Suppr超能文献

建立琼脂塞培养系统以用于放线菌菌株收集物的生物活性测定。

Development of an agar-plug cultivation system for bioactivity assays of actinomycete strain collections.

机构信息

Department of Microbiology/Biotechnology, Interfaculty Institute of Microbiology and Infection Medicine, Eberhard Karls University Tübingen, Tübingen, Germany.

German Centre for Infection Research (DZIF), Partner Site Tübingen, Tübingen, Germany.

出版信息

PLoS One. 2021 Nov 5;16(11):e0258934. doi: 10.1371/journal.pone.0258934. eCollection 2021.

Abstract

Natural products are an important source of lead compounds for the development of drug substances. Actinomycetes have been valuable especially for the discovery of antibiotics. Increasing occurrence of antibiotic resistance among bacterial pathogens has revived the interest in actinomycete natural product research. Actinobacteria produce a different set of natural products when cultivated on solid growth media compared with submersed culture. Bioactivity assays involving solid media (e.g. agar-plug assays) require manual manipulation of the strains and agar plugs. This is less convenient for the screening of larger strain collections of several hundred or thousand strains. Thus, the aim of this study was to develop a 96-well microplate-based system suitable for the screening of actinomycete strain collections in agar-plug assays. We developed a medium-throughput cultivation and agar-plug assay workflow that allows the convenient inoculation of solid agar plugs with actinomycete spore suspensions from a strain collection, and the transfer of the agar plugs to petri dishes to conduct agar-plug bioactivity assays. The development steps as well as the challenges that were overcome during the development (e.g. system sterility, handling of the agar plugs) are described. We present the results from one exemplary screening campaign targeted to identify compounds inhibiting Agr-based quorum sensing where the workflow was used successfully. We present a novel and convenient workflow to combine agar diffusion assays with microtiter-plate-based cultivation systems in which strains can grow on a solid surface. This workflow facilitates and speeds up the initial medium throughput screening of natural product-producing actinomycete strain collections against monitor strains in agar-plug assays.

摘要

天然产物是开发药物物质的重要先导化合物来源。放线菌在发现抗生素方面特别有价值。细菌病原体对抗生素的耐药性日益增加,重新激发了人们对放线菌天然产物研究的兴趣。与浸没培养相比,放线菌在固体生长培养基上培养时会产生不同的天然产物。涉及固体培养基的生物活性测定(例如琼脂塞测定)需要对菌株和琼脂塞进行手动操作。对于筛选几百或几千个菌株的较大菌株集合,这不太方便。因此,本研究的目的是开发一种基于 96 孔微孔板的系统,适用于琼脂塞测定中放线菌菌株集合的筛选。我们开发了一种高通量培养和琼脂塞测定工作流程,该流程允许方便地用放线菌孢子悬浮液接种固体琼脂塞,从菌株集合中,并将琼脂塞转移到培养皿中进行琼脂塞生物活性测定。描述了开发步骤以及在开发过程中克服的挑战(例如系统无菌性、琼脂塞的处理)。我们展示了一项针对鉴定 Agr 基于群体感应抑制化合物的示例筛选活动的结果,该工作流程成功应用于此。我们提出了一种新颖且方便的工作流程,将琼脂扩散测定与基于微孔板的培养系统相结合,其中菌株可以在固体表面上生长。该工作流程有助于加快和简化针对琼脂塞测定中的监测菌株对天然产物产生的放线菌菌株集合的初始高通量筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89a2/8570476/eea088eac731/pone.0258934.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验