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利用新的自动化和灵敏荧光检测方法筛选芽孢杆菌属的脂肽产生菌株。

Screening of Lipopeptide-Producing Strains of Bacillus sp. Using a New Automated and Sensitive Fluorescence Detection Method.

机构信息

University Lille, INRA, ISA, University Artois, Univ. Littoral Côte d'Opale, EA 7394-ICV Institut Charles Viollette, F-59000, Lille, France.

Faculty of Chemistry, Pontifical Catholic University of Campinas, Rod. D. Pedro I, km 136, Campinas, SP, 13086-900, Brazil.

出版信息

Biotechnol J. 2019 Apr;14(4):e1800314. doi: 10.1002/biot.201800314. Epub 2018 Nov 26.

Abstract

Lipopeptides, such as surfactins are important biosurfactants produced by Bacillus sp. that find applications in many areas (environment, medicine, and food industries). Giving their importance, the use of simple detection methods will facilitate screening and quantification. In the present work, the authors describe a completely automated workflow for the screening of lipopeptide-producing strains, including quantification. First, isolated colonies from environmental samples are automatically picked and inoculated in 96 wells growth plate. After overnight incubation, surfactin produced in the broth is quantified, using a new sensitive fluorescent method. The method uses fluorescein (FL), which is an anionic dye at neutral to alkaline pH and forms a stable complex with the cationic surfactant cetylpiridinium chloride (CPC), quenching fluorescence. Upon addition of surfactin or other lipopeptides, fluorescein is released from the CPC-FL complex and quantified. The robustness of this method is assessed by comparing the quantification results to those conventionally measured by RP-UPLC and the results of strain screening are confirmed by MALDI-ToF analysis. The authors report for the first time the successful application of this analytical method for high-throughput screening of novel lipopeptide-producing strains.

摘要

脂肽,如表面活性剂,是由芽孢杆菌属产生的重要生物表面活性剂,在许多领域(环境、医学和食品工业)都有应用。鉴于其重要性,使用简单的检测方法将有助于筛选和定量。在本工作中,作者描述了一种完全自动化的筛选产脂肽菌株的工作流程,包括定量。首先,从环境样本中分离的菌落被自动挑取并接种到 96 孔生长板中。过夜孵育后,使用新的灵敏荧光法定量测定发酵液中产生的表面活性剂。该方法使用荧光素(FL),在中性到碱性 pH 值下,FL 是一种阴离子染料,与阳离子表面活性剂十六烷基吡啶氯(CPC)形成稳定的配合物,使荧光猝灭。加入表面活性剂或其他脂肽后,荧光素从 CPC-FL 配合物中释放出来并被定量。通过将定量结果与传统的反相高效液相色谱法(RP-UPLC)测量的结果进行比较,评估了该方法的稳健性,通过 MALDI-ToF 分析确认了菌株筛选的结果。作者首次成功应用该分析方法对新型产脂肽菌株进行高通量筛选。

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