2-Aminoacetophenone — A hepatic skatole metabolite as a potential contributor to boar taint

The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to boar taint, which is an undesired off-flavor in pork. Therefore, backfat samples were screened by HS-SPME–GC/MS revealing a significant accumula...

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Published inFood research international Vol. 62; pp. 35 - 42
Main Authors Fischer, Jochen, Gerlach, Christoph, Meier-Dinkel, Lisa, Elsinghorst, Paul W., Boeker, Peter, Schmarr, Hans-Georg, Wüst, Matthias
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.08.2014
Elsevier
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Abstract The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to boar taint, which is an undesired off-flavor in pork. Therefore, backfat samples were screened by HS-SPME–GC/MS revealing a significant accumulation of the hepatic skatole metabolite 2-AAP in boar fat. Subsequently, a stable-isotope dilution assay (SIDA) was elaborated to precisely quantitate 2-AAP in a set of 130 backfat samples. The observed concentrations ranged between 34ng/g and 1178ng/g, resulting in a mean value of 100ng/g. In addition, the odor detection threshold of 2-AAP was evaluated by a trained sensory panel using a single-staircase, triple forced choice paradigm. The determined 2-AAP odor detection threshold is similar to the thresholds of the major boar taint compounds androstenone and skatole. Finally, a sensory evaluation of backfat samples spiked with 2-AAP was performed in a triangle test with untrained testers. Here, the 2-AAP spiked samples were frequently identified as the odd sample independent of their respective androstenone and skatole levels. In conclusion, the hepatic skatole metabolite 2-AAP was identified as a potential contributor to boar taint. •2-Aminoacetophenone (2-AAP) was identified as potential contributor to boar taint.•GC/MS analysis reveals significant accumulation of 2-AAP in back fat.•Odor threshold of 2-AAP is comparable to the androstenone/skatole threshold.•2-AAP spiked back fat samples are determined as the odd sample in triangle tests.
AbstractList The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to boar taint, which is an undesired off-flavor in pork. Therefore, backfat samples were screened by HS-SPME–GC/MS revealing a significant accumulation of the hepatic skatole metabolite 2-AAP in boar fat. Subsequently, a stable-isotope dilution assay (SIDA) was elaborated to precisely quantitate 2-AAP in a set of 130 backfat samples. The observed concentrations ranged between 34ng/g and 1178ng/g, resulting in a mean value of 100ng/g. In addition, the odor detection threshold of 2-AAP was evaluated by a trained sensory panel using a single-staircase, triple forced choice paradigm. The determined 2-AAP odor detection threshold is similar to the thresholds of the major boar taint compounds androstenone and skatole. Finally, a sensory evaluation of backfat samples spiked with 2-AAP was performed in a triangle test with untrained testers. Here, the 2-AAP spiked samples were frequently identified as the odd sample independent of their respective androstenone and skatole levels. In conclusion, the hepatic skatole metabolite 2-AAP was identified as a potential contributor to boar taint.
The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to boar taint, which is an undesired off-flavor in pork. Therefore, backfat samples were screened by HS-SPME-GC/MS revealing a significant accumulation of the hepatic skatole metabolite 2-AAP in boar fat. Subsequently, a stable-isotope dilution assay (SIDA) was elaborated to precisely quantitate 2-AAP in a set of 130 backfat samples. The observed concentrations ranged between 34 ng/g and 1178 ng/g, resulting in a mean value of 100 ng/g. In addition, the odor detection threshold of 2-AAP was evaluated by a trained sensory panel using a single-staircase, triple forced choice paradigm. The determined 2-AAP odor detection threshold is similar to the thresholds of the major boar taint compounds androstenone and skatole. Finally, a sensory evaluation of backfat samples spiked with 2-AAP was performed in a triangle test with untrained testers. Here, the 2-AAP spiked samples were frequently identified as the odd sample independent of their respective androstenone and skatole levels. In conclusion, the hepatic skatole metabolite 2-AAP was identified as a potential contributor to boar taint.
The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to boar taint, which is an undesired off-flavor in pork. Therefore, backfat samples were screened by HS-SPME–GC/MS revealing a significant accumulation of the hepatic skatole metabolite 2-AAP in boar fat. Subsequently, a stable-isotope dilution assay (SIDA) was elaborated to precisely quantitate 2-AAP in a set of 130 backfat samples. The observed concentrations ranged between 34ng/g and 1178ng/g, resulting in a mean value of 100ng/g. In addition, the odor detection threshold of 2-AAP was evaluated by a trained sensory panel using a single-staircase, triple forced choice paradigm. The determined 2-AAP odor detection threshold is similar to the thresholds of the major boar taint compounds androstenone and skatole. Finally, a sensory evaluation of backfat samples spiked with 2-AAP was performed in a triangle test with untrained testers. Here, the 2-AAP spiked samples were frequently identified as the odd sample independent of their respective androstenone and skatole levels. In conclusion, the hepatic skatole metabolite 2-AAP was identified as a potential contributor to boar taint. •2-Aminoacetophenone (2-AAP) was identified as potential contributor to boar taint.•GC/MS analysis reveals significant accumulation of 2-AAP in back fat.•Odor threshold of 2-AAP is comparable to the androstenone/skatole threshold.•2-AAP spiked back fat samples are determined as the odd sample in triangle tests.
Author Elsinghorst, Paul W.
Wüst, Matthias
Fischer, Jochen
Gerlach, Christoph
Meier-Dinkel, Lisa
Boeker, Peter
Schmarr, Hans-Georg
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Keywords Off-flavor
Skatole metabolism
SIDA
2-Aminoacetophenone
Boar taint
Metabolite
Liver
Metabolism
Pig
Vertebrata
Meat animals
Mammalia
Artiodactyla
Ungulata
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Snippet The major objective of the presented study was to evaluate whether the hepatic skatole metabolite 2-aminoacetophenone (2-AAP) is a potential contributor to...
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SubjectTerms 2-Aminoacetophenone
backfat
Biological and medical sciences
Boar taint
boars
detection limit
Food industries
Fundamental and applied biological sciences. Psychology
metabolites
odors
off flavors
Off-flavor
pork
sensory evaluation
SIDA
skatole
Skatole metabolism
stable isotopes
Title 2-Aminoacetophenone — A hepatic skatole metabolite as a potential contributor to boar taint
URI https://dx.doi.org/10.1016/j.foodres.2014.02.045
https://www.proquest.com/docview/1551615821
https://www.proquest.com/docview/1836631377
Volume 62
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