Organic acids,antioxidant capacity,phenolic content and lipid characterisation of Georgia-grown underutilized fruit crops

Four underutilized Georgia-grown fruit crops, namely loquat (Eriobotrya japonica), mayhaw (Crataegus sp.), fig (Ficus carica), and pawpaw (Asimina triloba), and their leaves were analysed for total polyphenols by Folin–Ciocalteau method, and antioxidant capacity by ferric-reducing antioxidant power (FRAP) and Trolox-equivalent antioxidant capacity (TEAC) assays. Organic acids and phenolic compounds were identified by RP-HPLC. For lipid profile, fruits were separated into two fractions – seed and fruit (i.e., without seed); lipid was extracted using the Folch method and analysed for fatty acids, phytosterols, tocopherols, and phospholipids. The major organic acid identified in all samples was malic acid (177–1918 mg/100 g FW). The predominant phenolic acids in all the fruits were gallic (1.5–6.4 mg/100 g FW) and ellagic (0.2–33.8 mg/100 g FW), and the most abundant flavonoid was catechin (12.2–37.8 mg/100 g FW). Total lipid content varied from 0.1% in mayhaw fruit to 21.5% in pawpaw seed. Linoleic acid was the predominant fatty acid in all of the samples (28.2–55.7%).     

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.     

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     

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.     

The lipids of young cassava (Manihot esculenta,Crantz) leaves

Lipids were extracted quantitatively from young cassava (Manihot esculenta Crantz) leaves with a chloroform-methanol mixture. Total lipids were purified by the Folch procedure and separated into non-polar lipid, glycolipid and phospholipid fractions by column chromatography. Lipids of each fraction were further subjected to thin layer chromatography and gas-liquid chromatography. Young cassava leaves were found to have low content of lipids (3.02%) of which 22.4, 25.1 and 48.2 were non-polar lipids, glycolipids and phospholipids, respectively. Pigments (11.5%), wax and hydrocarbons (1.2%), steryl esters (2.9%), methyl esters of fatty acids (2.0%), trigly-cerides (1.5%), fatty acids (2.1%), diglycerides (1.1%) and sterols (0.1%) constituted the leaf non-polar lipids. The leaf glycolipids were made up of esterified steryl glycosides (2.1%), monogalactosyl diglycerides (12.5%), steryl glycosides (1.1%), cerebrosides (4.2%) and digalactosyl diglycerides (5.2%). The leaf phospholipids were found to include cardiolipin (3.6%), phosphatidylglycerol (21.5%), phosphatidylethanolamine (16.4%), phosphatidylserine (0.7%), phosphatidylinositol (4.0%) and other unidentified phospholipids (2.5%). Phosphatidylcholine was present only in trace quantity. Analysis of the fatty acid composition of each of the leaf lipids revealed that, with the exception of steryl esters, all leaf lipids have high content of polyunsaturated fatty acids.     

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     

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).     

Tropical oils: nutritional and scientific issues.

Individually and in combination with other oils, the tropical oils impart into manufactured foods functional properties that appeal to consumers. The use of and/or labeling in the ingredient lists give the impression that these oils are used extensively in commercially processed foods. The estimated daily intake of tropical oils by adult males is slightly more than one fourth of a tablespoon (3.8 g), 75% of which consists of saturated fatty acids. Dietary fats containing saturated fatty acids at the beta-position tend to raise plasma total and LDL-cholesterol, which, of course, contribute to atherosclerosis and coronary heart disease. Health professionals express concern that consumers who choose foods containing tropical oils unknowingly increase their intake of saturated fatty acids. The saturated fatty acid-rich tropical oils, coconut oil, hydrogenated coconut oil, and palm kernel oil, raise cholesterol levels; studies demonstrating this effect are often confounded by a developing essential fatty acid deficiency. Palm oil, an essential fatty acid-sufficient tropical oil, raises plasma cholesterol only when an excess of cholesterol is presented in the diet. The failure of palm oil to elevate blood cholesterol as predicted by the regression equations developed by Keys et al. and Hegsted et al. might be due to the dominant alpha-position location of its constituent saturated fatty acids. If so, the substitution of interesterified artificial fats for palm oil in food formulations, a recommendation of some health professionals, has the potential of raising cholesterol levels. A second rationale addresses prospective roles minor constituents of palm oil might play in health maintenance. This rationale is founded on the following observations. Dietary palm oil does not raise plasma cholesterol. Single fat studies suggests that oils richer in polyunsaturated fatty acid content tend to decrease thrombus formation. Anomalously, palm oil differs from other of the more saturated fats in tending to decrease thrombus formation. Finally, in studies comparing palm oil with other fats and oils, experimental carcinogenesis is enhanced both by vegetable oils richer in linoleic acid content and by more highly saturated animal fats. The carotenoid constituents of red palm oil are potent dietary anticarcinogens. A second group of antioxidants, the tocotrienols, are present in both palm olein and red palm oil. These vitamin E-active constituents are potent suppressors of cholesterol biosynthesis; emerging data point to their anticarcinogenic and antithrombotic activities. This review does not support claims that foods containing palm oil have no place in a prudent diet.     

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.     

太平洋褶柔鱼内脏团营养成分分析与评价

目的 研究太平洋褶柔鱼(Todarodes pacificus)内脏团的营养成分和价值。方法 通过系统测定太平洋褶柔鱼内脏团的基本营养成分组成、脂肪酸组成、氨基酸组成、矿物质元素组成和脂溶性维生素含量,对其营养品质进行分析评价。结果 太平洋褶柔鱼内脏团的水分含量为(64.19±0.78)%,蛋白质、粗脂肪、碳水化合物和灰分的含量分别占干基的(49.68±1.89)%、(32.40±0.14)%、(10.31±1.94)%和(5.70±0.14)%;总脂质中甘油酯、磷脂和游离脂肪酸的含量分别为(55.42±2.65)%、(13.33±1.31)%和(22.64±0.70)%;总脂质中的多不饱和脂肪酸含量丰富,且主要为二十碳五烯酸(eicosapentaenoic acid, EPA)和二十二六烯酸 (docosahexaenoic acid, DHA),二者分别占总脂肪酸含量的(11.56±0.04)%和(27.86±0.09)%;氨基酸组成符合联合国粮农组织/世界卫生组织规定的优质蛋白标准;矿物质元素含量丰富,锌和铁等微量元素的含量较高;维生素D和维生素E等脂溶性维生素的含量较为丰富。结论 太平洋褶柔鱼内脏团是优质蛋白、Omega-3系列多不饱和脂肪酸、脂溶性维生素等营养成分的良好来源,值得进一步开发利用。     

C18 : 1, C18 : 2 and C18 : 3 trans and cis fatty acid isomers including conjugated cis δ9,trans δ11 linoleic acid (CLA) as well as total fat composition of German human milk lipids

In particular with respect to infant nutrition knowledge of the current contents of trans fatty acids (TFA) and of conjugated linoleic acid (CLA) in human milk lipids is of interest. After pre-separation by Ag-TLC 11 trans-C18 : 1 isomers could be quantified by GC with a mean total content of 2.40 ± 0.60 wt% in samples from 40 German women. For the positional isomers t4, t5, t6–8, t9, t10, t11, t12, t13, t14, t15 and t16 contents of 0.02, 0.02, 0.21, 0.37, 0.32, 0.68, 0.23, 0.15, 0.18, 0.09 and 0.14 wt% were established, with vaccenic acid being the predominant isomer. Further, small trans-C14 : 1 and trans-C16 : 1 contents of 0.08% and 0.15% on average were found. As the trans-C18 : 1 isomers also the trans-C16 : 1 isomers of human milk lipids could for the first time be baseline-resolved by GC to a great extent. Moreover, besides a mean CLA (c9,t11) content of 0.40 ± 0.09% further 6 cis/trans isomers of linoleic acid with a total content of 1.07 ± 0.56% on average (w/o CLA) were determined. Further, 4 trans isomers of α-linolenic acid could be baseline-resolved exhibiting a total content of 0.11%. Altogether German human milk lipids on average were found to contain 3.81 ± 0.97% TFA with a range of 2.38–6.03%. Direct connections between the dietary intake of trans-C18 : 1 isomers and the composition of human milk lipids could be established. The major fatty acids exhibited the following contents (wt%): C4: 0.16, C6: 0.18, C8: 0.06, C10: 0.58, C12: 3.12, C14: 6.43, C16: 25.28, C18: 7.41, C18 : 1 (total): 33.67, C18 : 2 (total): 10.63 and α-C18 : 3: 0.87.     

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.     

Composition and bioavailability of oxalates in baked taro (Colocasia esculenta var. Schott) leaves eaten with cows milk and cows milk and coconut milk

Taro leaves are an important food in the Pacific Islands but the overall oxalate composition and its nutritional effect has not been investigated. The oxalate contents of taro leaves were determined using chemical and in vitro extraction methods. Maori‐type taro leaves contained 524.2 ± 21.3 mg total oxalates 100 g^?1 fresh weight (FW) and 241.1 ± 20.9 mg soluble oxalates 100 g^?1 FW while the Japanese‐type leaves contained 525.6 ± 19.9 mg total oxalates 100 g^?1 FW and 330.4 ± 28.3 mg soluble oxalates 100 g^?1 FW. Maori‐type taro leaves contained 416.4 ± 1.5 mg gastric soluble oxalates 100 g^?1 FW and 212.4 ± 34.8 mg intestinal soluble oxalates 100 g^?1 FW while the Japanese‐type leaves contained 433.3 ± 9.7 mg gastric soluble oxalates 100 g^?1 FW and 224.2 ± 38.7 mg intestinal soluble oxalates 100 g^?1 FW). Human feeding experiments were conducted to determine the availability of the oxalates in the baked leaves following additions of cows milk and coconut milk. The consumption of a test meal of baked taro leaves resulted in a significant increase (P < 0.001) in the output of urinary oxalate in the following 6 h when compared to the output of oxalate during a reference collection. When the leaves were baked with cows milk or cows milk and coconut milk combined and consumed there was a small non‐significant reduction in urinary oxalate output which suggests that less soluble oxalate was absorbed from these mixtures.     

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

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

Nutritive value of the larvae of raphia palm beetle (Oryctes rhinoceros) and weevil (Rhyncophorus pheonicis)

The proximate nutrient composition, energy value, mineral concentrations, amino acid composition and chemical score of the larvae of raphia palm beetle (Oryctes rhinoceros) and weevil (Rhyncophorus pheonicis) were evaluated. Values of moisture, ash and crude protein were significantly (p < 0.05) higher in O rhinoceros than in R pheonicis while the reverse was the case for the values of crude fat, total carbohydrate and energy content. The crude protein content of both samples was high, with a value of 42.3 ± 0.84% for the palm beetle and 31.6 ± 0.59% for palm weevil, while crude fat was high (17.3 ± 1.2%) in palm weevil and very low (0.55 ± 0.10%) in palm beetle. The calorific value in kcal 100 g^?1 sample was 425 in R pheonicis and was significantly higher (p < 0.05) than the value of 285 in O rhinoceros, due to a relatively higher crude fat and total carbohydrate in the former compared with the latter. The mineral concentrations were high and differed for all the elements, with O rhinoceros having the higher level of many of the mineral elements (calcium, magnesium, potassium, manganese, iron and phosphorus) compared with R pheonicis, consistent with a significantly higher (p < 0.05) ash content of 12.7 ± 0.81% in O rhinoceros against the value of 4.2 ± 0.45% ash in R pheonicis. The amino acid profile showed both samples to be good sources of essential and non‐essential amino acids including cysteine and methionine, both of which contain sulfur. Valine, which had the lowest chemical score of 51.2%, was the most limiting amino acid for protein quality in both O rhinoceros and R pheonicis. Copyright © 2005 Society of Chemical Industry     

Characterization of nutritionally important phytoconstituents in bitter melon (<Emphasis Type="Italic">Momordica charantia</Emphasis> L.) fruits by HPLC–DAD and GC–MS

Bitter melon (Momordica charantia L.) is the traditional vegetable used as medicinal food, in different parts of the world, including Korea and China. Little is known about its bioactive composition aside from its health-promoting properties. Therefore, the present work aimed to determine the content of carotenoids, tocopherols, folates and fatty acids in bitter melon fruits. Using HPLC–DAD, six major carotenoids were quantified in fruits; all-E-lutein was recorded in highest quantity, followed by all-E-β-carotene and α-carotene, with 79.5, 17.6 and 1.5 % of total carotenoids, respectively. A high content of α-tocopherol (42.93 μg/g FW) and total folate (0.724 µg/g FW) was also recorded in fruits using HPLC–DAD and microbiological assay, respectively. The total lipid content of 1.79 % was recorded in fresh fruits (FW). Using GC–MS, sixteen fatty acids were identified in lipid fraction; α-linolenic acid (ALA; C18:3) was found in highest quantity (44.33 %) followed by palmitic acid (C16:0) (29.64 %), and linoleic acid (C18:2) (10.32 %). Melon fruits contain a low amount of saturated fatty acid and high-mono and polyunsaturated fatty acids, in the form of ALA. Knowledge of bioactive composition in bitter melon fruit will be useful for proper diet recommendations and also for nutrient database updating.     

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).     

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。     

Fatty acids distribution in different tissues of wild and reared Seriola dumerili

In this study, we compared the lipid and fatty acids content, between cultured and wild Seriola dumerili, in different edible portions. Results showed that cultured fish contained a higher level of lipids than wild fish. The fatty acids profiles revealed that, among all the split‐fish side, palmitic (C16:0) and oleic (C18:1n‐9) acid were the principal saturated and monounsaturated fatty acids, in cultured and wild S. dumerili. On the other hand, wild S. dumerili contained a higher level of saturated (38.12 ± 0.54% vs. 33.66 ± 0.15% in cultured fish), monounsaturated (33.13 ± 1.07% vs. 26.49 ± 0.17%), n‐3 polyunsaturated fatty acids (PUFA) (23.90 ± 1.02% vs. 19.77 ± 0.51%) particularly docosahexaenoic acid (DHA) (18.83 ± 0.48% vs. 11.77 ± 0.42%). However, the cultured fish showed a higher level of n‐6 PUFA due principally to the higher value of linoleic acid (C18:2n‐6). In fact, changes in fatty acids content between anatomical areas marked differences in the muscle quality of wild and cultured S. dumerili. According to this study, both groups of wild and farmed S. dumerili have nutritional benefits for human health. Cultured fish were characterised by higher hypocholesterolaemic and hypercholesterolaemic fatty acids ratio for all samples studied and a lower n‐3/n‐6 ratio due to the abundance of n‐3 PUFA particularly DHA in wild fish.     

Changes in Composition of Potatoes Solanum Tuberosum cv. Huinkul Stored in Clamps

Changes in tuber composition related to potato (Solanum tuberosum cv. Huinkul) storage in clamps for 120 days, were studied. Dry matter (22.5g ± 2.9) was unaffected by storage. Protein, vitamin C, total lipids and phospholipids were calculated on a 100g dry weight basis. Initial protein content (4.71 g ± 0.5) fluctuated during storage, having a similar percentage value at the end of the storage period. Vitamin C at harvest was 100 mg ± 8.1 and decreased to 55.8 mg ± 8.4 (120th day).Total lipids were 0.6g ± 0.15 and 0.25g ± 0.06 at the beginning and at the end of storage, respectively. Initial and final phospholipid content were 0.14g ± 0.02 and 0.16g ± 0.02, respectively.