Jc. Martin et al., EFFECT OF FATTY-ACID POSITIONAL DISTRIBUTION AND TRIACYLGLYCEROL COMPOSITION ON LIPID BY-PRODUCTS FORMATION DURING HEAT-TREATMENT - II - TRANS ISOMERS, Journal of the American Oil Chemists' Society, 75(9), 1998, pp. 1073-1078
This study examined the effect of the fatty acid positional distributi
on and of the triacylglycerol (TC) composition on heat-induced trans i
somerization of linoleic and linolenic acids. For this, we synthesized
diacid TG molecules that were acylated only with linoleic acid (L) or
with linolenic acid (Ln) along with palmitic acid (P). The fatty acid
of interest was positioned either in the central position (PLP and PL
nP, respectively) or in one of the two outer positions (PPL and PPLn,
respectively). Monoacid TG, i.e., trilinolein and trilinolenin, were a
lso synthesized and mixed with tripalmitin in a 1:2 ratio. This model
TG was also compared to another TC model, which consisted of a canola
oil and its randomized counterpart whose fatty acid positional distrib
ution and TC composition were determined by means of high-performance
liquid chromatography. After heating, the content of trans isomers was
determined by gas-liquid chromatography with a polar capillary column
. In model TG, polyunsaturated fatty acids in monoacid TC (LLL acid Ln
LnLn) exhibited the highest degree of isomerization, compared to diaci
d TC, and this effect was greatest at 220 degrees C At this temperatur
e, an effect of the TG structure was observed only with linolenic acid
. In that situation, 18:3n-3 acylated in the central position of the T
G molecule (PLnP) displayed the highest sensitivity to trans geometric
al isomerization. Although to a lesser extent, the same trends as for
the pure TC model were observed with the canola oil model with regard
to the influence of the fatty acid positional distribution and TC mole
cular species.