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Detection of the bacterial quorum-sensing signaling molecules N-Acyl-Homoserine Lactones (HSL) and N-Acyl-Homoserine (HS) with an Enzyme-Linked Immunosorbent Assay (ELISA) and via Ultrahigh-Performance Liquid Chromatography Coupled to Mass Spectrometry (UHPLC-MS).

Methods Mol. Biol. 1673, 61-72 (2018)
Postprint DOI PMC
Open Access Green
Quick and reliable quantitative methods requiring low amounts of sample volume are needed for the detection of N-acyl-homoserine lactones (HSL) and their degradation products N-acyl-homoserines (HS) in order to elucidate the occurrence and dynamics of these prevalent quorum-sensing molecules of Gram-negative bacteria in natural samples and laboratory model experiments. A combination of ELISA and UHPLC-MS is presented here which has proven to meet these requirements. Both methods can not only precisely detect and quantify HSLs but also their degradation products HS and thereby enable studying signaling dynamics in quorum sensing, which have been identified to play an essential role in bacterial communication.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Bacterial Signaling ; Elisa ; N-acyl-homoserine Lactone ; Quorum Sensing ; Uhplc-ms
Language english
Publication Year 2018
HGF-reported in Year 2017
ISSN (print) / ISBN 1064-3745
e-ISSN 1940-6029
Book Volume Title Quorum Sensing
Quellenangaben Volume: 1673, Issue: , Pages: 61-72 Article Number: , Supplement: ,
Publisher Springer
Publishing Place Berlin [u.a.]
Reviewing status Peer reviewed
Institute(s) Institute of Network Biology (INET)
Research Unit BioGeoChemistry and Analytics (BGC)
POF-Topic(s) 30203 - Molecular Targets and Therapies
30202 - Environmental Health
Research field(s) Environmental Sciences
PSP Element(s) G-506400-001
G-504800-001
Scopus ID 85033719317
PubMed ID 29130164
Erfassungsdatum 2017-11-22