一种改进的 CRISPR 和 CRISPR 干扰(CRISPRi)工具包,用于改造模式产甲烷古菌 Methanococcus maripaludis。

IF 4.3 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Qing Du, Yufei Wei, Liuyang Zhang, Derong Ren, Jian Gao, Xiuzhu Dong, Liping Bai, Jie Li
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引用次数: 0

摘要

背景:基于 II 型的 CRISPR-Cas 系统仍然仅限于在古细菌中使用,而古细菌是与细菌和真核生物并列的特色生命领域。Maripaludis 甲烷球菌(Methanococcus maripaludis)以快速生长和遗传可操作性著称,是研究古细菌生物学和探索二氧化碳生物技术应用的典范。然而,该古菌的基因调控工具仍然不足,CRISPR-Cas工具仍需改进,限制了其作为古菌模式细胞工厂的应用:本研究不仅改进了CRISPR-Cas9系统,优化了多重基因组编辑和CRISPR质粒构建的效率,而且还开创了一种有效的CRISPR干扰(CRISPRi)系统,用于M. maripaludis的可控基因调控。我们开发了两种平衡表达多个 sgRNA 的新策略,促进了高效的多重基因组编辑。我们还设计了一种基因组表达 Cas9 的菌株,从而简化了 CRISPR 质粒的构建,提高了基因组修饰的效率,包括无标记和无疤痕基因敲入。重要的是,我们利用无催化活性的 dCas9 建立了 CRISPRi 系统,实现了对目标基因高达 100 倍的抑制。其中,针对转录起始位点附近和下游区域以及 5'end ORF 的 sgRNA 抑制效果最好。此外,我们还开发了基于 TetR/tetO 平台的可诱导 CRISPRi-dCas9 系统。这促进了诱导性基因抑制,尤其是对重要基因的抑制:因此,这些进展不仅扩大了遗传操作的工具包,还弥补了马里斑马鱼中基因调控,尤其是重要基因调控的方法学空白。在此开发的强大工具包为将 Maripaludis 作为重要的模式古细 胞工厂铺平了道路,促进了古细菌的基础生物学研究和应用生物技术的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An improved CRISPR and CRISPR interference (CRISPRi) toolkit for engineering the model methanogenic archaeon Methanococcus maripaludis.

Background: The type II based CRISPR-Cas system remains restrictedly utilized in archaea, a featured domain of life that ranks parallelly with Bacteria and Eukaryotes. Methanococcus maripaludis, known for rapid growth and genetic tractability, serves as an exemplary model for studying archaeal biology and exploring CO2-based biotechnological applications. However, tools for controlled gene regulation remain deficient and CRISPR-Cas tools still need improved in this archaeon, limiting its application as an archaeal model cellular factory.

Results: This study not only improved the CRISPR-Cas9 system for optimizing multiplex genome editing and CRISPR plasmid construction efficiencies but also pioneered an effective CRISPR interference (CRISPRi) system for controlled gene regulation in M. maripaludis. We developed two novel strategies for balanced expression of multiple sgRNAs, facilitating efficient multiplex genome editing. We also engineered a strain expressing Cas9 genomically, which simplified the CRISPR plasmid construction and facilitated more efficient genome modifications, including markerless and scarless gene knock-in. Importantly, we established a CRISPRi system using catalytic inactive dCas9, achieving up to 100-fold repression on target gene. Here, sgRNAs targeting near and downstream regions of the transcription start site and the 5'end ORF achieved the highest repression efficacy. Furthermore, we developed an inducible CRISPRi-dCas9 system based on TetR/tetO platform. This facilitated the inducible gene repression, especially for essential genes.

Conclusions: Therefore, these advancements not only expand the toolkit for genetic manipulation but also bridge methodological gaps for controlled gene regulation, especially for essential genes, in M. maripaludis. The robust toolkit developed here paves the way for applying M. maripaludis as a vital model archaeal cell factory, facilitating fundamental biological studies and applied biotechnology development of archaea.

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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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