TY - JOUR
T1 - Characterization of Bitter Off-Taste Stimuli in Sunflower Press Cake Using the Sensomics Approach
AU - Huseynli, Lachinkhanim
AU - Gigl, Michael
AU - Müller, Jasmin
AU - Walser, Christoph
AU - Frank, Oliver
AU - Vene, Kristel
AU - Dawid, Corinna
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/9/17
Y1 - 2025/9/17
N2 - The Sensomics approach, including activity-guided fractionation and taste dilution analysis, was employed to identify the key compounds responsible for the bitter off-taste of sunflower press cake. A combination of liquid chromatography–tandem mass spectrometry, liquid chromatography–time-of-flight-mass spectrometry, one-/two-dimensional nuclear magnetic resonance spectroscopy, and dose-overthreshold factor calculation led to the identification of 9,12,13-trihydroxyoctadec-10-enoic acid, 9,10,11-trihydroxyoctadec-12-enoic acid, 11,12,13-trihydroxyoctadec-9-enoic acid, (10E,12E)-9-hydroxyoctadeca-10,12-dienoic acid, (10E,12Z)-9-hydroxyoctadeca-10,12-dienoic acid, (9E,11E)-13-hydroxyoctadeca-9,11-dienoic acid, (9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid, (9Z,11E)-13-oxooctadeca-9,11-dienoic acid, α-linolenic acid, linoleic acid, oleic acid, 2-hydroxyoleic acid, palmitic acid, stearic acid, and novel pinocarveol β-d-apiofuranosyl-(1→6)-β-d-(4-O-caffeoyl) glucopyranoside as contributors to the bitterness of sunflower press cake. The findings provide valuable insights into the sensory challenges associated with using sunflower press cake in food applications and offer pathways to enhance its palatability and potential as a sustainable protein alternative to meet future protein demands.
AB - The Sensomics approach, including activity-guided fractionation and taste dilution analysis, was employed to identify the key compounds responsible for the bitter off-taste of sunflower press cake. A combination of liquid chromatography–tandem mass spectrometry, liquid chromatography–time-of-flight-mass spectrometry, one-/two-dimensional nuclear magnetic resonance spectroscopy, and dose-overthreshold factor calculation led to the identification of 9,12,13-trihydroxyoctadec-10-enoic acid, 9,10,11-trihydroxyoctadec-12-enoic acid, 11,12,13-trihydroxyoctadec-9-enoic acid, (10E,12E)-9-hydroxyoctadeca-10,12-dienoic acid, (10E,12Z)-9-hydroxyoctadeca-10,12-dienoic acid, (9E,11E)-13-hydroxyoctadeca-9,11-dienoic acid, (9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid, (9Z,11E)-13-oxooctadeca-9,11-dienoic acid, α-linolenic acid, linoleic acid, oleic acid, 2-hydroxyoleic acid, palmitic acid, stearic acid, and novel pinocarveol β-d-apiofuranosyl-(1→6)-β-d-(4-O-caffeoyl) glucopyranoside as contributors to the bitterness of sunflower press cake. The findings provide valuable insights into the sensory challenges associated with using sunflower press cake in food applications and offer pathways to enhance its palatability and potential as a sustainable protein alternative to meet future protein demands.
KW - bitter taste
KW - fatty acid oxidation products
KW - liquid chromatography−tandem mass spectrometry
KW - off-flavor
KW - sunflower
UR - https://www.scopus.com/pages/publications/105016099457
U2 - 10.1021/acs.jafc.5c07283
DO - 10.1021/acs.jafc.5c07283
M3 - Article
C2 - 40908255
AN - SCOPUS:105016099457
SN - 0021-8561
VL - 73
SP - 23548
EP - 23559
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 37
ER -