Literature DB >> 21031320

High-performance liquid chromatography analysis of N-acyl homoserine lactone hydrolysis by paraoxonases.

John F Teiber1, Dragomir I Draganov.   

Abstract

Mammalian paraoxonases (PONs) are a unique, highly conserved family of calcium-dependent esterases consisting of PON1, PON2, and PON3. The PONs can hydrolyze the lactone ring of a range of N-acyl-L: -homoserine lactone (AHL) quorum sensing signaling molecules, rendering them inactive. This chapter describes a method that utilizes high-performance liquid chromatography analysis with UV detection for determining the rate of AHL hydrolysis in cell lysates, tissue homogenates, serum, and with purified proteins. Also described are the techniques used to prepare cell culture lysates and tissue homogenates for analysis and the use of class-specific enzyme inhibitors to determine the contribution of PONs to AHL hydrolysis in the samples.

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Year:  2011        PMID: 21031320     DOI: 10.1007/978-1-60761-971-0_21

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

Review 1.  Divergence and convergence in enzyme evolution: parallel evolution of paraoxonases from quorum-quenching lactonases.

Authors:  Mikael Elias; Dan S Tawfik
Journal:  J Biol Chem       Date:  2011-11-08       Impact factor: 5.157

2.  Novel Quorum Quenching YtnP Lactonase From Bacillus paralicheniformis Reduces Pseudomonas aeruginosa Virulence and Increases Antibiotic Efficacy in vivo.

Authors:  Lidija Djokic; Nada Stankovic; Ivana Galic; Ivana Moric; Natasa Radakovic; Sandra Šegan; Aleksandar Pavic; Lidija Senerovic
Journal:  Front Microbiol       Date:  2022-06-02       Impact factor: 6.064

  2 in total

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