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一种新型宏基因组来源的病毒 RNA 聚合酶及其在无细胞表达系统中用于宏基因组筛选的应用。

A novel metagenome-derived viral RNA polymerase and its application in a cell-free expression system for metagenome screening.

机构信息

Department of Microbiology and Biotechnology, University of Hamburg, Ohnhorststr. 18, 22609, Hamburg, Germany.

Institute for General Microbiology, Christian-Albrechts-University, 24118, Kiel, Germany.

出版信息

Sci Rep. 2022 Oct 25;12(1):17882. doi: 10.1038/s41598-022-22383-x.

Abstract

The mining of genomes from non-cultivated microorganisms using metagenomics is a powerful tool to discover novel proteins and other valuable biomolecules. However, function-based metagenome searches are often limited by the time-consuming expression of the active proteins in various heterologous host systems. We here report the initial characterization of novel single-subunit bacteriophage RNA polymerase, EM1 RNAP, identified from a metagenome data set obtained from an elephant dung microbiome. EM1 RNAP and its promoter sequence are distantly related to T7 RNA polymerase. Using EM1 RNAP and a translation-competent Escherichia coli extract, we have developed an efficient medium-throughput pipeline and protocol allowing the expression of metagenome-derived genes and the production of proteins in cell-free system is sufficient for the initial testing of the predicted activities. Here, we have successfully identified and verified 12 enzymes acting on bis(2-hydroxyethyl) terephthalate (BHET) in a completely clone-free approach and proposed an in vitro high-throughput metagenomic screening method.

摘要

利用宏基因组学从非培养微生物中挖掘基因组是发现新蛋白质和其他有价值生物分子的有力工具。然而,基于功能的宏基因组搜索通常受到在各种异源宿主系统中表达活性蛋白的耗时限制。我们在这里报告了从大象粪便微生物组获得的宏基因组数据集鉴定的新型单亚基噬菌体 RNA 聚合酶 EM1 RNAP 的初步特征。EM1 RNAP 和其启动子序列与 T7 RNA 聚合酶的关系较远。使用 EM1 RNAP 和具有翻译能力的大肠杆菌提取物,我们开发了一种高效的高通量流水线和方案,允许在无细胞系统中表达宏基因组衍生基因和蛋白质,足以进行预测活性的初步测试。在这里,我们已经成功地以完全无克隆的方法鉴定和验证了 12 种作用于双(2-羟乙基)对苯二甲酸酯 (BHET) 的酶,并提出了一种体外高通量宏基因组筛选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f95f/9596486/a2bd77aa6427/41598_2022_22383_Fig1_HTML.jpg

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