Tong Yaojun, Robertsen Helene Lunde, Blin Kai, Weber Tilmann, Lee Sang Yup
The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kgs. Lyngby, 2800, Denmark.
Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical and Biomolecular Engineering (BK21 Plus Program), Center for Systems and Synthetic Biotechnology, Institute for the BioCentury, BioInformatics Research Center, and BioProcess Engineering Research Center, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 305-701, Republic of Korea.
Methods Mol Biol. 2018;1671:163-184. doi: 10.1007/978-1-4939-7295-1_11.
Bacteria of the order Actinomycetales are one of the most important sources of bioactive natural products, which are the source of many drugs. However, many of them still lack efficient genome editing methods, some strains even cannot be manipulated at all. This restricts systematic metabolic engineering approaches for boosting known and discovering novel natural products. In order to facilitate the genome editing for actinomycetes, we developed a CRISPR-Cas9 toolkit with high efficiency for actinomyces genome editing. This basic toolkit includes a software for spacer (sgRNA) identification, a system for in-frame gene/gene cluster knockout, a system for gene loss-of-function study, a system for generating a random size deletion library, and a system for gene knockdown. For the latter, a uracil-specific excision reagent (USER) cloning technology was adapted to simplify the CRISPR vector construction process. The application of this toolkit was successfully demonstrated by perturbation of genomes of Streptomyces coelicolor A3(2) and Streptomyces collinus Tü 365. The CRISPR-Cas9 toolkit and related protocol described here can be widely used for metabolic engineering of actinomycetes.
放线菌目细菌是生物活性天然产物的最重要来源之一,这些天然产物是许多药物的来源。然而,它们中的许多仍然缺乏高效的基因组编辑方法,有些菌株甚至根本无法进行操作。这限制了用于促进已知天然产物发现和挖掘新型天然产物的系统代谢工程方法。为了便于放线菌的基因组编辑,我们开发了一种用于放线菌基因组编辑的高效CRISPR-Cas9工具包。这个基础工具包包括一个用于间隔序列(sgRNA)识别的软件、一个用于框内基因/基因簇敲除的系统、一个用于基因功能丧失研究的系统、一个用于生成随机大小缺失文库的系统以及一个用于基因敲低的系统。对于后者,采用了尿嘧啶特异性切除试剂(USER)克隆技术来简化CRISPR载体构建过程。通过对天蓝色链霉菌A3(2)和栖土链霉菌Tü 365的基因组进行扰动,成功证明了该工具包的应用。本文所述的CRISPR-Cas9工具包及相关方案可广泛用于放线菌的代谢工程。