LIPIDS OF CURED CENTENNIAL SWEET POTATOES

SUMMARY –Lipids isolated from cured Centennial sweet potatoes were identified and quantitated by a combination of column and thin layer chromatography. These lipids were shown to consist of 42.1% neutral lipids, 30.8% glycolipids and 27.1% phospholipids. Triglycerides and steryl esters were the major lipids of the neutral fraction. Among the phospholipids, phosphatidyl ethanolamine, phosphatidyl choline and phosphatidyl inositol were the most abundant. Galactolipids and the steryl glucosides were also present. The predominant fatty acids were stearic, palmitic, oleic, linoleic and linolenic.     

Oxidation of free and esterified linoleic and linolenic acids in bread doughs by wheat and soya lipoxygenases

Lipids containing ¹⁴C-labelled linoleic and linolenic acids were added to flour which was then made into bread doughs with or without 2% enzyme-active soya flour. The ¹⁴C-labelled lipids and their oxidation products were analysed as intact lipids or as ¹⁴C fatty acid methyl esters by thin-layer chromatography. In the control doughs wheat lipoxygenase oxidised free fatty acids and monoglycerides. In doughs containing soya flour, steryl esters, triglycerides, diglycerides, mono-galactosyl diglycerides, digalactosyl diglycerides and phosphatidyl choline were also oxidised, and the oxidation of these lipids is attributed to soya lipoxygenase.     

Identification and quantitative determination of the lipids of dried Origanum dictamnus leaves

The Origanum dictamnus plant was examined for its lipid and fatty acid compositions. A combination of chromatographic techniques has been employed for the qualitative and quantitative determination of the lipids of dried leaves of O. dictamnus. The following polar lipids were identified: mono-, di- and poly-digalactosyl diglycerides, sulpholipids, cerebrosides, phosphatidyl-ethanolamine, phosphatidylserine, phosphatidylglycerol, phosphatidylinositol, phosphatidyl choline and phosphatidic acid. The non-polar lipids identified were sterols, steryl esters, fatty alcohols, free fatty acid, waxes, traces of triglyceride, triterpenic acids and essential oil. The predominant fatty acids were palmitic, oleic and linoleic acids.     

The distribution of acyl lipids in the germ,aleurone, starch and non-starch endosperm of four wheat varieties

The quantitative distribution of 23 classes of acyl lipids was determined in the germ, aleurone, starch and endosperm non-starch fractions of Atou (Soft English), Flinor (Hard English), Waldron (US Hard Red Spring) and Edmore (US Amber Durum) wheats. All four wheats had similar proportions (dry basis) of pericarp (6.8–8.6%), germ (2.5–3.0%), starchy endosperm (78.7–84.5%) and starch (59.3–67.5%), and similar quantities of acyl lipids in the whole kernels (2.8–3.2%), germ (25.7–30.5%), starch (0.8–1.2%) and endosperm non-starch fractions (0.8–1.1%). Flinor, Waldron and Edmore had 7.3–10% aleurone containing 8.7–10.6% lipids, but Atou appeared to have an abnormally low aleurone weight (4.0%) and a correspondingly high lipid content (19.4%). Pericarp acyl lipids were studied only in Atou, where they comprised 1.3% of the dry weight and 3.8% of the total acyl lipids in the whole kernel. Lipids in the germ and aleurone consisted of triglycerides (60.3–79.3%), other nonpolar lipids (5.6–12.0%) and phospholipids (13.6–17.9%). Starch lipids were almost exclusively lysophospholipids (89.4–94.4%). Greater variation was found in the endosperm non-starch lipids which consisted of triglycerides (13.7–34.1%), other nonpolar lipids (33.2–48.5%), glycolipids (18.6–38.3%) and phospholipids (21.9–35.3%). Edmore had the highest levels of triglycerides and non-polar lipids, and the lowest levels of glycolipids (as expected in a tetraploid wheat). Atouresembled Edmore in its low levels of steryl esters and glycolipids, but it also had least phospholipids.     

Lipid levels in cabbage leaves (Brassica oleracea)

Cabbage (Brassica oleracea L, var Glory) is one of the cruciferous vegetables. The objective of this study was to investigate the neutral, glyco- and phospholipids of cabbage and their fatty acid composition. Lipids from its leaves were extracted and fractionated into neutral lipids, glycolipids and phospholipids. The fatty acids of each fraction were analysed by gas liquid chromatography.     

Selective extraction and quantitative analysis of non-starch and starch lipids from wheat flour.

Wheat flour non-starch lipids (lipids not bound to starch) were quantitatively extracted with water-saturated n-butanol (WSB), benzene-ethanol-water (10:10:1, by vol.) or ethanol-diethyl ether-water (2:2:1, by vol.) in 10min at 20 °C. Starch lipids (lipids bound to starch) were subsequently extracted with WSB at 90–100 °C. Carotenoid pigments were quantitatively extracted with the non-starch lipids. There was no significant hydrolysis of esterified fatty acids and no detectable autoxidation of unsaturated acids in the hot solvent extracts. Non-starch and starch lipids from a high grade spring wheat flour and three grades of winter wheat flour were separated by thin-layer chromatography and quantified as fatty acid methyl esters (FAME) by gas-liquid chromatography (g.l.c.) using heptadecanoic acid (or its methyl ester) as internal standard. Total flour and starch lipids after acid hydrolysis were also converted to FAME for quantitation by g.l.c. Non-starch lipids consisted of 59–63% non-polar (neutral) lipids, 22–27% polar glycolipids and 13–16% phospholipids. Steryl esters, triglycerides, and all the diacyl galactosylglycerides and phosphoglycerides were present only in non-starch lipids. Starch lipids consisted of 6–9% non-polar (neutral) lipids (mostly free fatty acids), 3–5 % polar glycolipids and 86–91 % phospholipids (mostly lysophosphatidyl choline). Starch lipids were almost exclusively monoacyl lipids. Factors are given for converting weight of FAME into weight of original lipid for all individual lipid classes in wheat which contain O-acyl groups. Factors for total lipids are: total starch lipids = FAME × 1.70, total non-starch lipids = FAME × 1.20, and total flour (non-starch + starch) lipids = FAME × 1.32. Similar factors could be used to convert weight of lipids obtained by conventional acid hydrolysis methods into weight of unhydrolysed lipids. Phospholipid contents are given by: total starch phospholipids = P × 16.51, total non-starch phospholipids = P × 23.90, total flour phospholipids = P × 17.91.     

Supercritical fluid extraction and characterization of lipids from algae Scenedesmus obliquus

Supercritical carbon dioxide (SC-CO2) extractions (with and without ethanol as an entrainer) were carried out to remove lipids and pigments from protein concentrate of green algae (Scenedesmus obliquus) cultivated under controlled conditions. The content and fatty acid composition of algal lipids using column, thin-layer (TLC) and gas-liquid chromatography (GLC) were determined. Absorption spectra of extracted fractions showed the predominance of chlorophyll A (lambda max at 410 nm). Single step supercritical carbon dioxide (SC-CO2) extraction resulted mostly in removal of neutral lipids and a part of glycolipids, but phospholipids were not extracted. Addition of ethanol to SC-CO2 increased the amount of glycolipids and phospholipids in the extract. TLC pattern of algal lipids showed that the main part of neutral lipids consisted of diglycerides, triglycerides, hydrocarbons, free sterols, and sterol esters. The glycolipids were mostly monogalactosyl diglyceride, digalactosyl diglyceride, esterified sterol glycoside, and sterol glycoside. In phospholipids, phosphatidyl choline, phosphatidyl glycerol, and phosphatidyl ethanolamine were the main compounds. Fatty acid composition patterns indicated the main fatty acids to be 16:0, 16:1, 16:2, 16:3, 16:4, 18:1, 18:2, and 18:3(a). Relatively high recovery of polyunsaturated fatty acids and essential fatty acids in supercritical fluid extracted algal lipids and proteins isolates were observed.     

Supercritical fluid extraction and characterization of lipids from algae scenedesmus obliquus

Supercritical carbon dioxide (SC‐CO₂) extractions (with and without ethanol as an entrainer) were carried out to remove lipids and pigments from protein concentrate of green algae (Scenedesmus obliquus) cultivated under controlled conditions. The content and fatty acid composition of algal lipids using column, thin‐layer (TLC) and gas‐liquid chromatography (GLC) were determined. Absorption spectra of extracted fractions showed the predominance of chlorophyll A (λ_max at 410nm). Single step supercritical carbon dioxide (SC‐CO₂) extraction resulted mostly in removal of neutral lipids and a part of glycolipids, but phospholipids were not extracted. Addition of ethanol to SC‐CO₂ increased the amount of glycolipids and phospholipids in the extract. TLC pattern of algal lipids showed that the main part of neutral lipids consisted of diglycerides, triglycerides, hydrocarbons, free sterols, and sterol esters. The glycolipids were mostly monogalactosyl diglyceride, digalactosyl diglyceride, esterified sterol glycoside, and sterol glycoside. In phospholipids, phosphatidyl choline, phosphatidyl glycerol, and phosphatidyl ethanolamine were the main compounds. Fatty acid composition patterns indicated the main fatty acids to be 16:0, 16:1, 16:2, 16:3, 16:4, 18:1, 18:2 and 18:3(a). Relatively high recovery of polyunsaturated fatty acids and essential fatty acids in supercritical fluid extracted algal lipids and protein isolates were observed.     

Lipids in cereals. 1. Pennisetum typhoideum

Two improved strains of Pennisetum typhoideum (‘bajra’) were found to have a free lipid content of about 5.0% and bound lipid content of about 0.5%. In the non-polar fraction, sterol esters and hydrocarbons, triglycerides, free fatty acids, free sterols and partial glycerides were present with triglycerides as the principal constituents. Polar lipids were separated by two-dimensional thin-layer chromatography and lecithin was found to be the major component. Sterol-containing glycolipids (sterol glycosides and esterified sterol glycosides) were present in appreciable amounts. Phosphatidyl ethanolamine, phosphatidyl glycerol, phosphatidyl inositol, lysophosphatidyl ethanolamine, lysolecithin, phosphatidic acid, poly-glycerophosphatide, mono- and di-galactosyl glycerides and cerebrosides have also been tentatively identified.     

六种鱼鱼头磷脂的组成及脂质脂肪酸分析

为研究海水鱼和淡水鱼鱼头磷脂及脂质脂肪酸组成的差异,以海水鱼(马鲛鱼、巴浪鱼、金鲳鱼)和淡水鱼(罗非鱼、鲫鱼、鲢鱼)鱼头为研究对象,利用Floch法提取6种鱼鱼头总脂;硅胶柱层析法将总脂分离收集中性脂、糖脂和磷脂;薄层层析(thin layer chromatography,TLC)分析比较6种鱼鱼头磷脂种类的分布、组成;气相色谱(Gas chromatography,GC)分析6种鱼鱼头脂质的脂肪酸组成。结果表明,6种鱼鱼头中提取率最高的脂质类型为中性脂,占总脂的48.98%~77.84%,其次为磷脂,占总脂的5.93%~22.86%,糖脂提取率最低,占总脂的3.67%~15.91%。鱼头磷脂中共检出4种磷脂组分,分别为磷脂酰乙醇胺(Phosphatidylethanolamine,PE)、磷脂酰胆碱(Phosphatidylcholine,PC)、鞘磷脂(Sphingomyelin,SM)、溶血磷脂酰胆碱(Lysophosphatidylcholine,LPC),其中PC明显高于其他磷脂组分。脂质中均含有较高含量的多不饱和脂肪酸(Poly-unsaturated fatty acid,PUFA),其中以二十二碳六烯酸(docosahexaenoic acid,DHA)为主,且均含有二十碳五烯酸(eicosapntemacnioc acid,EPA),海水鱼和淡水鱼鱼头磷脂中DHA和EPA占总脂肪酸的比例最高,分别为18.39%~21.43%和5.61%~10.38%,且海水鱼鱼头中以DHA和EPA为主的PUFA含量高于淡水鱼鱼头。因此,海水鱼鱼头是提取n-3多不饱和脂肪酸的潜在资源,尤其是制备n-3多不饱和脂肪酸型磷脂的良好来源。     

Lipid Composition of Field Pea (Pisum sativum cv Trapper) Seed and Starch

The total lipids in field pea seeds and refined starch were extracted by five aqueous/organic solvent systems and the greatest yield of total. neutral and polar lipids was obtained with hot n-propanol-water (3:1 v/v). Lipids extracted from field pea seeds represented 2.9% of the seed weight and consisted of 43.2% neutral lipids, 3.2% glycolipids and 53.6% phospholipids. The major components of the three fractions were 70% triacylglycerol in neutral lipid, 28% esterified sterol glycoside in glycolipid and 55% phosphatidylcholine in phospholipid. The purified starch fraction contained 0.22% surface lipids and 0.09% internal lipids. The surface lipids were primarily sterol esters and free fatty acids while only free fatty acids were found in the internal lipids. The ability of lysophospholipids and fatty acids to complex with field pea starch was demonstrated by differential scanning calorimetry and X-ray diffraction, respectively.     

Changes in lipid composition and fatty acid profile of Nham,a Thai fermented pork sausage,during fermentation

Changes in lipid composition and fatty acid profile of Nham during fermentation were investigated. Total lipids of Nham were in the range 2–3%. The extracted lipid of initial Nham mix consisted mainly of triglycerides (TG), accounting for more than 75% of the total lipid, followed by phospholipids (PL) and a trace amount of diglycerides (DG) and free fatty acid (FFA). During fermentation, TG, DG and PL decreased with a concomitant increase in FFA, indicating lipolysis of Nham lipids during fermentation. Changes in fatty acids of the total lipids, non-polar and polar lipid fractions were observed during fermentation. In both total and non-polar lipid fractions, the major fatty acids found in a descending order were oleic (C18:1), linoleic (C18:2) and palmitic (C16:0) acids, which together accounted for 90% of the total fatty acids. Increases in fatty acid contents in both total and non-polar lipid fractions, were observed with a corresponding decrease in the quantity of fatty acids of phospholipids. As the fermentation proceeded, peroxide value generally increased while TBARS values decreased. Overall, lipid oxidation in Nham occurred during fermentation but did not cause the objectionable odour and taste in any Nham tested.     

Lipids of berseem (Trifolium alexandrinum) seed

Berseem seed oil was fractionated into non-polar and polar components. Tentative identification was made of hydrocarbons, sterol esters, triglycerides, free fatty acids and partial glycerides in the non-polar fraction and of lysophosphatidyl choline, phosphatidyl inositol, lysophosphatidyl ethanolamine, phosphatidyl choline, phosphatidyl glycerol, phosphatidyl ethanolamine, digalactosyl diglycerides, sterol glycosides, phosphatidic acid, monogalactosyl diglycerides, cerebrosides and esterified sterol glycosides in the polar fraction. The fatty acid constituents of the major polar and of all the non-polar lipid components are also reported.     

Lipid content and fatty acid composition of green algae Scenedesmus obliquus grown in a constant cell density apparatus

The lipids of alga Scenedesmus obliquus grown under controlled conditions were separated and fractionated by column and thin-layer chromatography, and fatty acid composition of each lipid component was studied by gas-liquid chromatography (GLC). Total lipids were 11.17%, and neutral lipid, glycolipid and phospholipid fractions were 7.24%, 2.45% and 1.48% on a dry weight basis, respectively. The major neutral lipids were diglycerides, triglycerides, free sterols, hydrocarbons and sterol esters. The glycolipids were: monogalactosyl diglyceride, digalactosyl diglyceride, esterified sterol glycoside, and sterol glycoside. The phospholipids included: phosphatidyl choline, phosphatidyl glycerol and phosphatidyl ethanolamine. Fourteen fatty acids were identified in the four lipid fractions by GLC. The main fatty acids were C18:2, C16:0, C18:3(alpha), C18:1, C16:3, C16:1, and C16:4. Total unsaturated fatty acid and essential fatty acid compositions of the total algal lipids were 80% and 38%, respectively.     

Fumgal lipids. I. Effect of different nitrogen sources on the chemical composition

The effect of three nitrogen sources on the chemical composition of seven fungi, namely: Aspergillus niger, A. luchuensis, Penicillium crustosum, Alternaria tenuis, Rhizoctonia solani, Mucor sp. and Pythium irregulare has been studied. The various fungi showed a great variation with respect to lipid percentage and total lipid content. Lipid content varied from 3.2 to 41.5%. Non-polar lipids were comprised of monoglycerides, diglycerides, free sterols, free fatty acids and triglycerides. The quantitative make-up of the non-polar lipid varied with different nitrogen sources. Palmitic, stearic, oleic and linoleic acids were the major fatty acids while lauric, myristic, palmitoleic, linoleic and arachidic were the minor ones. The fatty acid composition was dramatically changed by changing the nitrogen source. Since different fungi responded differently to changes in nitrogen source, no generalisation could be made. Two-dimensional thin-layer chromatography of the polar lipid fraction of these fungi revealed the presence of a maximum of fifteen spots. Phosphatidyl choline, phosphatidyl ethanolamine and phosphatidyl inositol were the major spots while lysophosphatidyl choline, lysophosphatidyl ethanolamine and phosphatidyl glycerol were present in smaller quantities. In comparison to phospholipids, glycolipids (except sterol glycoside) were present in relatively lower concentration. Pythium irregulare was very characteristic in having no glycolipids at all.     

Effect of crop maturity on leaf lipids

Studies extending throughout a period of 100 days' growth have been made on the total lipids of ryegrass, kale and fodder radish. Expressed in terms of % dry matter, lipids are at a maximum of about 10 to 11% during the period of vegetative growth. Lipid yields in absolute terms are maximal at 200–300 kg/ha after 56 to 70 days from sowing, at which stage lipids have fallen to 7 to 9% of total dry matter, according to species. Considering the fatty acids as a whole, dominant components are linolenic and palmitic, the latter rising and the former falling as maturation progresses. Minor fatty acids show no clear trend. More specific changes in fatty acid profiles are revealed when individual lipid classes are studied separately. Lipid classes display a predictable change in pattern as maturation progresses. New growth is rich in partial glycerides and free sterols, and particularly in mono- and digalactosyl diglycerides and sulphoquinovosyl diglyceride. Leaves from mature or senescing crops show progressive falls in these components, accompanied by the appearance of triglycerides, free fatty acids and steryl glycosides. In the case of fodder radish the accumulation of the hydrocarbon, n-nonacosane, is a noteworthy feature. The principal phospholipids do not change appreciably with maturation. The trends observed on maturation show common general patterns for all the leafy crops so far studied. They do emphasise, however, the crucial importance of specifying both species and duration of growth when quoting data on leaf lipid compositions.     

Identification and quantitative determination of the lipids of Alocasia macrorrhiza tubers

The identity, composition and concentration of each of the major lipids found in Alocasia tubers were investigated using a combination of chromatographic procedures. On a weight to weight basis, the neutral lipids, glycolipids and phospholipids comprised 60.5, 19.0 and 20.5% respectively while the total extractable lipids accounted for 0.6% of the dry weight. In addition to the conventional lipid classes of tubers, the presence of tri- and tetragalactosyl diglycerides was confirmed. The predominant fatty acid in each lipid class was linoleic acid with palmitic, oleic and linolenic acids being the other ones. In general, a high degree of unsaturation (66%), similar for most tuber lipids, was established for the component fatty acids of Alocasia.     

The fatty acid composition of the lipids of earthworms.

Lipids were freshly extracted from earthworms from agricultural pasture land, and fatty acid compositiona analyses were carried out on the total lipids; phospholipids; triglycerides; free fatty acids; mixed sterol esters, wax esters, free methyl esters, etc.; glycolipids; and neutrallipids. A wide variety of fatty acids ranging from C₁₀ to C₃₂ were identified. In the fatty acids of the total lipids, polyunsaturated constituents predominated in amount, while monomethyl branched, isoprenoid and n-odd-numbered acids were present in appreciable proportions. Eicosa-5,8,11,14,17-pentaenoic acid and arachidonic acid occurred at higher levels than any other components and were located mostly in the phospholipids. Significant contents of linoleic and linolenic acids were also detected. Earthworms collected in spring had a fatty acid composition which differed noticeably from that of worms from other seasons. The content of lauric acid during spring was much higher than that normally found in animals or pasture plants. The composition of the free fatty acids indicated that these components were the products of lipolysis and were derived from all the lipid classes. The results of this investigation suggest that the diet of local earthworms, which is reported to consist mainly of dead plant material, is supplemented by living and dead microorganisms from ingested soil.     

LIPID CLASSES, FATTY ACID COMPOSITIONS AND TRIACYLGLYCEROL MOLECULAR SPECIES FROM ADZUKI BEANS (VIGNA ANGULARIS)

The lipids extracted from adzuki beans grown in Japan were classified by thin-layer chromatography (TLC) into eight fractions. Molecular species and fatty acid distributions of triacylglycerols (TAGs) isolated from the total lipids in the beans were determined from a combination of argentation-TLC and gas chromatography. The major lipid components were phospholipids (PL; 63.5%) and TAG (21.2%), while hydrocarbons (5.1%), steryl esters (7.5%), free fatty acids (0.9%), diacylglycerols (1.3%) and monoacylglycerols (0.5%) were also present in minor proportions. Both major samples had high amounts of total unsaturated fatty acids, representing 62.1% for TAG and 65.9% for PL. Seventeen different molecular species were detected. The major TAG components were SMD (5.0%), S₂T (19.3%), SD₂ (13.8%), SMT (9.3%), MD₂ (4.5%), SDT (7.0%), D₃ (8.8%) and ST₂ (15.9%), where S, M, D and T denote a saturated fatty acid, a monoene, a diene and a triene, respectively.

PRACTICAL APPLICATIONS

This article describes the characteristics of lipid components, fatty acid compositions as well as the profiles of triacylglycerol (TAG) molecular species of adzuki beans. α-Linolenic (18:3 n -3) acid was detected as 24.8, 21.2 and 15.2% in the TAG, total lipids and phospholipids, respectively. The oil from legumes, except the profitable fatty acid content, could be a potential source of tocopherols. The data obtained in this study would be useful to both consumers and producers for manufacturing traditional adzuki confectionaries ( wagashi ) in Japan and elsewhere.     

A Research Note Lipid Composition of Cumin (Cuminum cyminum L.) Seeds

Total lipids extracted from Cumin (Cuminum cyminum L., Umbelliferae) amounted to 14.5% of the dry seeds. The total lipids consisted of 84.8% neutral lipids, 10.1% glycolipids, and 5.1% phospholipids. Neutral lipids consisted mostly of triacylglycerols (89.4%) and small amounts of diacylglycerols, free fatty acids, sterols, sterolesters, and hydrocarbons. At least five glycolipids and five phospholipids were identified. Acylmonogalactosyldiacylglycerol and acylatedsterylglucoside were the major glycolipids, while monogalactosyldiacylglycerol, monogalactosylmonoaclycerol, and digalactosyldiacylglycerol were present in small quantities. Phosphatidylethanolamine and phosphatidylcholine were the major phospholipids, while phosphatidylinositol, lysophosphatidylethanolamine, and phosphatidylglycerol were present in small amounts. The fatty acid composition of these different neutral lipids, glycolipids, and phospholipids was determined