OXIDATIVE STABILITIES OF SOYBEAN OILS THAT LACK LIPOXYGENASES

Citation
N. Shen et al., OXIDATIVE STABILITIES OF SOYBEAN OILS THAT LACK LIPOXYGENASES, Journal of the American Oil Chemists' Society, 73(10), 1996, pp. 1327-1336
Citations number
36
Categorie Soggetti
Food Science & Tenology","Chemistry Applied
ISSN journal
0003021X
Volume
73
Issue
10
Year of publication
1996
Pages
1327 - 1336
Database
ISI
SICI code
0003-021X(1996)73:10<1327:OSOSOT>2.0.ZU;2-Y
Abstract
Lipoxygenase (LOX)-null soybean lines that lack LOX 2, or LOX 2 and 3, and contain normal (8.0-8.6%) or low (2.0-2.8%) linolenate (18:3) amo unts were evaluated for their oil qualities and storage stabilities. S oybean oils of six genotypes were extracted by both laboratory-scale a nd pilot-plant systems and were refined, bleached, and deodorized in t he laboratory. Citric acid was added to oils during the cool-down stag e of deodorization. Two replications, separated at the point oi condit ioning, were evaluated for each genotype. Under storage conditions of 55-60 degrees C in the dark, soybean oils with low 18:3 contents were significantly (P less than or equal to 0.05) more stable as measured b y peroxide values than were oils with normal 18:3 contents, regardless of the LOX content of the beans. The volatile analysis showed few dif ferences between oils with low and high 18:3 contents or among oils fr om beans that lack different LOX enzymes. After 16 d of storage, the a mount of 1-octen-3-ol was significantly greater in oils with low 18:3 content, and soybean oils from beans with normal LOX content had a sig nificantly (P less than or equal to 0.05) lower amount of 1-octen-3-ol than did the oils that lacked LOX enzymes. Storage at 35 degrees C un der light showed no differences in volatile amounts or sensory evaluat ions after 14 d of storage. During storage, peroxide values tended to be lower in oils from beans with normal 18:3 content and in oils from beans with normal LOX content. Generally, the absence of LOX 2 or LOX 2 and 3, although having a small effect on lipid oxidation, was not as important to oil quality as was the 18:3 content.