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在细菌中通过 Golden Gate 克隆表达质粒用于合成小 RNA。

Golden Gate Cloning of Expression Plasmids for Synthetic Small RNAs in Bacteria.

机构信息

Institute for Microbiology and Molecular Biology, Justus-Liebig University Giessen, Giessen, Germany.

出版信息

Methods Mol Biol. 2025;2850:307-328. doi: 10.1007/978-1-0716-4220-7_17.

Abstract

Bacterial small RNAs (sRNAs) are well known for their ability to modulate gene expression at the post-transcriptional level. Their rather simple and modular organization provides the user with defined building blocks for synthetic biology approaches. In this chapter, we introduce a plasmid series for Escherichia coli and describe protocols for fast and efficient construction of synthetic sRNA expression plasmids based on Golden Gate assembly. In addition, we present the G-GArden tool, which assists with the design of oligodeoxynucleotides and overhangs for scarless assembly strategies. We propose that the presented procedures are suitable for many applications in different bacteria, which are related to E. coli and beyond.

摘要

细菌小 RNA(sRNA)以其在转录后水平调节基因表达的能力而闻名。它们相对简单和模块化的结构为合成生物学方法提供了定义明确的构建模块。在本章中,我们介绍了一系列用于大肠杆菌的质粒,并描述了基于 Golden Gate 组装的快速高效构建合成 sRNA 表达质粒的方案。此外,我们还介绍了 G-GArden 工具,它可以辅助设计无痕组装策略的寡脱氧核苷酸和突出端。我们认为,所提出的程序适用于与大肠杆菌相关的不同细菌中的许多应用。

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