Lipid quality and filleting yield of reared meagre (Argyrosomus regius)

Reared meagre (Argyrosomus regius) of average weight 1278 g was evaluated for its filleting yield and fillet lipid quality. Filleting yield averaged 42.2%, while very low levels of muscle fat deposits were measured (1.06%). Analysis of lipid classes revealed a high proportion of polar lipids (48.3–59.1%) and low levels of neutral fatty acids (40.9–51.7%) when compared to corresponding values of other farmed fish species. Phosphatidyl‐choline (PC) was the dominant polar lipid (2.92 mg g^?1 muscle), while cholesterol the most abundant neutral lipid (1.68 mg g^?1 muscle). The fatty acid composition of meagre fillet generally reflects the dietary fatty acids. Among n‐3 fatty acids, eicosapentaenoic (4.58%) and docohexaenoic (15.0%) were measured to be the most abundant ones, and 18:2n‐6 (11.9%) was the most common n‐6 fatty acid. The fatty acid profiles of polar and neutral fractions differ, with monounsaturated fatty acids being predominant in the neutral and n‐3 polyunsaturates in the polar lipids. The high polar lipid contents and n‐3 fatty acids and the low atherogenic and thrombogenic indexes indicate a high quality of this species’ lipids.     

Biochemical composition and storage of Jamaican yams (Dioscorea sp)

Dioscorea yam tubers of 11 cultivars from five common species grown in Jamaica were analysed for the following: protein content, total phenolics, vitamin C, total lipids, fatty acid composition and activity of the polyphenol oxidase enzyme. The results show that the yams grown in Jamaica are of good nutritional value with considerable amounts of protein, vitamin C, low lipids with only one cultivar ‘renta yam’ (D alata) possessing high levels of phenolic compounds. The fatty acids present in the total lipid extracts show that yam tubers generally possess high levels of saturated fatty acids mainly palmitic acid. However, the species D alata (cv white yam) and the species D trifida (cv yampie) have high levels of the unsaturated fatty acid, linolenic. All the polyphenol oxidases from the 11 cultivars show activities towards the diphenol substrates, catechol and DL-DOPA (DL-3,4-dihydroxyphenylalanine). However, no oxidation was observed with L-tyrosine, a monophenol substrate. All cultivars studied were found to have different lengths of dormancy which varied with storage conditions. When the harvested tubers were washed, sunned and stored at 20?C in a dark cupboard, it was possible to extend their lengths of dormancy by a further 11 weeks.     

Fatty Acids in the American Groundnut (Apios americana)

The fatty acid profiles of lipids extracted from groundnut (Apios americana Medikus) seeds and tubers were analyzed using gas-liquid chromatography. Groundnut seeds contained 12.1–18.4% lipids and groundnut tubers 4.1–4.6%, on a dry weight basis. Fatty acid profiles of seed and tuber lipids differred; however, linoleic acid predominated. The fatty acid profiles of seeds and tubers varied between plants collected in two different locations, suggesting genetic variability.     

Quantitative and qualitative analysis of lipids in genetically modified potato tubers with varying rates of 14–3–3 protein synthesis

In six transgenic lines of potatoes with the varying rates of 14–3–3 protein synthesis as well as in control cultivar Desiree the content and composition of the lipids extracted from the mature tubers from three years field trials (1998–2000) were analyzed. The transgenic lines J2 and J1 are both overexpressing gene encoding 14–3–3 protein. The J2 exhibited an overexpression of the protein 14–3–3 derived from pumpkin (Cucurbita pepo) cDNA and in J1 the 14–3–3 overexpression resulted from modifying of ADP‐ribosylation factor synthesis. In the remaining lines, synthesis of the protein 14–3–3 was modified by the antisense technology. In tubers from 1998, the content of total lipids was within the range of 0.45–0.88% of tuber dry matter. The highest amount of fat was in tubers of line J2 (69% more than in the control). The content of lipids in tubers from subsequent years ranged from 0.36 to 0.63% of dry matter. Consistently the highest amount of fat was in tubers of line J2, however, the increase was very slight (8.6% more than in the control). The fractionation of lipids into polar and nonpolar fractions showed that all transgenic lines from field trials 1998 and 2000 contained more nonpolar lipids than the control (up to 270% in line J2). The percentage of nonpolar fractions in fats of tubers from all transgenes harvested in 1999 were similar, but they were higher than in tubers from the previous years, and they amounted to 44.4–49.1%. Chromatographic separation of methyl esters of fatty acids demonstrated that cis‐α‐linoleic acid was the main fatty acid present in potato tubers. This acid composed the biggest part of all lipids in G2 line. In the nonpolar fraction of lipids, palmitic acid followed by cis‐α‐linoleic acid showed the highest amounts.     

Species‐specific differences in the fatty acid profiles of the lipids of the yolk and of the liver of the chick

Differences between four avian species of commercial importance (chicken, turkey, duck and goose), in terms of the relationship between the dietary fatty acids supplied in the diet of the layers and the fatty acid composition of the egg yolk lipids, were investigated. Laying hens of the four species were provided with diets with very similar fatty acid compositions. The polyunsaturated fatty acid content of the diets consisted of linoleic and α‐linolenic acids at approximately 50% and 6% (w/w of total fatty acids), respectively, for all four species. In spite of the very similar dietary provision of fatty acids, the subsequent fatty acid profiles of the yolk lipids differed markedly between the four species. In particular, the proportion of docosahexaenoic acid in the total lipid of the yolk was three to five times greater for the chicken compared to the other three species. By contrast, the proportion of arachidonic acid in total yolk lipid was approximately two times greater for the goose and duck than for the chicken and turkey. Thus the chicken was more efficient at incorporating long‐chain (C₂₂ ) fatty acid of the n‐3 series into yolk lipid whereas the duck and goose preferentially incorporated C₂₀ fatty acid of the n‐6 series. The turkey eggs contained a similar proportion of arachidonic acid but less docosahexaenoic acid than the chicken eggs. The main differences between the avian species in terms of the yolk levels of C_{20 –22} polyunsaturated fatty acids were in the phospholipid fraction since only low levels of these fatty acids were present in the triacylglycerol fraction. The relative proportions of docosahexaenoic acid in the phospholipid and triacylglycerol fractions of the livers of the newly‐hatched chicks of the four species reflected the differences displayed by the yolks. The proportions of arachidonic acid in these liver lipid fractions, however, did not reflect the species differences in yolk lipid composition. © 1999 Society of Chemical Industry     

Winter season krill (Euphausia superba D.) as a source of n-3 polyunsaturated fatty acids

Krill (Euphausia superba D.) caught in winter near South Georgia were examined as a raw, intermediate product, precipitate and by product. The following assayes were performed: lipid composition (TLC), fatty acid composition (GC), lipid susceptibility to oxidation, and carotenoids content. The krill harvested in July/August was found to contain about 3% of lipids. The amount of n-3 polyunsaturated fatty acids (PUFA; eicosapentaenoic and docosahexaenoic acids) in total lipids of whole krill accounts for 19.0 ± 1.7% of fatty acids. There was no any lost of n-3 PUFA during processes used to obtain the precipitate and the lipid formula. Euphausia superba is a valuable source of n-3 PUFA, primarily because of their stability in krill.     

Phospholipids of marine origin—the squid (Loligo vulgaris)

Squid (Loligo vulgaris) was found to contain 25 g kg^?1 lipids of which approximately 75% were phospholipids. The phospholipids were shown to consist of phosphatidylcholine (56% of total phospholipids), phosphatidylethanolamine (29%), phosphatidylserine (2%), phosphatidylinositol (2%). sphingomyelin (5%), lyso-phosphatidylcholine(3%) and the unusual lipid ceramide aminoethylphosphonic acid (3%). The major saturated fatty acid in both phospholipids and non-phosphorylated lipid was C16:0 (26% and 21%, respectively, of total fatty acids), while the major unsaturated fatty acid in both lipid fractions was C22:6n-3 (34% and 23%, respectively) followed by C20:5n-3 (14% in both lipids).     

The influence of dietary branched-chain fatty acids on the fatty acid composition of tissue lipids of rats

Branched-chain fatty acids (BCFA) were prepared as a concentrate from the adiposetissue lipids of barley-fed lambs. The BCFA was included in a stock Oxoid ration at levels of 2.5–15% by weight and these diets were given to appetite to female weanling rats for up to 14 days. The influence of the diets on inter alia growth-rate and fatty acid composition of tissue lipids was compared with the effect of the same stock diet with inclusions at a level of 5% by weight of 3-methylhexadecanoic acid (3-MHD), 4-methylhexadecanoic acid (4-MHD), 3,7,11,15-tetramethylhexadecanoic (phytanic) acid and n-hexadecanoic (palmitic) acid which, with the stock ration, served as control. Rats receiving diets containing up to 7.5% BCFA grew almost as well as did those given palmitic acid whereas the animals offered the diets containing 3-MHD, 4-MHD or 10% BCFA barely subsisted. Rats given 10% BCFA or phytanic acid became moribund within 3 days. BCFA accumulated to widely varying degrees in the lipids of the main internal organs. The higher proportions of these acids constituted some 40–60% of the total fatty acids of the lipids of kidney, liver and heart and were associated with diets containing 10% and 15% BCFA and 5% 3-MHD. The lower proportions of the branched acids in the lipids of these organs were in the range 15–25% of the total fatty acids and related to diets that included 2.5% BCFA and 5% 4-MHD. In contrast to the changes in fatty acid composition of the lipids of the main internal organs, those of the central and peripheral nervous systems were only minor, the proportions of branched acids amounting to some 3% in brain tissue and up to 14% in sciatic nerve. Clearance of branched acids from tissue lipids of the main internal organs was almost complete after the animals were returned to the basal diet for 14 days but the loss of branched acids from nerve tissue was evidently less rapid.     

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.     

Original article: Extraction of lipid from scallop (Patinopecten yessoensis) viscera by enzyme‐assisted solvent and supercritical carbon dioxide methods

In the present study, lipid was extracted from scallop (Patinopecten yessoensis) viscera by using the enzyme‐assisted solvent method and the supercritical carbon dioxide (SC‐CO₂) method. Soxhlet extraction with ethyl ether produced a yield of 23.7 ± 0.6 g of lipid 100 g^?1 of dry matter. Enzyme‐assisted solvent extraction allowed recovering 60.6 ± 1.5% of P. yessoensis viscera lipid from the samples treated with papain, whereas a lipid recovery rate of 78.3 ± 0.6% was achieved by SC‐CO₂ extraction. The lipid extracted was divided into the unsaponifiable fraction (sterol) and the saponifiable fraction (fatty acid) and analysed by gas chromatography mass spectrometry. Results indicated that the fatty acid composition and sterol composition for lipids extracted by different methods were slightly different. Eicosapentaenoic acid and docosahexaenoic acid were dominant polyunsaturated fatty acids accounting for 35–40% of the total fatty acid.     

Fatty acids of a whitefish (Coregonus albula) flesh lipids

Using gas chromatographic-mass spectrometric methods 50 fatty acid components of the flesh lipids of a fresh-water whitefish have been examined in detail. The total lipids represented, on average, 3.0% of the wet weight of whitefish fillets. Saturated, monoenoic and polyenoic fatty acids were present in proportions of 31.4, 22.4 and 44.2%, respectively. About half of the total saturated acids was composed of palmitic acid (16:0, 16.1 %), which is generally abundant in fish lipids. The proportion of saturated iso- and anteiso-acids was 2.9%. The major monoenoic acid was oleic acid (18:1,ω9 10.6%), whereas the monoenoic C₂₀-acids were present only in minor amounts and the monenoic C₂₂-acids were not detected at all. The polyenoic fatty acids were predominantly of ω3 series with docosahexaenoic (22:6ω3, 9.4%) and cicosapentaenoic (20:5ω3, 7.7%) acids as the major components. Linoleic (18:2ω6), linolenic (18:3ω3), octadecatetraenoic (18:4ω3) and arachidonic (20:4ω6) acids were also present in remarkable proportions each amounting to about 4.5% of the total fatty acids.     

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.     

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.     

Changes in lipid components during the development of the french bean seed (Phaseolus vulgaris)

Changes in lipid classes, fatty acid composition and distribution have been monitored during the germination, development and maturation of the French bean seed Phaseolus vulgaris. A lipase activity profile over time was also determined. Ungerminated seeds contained high levels of triglycerides and free fatty acids, but low levels of polar lipids, monoglycerides, and diglycerides. Five days after germination there was a decrease in the quantity of triglycerides and free fatty acids and a concomitant increase in the levels of monoglycerides, diglycerides, and polar lipids. As development and maturation progressed, triglycerides increased substantially at the expense of mono- and diglycerides. Ungerminated seeds contained high levels of C₂₀-C₂₂ fatty acids which decreased after germination with a concomitant increase in C₁₆-C₁₈ unsaturated fatty acids. A study of the fatty acid distribution among the different classes of lipids demonstrated that 55% of the unsaturated fatty acids in the ungerminated seeds were present in the triglycerides, whereas the remainder were distributed among the mono- and diglycerides as well the other lipid classes (free fatty acids, polar lipid, and sterols). Five days after germination, the majority of these unsaturated fatty acids were found in the glyceride form. Overall the lipid classes, fatty acid composition and distribution changes during development and maturation of the French bean seed indicated that it shares many of the characteristics of soya bean development.     

The fatty acid composition of the lipids from two species of hake

The fatty acid composition of lipids extracted from the livers, muscle and skin of two hake species Merluccius capensis and M. paradoxus were studied. In one instance a comparison was made between the fatty acid composition of the phospholipid and triglyceride fractions of the lipids. In pre-spawning fish there appears to be a tendency for M. capensis to have fat of higher unsaturation than M. paradoxus. The only consistent species difference found was the high level of unsaturation of skin lipids relative to muscle lipids in M. paradoxus, a species living at greater depth and lower water temperatures. The major saturated fatty acid in hake lipids is that with 16 carbon atoms, the major monoenoic acid the one with 18 carbon atoms, while C_22:6 is the dominant polyenoic fatty acid and C_20:5 the second most plentiful in hake lipids. Phospholipids form a small proportion of the lipid from dark muscle. They are particularly rich in the fatty acids C_16:0 and C_22:6.     

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.     

Stereospecific Positional Distribution of Fatty Acids of Camellia (Camellia japonica L.) Seed Oil

Abstract: The stereospecific positional distribution of fatty acids of camellia seed oil (also called camellia oil) was determined. The camellia oil was mainly composed of neutral lipids (88.2%), and the oleic acid (86.3%) was found to be a major fatty acid of neutral lipids. In the glycolipids and phospholipids, the oleic acid was also found to be a major fatty acid at 62.5% and 54.2%, respectively. The oleic acid was distributed abundantly in all sn‐1, 2, and 3 positions. It was found that the oleic acid was present more at sn‐2 (93.6%) and 3 positions (94.7%), than at sn‐1 position (66.0%). Practical Application: The information of stereospecific positional distribution of fatty acids in the camellia oil can be used for the development of the structured lipids for food, pharmaceutical, and medical purposes.     

Lipids and fatty acids of a whitefish (Coregonus albula) flesh and roe

The total lipids of whitefish flesh and roe averaged 3.0 and 9.8% fresh weight, respectively. Although neutral lipids dominated in both tissues the polar lipid content of fresh roe was unexceptionally high (2.5%). The fatty acid patterns of the total lipids from flesh and roe and of neutral lipids were similar to each other. Polyenoic acids constituted about half of the total fatty acids and monoenoic and saturated components existed in equal amounts. The calculated iodine values for the total lipids from flesh and roe indicated a slightly higher degree of unsaturation for roe fatty acids. The polar lipids were enriched in polyenoic and saturated fatty acids. Similarities in the composition and content of fatty acids from flesh and roe suggest that storage problems, apparent as a rancidity of roe products, may result from the high content of polar lipids readily hydrolysed during storage.     

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.     

Production and composition of microbial fat from Rhodotorula glutinis

The fatty acid, sterol and hydrocarbon compositions of oil produced by a new strain of Rhodotorula glutinis isolated from soil and grown on molasses, were determined. The major constituent fatty acids were: palmitic (37%) oleic (47%) and linoleic (8%). The major sterols were campesterol (42%) and stigmasterol (27%) and the major hydrocarbons were n-C₂₃ (37%), iso-C₂₉ (30%) and n-C₂₁ (19%). Minor constituents in each class of lipids were also detected and estimated. The oil produced was 54% on a dry weight basis. The fatty acid composition was found to be close to that of palm oil.