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Effect of Positional Distribution of Linoleic Acid on Oxidative Stability of Triacylglycerol Molecules Determined by 1 H NMR
Author(s) -
Wang XiangYu,
Yang Dan,
Gan LuJing,
Zhang Hua,
Shin JungAh,
Lee YongHwa,
Jang YoungSeok,
Lee KiTeak
Publication year - 2015
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-015-2590-y
Subject(s) - autoxidation , chemistry , linoleic acid , polyunsaturated fatty acid , fatty acid , interesterified fat , oxidative phosphorylation , oxidation process , organic chemistry , biochemistry , pulp and paper industry , lipase , engineering , enzyme
Abstract 1 H nuclear magnetic resonance ( 1 H NMR) was used to determine the effect of positional distribution of linoleic acid (L) on the oxidative stability of triacylglycerols. For this purpose, structured soybean oil (SSO), which had a similar total fatty acid composition but a different L positional distribution than soybean oil (SO), was produced by interesterification reaction. The SO and SSO were oxidized in the dark at 40 °C. Afterwards, 1 H NMR was used to monitor the oxidation process and quantify the main polyunsaturated fatty acid, Z , E ‐ and E , E ‐conjugated forms, hydroperoxides, and aldehydes at different oxidation periods in a single run. After 45 days of oxidation, SSO showed lower L content than SO (9.9 ± 1.1 and 16.8 ± 0.5 %, respectively). Additionally, secondary oxidation products in SSO were shown to be more abundant than in SO (82.3 ± 4.9 and 43.6 ± 0.9 mmol/L oil, respectively). This study indicated that SO, which contains a higher distribution of L at the sn ‐2 position, was more resistant to autoxidation than SSO.