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
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.