Phospholipids of marine origin. The lantern fish (Lampanyctodes hectoris)

Lantern fish of the species Lampanyctodes hectoris were shown to contain phospholipids (10 g kg^?1) and non-phosphorylated lipids (140 g kg^?1). The phospholipid fraction consisted of phosphatidyl choline (47% of total phospholipids), phosphatidyl ethanolamine (42%), phosphatidyl serine (3%), phosphatidyl inositol (1%), sphingomyelin (4%), lyso-phosphatidyl choline (1%) and cardiolipins (2%). Lantern fish (L hectoris) meals normally contain unacceptably high lipid contents (150 g kg^?1 and over); this characteristic was found not to be due to a high phospholipid level in the lantern fish. The major fatty acid of the phospholipids was C22:6n-3 (25% total fatty acids) followed by C16:0 (18%), C18:ln-9 (16%) and C20:5n-3 (8%). This distribution was different from that of the non-phosphorylated lipids where the major fatty acid was C16:0 (21%) followed by C18:ln-9 (19%), C20:5n-3 (11%), C20:l (7%) and C22:6n-3 (7%). The lantern fish press oil and residual meal lipids had fatty acid distributions similar to those of the non-phosphorylated lipids.     

Fatty acid and lipid class composition of the eicosapentaenoic acid-producing microalga, Nitzschia laevis

The diatom Nitzschia laevis is a potential producer of eicosapentaenoic acid (EPA, C20:5n − 3). In order to further adopt this alga in the functional food and aquaculture industries, the lipid class composition and fatty acid distribution in the lipid pool of N. laevis were studied using thin-layer chromatography and gas chromatography. The total lipids of N. laevis were fractionated into neutral lipids (NLs), glycolipids (GLs) and phospholipids (PLs). NLs were the major constituents and accounted for 78.6% of the total lipids. Triacylglycerol (TAG) was the predominant component of NLs (87.9%). GLs and PLs accounted for 8.1% and 11.6% of the total lipids, respectively. Phosphatidylcholine (PC) was the major component of PLs (69.7%). The principal fatty acids identified in most lipid classes were tetradecanoic acid (C14:0), hexadecanoic acid (C16:0), palmitoleic acid (C16:1) and EPA. EPA was distributed widely among the various lipid classes with the major proportion (75.9% of the total EPA) existing in TAG, monoacylglycerol and PC.     

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.     

Seasonal changes in phospholipids of mussel (Mytilus edulis Linne)

The phospholipids of mussels (Mytilus edulis Linne) from the coast of Qingdao were extracted, fractionated and analysed over a 12 month period. The contents of total lipids, neutral lipids, polar lipids and phospholipids were measured. The composition of phospholipids was determined by high‐performance liquid chromatography, and their fatty acid composition was analysed by gas chromatography. The phospholipid content ranged from 3.6 to 6.4 g kg^?1 soft tissue. PE (phosphatidyl ethanolamine) and PC (phosphatidyl choline) were the major constituents. C16:0, C20:5 and C22:6 were the major fatty acids. C20:5 (5.25–23.10%) and C22:6 (6.05–20.42%) varied regularly with the seasonal factors. Their total amounts were high from January to June, which would be an optimal time for the utilisation of the phospholipids of mussels. © 2002 Society of Chemical Industry     

3种经济类海胆的脂质组成差异分析

目的 对比分析国内3种常见经济类海胆的脂质组成。方法 以性腺基本指数、总脂含量、胆固醇含量、磷脂含量、甘油酯含量、脂肪酸组成、磷脂组成等为评价指标,结合统计分析技术比较不同种类海胆脂质组成的差异。结果 光棘球紫海胆、黄海胆和虾夷马粪海胆总脂占干基的(21.83±0.12)%～(27.21±0.10)%;其中磷脂和甘油酯是最主要的脂类组分,分别占(39.62±0.49)%～(49.39±0.73)%和(30.08±0.01)%～(38.65±0.03)%;磷脂中的主要组分为磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰肌醇;总脂中脂肪酸主要为C16:0、C18:0、C20:1。对脂类相关数据进行标准化处理,并结合聚类分析和主成分分析,结果显示3种海胆性腺脂类物质中脂质组成、磷脂组成及脂肪酸组成差异明显。结论 光棘球紫海胆相对于其他两种海胆具有较高的营养价值和脂质优势,可作为C20:5n3、C22:6n3及磷脂等功能性脂质分子的重要膳食来源。     

Seasonal variations in lipid composition of spanish wild rabbit (Oryctolagus cuniculus) meat

Four batches of wild rabbit (Oryctolagus cuniculus: winter, spring, summer and autumn) were caught at the end of the respective season of the year. A study of the meat chemical composition of these animals was carried out. The classes and amounts of total, apolar and polar lipid fractions, and their fatty acids, have been extensively studied. The total, apolar and polar lipid contents from the muscle of the four batches ranged from 37 to 14, 30-1 to 8–4 and 9–0 to 4–8 g kg^?1 FW respectively. Triglycerides accounted for more than 59% of the apolar lipids, and phosphatidylcholine and phosphatidyl-ethanolamine were the major phospholipids (>44% and >35% of total phospholipids, respectively). Almost always, 16:0, 18:0, 18:1 and 18:2 were the more abundant fatty acids of the total lipid fraction. Many seasonal differences may be observed in the fatty acid composition of total and apolar lipid fractions which are obviously related to the kinds of feed available in each season. One of the most significant differences is in 18:1 concentration. This fatty acid accounted for more than 50% in the apolar lipids from rabbits caught in autumn whereas the same fatty acid never reached 30% in other seasons. On the contrary, 18:2 and 20:0 showed a lower concentration in the autumn batch by comparison with those of the other seasons.     

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.     

Phospholipids of marine origin. VI. The octopus (Octopus vulgaris)

The composition of octopus (Octopus vulgaris) phospholipids was determined by analysis of hydrolytic breakdown products and by chromatography on silicic acid. The most remarkable feature of octopus phospholipids was the high content (13%) of ceramide aminoethylphosphonic acid. In addition the phospholipids contained phosphatidylcholine (42%), phosphatidylethanolamine (30%), phosphatidylserine (5%), phosphatidylinositol (4%) and sphingomyelin (3%). The fatty acid distribution of the phospholipids and the non-phosphorylated lipids was determined by gas chromatography. The major saturated fatty acids in the phospholipids and non-phosphorylated lipids were 16:0 (24 and 23%, respectively) and 18:0 (10 and 15%, respectively). The major highly unsaturated fatty acids in phospholipids and non-phosphorylated lipids were 20:5 (18 and 7%, respectively) and 22:6 (23 and 9% respectively).     

Characteristics of lipid composition differences between cultured and wild ayu (Plecoglossus altivelis)

The lipid levels and fatty acid compositions of the muscle and liver of ayu (sweetfish), Plecoglossus altivelis, and those of its stomach contents were investigated to clarify the difference in the lipid characteristics between aquacultured and wild samples. The lipid levels of the cultured P. altivelis (2.0-3.7%) were significantly higher than were those of the wild ones (1.1-1.4%). Triacylglycerols were the dominant depot lipids of both the cultured and wild samples, while phospholipids were the major components in the polar lipids. The major fatty acids in the muscle and liver triacylglycerols were 14:0, 16:0, 16:1n-7, 18:1n-9, 18:2n-6 (linoleic acid for cultured), 18:3n-3 (linolenic acid for wild), 20:5n-3 (icosapentaenoic acid), and 22:6n-3 (docosahexaenoic acid for cultured). In spite of similar levels of many fatty acids for cultured and wild triacylglycerols, the cultured samples had markedly higher levels of 18:1n-9, 18:2n-6, and 22:6n-3 while the wild ones had significantly higher levels of 18:3n-3 and 20:5n-3, which originate from their dietary lipids. The ratio (R_LA/LN) of linoleic acid (18:2n-6) to linolenic acid (18:3n-3) in the cultured samples was markedly higher than were those of the wild samples, and we can easily determine whether P. altivelis is cultured or wild by fatty acid analysis. Moreover, a significant difference in the long-chain PUFA levels, between the cultured and wild samples, was found: higher 22:6n-3 levels were found in the cultured samples while higher 20:5n-3 and 22:5n-3 levels were observed in the wild ones. This finding suggests a limitation of desaturation enzymes in P. altivelis and high 22:6n-3 levels in artificial feedstuff lipids.     

Lipid distribution and composition of commercially farmed atlantic salmon (salmosalar)

Skin, red and white muscle, belly flap, dorsal fat depot, backbone, head, visceral tissue and liver of commercially farmed Atlantic salmon (Salmo salar) were analysed for total lipid content, lipid classes and fatty acid composition. The fat is deposited in a number of tissues and organs with the highest level in the dorsal fat depot (38.4% of wet weight), red muscle (27.2%) and belly flap (28.1%). The fat content in white muscle is 9.6% of wet weight. The lipid class distribution is nearly uniform throughout the fish body. The belly flap contains the highest amount of triacylglycerols (98.8% of total lipid) and white muscle and visceral tissue have the lowest levels, 93.3% and 93.1%, respectively. The variation in total saturates, monoenes, polyenes, n-6 and n-3 fatty acids was much less between tissues than the variation in total lipid content. In the edible part, the belly flap (16.7%) contained significantly lower levels of n-3 fatty acids than red (18.4%) and white muscle (19.7%) mainly due to lower level of 22: 6n-3 and 20: 5n-3 fatty acids.     

Lipids and of fatty acids of edible crabs of the north-western Pacific

Analyses of lipids and fatty acids in muscles and hepatopancreas of five commercially exploited crabs inhabiting the Sea of Japan and the Okhotsk Sea, namely Paralithodes camtschaticus, Paralithodes platypus, Chionoecetes opilio, Chionoecetes angulatus and Chionoecetes japonicus, have been carried out. The total lipid level (TL) in muscles ranged from 0.53% of wet weight (ww) to 1.57% of ww and the amount of phospholipids exceeded that of triglycerides. The TL contents in the hepatopancreas of all crabs were higher than in muscles and varied between 10.2% ww in C. angulatus and 19.8% ww in P. platypus, the major class of lipids being triglycerides. The main polar lipids in the hepatopancreas and muscles were phosphatidylcholine (PC) and phosphatidylethanolamine (PE). Among polyunsaturated fatty acids (PUFAs), the n-3 fatty acids have dominated; 16:0, 18:1n-9, 20:5n-3 and 22:6n-3 were the main fatty acids contained in the tissues studied. In all the crabs, excluding C. angulatus, the PUFAs n-3/n-6 ratio in muscles varied between 7.02 and 10.3 while, in the hepatopancreas, the ratio varied between 4.00 and 6.62.     

The Fatty Acid Composition in Tuna (Bonito,Euthynnus pelamis) Caught at Three Different Localities from Tropics to Temperate

The present paper describes the effect of habitat on the fatty acid composition of the lipid of bonito (Euthynnus pelamis), which was caught at three different localities, Philippine Sea (the tropical zone; seawater temperature at the fishing ground was 27·8°C), East China Sea (the subtropical zone; seawater temperature was 29·7°C), and the Pacific coast of Japan (the temperate zone; sea-water temperature was 20·3°C). The total lipids of various organs and stomach contents were extracted and their fatty acid composition analysed by gas chromatography (GC). Docosahexaenoic acid (DHA; 22: 6n-3) was the major unsaturated fatty acid in the lipid of all specimens examined from all localities. The mean DHA content accounted for more than 25% (mean±standard error: 26·0±0·6%) of the total fatty acids (TFA) in the lipids of all organs, a lipid profile markedly different from that of other fish species whose fatty acid composition is generally variable. Particularly, the mean DHA content of lipids in bonito caught in the northern sea-area sample (the temperate zone) was always high (28·4±0·7% TFA) in the lipid of every organ. Because the DHA contents of lipids of the stomach contents fluctuated between 9·9 and 31·9% TFA, bonito did not simply incorporate the fatty acid profile of the lipids of its prey fishes, but selectively accumulated the DHA. Though the mean DHA content in the lipid of all bonito from the tropical to the temperate zone was markedly higher than other marine fish species such as sardines and herrings, there was a small difference between those in the northern (28·4±0·7% TFA) and southern samples (the subtropical and tropical samples, 24·7±0·8% TFA) (P<0·05). It is suggested that the difference between them may be due to environmental effects, for example, the temperature of the seawater and the fatty acid composition of the lipids of prey organisms. © 1997 SCI.     

Changes in Soya Bean Lipid Profiles during Kinema Production

The influence of processing on soya bean lipids during kinema production was studied. The crude lipid (CL), free fatty acid (FFA) and phytosterol contents of raw beans were 121 g, 6·9 g and 0·8 g kg⁻¹ dry matter, respectively. After soaking and cooking the moisture content of beans increased significantly from 121 to 749 g kg⁻¹, whilst the lipid contents were unchanged. During a 2 day fermentation at 37°C, the lipid contents increased significantly as indicated by capillary column gas chromatography (GC) analysis of petroleum ether extracts of lyophilised samples of unfermented and fermented beans. The fatty acids, palmitic (C16:0), stearic (C18:0), oleic (C18:1), linoleic (C18:2), linolenic (C18:3) and arachidic (C20:0) acids were identified. The major fatty acid present in all samples was the essential fatty acid, linoleic acid. All of the aforementioned fatty acids (except arachidic) were liberated during fermentation by microbial lipases, yielding approximately the same proportion of fatty acids found in unfermented beans. The unsaponifiable soya bean lipids identified by GC were campesterol, stigmasterol and β-sitosterol (ratio 1·2:1:3·4). Levels of these increased during fermentation by 50–61%, but remained in approximately the same proportions.     

Camphor Tree Seed Kernel Oil Reduces Body Fat Deposition and Improves Blood Lipids in Rats

The total and positional fatty acid composition in camphor tree (Cinnamomum camphora) seed kernel oil (CKO) were analyzed, and for the first time, the effect of CKO on body fat deposition and blood lipids in rats was studied. The major fatty acids in CKO were determined to be decanoic acid (C10:0, 51.49%) and dodecanoic acid (C12:0, 40.08%), and uniformly distributed at Sn‐1, 3, and Sn‐2 positions in triglyceride (TG). Rats were randomly divided into control, CKO, lard, and soybean oil groups. At the end of the experiment, levels of blood lipids and the fats of abdomen in the rats were measured. The main organ were weighted and used for the histological examination. The results showed that body weight and fat deposition in CKO group were significantly lower than the lard and soybean groups. Moderate consumption of CKO was found to improve the levels of blood TG and low density lipoprotein cholesterol.     

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.     

Distribution of fatty acids in triacylglycerols and phospholipids from peas (Pisum sativum L.)

BACKGROUND: The fatty acid distribution of triacylglycerols (TAG) and major phospholipids (PL) obtained from four varieties of peas (Pisum sativum) was investigated. The total lipids extracted from the peas were separated by thin layer chromatography into seven fractions. RESULTS: The major lipid components were PL (52.2–61.3%) and TAG (31.2–40.3%), while hydrocarbons, steryl esters, free fatty acids and diacylglycerols (sn‐1,3 and sn‐1,2) were also present in minor proportions (5.6–9.2%). The main PL components isolated from the four varieties were phosphatidylcholine (42.3–49.2%), phosphatidylinositol (23.3–25.2%) and phosphatidylethanolamine (17.7–20.5%). Significant differences (P < 0.05) in fatty acid distribution were found for different pea varieties. Phosphatidylinositol was unique in that it had the highest saturated fatty acid content among the three PL. However, the principal characteristics of the fatty acid distribution in the TAG and three PL were evident among the four varieties: unsaturated fatty acids were predominantly located in the sn‐2 position while saturated fatty acids primarily occupied the sn‐1 or sn‐3 position in the oils of the peas. CONCLUSION: These results should be useful to both producers and consumers for the manufacture of pea foods in Japan. Copyright © 2007 Society of Chemical Industry     

Fatty acid composition of the total, neutral and phospholipids of pond-raised Brazilian Piaractus mesopotamicus

Seven sample lots of farmed Piaractus mesopotamicus , fed a set diet, collected at different times during the year were analysed. The total lipids (11 ± 3% fresh weight, muscle) consisted of 94% neutral lipids and 5% phospholipids. Sixty-seven fatty acids and dimethylacetals were detected in the total lipids, the principal acids being 18:1ω9±ω7 (41.0 ± 1.7%), 16:0 (24.2 ± 1.2%), 18.2ω6 (9.1 ω 0.5%), 16:1ω7 (8.9 ± 0.7%), 18:0 (7.7 ± 0.5%) and 14:0 (3.2 ± 0.5%). The neutral lipids exhibited a similar profile. The phospholipids had a higher proportion of polyunsaturated fatty acids, the major components being 18:1ω6 (9.1 ± 0.7%) (17.5 ± 1.8%), 16:0 (16.7 ± 2.0%), 20:4ω6 (11.6 ± 1.3%), 22:6ω3 (11.0 ± 1.3%), 18:2ω6 (9.1 ± 0.7%), 18:0 (8.9 ± 1.1%), 22:5ω (5.8 ± 0.7%). No definite trend was seen in relation to season (water temperature, 7–26°C). The fish samples analysed were poor in ω3 fatty acids, which appeared to reflect the low ω3 fatty acid content of the diet.     

Evaluating nutritional quality of pacific fish species from fatty acid signatures

Eight fish species common to the Pacific Northwest coastal waters were categorised according to total lipids in a ranking from lean fish (e.g. walleye pollock) to oily fish (e.g. herring) species. Comprehensive fatty acid signatures were compared on both the relative proportion of total fatty acids and the proportion of total carcass lipid content. Generally, fish species from the Pacific coast had a relatively high proportion of n-3 highly polyunsaturated fatty acids (n-3 HUFAs), of which more than 80% was accounted for by C20:5n-3 (EPA) and C22:6n-3 (DHA), with species-specific and lower proportions of oleic acid (C18:1n-9) and palmitic acid (C16:0) also dominating. The MUFA contents of fish were lower (P < 0.05) in the lipids of lean and low-fat fish compared to those of fattier species. In contrast, higher (P < 0.05) proportions of polyunsaturated fatty acids (PUFAs) existed in the low-fat species with DHA contents ranging from 18% to 29% in the low-fat fish and from 8% to 10% in the fattier fish, such as herring and capelin. Expressing the same fatty acid content data in terms of absolute amount of fatty acids (e.g. gFA/100 g wet tissue) showed that both EPA and DHA contents in the flesh of pollock and hake were indeed many fold lower than those found in fatty fish, such as herring. The findings confirm that it is important that both the total lipid content and the fatty acid composition of these Pacific fish food sources be considered when making evaluations on the nutritional quality.     

LIPID CONTENT AND FATTY ACID PROFILES OF SOME LESSER KNOWN NIGERIAN FOODS

The lipid content and fatty acid profiles of seven lesser known protein foods in Nigeria, which include raffia palm and oil palm weevils (Rhynchophorus sp.), shrimps (Palaemonetes sp.), periwinkles (Pachynelania byronesis), snails (Vicapara quadrata), tropical oysters (Thais haemastrama) and crayfish (Palaemonetes varians), were determined. The total lipid content (% fresh weight, FW) ranged between 1.8 ± 0.1 and 9.8 ± 0.1. The range of values for neutral lipids, total phospholipids, and glycolipids (mg/g FW) was 10.1 ± 0.7 to 53.6 ± 1.5, 6.1 ± 1.3 to 30.1 ± 1.5, and 2.5 ± 0.2 to 13.1 ± 0.9, while those of total cholesterol and triacylglycerol content (mg/g neutral lipids) were 1.4 ± 0.1 to 7.1 ± 0.2 and 8.3 ± 1.1 to 47.0 ± 1.5, respectively. Crayfish and palm weevils contained higher amounts of total cholesterol and phospholipids, compared with the rest of the foods. The fatty acid profiles showed variation among the different foods. Palm weevils, periwinkles, snails and tropical oysters were shown to contain substantial amounts of essential fatty acids, especially linolenic acid (C18:3n3).     

Fatty acids from Macoma sp. of bivalve mollusc

Fatty acids of the total lipids of flesh and hepatopancreas of Macoma sp. have been determined. The level of 20:5w3 (ca 17%), a biologically important fatty acid, was found to be considerably high. Other major component fatty acids were 16:0, 16:1, 18:1 and 22:4w6. High levels of 22:5w6 (8%), 22:5w3 (8%) and 22:6w3 (ca 15%) were found in flesh lipid. Nonsaponifiables were also high (28–30%). Alkyl ether acyl glycerols were found in flesh (1.3%) and hepatopancreas (3.8%).