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在恶臭假单胞菌中基于 yTREX/Tn5 的基因簇表达的方案。

Protocols for yTREX/Tn5-based gene cluster expression in Pseudomonas putida.

机构信息

Institute of Molecular Enzyme Technology, Heinrich-Heine-University Düsseldorf, Forschungszentrum Jülich, Jülich, Germany.

Institute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University, Düsseldorf, Germany.

出版信息

Microb Biotechnol. 2020 Jan;13(1):250-262. doi: 10.1111/1751-7915.13402. Epub 2019 Jun 4.

DOI:10.1111/1751-7915.13402
PMID:31162833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6922528/
Abstract

Bacterial gene clusters, which represent a genetic treasure trove for secondary metabolite pathways, often need to be activated in a heterologous host to access the valuable biosynthetic products. We provide here a detailed protocol for the application of the yTREX 'gene cluster transplantation tool': Via yeast recombinational cloning, a gene cluster of interest can be cloned in the yTREX vector, which enables the robust conjugational transfer of the gene cluster to bacteria like Pseudomonas putida, and their subsequent transposon Tn5-based insertion into the host chromosome. Depending on the gene cluster architecture and chromosomal insertion site, the respective pathway genes can be transcribed effectively from a chromosomal promoter, thereby enabling the biosynthesis of a natural product. We describe workflows for the design of a gene cluster expression cassette, cloning of the cassette in the yTREX vector by yeast recombineering, and subsequent transfer and expression in P. putida. As an example for yTREX-based transplantation of a natural product biosynthesis, we provide details on the cloning and activation of the phenazine-1-carboxylic acid biosynthetic genes from Pseudomonas aeruginosa in P. putidaKT2440 as well as the use of β-galactosidase-encoding lacZ as a reporter of production levels.

摘要

细菌基因簇代表了次生代谢途径的遗传宝库,通常需要在异源宿主中被激活,以获得有价值的生物合成产物。我们在这里提供了一个详细的协议,用于应用 yTREX“基因簇移植工具”:通过酵母重组克隆,可以将感兴趣的基因簇克隆到 yTREX 载体中,这使得基因簇能够有效地通过接合转移到 Pseudomonas putida 等细菌中,然后通过转座子 Tn5 将其插入宿主染色体。根据基因簇的结构和染色体插入位点,相应的途径基因可以从染色体启动子有效地转录,从而能够合成天然产物。我们描述了设计基因簇表达盒的工作流程,通过酵母重组克隆将盒克隆到 yTREX 载体中,然后在 P. putida 中进行转移和表达。作为基于 yTREX 的天然产物生物合成移植的一个例子,我们提供了在 P. putidaKT2440 中克隆和激活来自铜绿假单胞菌的苯并嗪-1-羧酸生物合成基因的详细信息,以及使用β-半乳糖苷酶编码 lacZ 作为产量水平的报告基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/da6337b1b126/MBT2-13-250-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/f1d31278d241/MBT2-13-250-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/bdcc87b823a1/MBT2-13-250-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/f77b66147bb4/MBT2-13-250-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/da6337b1b126/MBT2-13-250-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/f1d31278d241/MBT2-13-250-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/bdcc87b823a1/MBT2-13-250-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/f77b66147bb4/MBT2-13-250-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ea/6922528/da6337b1b126/MBT2-13-250-g004.jpg

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