Synthesis and analysis of stable isotope-labelled N-acyl homoserine lactones?

RSC Advances Pub Date: 2016-07-28 DOI: 10.1039/C6RA17797B

Abstract

Aliphatic aldehydes were deuterated at the α-position via a base-catalyzed exchange reaction with D2O. These deuterated building blocks were used for the synthesis of labelled analogues of quorum sensing signal molecules belonging to the three major classes of naturally occurring N-acylated homoserine lactones (AHLs), with the label on a non-enolizable and therefore stable position. Besides the application of these stable isotope-labelled AHLs as a labelled standard for analysis via isotope dilution mass spectrometry, these compounds can be used to study the metabolic fate of the fatty acid tail of the AHL-molecule. These isotope-labelled compounds were fully characterized and used to synthesize the deuterated analogues of two commonly occurring AHL-degradation products, a tetramic acid and a ring opened N-acyl homoserine.

Graphical abstract: Synthesis and analysis of stable isotope-labelled N-acyl homoserine lactones
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