Journal of Agricultural and Food Chemistry · 2009 · 65 citations · 18 references
AgricultureChemistryFood ScienceCarbohydrate ChemistryMetabolomicsNatural Product BiosynthesisAroma CompoundsFlavor ChemistryFlavor EvaluationFlavoring PlantsOrganic AcidsVolatile Aroma AnalysisBeer Flavor ChemistryBitterness CompoundsBoilingChemical Structure ClassificationFlavor Compound AnalysisFlavor Formation From Lipid HydrolysisFlavor IdentificationMultidimensional Nmr Spectroscopy
Thermal treatment of the hop beta-acid colupulone under wort boiling conditions, followed by LC-TOF-MS and 1D/2D NMR spectroscopy, revealed cohulupone, hulupinic acid, nortricyclocolupone, two tricyclocolupone epimers, two dehydrotricyclocolupone epimers, two hydroxytricyclocolupone epimers, and two hydroperoxytricyclocolupone epimers as the major bitter-tasting beta-acid transformation products. Among these compounds, the chemical structures of the hydroxy- as well as the hydroperoxytricyclocolupone epimers have not previously been confirmed by 1D/2D NMR experiments. Depending on their chemical structure, these compounds showed rather low recognition thresholds ranging from 7.9 to 90.3 micromol/L. The lowest thresholds of 7.9 and 14.7 micromol/L were found for cohulupone, imparting a short-lasting, iso-alpha-acid-like bitter impression, and for hydroxytricyclocolupone, exhibiting a long-lasting, lingering, and harsh bitterness perceived on the posterior tongue and throat. Furthermore, HPLC-ESI-MS/MS analysis allowed for the first time a simultaneous detection and quantitation of these bitter-tasting beta-acid transformation products in a range of commercial beer samples without any sample cleanup. Depending on the type of beer, these studies revealed remarkable differences in the concentrations of the individual beta-acid transformation products.
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