| Literature DB >> 26456773 |
Daniel Shin1, Nicole D Frane1, Ryan M Brecht1,2, Jesse Keeler3,4, Rajesh Nagarajan5.
Abstract
Quorum sensing is cell-to-cell communication that allows bacteria to coordinate attacks on their hosts by inducing virulent gene expression, biofilm production, and other cellular functions, including antibiotic resistance. AHL synthase enzymes synthesize N-acyl-l-homoserine lactones, commonly referred to as autoinducers, to facilitate quorum sensing in Gram-negative bacteria. Studying the synthases, however, has proven to be a difficult road. Two assays, including a radiolabeled assay and a colorimetric (DCPIP) assay are well-documented in literature to study AHL synthases. In this paper, we describe additional methods that include an HPLC-based, C-S bond cleavage and coupled assays to investigate this class of enzymes. In addition, we compare and contrast each assay for both acyl-CoA- and acyl-ACP-utilizing synthases. The expanded toolkit described in this study should facilitate mechanistic studies on quorum sensing signal synthases and expedite discovery of antivirulent compounds.Entities:
Keywords: acyl-homoserine lactone synthase; enzyme assays; methylthioadenosine nucleosidase; quorum sensing; xanthine oxidase
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Year: 2015 PMID: 26456773 PMCID: PMC5002224 DOI: 10.1002/cbic.201500387
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164