomes studies that explore their practical applications. This may include research on microbial diseases, biotechnology, or environmental remediation. In summary, Nature Microbiology is interested in research related to the evolution, physiology and cell biology of microorganisms, their interactions, and their societal relevance.
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