细菌中合成小 RNA 的表达质粒的金门克隆。

Q4 Biochemistry, Genetics and Molecular Biology Methods in molecular biology Pub Date : 2025-01-01 DOI:10.1007/978-1-0716-4220-7_17
Sophie Dittmar, Bork A Berghoff
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引用次数: 0

摘要

众所周知,细菌小核糖核酸(sRNA)具有在转录后水平调节基因表达的能力。它们相当简单的模块化组织为用户提供了合成生物学方法的定义构件。在本章中,我们介绍了大肠杆菌质粒系列,并描述了基于金门组装技术快速高效构建合成 sRNA 表达质粒的方案。此外,我们还介绍了 G-GArden 工具,该工具可协助设计寡去氧核苷酸和悬臂,用于无痕组装策略。我们认为所介绍的程序适用于与大肠杆菌有关的不同细菌及其他细菌的许多应用。
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Golden Gate Cloning of Expression Plasmids for Synthetic Small RNAs in Bacteria.

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.

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来源期刊
Methods in molecular biology
Methods in molecular biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.00
自引率
0.00%
发文量
3536
期刊介绍: For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.
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