Fatty Acid Composition of Crude and Refined Cottonseed Oils

1969 ◽  
Vol 52 (6) ◽  
pp. 1146-1150 ◽  
Author(s):  
John L Iverson

Abstract The fatty acid composition of 20 cottonseed oils was determined by isothermal GLC analysis of the total esters. A urea fractionation procedure, combined with modified programmed temperature GLC, was used to detect esters present in trace amounts (0.001–0.1%) in four refined and three crude oils. The odd a n d even chain length saturated acids from C8 to C26 were present. Mono-unsaturated acids from C15 to C20 were also detected. The crude and refined oils did not differ markedly in their fatty acid composition. The presence of malvalic and sterculic acids and the possible presence of shorter and longer chain length cyclopropenoid acids with their interfering GLC peaks make it impossible to detect and quantitatively estimate the branched and multiple branched acids.

1969 ◽  
Vol 52 (4) ◽  
pp. 685-688
Author(s):  
John L Iverson ◽  
P G Harrill ◽  
Robert W Weik

Abstract This proposed urea fractionation procedure concentrates esters with similar GLC retention times in separate fractions. GLC peaks of esters present in cocoa butter oil in trace amounts (0.001–0.1%), which are normally hidden under major peaks, can then be detected. By modified programmed temperature GLC techniques, it is possible to detect the short and long chain length fatty acids present in cocoa butter oil. The odd and even chain length saturated acids from C10 to C28, mono-unsaturates C16 to C24, branched acids C16 to C24, and linoleic and linolenic acids were detected.


1967 ◽  
Vol 102 (3) ◽  
pp. 637-647 ◽  
Author(s):  
E. F. Annison ◽  
J. L. Linzell ◽  
S Fazakerley ◽  
B. W. Nichols

1. Measurements were made of milk yield, mammary blood flow and arteriovenous differences of each plasma lipid fraction, and their specific radioactivities, during the infusion of [U-(14)C]stearate, [U-(14)C]oleate, [U-(14)C]palmitate and [1-(14)C]acetate into fed lactating goats. 2. Entry rates of fatty acids into the circulation were 4.2mg./min./kg. body wt. for acetate, and 0.18, 0.28 and 0.42mg./min./kg. for stearate, oleate and palmitate respectively. Acetate accounted for 23% of the total carbon dioxide produced by the whole animal, and contributed to the oxidative metabolism of the mammary gland to about the same extent. Corresponding values for each of the long-chain acids were less than 1%. 3. There were no significant arteriovenous differences of phospholipids, sterols or sterol esters, and their fatty acid composition showed no net changes during passage through the mammary gland. 4. There were large arteriovenous differences of plasma triglycerides, and their fatty acid composition showed marked changes across the gland. The proportions of palmitate and stearate fell, and that of oleate increased. 5. Arteriovenous differences of plasma free fatty acids (FFA) were small and variable, but a large fall in the specific radioactivity of each of the long-chain acids examined indicated substantial uptake of plasma FFA, accompanied by roughly equivalent FFA release from mammary tissue. The uptake of FFA was confirmed by the extensive transfer of radioactivity into milk. The FFA of milk were similar in composition and radioactivity to the milk triglyceride fatty acids, and quite unlike plasma FFA. 6. The formation of large amounts of oleic acid (18-21 mg./min.) from stearic acid was demonstrated. 7. During the terminal stages of the [(14)C]acetate infusion, milk triglyceride fatty acids of chain length C(4)-C(14) showed specific radioactivities that were 75-90% of that of blood acetate, and that of palmitate was roughly one-quarter of this value. Oleate and stearate were unlabelled. 8. The results confirmed that milk fatty acids of chain length C(4)-C(14) arise largely from blood acetate, and palmitate is derived partly from acetate and partly from plasma triglyceride, the latter fraction being almost the sole precursor of oleate and stearate.


1972 ◽  
Vol 55 (3) ◽  
pp. 645-647
Author(s):  
G C Tsatsaronis ◽  
D G Boskou

Abstract The fatty acid composition of the oil extracted from tomato seeds was determined by GLC. A urea fractionation procedure and preparative GLC were used to detect esters present in small or trace amounts. Linoleic, oleic, and palmitic acids were predominant. Odd- and even-chain length saturated acids from C12-C28 were present. Hexadecenoic, heptadecenoic, and eicosenoic acids were also detected. Minor chromatographic peaks preceding some of the saturated esters were attributed to branched acids.


1966 ◽  
Vol 49 (2) ◽  
pp. 332-336
Author(s):  
John L Iverson

Abstract The detection of C20 to C26 polyunsaturated fatty acids in a Cruciferae seed oil (white mustard) is possible when these methyl esters are concentrated by urea fractionation. The detection and estimation of fatty acids present in trace amounts (< 0.1%) was simplified by quantitative removal of other fatty acids with similar gas chromatographic retention times. Odd and even chain length di- and tri-unsaturated fatty acids were tentatively identified in white mustard seed oil. A tetraenoic acid, presumably arachidonic acid, was tentatively identified for the first time in a plant lipid of the highest evolutionary level, i.e., angiospermae. More easily extracted “free” lipids have a significantly different fatty acid composition than the more difficult to extract “bound” lipids.


1979 ◽  
Vol 46 (1) ◽  
pp. 75-81 ◽  
Author(s):  
Peter W. Parodi

SUMMARYPancreatic lipase deacylation was used to study the variation in distribution of the fatty acids at position sn-2 of milk fat triglycerides of a series of butters and of the milk obtained from a cow on a restricted feeding regimen. Selected samples were analysed for stereospecific distribution of their triglyceride fatty acids which were found to be esterified in a non-random manner. The percentage of a fatty acid at position sn-3 generally decreased with increase in the chain length of the acid; the reverse occurred at position sn-1. There was no major variation in the stereospecific distribution of fatty acids throughout the year; the variation that did occur was exhibited mainly by the medium chain length acids. Variation was greater at positions sn-1 and sn-3 than at position sn-2 and when the proportion of an acid varied at position sn-1 it usually varied at position sn-3 in the reverse manner.For the milk samples it was found that change in triglyceride fatty acid composition was not associated with random increases or decreases of fatty acids at the 3 stereospecific positions. With changing triglyceride fatty acid composition (6:0, 8:0, 10:0, 12:0, 14:0, and 16:0 decreasing and 18:1 increasing) the percentage of 6:0, 8:0, 10:0, 12:0, 14:0 and 16:0 acids at position sn-3 decreased while the percentage of 18:0 and 18:1 acids increased. These changes were compensated for by changes in the opposite direction at positions sn-1 and sn-2.


1995 ◽  
Vol 269 (5) ◽  
pp. R1060-R1067 ◽  
Author(s):  
T. Raclot ◽  
E. Mioskowski ◽  
A. C. Bach ◽  
R. Groscolas

This study extends our earlier work (T. Raclot and R. Groscolas. J. Lipid Res. 34: 1515-1526, 1993), which showed that, under norepinephrine-stimulated lipolysis, fatty acids of rat retroperitoneal fat cells are selectively mobilized. The present study examines whether this selective mobilization of fatty acids 1) is based on their proportions in adipose tissue, 2) is a metabolic feature common to all adipose tissues, and/or 3) depends on the lipolysis-stimulating agent. Rat fat cells with two markedly different fatty acid compositions were isolated from four white adipose tissues and treated with three lipolytic agents. Fatty acid composition of in vitro released free fatty acids was compared with that of fat cell triacylglycerols, the ratio of percent in free fatty acid to percent in triacylglycerol being defined as the relative mobilization rate (RMR). The RMR of individual fatty acids was related to their molecular structure. It increased exponentially with unsaturation for a given chain length and decreased with increasing chain length for a given unsaturation. The selectivity of fatty acid mobilization was similar regardless of the fatty acid composition of adipose tissue, the tissue location, and the lipolytic agent used. Under conditions of stimulated lipolysis, the selectivity of fatty acid mobilization is therefore a general metabolic feature of adipose tissue. Fatty acids with 16-20 carbon atoms and 4 or 5 double bonds had the highest RMR (from 1.4 to > 5), whereas fatty acids with 20-22 carbon atoms and 0 or 1 double bond had the lowest RMR (from 0.3 to 0.7). For the other fatty acids, RMR was close to unity.(ABSTRACT TRUNCATED AT 250 WORDS)


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