TY - JOUR
T1 - New Degradation Pathways of the Key Aroma Compound 1-Penten-3-one during Storage of Not-from-Concentrate Orange Juice
AU - Mall, Veronika
AU - Sellami, Ines
AU - Schieberle, Peter
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/10/24
Y1 - 2018/10/24
N2 - 1-Penten-3-one with its fresh and pungent smell at a very low odor threshold of 0.94 μg/L water has been characterized as impact aroma compound in many foods, such as grapefruit, orange juice, black tea, olive oil, or tomatoes. While its importance to the fresh sensation of unstored not-from-concentrate (NFC) orange juice was recently confirmed by aroma recombinates, a total loss was determined already after 4 weeks in NFC orange juice stored at 0 °C. Until now, the degradation pathway of this compound has not been clarified. Systematic model studies resulted in the identification of 1-hydroxy-3-pentanone and 4-hydroxy-3,8-decanedione as degradation products as well as S-(3-oxopentyl)-l-cysteine in the presence of the amino acid. In orange juice samples, it was found that the elevated content of 1-hydroxy-3-pentanone indicates a thermal processing, while S-(3-oxopentyl)-l-cysteine showed a significant increase during cold storage. Additionally, both compounds were identified in other food samples, such as commercial orange juices, pickled olives and olive oil, fresh tomatoes and commercial tomato juice, and black tea.
AB - 1-Penten-3-one with its fresh and pungent smell at a very low odor threshold of 0.94 μg/L water has been characterized as impact aroma compound in many foods, such as grapefruit, orange juice, black tea, olive oil, or tomatoes. While its importance to the fresh sensation of unstored not-from-concentrate (NFC) orange juice was recently confirmed by aroma recombinates, a total loss was determined already after 4 weeks in NFC orange juice stored at 0 °C. Until now, the degradation pathway of this compound has not been clarified. Systematic model studies resulted in the identification of 1-hydroxy-3-pentanone and 4-hydroxy-3,8-decanedione as degradation products as well as S-(3-oxopentyl)-l-cysteine in the presence of the amino acid. In orange juice samples, it was found that the elevated content of 1-hydroxy-3-pentanone indicates a thermal processing, while S-(3-oxopentyl)-l-cysteine showed a significant increase during cold storage. Additionally, both compounds were identified in other food samples, such as commercial orange juices, pickled olives and olive oil, fresh tomatoes and commercial tomato juice, and black tea.
KW - 1-hydroxy-3-pentanone
KW - 1-penten-3-one
KW - S-(3-oxopentyl)-L-cysteine
KW - black tea
KW - degradation products
KW - ethyl vinyl ketone
KW - olive oil
KW - tomato juice
UR - http://www.scopus.com/inward/record.url?scp=85055006607&partnerID=8YFLogxK
U2 - 10.1021/acs.jafc.8b04334
DO - 10.1021/acs.jafc.8b04334
M3 - Article
C2 - 30240205
AN - SCOPUS:85055006607
SN - 0021-8561
VL - 66
SP - 11083
EP - 11091
JO - Journal of agricultural and food chemistry
JF - Journal of agricultural and food chemistry
IS - 42
ER -