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.
| Original language | English |
|---|---|
| Pages (from-to) | 2651-2659 |
| Number of pages | 9 |
| Journal | ChemBioChem |
| Volume | 16 |
| Issue number | 18 |
| DOIs | |
| State | Published - 14 Dec 2015 |
Keywords
- acyl-homoserine lactone synthase
- enzyme assays
- methylthioadenosine nucleosidase
- quorum sensing
- xanthine oxidase
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