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easyPACId,一种诱导生产、分离、鉴定和测试变形菌门天然产物的简单方法。

easyPACId, a Simple Method for Induced Production, Isolation, Identification, and Testing of Natural Products from Proteobacteria.

作者信息

Bode Edna, Assmann Daniela, Happel Petra, Meyer Elmar, Münch Karin, Rössel Nicole, Bode Helge B

机构信息

Department of Natural Products in Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Molecular Biotechnology, Goethe University Frankfurt am Main, Frankfurt am Main, Germany.

出版信息

Bio Protoc. 2023 Jul 5;13(13):e4709. doi: 10.21769/BioProtoc.4709.

Abstract

The easyPACId (easy Promoter Activation and Compound Identification) approach is focused on the targeted activation of natural product biosynthetic gene clusters (BGCs) encoding non-ribosomal peptide synthetases (NRPS), polyketide synthases (PKS), NRPS-PKS hybrids, or other BGC classes. It was applied to entomopathogenic bacteria of the genera Xenorhabdus and Photorhabdus by exchanging the natural promoter of desired BGCs against the L-arabinose inducible PBAD promoter in ∆hfq mutants of the respective strains. The crude (culture) extracts of the cultivated easyPACId mutants are enriched with the single compound or compound class and can be tested directly against various target organisms without further purification of the produced natural products. Furthermore, isolation and identification of compounds from these mutants is simplified due to the reduced background in the ∆hfq strains. The approach avoids problems often encountered in heterologous expression hosts, chemical synthesis, or tedious extraction of desired compounds from wild-type crude extracts. This protocol describes easyPACId for Xenorhabdus and Photorhabdus, but it was also successfully adapted to Pseudomonas entomophila and might be suitable for other proteobacteria that carry hfq.

摘要

简易PACId(简易启动子激活与化合物鉴定)方法专注于对编码非核糖体肽合成酶(NRPS)、聚酮合酶(PKS)、NRPS-PKS杂合体或其他BGC类别的天然产物生物合成基因簇(BGC)进行靶向激活。通过将相应菌株的∆hfq突变体中所需BGC的天然启动子替换为L-阿拉伯糖诱导型PBAD启动子,该方法被应用于嗜线虫致病杆菌属和发光杆菌属的昆虫病原细菌。培养的简易PACId突变体的粗(培养)提取物富含单一化合物或化合物类别,无需对产生的天然产物进行进一步纯化,即可直接针对各种靶标生物进行测试。此外,由于∆hfq菌株中的背景减少,从这些突变体中分离和鉴定化合物变得更加简便。该方法避免了在异源表达宿主、化学合成或从野生型粗提物中繁琐提取所需化合物时经常遇到的问题。本方案描述了嗜线虫致病杆菌属和发光杆菌属的简易PACId,但它也成功应用于嗜昆虫假单胞菌,可能适用于其他携带hfq的变形菌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc9/10336570/d9128870da7e/BioProtoc-13-13-4709-g001.jpg

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