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.     

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.     

Composition of wheat-flour lipids

Lipids were extracted from a single sample of wheat flour using three solvent systems: ethanol–diethyl ether–water (2:2:1 by vol.); chloroform–methanol (2:1 by vol.); and water-saturated n-butanol. Analysis of the extracts and of residual lipid in the extracted flour showed that water-saturated n-butanol was the most efficient solvent. Wheat-flour lipids were extracted with water-saturated n-butanol and separated by chromatographic procedures into individual components. The lipid classes which were isolated and studied were steryl ester, free sterol, 6-O-acyl steryl glucoside, steryl glucoside, triglyceride, diglyceride, monoglyceride, free fatty acid, monogalactosyl diglyceride, 6-O-acyl monogalactosyl diglyceride, digalactosyl diglyceride, digalactosyl monoglyceride, monoglycosyl ceramide, diglycosyl ceramide, N-acyl phosphatidyl ethanolamine, N-acyl lysophosphatidyl ethanolamine, phosphatidyl ethanolamine, lysophosphatidyl ethanolamine, phosphatidyl choline, lysophosphatidyl choline, phosphatidyl serine and phosphatidyl inositol. Monogalactosyl monoglyceride was also tentatively identified. The quantitative distributions of the lipid classes were determined. Monoglycosyl ceramide contained small amounts of normal fatty acids (12:0–24:0) and large amounts of 2-hydroxy fatty acids (principally 16:0 and 20:0), with similar amounts of dihydroxy long-chain bases (18:0 and 18:1) and trihydroxy long-chain bases (18:0, 18:1, 19:0, 19:1, 20:0, 22:0). The principal sterols were identified as β-sitosterol, campesterol, and C₂₈ and C₂₉ saturated sterols. The fatty acids in the sterol lipids were principally 16:0 (50–60%) and 18:2 (28–30%) with small amounts of 16:1, 18:0, 18:1 and 18:3. The fatty acids in all the glycerides were principally 18:2 (51–84%) with lesser amounts of 16:0, 18:0, 18:1 and 18:3.     

EFFECT OF POSTMORTEM AGING ON CHICKEN MUSCLE LIPIDS

Neutral lipids of fresh chicken breast muscles are shown to be triglycerides, sterols and sterol esters with only traces of mono- and diglycerides and free fatty acids. Phospholipids include measurable quantities of phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl inositol, phosphatidyl serine, sphingomyelin, diphosphatidyl glycerol, lysophosphatidyl choline and lysophosphatidyl ethanolamine. Fatty acid analyses of several of the lipid fractions are also included. Decreases in phosphatidyl choline and phosphatidyl ethanolamine coupled with increases in lysophosphatidyl choline, lysophosphatidyl ethanolamine and free fatty acids after 48 hr postmortem in the cold indicate phospholipase A activity concurrent with other postmortem changes. The significance of the results is discussed.     

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.     

Mesocarp,seed and pollen lipids of Raphia palms

The lipid classes, fatty acids and sterols of the mesocarp, seed and pollen lipids of five species of Raphia palms endemic to Nigeria were analysed. Apart from quantitative differences in the fatty acid compositions, chromatographic analyses demonstrated very little change in the patterns of the characteristic lipids associated with either the mesocarps, seed endosperms or pollens. Mesocarp lipids contained mainly triglycerides, while palmitic, oleic and linoleic acids were the major acids. Contrary to published data for seed lipids, Raphia seed endosperms contained a relatively small amount of triglycerides and a high proportion of polar lipids. Fatty acids associated with this tissue were not only highly unsaturated, but were significantly different from typical fatty acids of seed lipids. Raphia pollens, on the other hand, showed a complex array of lipid types. Triglycerides, sterols and sterol esters constituted the main neutral lipids while phosphatidyl choline, phosphatidyl inositol, phosphatidyl ethanolamine and galactosyl diglycerides represented the polar fraction. Apart from minor trends, palmitic, oleic and linoleic acids constituted the major fatty acids in all species. The biological importance of the steroidal sapogenins found in all organs is discussed.     

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.     

Changes in the composition of the rumen and abomasum lipids of sheep from birth to maturity

The composition of the lipids of the rumen and abomasum tissues of foetal (at term), 1 month, 2 month and 1-2-year old sheep grazed on pasture has been determined. The lipid content of the rumen tissues increased from 2.0% at birth to 3.4% in 1-2-year old sheep While that of the abomasum tissues increased from 2.6 to 5.7%. The main change in the neutral lipid fraction was a decrease in the hydrocarbon content from 0.13 % in the rumen tissues and 0.08 % in the abomasum tissues at birth to 0.003% and 0.006% respectively in the 1-2-year old sheep. The main components of the phospholipid fraction of the rumen and abomasum tissues were 34.9- 46.8% phosphatidyl choline; 14.623.5 % phosphatidyl ethanolamine; 14.3-21.1 % sphingomyelin; with smaller amounts of lysophosphatidyl choline (4 13-12.6 %), acidic phospholipids (cardiolipin) (4.1-8 -5 %) and phosphatidyl inositol/phosphaticlyl serine (3.0-5.5 %). No marked changes in phos- pholipid composition with age were noted. The amounts of phosphatidyl choline and phosphatidyl ethanolamine tended to be higher in the abomasum than in the rumen whereas the sphingomyelin content of the rumen tissue phospholipids was generally greater than that of the abomasurn tissue phospholipids. From the fatty acid composition of the triglycerides of the rumen and abomasum tissues it appeared that the foetal triglycerides were largely, though not entirely, of endogenous origin. In contrast the phospholipids of the foetal rumen and abomasum tissues contained di- and poly-unsaturated as well as branched-chain fatty acids in proportions similar to those found in older animals having access to pasture. From these results it is suggested that the phospholipids of the foetus are derived to a considerable extent from the maternal phospholipids.     

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.     

Role of seed phosphatides as antioxidants for ghee (butter fat)

Antioxidant potentiality of seed phospholipids for stored ghee was found to be in the order of sunflower (Helianthus annuus L.), groundnut (Arachis hypogea), soybean (Glycine max) and cotton seed (Gossypium sp.), possibly corresponding to their phosphatidyl ethanolamine content. Out of phosphatidyl choline, phosphatidyl ethanolamine and phosphatidic acid, phosphatidyl ethanolamine was found to be the most effective antioxidant. Antioxidant property of phosphatidyl ethanolamine did not vary with the seed source, indicating that the fatty acid portion of the molecule played no role in protecting ghee against oxidation. In stored ghee addition of phosphatidyl ethanolamine and phosphatidyl choline reduced lipolysis, probably by interacting with the lipase system. During storage, phosphatidyl ethanolamine afforded better protection against the oxidation of unsaturated fatty acids.     

Phospholipids of marine origin. IV. The abalone (Haliotis midae)

Phospholipids of the abalone were separated into component fractions by chromatography on silicic acid. The phospholipids were remarkable for the presence (6%) of an unusual sphingolipid liberating 2-amino-ethylphosphonic acid on hydrolysis, and for the high proportion of plasmalogens (23%). The presence of phosphatidyl ethanolamine plus ethanolamine plasmalogen (32%), phosphatidyl serine (5%), phosphatidyl inositol (5%), phosphatidyl choline (41%) and sphingomyelin (1%) were also demonstrated. The fatty acid distribhion in the phospholipids, the non-phosphorylated lipids and the unusual sphingolipid was determined by gas chromatography. In general these results show a similarity between the phospholipid and the non-phosphorylated lipid fatty acids, the former being richer in long chain polyunsaturated fatty acids. Fatty acids of the unusual sphingolipid were outstanding for the high palmitic (53%) and stearic acid (15%) content.     

Lipid composition of five species of Indian prawns

The lipid and fatty acid compositions of five Indian species of prawns, Metapenaeus monoceros, M. dobsoni, M. affinis, Penaeus indicus and Parapenaeopsis stylifera, were examined. Phospholipids constituted 50–70% of the total lipids, with phosphatidyl choline (50%) and phosphatidyl ethanolamine (29%) as their chief components. Unsaponifiable matter comprised 21–40%, chiefly cholesterol: triglycerides only constituted 9–14.5%. In the total lipids (I.V. 90–112), saturated, monoenoic and polyenoic fatty acids averaged 42, 24 and 34%. Palmitic acid is high, oleic low, and 20:5 generally, but not always, higher than 22:6. The only brackish water prawn, M. monoceros, though generally in conformity, was distinctive in several respects.     

Composition of the lipids of lupin seed (Lupinus angustifolius L. var. “uniwhite”)

The total lipids (8.6%) extracted from whole lupin seeds (Lupinus angustifolius L. var. “Uniwhite”) were found to be comprised of triglycerides (71.1%), phospho-lipids (14.9%), free sterols (5.2%), glycolipids (3.5%), sterol and wax esters (0.5%), free alcohols (0.4%), hydrocarbons (0.4%) and unidentified waxy material (4.0%). The main fatty acids in the total lipid extract were linoleic (48.3%), oleic (31.2%), palmitic (7.6%) and linolenic (5.4%). Erucic acid was not present, nor were cyclopropenoid acids. Seed coatings constituted 23.9% of the weight of the whole seeds and contained 1.5% lipids, the main classes of which were triglycerides (38.4%), free sterols (28.0%), phospholipids (9.7%), glycolipids (9.1%) and free alcohols (3.7%). The seed coatings and kernels contained the same fatty acid constituents, but the proportions of oleic, linoleic and linolenic acids were markedly different. β-Carotene was present, although at low concentration. When evaluated on its lipid composition, “Uniwhite” lupin seed appears suitable as a supplement for pig, poultry and stock feeding.     

Lipid Content and Fatty Acid Composition in Bamboo Shoots

Lipids from bamboo shoots (Phyllostachys pubescens), peeled and divided from top to base, were extracted and fractionated into three classes, and each class separated into constituent components by thin-layer chromatography (TLC). Fatty acid composition and amount of separated lipids were determined. Total lipids (TL) ranged from 800 (top) to 380 mg (base) per 100g fresh weight and the ratio of nonpolar lipids (NPL):glycolipids (GL):phospholipids (PL) was about 17:27:56. The main fatty acids of the three lipid classes were palmitic, linoleic and linolenic acids, but composition was remarkably different among these fractions. The fatty acid composition of triglycerides (TG) was similar to the original NPL. Palmitic acid was almost all located in 1-, 3-position, linoleic acid mainly located in 2-position of TG, while linolenic acid was distributed in each position. Digalactosyl diglyceride (DGDG) and monogalactosyl diglyceride (MGDG) were the main components of GL; the average of the former had about 37% linoleic and 29% linolenic acids, while the latter had about 25% linoleic and 62% linolenic acids. Bamboo shoots contained 9 PL fractions, the major being phosphatidyl choline (PC) and phosphatidyl ethanolamine (PE). PC contained about 48% linoleic, 31% palmitic and 11% linolenic acids, and PE also had the similar tendency as PC.     

INHIBITION OF ASPERGILLUS GROWTH AND EXTRACELLULAR AFLATOXIN ACCUMULATION BY SORBIC ACID AND DERIVATIVES OF FATTY ACIDS

A study was conducted to determine the effects of sorbic acid and several derivatives of fatty acids (amides, aminimides, and monoglycerides) upon toxigenic cultures of Aspergillus flavus and A. parasiticus. A synthetic medium was inoculated with spores, incubated for 48 h at 27°C, and then supplemented with sorbic acid and fatty acid derivatives. Cultures were then incubated for an additional 5 days. Aflatoxins were extracted, separated, and quantitated. Mycelial mats were dried, weighed, and analyzed for lipid and mineral content. Cerulenin (8 μg/ml) was the most effective fatty acid derivative examined, reducing mycelial growth by 37% and completely inhibiting extracellular accumulation of aflatoxins. Other derivatives, in decreasing order of effectiveness, included M-20 (an aminimide), lauribic, and lauricidin. Mycelia grown in the presence of fatty acid derivatives contained less phosphorus, potassium, magnesium, phosphatidyl ethanolamine, phosphatidyl serine, cholesterol, and triglycerides, but more cardiolipin, phosphatidyl choline, free fatty acids, fatty acid esters, and diglycerides. Levels of monoglycerides and cholesterol esters remained essentially unchanged. Inhibition by sorbic acid was nonspecific, affecting both mycelial growth and extracellular aflatoxin accumulation to approximately the same extent. Utilization of fatty acid derivatives for determining mechanisms of aflatoxin accumulation and lipid biosynthesis appears promising.     

Neutral Lipids Present in Starch of Uruchi and Mochi Rice

The total lipid contents of rice starch were 1.30 and 0.92%, and the ratios of neutral lipid to polar lipid were 56:44, and 77:23 in the case of Urichi and Mochi, respectively. The main classes of neutral lipids were free fatty acids, triglycerides, free sterols and sterolesters. The major components of free fatty acids and triglycerides were linoleic, palmitic and oleic acids. Among the component fatty acids of rice starch triglycerides, palmitic acid occupied almost exclusively 1-C and 3-C positions, 2-C position was rich in linoleic acid, and oleic acid was equally distributed in 1-C, 2-C and 3-C positions. The fatty acids in Uruchi triglycerides were symmetrically distributed in 1-C and 3-C positions, but Mochi triglycerides were of asymmetrical distribution. There was no appreciable difference in the sterol compositions of free sterols and sterolesters.     

Effect of ripening stage and technological treatments on the lipid composition,lipase and lipoxygenase activities of chickpea (Cicer arietinum L.)

Lipid composition, lipase and lipoxygenase activities of chickpea seeds were determined in the green (Malana) and fully ripe (dry) chickpea seeds for Giza 1 and Giza 2 cultivars before and after some technological treatments (decortication, cooking and parching). Ripening resulted in marked increase in the content of triglycerides, phosphatidyl choline and phosphatidyl ethanolamine as major components of chickpea lipids. Also, there was a marked rise in lipase and lipoxygenase activities with slight changes in fatty acid composition of chickpea lipids. Minor changes in lipid composition owing to the decortication process applied to the two tested chickpea cultivars (Giza 1 and 2) were also noticed. Cooking and parching caused only slight changes in lipid classes and fatty acids composition, but yielded a significant increase in peroxide value of chickpea lipids. There was a marked drop in lipoxygenase activity with complete inhibition of lipase activity due to cooking and parching.     

Characterization of Shrimp Lipids

Edible shrimp (Penaeus aztecus) tissue contains approximately 1.2% extractable lipids, the majority of which are phospholipids. Data from the gravimetric quantitation of lipid classes isolated by column chromatography indicated that phosphatidyl choline was the predominant phospholipid and cholesterol the predominant neutral lipid in edible shrimp tissue. Fatty acid distribution data indicated that sphingomyelins contained the greatest percent by weight of unsaturated fatty acids while cholesterol esters contained the greatest proportion of saturated fatty acids. Enzymatic hydrolysis followed by gas liquid chromatography of phosphatidyl choline, phosphatidyl ethanolamine, and phosphatidyl serine indicated that fatty acids located at the β position were more highly unsaturated than those at the α position.     

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.     

Chemical and Enzymic Changes During the Fermentation of Bacteria-Free Soya Bean Tempe

Amounts of dry matter, ash, protein, free ammonia, crude lipid, glyceride–glycerol, free fatty acids, free glycerol, glucosamine, protease activity and lipase activity were monitored during the fermentation of bacteria-free tempe made with acidified soya bean cotyledons and Rhizopus oligosporus NRRL 2710 at 30°C. During the phase of mycelial growth (0–32 h) the total dry matter decreased by approximately 10% (w/w), accounted for by losses of crude lipid (3% of initial dry matter), protein/amino acids (0·5%), and unidentified compounds (6·5%). During the phase of mycelial senescence (60–180 h), decrease in dry matter (12% of initial dry matter) was due almost entirely to loss of crude lipid. Lipase activity and the production of free fatty acids occurred from the earliest stages of the fermentation. The production of only small amounts of free glycerol indicates that triglycerides were primarily hydrolysed to partial glycerides and free fatty acids. Protease activity and production of free ammonia were also detected at the earliest stages of the fermentation. During the phase of mycelial senescence, amounts of crude lipid and glycerol decreased in the absence of fungal growth, possibly due to the activity of enzymes released from senescent mycelium.