Lipid composition ofCalophyllum inophyllum kernel

Total kernel lipids extracted fromCalophyllum inophyllum, Guttifereae amounted to 60.1% of the dry kernel. The total lipids consisted of 92.0% of neutral lipids, 6.4% glycolipids and 1.6% phospholipids. Neutral lipids consisted of triacylglycerols (82.3%), free fatty acids (7.4%) and small amounts of diacylglycerols, monoacylglycerols and sterols. At least four glycolipids and five phospholipids were identified. Acylmonogalactosyldiacylglycerol and monogalactosylmonoacylglycerol were major glycolipids; while monogalactosyldiacylglycerol and an acylated sterolglucoside were present in small amounts. The phospholipids consisted of phosphatidylethanolamine and phosphatidylcholine as major phospholipids, and minor amounts of phosphatidic acid, phosphatidylserine and lysophosphatidylcholine. The fatty acid composition of these different neutral lipids, glycolipids and phospholipids was determined.     

The lipid components of white potato tubers (Solanum tuberosum)

Four Canadian varieties of potatoes were examined for their lipid composition. Lipids, extracted with chloroformmethanol, were shown by TLC and column chromatography to consist of 16.5% neutral lipids, 45.5% phospholipids and 38.1% glycolipids. Among the phospholipids and glycolipids, phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl inositol, the galactolipids and the sterol glucosides were the major lipids. The predominant fatty acids were palmitic (19.5%), linoleic (44.8%) and linolenic (30.4%, in Kennebec). Analyses of the fatty acids of stored potatoes showed a marked decrease in linoleic acid and an increase in linolenic acid, in the Irish Cobbler and Sebago potatoes. β-sitosterol comprised 85.0% of total sterols. Nearly half of the carotenoids was lutein (xanthophyll), the others being α-carotene, β-carotene, an unidentified pigment and lutein epoxide. Contribution No. 101 of the Food Research Institute, Canada Department of Agriculture.     

Lipid composition of murraya koenigii seed

Total seed lipids extracted fromMurraya koenigii (Linn), Rutaceae amounted to 4.4% of the dry seed. The total lipids consisted of 85.4% neutral lipids, 5.1% glycolipids and 9.5% phospholipids. Neutral lipids consisted of 73.9% triacylglycerols, 10.2% free fatty acids and small amounts of diacylglycerols, monoacylglycerols and sterols. At least five glycolipids and seven phospholipids were identified. Sterylglucoside and acylated sterylglucoside were major glycolipids, while digalactosyldiacylglycerol, monogalac-tosyldiacylglycerol and monogalactosylmonoacylglycerol were present in small quantities. The phospholipids consisted of phosphatidylethanolamine, phosphatidylcholine, lysophosphatidylethanolamine and lysophosphatidylcholine as major phospholipids and minor quantities of phosphatidylinositol, phosphatidylglycerol and phosphatidic acid. The fatty acid composition of these different neutral lipids, glycolipids and phospholipids were determined.     

Fatty Acid Composition of Winged Bean Seed Oil (Psophocarpus tetragonolobus)

Winged bean seeds (Psophocarpus tetragonolobus) were shown to contain 14.4% of oil on a dry weight basis. Fractionation of this oil by silicic acid column chromatography showed 72.7% neutral lipids, 2.8% of glycolipids and 24.5% of phospholipids. Fatty acid composition of total lipid, neutral and glycolipid showed palmitic acid (12.2-14.0%), stearic acid (3.5-4.3%), oleic acid (36-39%) and linoleic acid (39-42%) as major fatty acids. The phospholipid fraction was slightly different from the rest in containing higher palmitic and lower oleic and linoleic acids.     

Lipid composition of perilla seed

The composition of lipids and oil characteristics from perilla [Perilla frutescens (L.) Britt.] seed cultivars are reported. Total lipid contents of the five perilla seed cultivars ranged from 38.6 to 47.8% on a dry weight basis. The lipids consisted of 91.2–93.9% neutral lipids, 3.9–5.8% glycolipids and 2.0–3.0% phospholipids. Neutral lipids consisted mostly of triacylglycerols (88.1–91.0%) and small amounts of sterol esters, hydrocarbons, free fatty acids, free sterols and partial glycerides. Among the glycolipids, esterified sterylglycoside (48.9–53.2%) and sterylglycoside (22.1–25.4%) were the most abundant, while monogalactosyldiacylglycerol and digalactosyldiacylglycerol were present as minor components. Of the phospholipids, phosphatidylethanolamine (50.4–57.1%) and phosphatidylcholines (17.6–20.6%) were the major components, and phosphatidic acid, lysophosphatidylcholine, phosphatidylserine and phosphatidylinositol were present in small quantities. The major fatty acids of the perilla oil were linolenic (61.1–64.0%), linoleic (14.3–17.0%) and oleic acids (13.2–14.9%). Some of the physicochemical characteristics and the tocopherol composition of perilla oil were determined.     

Neutral Lipid Characterization of Non-Water-Soluble Fractions of <Emphasis Type="Italic">Carica Papaya</Emphasis> Latex

The non-water-soluble fraction of Carica papaya latex (CPL) constitutes a waste material from papain production; very little information exists regarding its chemical composition. The non-water-soluble fraction of CPL was fractionated by liquid chromatography into neutral lipids, glycolipids and phospholipids. The most abundant compounds were found to be the polar lipids, accounting for 79.2% (w/w) of the total extractible matter, while the total amount of neutral lipids was only around 20%. It was composed of free fatty acids, sterols and triterpenic alcohols, but no glycerides were detected. A high content of saturated fatty acids was measured; these saturated fatty acids were represented by very long chains with C24:0, C26:0 and C28:0 accounting for 6.3, 11.0 and 6.3%, respectively, in the total extractible matter and 7.3, 9.0 and 3.9% in the FFA fraction. The monounsaturated fatty acids were about 23–25% in both samples, with oleic acid (C18:1) being the most abundant. The polyunsaturated fatty acids that were 25.1% in the total matter and 21.6% in the FFA fraction were mainly represented by linoleic acid (C18:2n-6). Finally, a very interesting characteristic of the FA composition of this latex concerns the presence of odd-numbered fatty acids in significant amounts (around 22% in the total extract and 24.3% in the FFA fraction).     

Varietal difference in lipid content and fatty acid composition of highbush blueberries

Lipids from five cultivars of highbush blueberries (Vaccinium corymbosum L.) were extracted and fractionated into neutral lipids (60–66%), glycolipids (20–22%) and phospholipids (14–18%). The major fatty acids in all fractions were palmitic (16∶0), oleic (18∶1), linoleic (18∶2), and linolenic (18∶3) acids. All lipid classes had a large concentration of C₁₈ polyunsaturated acids (84–92%), indicating that blueberries are a rich source of linoleic and linolenic acids. Changes in the fatty acid composition of neutral lipids and phospholipids were not significantly different among the five cultivars, but significant differences were noted in the ratios of linoleic and linolenic acids in the glycolipids fraction.     

Lipid Profile and Fatty Acid Composition of Moth Bean (Vigna aconitefolia) Seeds

The seeds of moth bean (Vigna aconitefolia) were found to contain 4.5 % of lipid. Fractionation of this lipid by silicic acid column chromatography yielded 44.5 % neutral lipids (NL), 23.4 % glycolipids (GL) and 32.1 % phospholipids (PL). Fatty acid composition of the total lipid and lipid fractions showed that palmitic acid (37.3-54.7 %), stearic acid (7.8-8.0%) oleic acid (6.8-13.9 %) linoleic acid (23.1-35.6 %) and linolenic acid (3.0-10.0%) are the major fatty acids. The phospholipid fraction was found to be different from the rest in containing higher palmitic acid (54.7%) and lower unsaturated fatty acids.     

Characteristics of Oil from Hulless Barley (<Emphasis Type="Italic">Hordeum vulgare</Emphasis> L.) Bran from Tibet

The bran of hulless barley (Hordeum vulgare L.) from Tibet was investigated. This paper reports on the physicochemical characteristics, lipid classes and fatty acids of the oil from the bran. The petroleum (60–90 °C) extract of hulless barley bran was found to be 8.1%. The investigated physiochemical parameters included density at 40 °C (0.96 g/cm³), refractive index at 40 °C (1.41), melting point (30.12 °C), acid value (11.6 mg KOH/g), peroxide value (19.41 μg/g), saponification value (337.62 mg KOH/g), iodine value (113.51 mg iodine/g) and unsaponifiable matter (4.5% of total lipids).The amount of neutral lipids in the crude oil was the highest (94.55% of total lipids), followed by glycolipids (4.20% of the total lipid) and phospholipids (1.25% of the total lipid). Linoleic acid (75.08% of total fatty acids) followed by palmitic acid (20.58% of total fatty acids), were the two major fatty acids in the oil. The results show that the oil from the hulless barley bran could be a good source of valuable essential fatty acids.     

Polar lipids ofMacrophomina phaseolina

Macrophomina phaseolina was grown on a defined medium at three different carbon/nitrogen ratios. The lipids of the mycelia and the sclerotia were extracted; fractionated into polarity groups; and separated by thin layer, column, and gas liquid chromatographies. Sclerotia contained higher levels of neutral lipids and lower amounts of polar lipids than mycelia. The neutral lipid content of sclerotia increased, up to 77% of total lipids, and phospholipids decreased as carbon/nitrogen ratio increased from 10 to 320. The glycolipid content was not altered significantly by changes in carbon/nitrogen ratios. Although cardiolipin could not be detected in sclerotial polar lipids, both sclerotia and mycelia contained similar phospholipid profiles with major quantitative differences. Phosphatidic acid and phosphatidyl glycerol were major components of sclerotia, whereas phosphatidyl ethanolamine and phosphatidyl inositol were the major phosphatides of mycelia. Phosphatidyl choline was present in both mycelia and sclerotia. The fatty acid distribution did not show any particular pattern of saturation or unsaturation due to differences in carbon/nitrogen ratio. However, mycelial lipids tended to contain C24∶1, C18∶3, and C22∶1 as major fatty acids, whereas the major fatty acids in sclerotial lipids were C18∶2, C18∶1, C22∶1, C20∶0, and C16∶1. Saturated fatty acids were present in lesser concentrations.     

Fungi pathogenic to insects: III. Neutral and polar lipids ofEntomophthora coronata

The neutral and polar lipid composition ofEntomophthora coronata was determined qualitatively. The fungus was grown on a chemically nondefined medium (Sabouraud dextrose yeast extract) and a chemically defined medium for a period up to 26 days. The lipids were characterized by thin-layer, column, gas chromatography, and selective sprays,³²P-labeling, and mass spectrometry. The neutral lipids consist of monoglycerides, diglycerides, cholesterol, free fatty acids, triglycerides, and cholesteryl esters. The polar lipids consist of phospholipids (phosphatidyl ethanolamine, phosphatidyl choline, lysophosphatidyl ethanolamine, lysophosphatidyl choline, and spingomyelin), a number of glycolipids including cerebrosides, and many unrecognizable lipids, most of which are present in trace amounts. The cerebrosides and spingomyelin are present in significant amounts, and their concentration increased with age of the culture. The major fatty acids (>10%) of the total, neutral, and polar lipids of the mycelia are 14∶0, 16∶0, 18∶1, 18∶3(γ), and 24∶1. The polar lipids of total culture (unsaturation index 0.88) and of the conidia (unsaturation index 1.48) are considerably more unsaturated than the corresponding neutral lipids (unsaturated index 0.50 and 0.49). The mycelial polar lipids, compared to the neutral lipids, possess less 14∶0 and 18∶1 but contain a greater percentage of 16∶0, 18∶2, 18∶3(γ), 24∶0, and 24∶1. The major fatty acid of the conidia (>10%) are 13∶0, 14∶0, 18∶1, 18∶2, 18∶3(γ), and 20∶4. Their polar lipids have a higher proportion of 18∶2, 18∶3(γ), and 20∶4. The cerebrosides possess 24.1 in high relative proportion (30.1%). Presented at the AOCS Meeting, Atlantic City, October 1971.     

Lipids of six cultivated barley (Hordeum vulgare L.) varieties

The lipids of representative varieties of 2-row spring, 6-row spring, and 6-row winter-type barleys were studied. Total barley lipids were classified by silicic acid gel column chromatography and separated by thin layer chromatography, and the fatty acid composition was determined by gas liquid chromatography. Total lipid content of the 6 barley varieties ranged from 3.12%–3.56% (dry wt basis). The average values for neutral lipids, glycolipids, and phospholipids were 71, 9, and 20%, respectively. The fatty acid composition of barley was rather typical of plant tissue. The neutral lipids and glycolipids from all the varieties contained a higher percent of linoleic and linolenic (C 18∶2 and C 18∶3) acids than the phospholipid fraction. South Dakota Experiment Station Paper 1248.     

Lipid composition of oats (Avena sativa L.)

Compositions of lipids extracted from a sample of Hinoat oat by seven solvent systems and that extracted with chloroform/methanol (2:1 v/v) from six selected cultivars representing high and low lipid contents are reported. Lipid components (steryl esters, triglycerides, partial glycerides, free fatty acids, glycolipids and phospholipids) were separated by silicic acid column chromatography and thin layer chromatography and quantitated by GLC analysis of fatty acids and phosphorus determinations. Twelve oat cultivars were examined for the fatty acid composition of lipid extracted with n-hexane. Lipids extracted from Hinoat by different solvent systems ranged from 5.6 to 8.8%. Quantitative distribution of lipid components extracted with chloroform/methanol from six cultivars containing 4.6 to 11.6% lipid showed a significant correlation (γ=0.99) between the total lipid and the neutral lipid content. Phospholipid content was similar in all cultivars, but glycolipids showed a two-fold increase in high lipid oats. Triglycerides contained less palmitic and more oleic acid than the glycolipids or phospholipids. Nine glycolipids and 11 phospholipids have been identified, and the polar lipid composition of Hinoat oat is presented.     

Effect of vacuum‐packaging on the changes of Russian sturgeon muscle lipids during frozen storage

The changes in fatty acid composition, non‐polar (triglycerols) and polar lipids (phospholipids), total free fatty acids and total cholesterol of Russian sturgeon (Acipenser gueldenstaedtii) were studied during 360 days of storage at ?18°C. It was established that total neutral lipids and phospholipids content decreased and total free fatty acids concentration increased significantly during the frozen storage. Lower non‐polar and polar lipids content and higher free fatty acids concentration of vacuum‐packaged samples in comparison with air‐packaged samples were found. The changes in total cholesterol concentration and phospholipid classes of frozen stored sturgeon were not influenced by the frozen storage period and the type of packaging. It was established that the sturgeon polar lipids consisted mainly of phosphatidylcholine – 54.98 ± 0.85%, phosphatidylethanolamine – 28.42 ± 0.61%, and phosphatidylserine – 8.64 ± 0.45%. The increase of the total free fatty acids concentration was associated with the free n ? 3 PUFA accumulation as a result of hydrolysis of non‐polar and polar lipids. During the frozen storage DHA percentage of non‐polar lipids and phospholipids decreased approximately 3 and 1.75%, respectively. After 360 days of storage at ?18°C the n ? 3/n ? 6 PUFA ratio of total lipids decreased 4.9%.     

Free Fatty Acids in Commercial Krill Oils: Concentrations,Compositions, and Implications for Oxidative Stability

The concentrations and pro-oxidative effects of free fatty acids in commercial krill oil are not well defined. We now report that krill oil free fatty acids account for 2–13% of total lipids in commercial krill oil (n = 8) that these compounds are enriched in eicosapentaenoic acid (+7.1%) and docosahexaenoic acid (+6.3%) relative to whole oils; and that this composition make them highly pro-oxidizing in marine triacylglycerol oils, but not in krill oil, which derives oxidative stability from both its phospholipids, and neutral lipids (the latter because of astaxanthin). Specific fatty acid esterification patterns showed that krill oil free fatty acids predominantly (88–93%) originated from phospholipids, mainly from the sn-2 position, which was eight-fold more hydrolyzed than the sn-1 position. Lipolysis was not ongoing in stored oils. Adding small amounts of krill oil (1–5%) to marine triacylglycerol oils significantly increased their oxidative stability and also their resistance to free fatty acid-mediated pro-oxidative effects.     

Lipid composition of beef and human pituitary glands

The lipid composition of beef and human pituitary was determined by chromatographic and spectrophotometric methods. Beef pituitary lipid contained about 25% nonpolar lipids and 75% phospholipids whereas nonpolar lipids made up approximately 60% of the total in human pituitaries. The main nonpolar (i.e., low polarity) lipids in human pituitary were triglycerides, cholesterol, free fatty acids and an unidentified component in the triglyceride fraction. Cholesterol was the major nonpolar lipid component in freshly collected beef anterior and posterior pituitary, but the amount of free fatty acids appeared to increase during storage. Preliminary investigation of the unknown nonpolar lipid in human pituitaries suggested that it was an unsaturated hydroxy compound with no carbonyl functions. Thin layer chromatography indicated that it was also present in smaller amounts in freshly collected beef pituitaries. The main phospholipids of beef anterior, posterior and human pituitary were phosphatidyl ethanolamine, phosphatidyl choline, phosphatidyl inositol, phosphatidyl serine and sphingomyelin. The fatty acid composition of total nonpolar lipids, free fatty acids, total phospholipids, phosphatidyl ethanolamine and phosphatidyl choline of beef anterior and posterior pituitary was determined by gas liquid chromatography. Mixtures of saturated and unsaturated fatty acids ranging from C₁₂ to C₂₂ were present; the main fatty acids were palmitic, stearic, oleic, linoleic and arachidonic.     

Lipid composition of rice (Oryza sativa L.) bran

The composition of lipids of bran from three varieties of rice is reported. Lipids extracted amounted to 21.9–23.0% of the bran dry weight and consisted of 88.1–89.2% neutral lipids, 6.3–7.0% glycolipids and 4.5–4.9% phospholipids. Neutral lipids consisted mostly of triacylglycerols (83.0–85.5%), monoacylglycerols (5.9–6.8%) and small amounts of diacylglycerols, sterols and free fatty acids. Three glycolipids and eight phospholipids were separated and characterized. Acylated steryl glucoside and digalactosyldiacylglycerol were the main glycolipids, while monogalactosylmonoacylglycerol was present in small amounts. The major phospholipids were phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol and phosphatidic acid. Phosphatidylglycerol, lysophosphatidylcholine, lysophosphatidylethanolamine and acyl-phosphatidylethanolamine were present in small quantities.     

Composition of the lipids in cabbage

Cabbage leaves contain 0.16% total lipids of which 51.02% are neutral lipids, 40.78% glycolipids, and 8.18% phospholipids. The predominant fatty acids in the total lipid analysis are linolenic, linoleic, oleic, palmitic, and stearic acids. Linolenic, palmitic, tridecanoic, and oleic are the principal components in the neutral lipid fraction while glycolipids are composed mainly of linolenic, palmitic, lauric, myristic, and tricosanoic acids. Phospholipids are high in palmitic, linolenic, and linoleic acids. Both glucose and galactose were observed in the glycolipid fraction.     

Lipid profile of process streams of palm oil mill

During palm oil extraction, oil loss occurs mainly at three stages of processing, namely sterilization, pressing and clarification. Samples from a semi-commercial palm oil mill were analyzed for their lipid composition (triacylglycerol, diacylglycerol, monoacylglycerol, free fatty acid, phospholipid and glycolipid contents and fatty acid compositions of these lipid classes) and compared with the end product,viz., raw palm oil. The results indicate significant variations between the samples with respect to oil quality and lipid profile. Data relating to the lipid classes showed that sterilizer condensate had the highest levels of free fatty acids (24%), followed by press fiber (12.5%) and sludge effluent (10.9%), as compared to raw oil (1.5%). Diacylglycerol and monoacylglycerol contents were also markedly higher for these streams. Press fiber was characterized by extremely high proportions of phospholipids and glycolipids. Distribution of fatty acids (16:0, 18:1, 18:2 and 18:3) also varied among lipid classes of the process streams, particularly between polar lipids. This paper discusses the compositional aspects of lipids relating to quality of oils of the palm oil mill streams.     

Lipid Composition of Garlic

Neutral, glyco- and phospholipids of garlic were resolved into their component fractions by thin layer chromatography. Neutral lipids contained considerable quantities of monoglycerides (18.5%), diglycerides (14.2%), sterols (16.3%) and triglycerides (41.5%) respectively. The phospholipid fraction was rich in phosphatidyl choline (23.5%), phosphatidyl ethanolamine (17.9%), lysophosphatidyl choline (11.8%) and lysophosphatidyl ethanolamine (8.2%). Digalactosyl diglyceride (10.1%), sterol glycoside (15.6%), cerebrosides (8.1%), acylsterol glycoside (38.6%) and monogalactosyl diglyceride (22.5%) were the major components of the glycolipids of garlic. Lauric, myristic, palmitic and linoleic acids constituted the major fatty acids of monoglycerides, diglycerides and free fatty acid fractions whereas palmitic, linoleic and linolenic acids were the major fatty acids of triglycerides. Palmitic and linoleic acids were the major fatty acids of garlic phospholipids. Except the acylsterol glycoside fraction glycolipids were rich in lauric, palmitic, linoleic and linolenic acids; palmitic acid was the only major fatty acid of acylsterol glycosides.