32
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Usage of FT-ICR-MS Metabolomics for Characterizing the Chemical Signatures of Barrel-Aged Whisky

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Whisky can be described as a complex matrix integrating the chemical history from the fermented cereals, the wooden barrels, the specific distillery processes, aging, and environmental factors. In this study, using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) and liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS), we analyzed 150 whisky samples from 49 different distilleries, 7 countries, and ranging from 1 day new make spirit to 43 years of maturation with different types of barrel. Chemometrics revealed the unexpected impact of the wood history on the distillate's composition during barrel aging, regardless of the whisky origin. Flavonols, oligolignols, and fatty acids are examples of important chemical signatures for Bourbon casks, whereas a high number of polyphenol glycosides, including for instance quercetin-glucuronide or myricetin-glucoside as potential candidates, and carbohydrates would discriminate Sherry casks. However, the comparison of barrel aged rums and whiskies revealed specific signatures, highlighting the importance of the initial composition of the distillate and the distillery processes.

          Related collections

          Most cited references39

          • Record: found
          • Abstract: not found
          • Article: not found

          Metabolomic analysis in food science: a review

            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Evolution of Complex Maillard Chemical Reactions, Resolved in Time

            In this study, we monitored the thermal formation of early ribose-glycine Maillard reaction products over time by ion cyclotron resonance mass spectrometry. Here, we considered sugar decomposition (caramelization) apart from compounds that could only be produced in the presence of the amino acid. More than 300 intermediates as a result of the two initial reactants were found after ten hours (100 °C) to participate in the interplay of the Maillard reaction cascade. Despite the large numerical variety the majority of intermediates follow simple and repetitive reaction patterns. Dehydration, carbonyl cleavage, and redox reactions turned out to have a large impact on the diversity the Maillard reaction causes. Although the Amadori breakdown is considered as the main Maillard reaction pathway, other reactive intermediates, often of higher molecular weight than the Amadori rearrangement product, contribute to a large extent to the multitude of intermediates we observed.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Wood maturation of distilled beverages

                Bookmark

                Author and article information

                Contributors
                Journal
                Front Chem
                Front Chem
                Front. Chem.
                Frontiers in Chemistry
                Frontiers Media S.A.
                2296-2646
                22 February 2018
                2018
                : 6
                : 29
                Affiliations
                [1] 1Comprehensive Foodomics Platform, Technische Universität München , Freising, Germany
                [2] 2Research Unit Analytical BioGeoChemistry, Department of Environmental Sciences, Helmholtz Zentrum München , Neuherberg, Germany
                [3] 3Independent Spirit Consultant , Nuremberg, Germany
                [4] 4UMR PAM Université de Bourgogne, AgroSupDijon, Institut Universitaire de la Vigne et du Vin , Dijon, France
                Author notes

                Edited by: Holger Hintelmann, Trent University, Canada

                Reviewed by: Michaela Schafberg, Federal Maritime and Hydrographic Agency of Germany, Germany; Viduranga Y. Waisundara, Rajarata University of Sri Lanka, Sri Lanka

                *Correspondence: Chloé Roullier-Gall c.roullier.gall@ 123456gmail.com

                This article was submitted to Food Chemistry, a section of the journal Frontiers in Chemistry

                Article
                10.3389/fchem.2018.00029
                5827162
                29520358
                fcb1ed46-b92a-477c-b26c-8ad624314514
                Copyright © 2018 Roullier-Gall, Signoret, Hemmler, Witting, Kanawati, Schäfer, Gougeon and Schmitt-Kopplin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 28 June 2017
                : 05 February 2018
                Page count
                Figures: 5, Tables: 2, Equations: 0, References: 51, Pages: 11, Words: 7051
                Categories
                Chemistry
                Original Research

                whisky,ft-icr-ms,barrel,wood,rum,distillate,lc-ms
                whisky, ft-icr-ms, barrel, wood, rum, distillate, lc-ms

                Comments

                Comment on this article