超高效液相色谱-静电场轨道阱高分辨质谱鉴定核桃仁的脂质构成

利用超高效液相色谱-静电场轨道阱高分辨质谱系统鉴定了核桃的脂质组.在正负离子模式下获得脂质的一级质谱和二级质谱信息后,共鉴定出4大类525种脂质分子,包括250种甘油酯、221种磷脂、18种糖脂、36种鞘脂类,含量分别占总脂质的87％、12.97％、0.02％和0.01％.甘油二酯(diacylglycerol,DG)...     

Changes in lipid content and composition during germination of groundnuts

The cotyledons of two varieties of germinating groundnut seeds (Runner and Bunch) were analysed periodically for their lipid content and fatty acid composition over a period of 132 h. The lipid content decreased drastically during germination. More drastic changes in lipid constituents were observed for light-grown seedlings than for dark-grown ones. In general, the non-polar lipids (NPL) were metabolised faster than the polar ones (P > 0.05) especially in those seeds grown in the dark. The rate of decrease in NPL content almost paralleled that of increase in glycolipid (GL) content. Triacyl glycerol content decreased noticeably during germination while other NPL tended to increase. Among the GL, sterylglucoside increased rapidly during early germination under darkness, only to decrease steadily thereafter. A converse effect was observed for acyl sterylglucoside which, in the dark, decreased rapidly at early germination only to increase equally rapidly later on. Among the phospholipids (PL), only phosphatidic acid showed a marked increase during germination, under both growth conditions, while others tended to decrease in varying degrees. The changing patterns of GL and PL during germination seem to follow the pattern of the formation of photosynthetic tissues and the metabolic conversion of PL. The major fatty acids of the three lipid groups, which more or less decreased or increased in varying degrees with germination in light-grown seeds were oleic, linoleic, palmitic, stearic, arachidic and lignoceric acids in decreasing order of prominence at early germination.     

Effect of grass or concentrate feeding systems and rate of growth on triglyceride and phospholipid and their fatty acids in the M. longissimus thoracis of lambs

Thirty-two male Ile-de-France lambs were used in a factorial 2×2 design to analyse the effects of feeding systems (grass outdoor, G, or concentrate and hay indoor: stall, S) and of growth rate (low, L, or high, H) on total lipids, triglyceride (TG) and phospholipid (PL) contents and their fatty acid composition in the longissimus thoracis muscle (L.T.). Contents were lower for TG (10.4 vs. 15.8 mg/100 g fresh tissue, P<0.05) and higher for PL (6.4 vs. 5.8 mg/100 g fresh tissue, P <0.05) in grass-fed lambs compared to stall-fed ones. TG of grass fed lambs displayed lower proportions of palmitic acid (C16:0), monounsaturated fatty acids (MUFAs), linoleic acid (C18:2n-6) and other (n-6) polyunsaturated fatty acids (PUFA) and higher proportions of stearic acid (C18:0), linolenic acid (C18:3n-3), cis 9, 11 trans C18:2 and trans monounsaturated fatty acids. In PL of the same lambs only lower MUFA, C18:2n-6 and (n-6) PUFA and higher C18:3n-3, (n-3) PUFA and cis 9, 11 trans C18:2 were observed. Growth rate had no effect on lipid, TG or PL contents of longissimus thoracis. However C18:0 proportions were higher in TG and lower in PL for low growth rate lambs. Low growth rate lambs had also lower cis 9, 11 trans C18:2 in TG. Thus, irrespective of growth rate, the muscle lipids characteristic of grass fed lambs fulfilled the recommended features of human food components much better than that of stall fed lambs, namely for CLA and C18:3n-3. The lower ratios of (n-6) to (n-3) PUFA displayed in grass fed lambs both in TG and in PL were also useful to discriminate all the grass fed lambs from all the stall fed animals.     

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.     

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.     

Changes in lipid composition,fatty acid profile and lipid oxidative stability during Cantonese sausage processing

Lipid composition, fatty acid profile and lipid oxidative stability were evaluated during Cantonese sausage processing. Free fatty acids increased with concomitant decrease of phospholipids. Total content of free fatty acids at 72 h in muscle and adipose tissue was 7.341 mg/g and 3.067 mg/g, respectively. Total amount of saturated, monounsaturated and polyunsaturated fatty acids (SFA, MUFA, and PUFA) in neutral lipid exhibited a little change during processing, while the proportion of PUFA significantly decreased in the PL fraction. The main triacylglycerols were POO + SLO + OOO, PSO (P = palmitic acid, O = oleic acid, L = linoleic acid, S = stearic acid), and a preferential hydrolysis of palmitic, oleic and linoleic acid was observed. Phosphatidylcholines (PC) and phosphatidylethanolamines (PE) were the main components of phospholipids and PE exhibited the most significant degradation during processing. Thiobarbituric acid values (TBARS) increased while peroxide values and hexanal contents varied during processing.     

Relative Role of Individual Phospholipids on Thiobarbituric Acid Reactive Substances Formation in Chicken Meat, Skin and Swine Aorta

Fatty acid profiles and distribution of individual phospholipids (PL) in the total PL were determined in chicken meat and skin and swine aortas, and the contribution of each PL to malondialdehyde (MDA) formation was studied. Results indicate that phosphatidyl choline (PC) and phosphatidyl ethanolamine (PE) produced 70-77% of the total PL MDA while 16-25% of the MDA was formed by phosphatidyl inositol (PI) and phosphatidyl serine (PS). Much lower concentrations of MDA (3-6%) were formed by sphingomyelin (SP), cardiolipin (CL) and lysophosphatidyl choline (LyPC). In all analyzed tissues, both the MDA concentration and the percentage of polyenoic fatty acids, especially arachidonic acid, were highest in PI followed by PE, PS, PC, CL LyPC, and SP.     

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.     

The fatty acid composition of the main phospholipid fractions of the rumen and abomasum tissues of foetal and adult sheep

The fatty acid composition has been determined on phosphatidyl choline, phos-phatidyl ethanolamine and sphingomyelin fractions earlier isolated from the rumen and abomasum tissues of foetal and of adult Romney sheep. The major proportion of polyunsaturated fatty acids was found in the phosphatidyl ethanolamine (17 to 43%) fraction and this was reduced in the phosphatidyl choline (7 to 25%) and sphingomyelin (1 to 4%) fractions. These features are in keeping with the results for mammalian tissues generally. The phosphatidyl ethanolamine fractions were further characterised by the low content of palmitic acid (<8%) compared with 25 to 30 % in the phosphatidyl choline fractions and 29 to 52% in the sphingomyelin fractions and by the occurrence of cyclopropane fatty acids. Consistent with the findings of other workers on mammalian tissues, the sphingomyelin fractions contained a relatively high content (16 to 27%) of higher w-saturated fatty acids including 22:0,23:0,24:0 and 25:0 and of tetracos-14-enoic (24:1 ω9) acid (5 to 16%). The total amounts of acids above C₂₀ tended to vary inversely with the levels of palmitic acid whereas the levels of stearic acid were relatively constant at 13 to 17%. Changes in fatty acid composition with age were generally not marked but the tissues of the foetus were distinguished from those of the foetus were distinguished from those of the adult by their substantial amount of eicosa-5,8,11-trienoic (20:3 ω9) acid together with relatively low contents of linoleic (18:2 ω6) and linolenic (18:3 ω3) acids and to a leser extent by reduced level of acids of the ω3 series. This was particularly reflected by the ratios of ω6/ω3 C₂₀ + C₂₂ acids in the phosphatidyl ethanolamine fractions, the valucs for the foetal rumen and abomasum tissues being 1.03 and 1.07, respectively, compared with corresponding values of 0.78 and 0.72 found in adult sheep. The results are consistent with a requirement for C₂₀ and C₂₂ polyunsaturated acids of the ω3 and ω6 series and some penetration of maternal fatty acids through the placenta. The resemblance between the fatty acid make-up and composition of foetal and maternal phospholipids suggests the possibiligy of transference of intact or lyso-phospholipids from the mother to the foetus through the placenta. However, such a possibility is counter-indicated by consideration of previous work using labelled intermediates and by the mechanism of conversion of linoleic and linolenic acids requiring their CoA derivatives in the formation of the corresponding polyunsaturated C₂₀ + C₂₂ acids. Nevertheless, the sharp cut-off of exogenous maternal fatty acids from the foetal triglycerides and their inclusion in the foetal phospholipids are not readily explainable.     

GLC-MS Analysis of Fatty Acids From Five Black Walnut Cultivars

The lipids from kernels of five black walnut cultivars were extracted by solvent extraction and the fatty acids were analyzed as their methyl esters by GLC-MS analyses. Twenty-one fatty acids were identified in each cultivar. Five acids, palmitic, stearic, oleic, linoleic and linolenic, were present in quantities greater than 1% of total lipids present. Quantities of the individual fatty acids varied significantly among cultivars (P > 0.05) except for palmitic. Linoleic was the predominant fatty acid in all cultivars. Oleic and linoleic comprised greater than 85% of the lipids present in the walnut kernels.     

Analysis of lipid classes and the fatty acid composition of the salted fish roe food products,Ikura, Tarako,Tobiko and Kazunoko

This study was designed to clarify the content of lipid classes and the fatty acid composition of total lipids (TL), sterol esters (SE), triacylglycerols (TG), phospholipids (PL), phosphatidylcholine (PC), and phosphatidylethanolamine (PE) of the Japanese fish roe products, Ikura, Tarako, Tobiko and Kazunoko. The TL, total cholesterol, TG, and PL content of Ikura were higher than those of Tarako, Tobiko and Kazunoko. Kazunoko had the lowest cholesterol content among these roe products. PC was the main component in the PL class of each fish roe product. The main fatty acids of all roe products were 16:0, 18:1n−9, 20:5n−3, and 22:6n−3. Docosahexaenoic acid (22:6n−3) was rich in the TL, SE, TG, PL, PC and PE fractions of all roe products. In particulars the 22:6n−3 percentage of PC and PE fractions in Tobiko were higher than those of Ikura, Tarako and Kazunoko. These results indicate that the lipid from fish roe products may be a useful food source for maintaining human health.     

EFFECT OF FERMENTATION ON THE FATTY ACID CONTENT AND COMPOSITION OF CASSAVA TUBER MEAL

The effect of fermentation on the fatty acids (FA) content and composition of cassava tuber meal has been investigated. The major FA of the cassava tuber meal (CTM) lipid were oleic and palmitic acids. Other FA found in decreasing order were linoleic, linolenic, palmitoleic, stearic, myristic, pentadecanoic, heptadecanoic and nonadecanoic acids. Fermentation of the CTM resulted in substantial increases in the absolute quantities of the individual FA detected except linolenic acid. However fermentation did not alter the pattern of composition of the FA, but it caused increases in the composition of saturated FA and decreases in certain unsaturated ones. Stearic acid increased in composition by about 92.6% and pentadecanoic by about 50%. A reduction of about 72% of the linolenic acid and 24.2% of the palmitoleic acid composition were obtained in the fermented CTM lipid.     

Metabolic fate of long-chain unsaturated fatty acids and their effects on palmitic acid metabolism and gluconeogenesis in bovine hepatocytes

The objectives were to determine the metabolic fate of different long-chain fatty acids, and their effects on palmitic acid metabolism and gluconeogenesis in bovine hepatocytes. Hepatocytes were isolated from four ruminating calves and exposed in suspension for 3 h to one of the following treatments: 1 mM palmitic acid (1C16), 2 mM palmitic acid (2C16), or 1 mM palmitic acid plus either 1 mM oleic (C18:1), linoleic (C18:2), linolenic (C18:3), eicosapentaenoic (C20:5), or docosahexaenoic acid (C22:6). Oxidation of [1-(14)C]palmitic acid or one of the [1-(14)C]-labeled treatment fatty acids to CO2 or incorporation into cellular triglycerides (TG), phospholipids, cholesterol, and cholesterol esters were measured. Rates of oxidation to CO2 were 3- to 4-fold higher for C22:6 than for other fatty acids, with the exception of C20:5, which had intermediate rates of oxidation to CO2. In general, treatments 2C16 and C18:1 yielded the highest rates of incorporation into most cellular lipids, whereas the polyunsaturated fatty acids were poor substrates for incorporation into cellular lipids. The most pronounced change was a large reduction of polyunsaturated fatty acid incorporation into cellular TG compared to 1C16, 2C16, and C18:1. The unsaturated fatty acids also influenced palmitic acid metabolism. The addition of C20:5 yielded the highest rates of palmitic acid oxidation to CO2 followed by addition of C18:1 and C22:6. Treatments containing polyunsaturated fatty acids decreased palmitic acid metabolism to TG and total cellular lipids compared with treatments 2C16 and C18:1. Rates of gluconeogenesis from propionate were significantly higher for the treatment containing C18:1. Long-chain fatty acids vary in their routes of metabolism and influence palmitic acid metabolism and gluconeogenesis in bovine hepatocytes.     

Determination of phospholipid molecular species in pork meat by high performance liquid chromatography-tandem mass spectrometry and evaporative light scattering detection

Normal phase high performance liquid chromatography has been optimized for both evaporative light scattering detection and tandem mass spectrometry in order to characterize the natural phospholipids (PL) (classes and molecular species) of raw and cooked pork meat. The PL fraction included phosphatidylcholine (PC) (42.9%±4.5 for raw vs 42.6%±8.0 for cooked meat), plasmalogen-phosphatidylethanolamine (pPE) and phosphatidylethanolamine (PE) (26.7%±3.1 vs 28.5%±2.3), cardiolipin (CL) (8.3%±2.9 vs 6.3%±0.7), sphingomyelin (Sph) (7.5%±0.9 vs 8.3%±2.1), phosphatidylinositol (PI) (6.8%±0.7 vs 6.5%±2.1) phosphatidylserine (PS) (4.9%±0.5 vs 4.6%±1.4) and lysophosphatidylcholine (LPC) (2.9%±1.3 vs 3.3%±2.6). Arachidonic acid (absent in Sph) was mainly present in pPE and PI and formed molecular species with a saturated fatty acid, such as stearic (as in PI, PS, PE and PC) or palmitic acid (as in PE and PC), or the respective vinyl ethers in pPE (p18:0 and p16:0); however, in PC, arachidonic acid also formed combinations with oleic and linoleic acid. Palmitic acid formed the most abundant molecular species in PC, but not in CL, PE, PI and PS. Unexpectedly, the cooked pork meat showed an increased content of the molecular species of PI and LPC with more unsaturated fatty acids (18:0/20:4 and 18:2, respectively) with respect to raw meat.     

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.     

Capillary gas chromatography analysis of Ethiopian mustard to determine variability of fatty acid composition

Ethiopian mustard (Brassica carinata A. Braun) is an oil crop grown in Ethiopia. However, the oil is considered low quality, as it contains long chain monounsaturated fatty acids, mainly erucic acid. High erucic acid content is beneficial for the polymer industry, whereas low erucic acid is recommended for food purposes. Both linoleic and linolenic acids are essential fatty acids; however, less than 3% linolenic acid is preferred for oil stability. The objectives of this study were to determine fatty acid composition of Ethiopian mustard to determine the range of genetic diversity for these traits. The genotypes were analysed by capillary gas chromatography (CGC). Twenty‐six fatty acids were identified. In all accessions, the predominant fatty acids were erucic, linoleic, α‐linolenic and oleic, followed by gadoleic and palmitic. To a lesser extent stearic, vaccinic, nervonic and behenic acids were found in all accessions. Significant correlations were found between palmitic acid and stearic acid (positive), between erucic acid and palmitic, stearic, vaccinic, oleic, linoleic and α‐linolenic acids (negative) and eicosenoic acid (positive). Selection and hybridization techniques can be applied to modify the oil content of Ethiopian mustard, considering the variability observed. Copyright © 2004 Society of Chemical Industry     

Characterization of phospholipid composition of black cumin (Nigella sativa L.) seed oil

Black cumin (Nigella sativa L.) seed oil was extracted with two different solvents, n-hexane (H) and a mixture of chloroform/methanol (CM) (2:1, by volume). Amount of total lipid (TL) was higher in the CM miscelle (39.2% of seed fresh weight) than in the H extract (37.9%). Chemical characteristics as well as fatty acid profile of the TL extracts were compared and the analysis revealed that the major fatty acid was linoleic acid C18:2n-6 (ca. 57% of total fatty acid methyl esters (FAME)) followed by oleic acid C18:1n-9. Palmitic acid C16:0 was the major saturated fatty acid and detected in appreciable level. Chromatography on a silica column with solvent of increasing polarity yielded 96.1-97.2% neutral lipids (NL) and ca. 3% of polar lipids. Gas liquid chromatography with flame ionization detector (GLC/FID) showed that the major fatty acid present in all lipid classes was C18:2n-6 followed by C18:1n-9 and C16:0 acids, respectively. Phospholipid (PL) classes were separated via normal-phase HPLC. Separation was achieved on a silica column by gradient elution from isooctane/2-propanol (6:8, by volume) to isooctane/2-propanol/water (6:8:0.6, by volume) lasting 35 min with UV detection at 205 nm. The major individual PL classes were found to be phosphatidylcholine (PC; ca. 46-48% of total PL) followed by phosphatidylethanolamine (PE), phosphatidylserine (PS) and phosphatidylinositol (PI), respectively. Phosphatidylglycerol (PG), lysophosphatidylethanolamine (LPE) and lysophosphatidylcholine (LPC) were isolated in smaller quantities. The level of saturated fatty acids, namely palmitic C16:0 and stearic C18:0 acids, was considerably higher in PL classes than in the corresponding triacylglycerols. Characterization of PL profile from Nigella sativa L. seed oil as well as the development of new source of PL was the primary aim of this study.     

新疆野蔷薇种子油的脂肪酸组成分析

采用超声辅助提取法提取野蔷薇种子油,以气相色谱-质谱联用技术对油脂进行脂肪酸组成分析.结果表明:野蔷薇种子油中的主要脂肪酸为棕榈酸、油酸、亚油酸、亚麻酸,其中不饱和脂肪酸占总量的92.41%;主要成分棕榈酸占5.88%,油酸占12.39%,亚油酸占56.52%,亚麻酸占23.50% .     

蝉花菌质的营养及脂质成分分析

本研究以蝉花菌质为试材,采用常规分析法测定一般营养成分;氯仿-甲醇改良法提取总脂肪,硅胶柱层析法分离总脂肪中的极性、中性脂质,TLC分析鉴定其功能性脂质成分;高效液相色谱法和气相色谱法分别测定氨基酸及脂肪酸组成。结果表明:蝉花菌质干物质中的粗蛋白、总脂肪、灰分和粗纤维含量分别为15.22%、1.47%、1.33%和5.54%。钙和磷以及维生素A和维生素E含量分别为0.27%、0.13%、266.59 mg/100 g、62.98 mg/100 g。TLC分析表明脂肪成分中含有鞘磷脂(SM)、卵磷脂(PC)、脑磷脂(PE)和甘油三酯(TG)等功能性脂肪。蝉花菌质富含多不饱和脂肪酸,占脂肪酸总量的48.06%,其中亚油酸含量高达47.94%。蝉花菌质含17种氨基酸,总量为88.27mg/g,其中必需氨基酸占氨基酸总量的53.11%。综上结果,蝉花菌质富含各类营养素,可作为食品或动物饲料添加剂开发利用。     

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.