Fatty acid composition of melon seed oil lipids and phospholipids

Fatty acid compositions of crude melon seed oil from two different sources were compared. Melon seeds fromCitrullus vulgaris (syn.C. lanatus) contained phosphatidylcholine (PC), lysophosphatidylcholine (LPC) and phosphatidylserine (PS), whereas melon seeds fromCitrullus colocynthis contained only PC and LPC, but not PS. Analysis of the total lipids revealed that the major fatty acid of the oils was 18:2n-6.Citrullus vulgaris seed oil contained 71.3% andC. colocynthis contained 63.4% of 18:2n-6. The predominant fatty acids in theC. vulgaris PC were 18:2n-6 (32.2%), 18:1n-9 (26.4%) and 16:0 (22.2%), whereas theC. colocynthis PC contained 44.6% of 18:1n-9 as the major fatty acid. The level of monoenes in theC. colocynthis variety (46.2%) was different from theC. vulgaris (27.3%). The major fatty acid in the LPC was 18:1n-9 for both varieties. Notably, theC. colocynthis variety did not contain any PS. The major fatty acids in theC. vulgaris PS were 18:1n-9 (37.9%) and 18:2n-6 (33.7%). Of all the phospholipids, LPC contained the greatest amount of monoenes, 48.6–52.4%.     

Chemical examination ofClitoria ternatea seeds

Fatty acid composition determined by paper, thin layer and gas liquid chromatography revealed the presence of palmitic, stearic, oleic, linoleic and linolenic acids in the weight ratio of 18.5, 9.5, 51.4, 16.8 and 3.8%, respectively, inClitoria ternatea seed oil. Protein constitutes 38.4% and consists of 18 amino acids. Essential amino acid pattern is (%): lysine (6.55), histidine (2.03), threonine (3.13), phenylalanine+tyrosine (5.5), valine (5.8), methionine+cystine (1.16) and leucine+isoleucine (15.4). The seeds have been found to be rich in calories (500.5 cal/100 g).     

Characteristics and composition of six malvaceae seeds and the oils

The seeds ofSida veronicifolia Linn., syn.S. bumilis cav.,S. cordifolia Linn.,S. ovata Forsk.,S. mysorensis W & A., syn.S. urticaefolia W & A,S. rhombifolia var.retusa Masters andAbutilon crispum Medik. (Malvaceae) contained 15.5%, 11.5%, 12.1%, 13.2%, 20.2% and 12.5% oil, and 15.0%, 14.1%, 17.3%, 13.6%, 12.6% and 18.4% protein, respectively. Linoleic acid predominated (54.9–69.4%) as the fatty acid of all the oils, and malvalic (1.3–11.4%) and sterculic acids (0.4–1.1%) were significant.     

The composition of the oil of starfruit (Averrhoa carambola,Linn.) seeds

The starfruit (Averrhoa carambola, Linn.) seeds were found rich in oil. The oil was examined for its refractive index, iodine value, acid value, saponification number, unsaponifiable matter, and fatty acid composition by gas liquid chromatography. The values (area percent) for fatty acids as methyl esters were: C14:0 (0.67%); C16:0 (21.34%); C18:0 and C24:0 (trace).     

Studies on Apocynacea Seed Oils

The fatty acid composition of three seed oils of Apocynaceae has been studied in this investigation. The seed oils of Apocynaceae were examined for their component acids and were found to contain the following acids: Rauwolfia serpentina, Benth, (wt.%) lauric 0.2 %, myristic 0.8 %, palmitic 17.7%, stearic 4.9 %, arachidic 0.9 %, behenic 0.6 %, oleic 34.4 %, and linoleic 40.5 %. Rauwolfia tetraphylla, Linn. syn. Rauwolfia canescens, Linn., Rauwolfia heterophylla, Roem and Schult, (wt.%) lauric 0.9 %, myristic 3.4 %, palmitic 25.7 %, stearic 10.3%, arachidic 1.6%, behenic 1.4%, oleic 36.5 %, and linoleic 20.2 %. Vinca rosea Linn syn. Lochnera rosea, Linn. (wt.%) lauric 0.2%, myristic 1.0%, palmitic 1.4 %, stearic 6.8 %, arachidic 1.3 %, behenic 0.6 %, oleic 73.6 %, and linoleic 15.1 %.     

Characterization and Authentication of Significant Chinese Edible Oilseed Oils by Stable Carbon Isotope Analysis

The ratios of stable carbon isotopes (δ¹³C) of 12 oils extracted from Chinese edible oilseed samples and their individual fatty acids were determined by elemental analysis-isotope ratio mass spectrometry (EA-IRMS) and gas chromatography-isotope ratio mass spectrometry (GC-IRMS). The results have demonstrated that the δ¹³C ratios of the oils from C3-plant seeds range from ?26.8 to ?30.7‰, while the δ¹³C ratios of C4-plant maize oil are in the interval of ?14.1 to ?16.2‰. Eighteen fatty acids were identified and their abundances were measured by gas chromatography–mass spectrometry (GC–MS) in these oils with C_16:0, C_18:0, C_18:1 and C_18:2 as the major constituents. From the data on fatty acids and stable carbon isotopes, several sensitive markers were developed to detect the adulteration of Chinese edible oilseed oils. Examples are provided with pre-blended samples to illustrate the discrimination procedures and corresponding sensitive markers with emphasis on camellia seed oil, flax seed oil and perilla seed oil.     

Investigating Some Physicochemical Properties and Fatty Acid Composition of Native Black Mulberry (<Emphasis Type="Italic">Morus nigra</Emphasis> L.) Seed Oil

The physicochemical properties of seed and seed oil obtained from the native black mulberry (Morus nigra L.) were investigated in 2008 and 2009. The results showed that the seed consisted of 27.5–33% crude oil, 20.2–22.5% crude protein, 3.5–6% ash, 42.4–46.6% carbohydrate and 112.2–152.0 mg total phenolics/100 g. Twenty different fatty acids were determined, with the percentages varying from 0.02% myristic acid (C14:0) to 78.7% linoleic acid (C18:2). According to the GC analysis of fatty acid methyl esters, linoleic acid (C18:2), followed by palmitic acid (C16:0), oleic acid (C18:1) and stearic acid (C18:0) were the major fatty acids, which together comprised approximately 97% of the total identified fatty acids. High C18:2 content (average 73.7%) proved that the black mulberry seed oil is a good source of the essential fatty acid, linoleic acid. Linolenic acid (C18:3) was also found in a relatively lower amount (0.3–0.5%). The α-tocopherol content was found to be between 0.17 and 0.20 mg in 100 g seed oil. The main sterols in the mulberry seed oil were β-sitosterol, Δ5-avenasterol, Δ5, 23-stigmastadienol, clerosterol, sitosterol and Δ5, 24-stigmastadienol. The present study stated that the native black mulberry seed oil can be used as a nutritional dietary substance and has great usage potential.     

Determination of the Fatty Acid Composition in Tree Peony Seeds Using Near-Infrared Spectroscopy

Tree peonies (Paeonia Sect Moutan DC) are an emerging oil crop because of their high oil and α‐linolenic acid (ALA) content. This research was to investigate the potential use of near infrared reflectance spectroscopy (NIRS) for estimating the major fatty acids contents, such as palmitic acid (C16:0), oleic acid (C18:1), linoleic acid (C18:2) and linolenic acid (C18:3) in tree peonies. A total of 115 small seed samples and 447 single seeds were selected to calibrate the predictive models. NIRS absorbance spectra were collected using a Fourier transform near infrared (FT‐NIR) spectrometer for the small seed samples, and acousto‐optic tunable filter‐near infrared (AOTF‐NIR) for the single seed samples. Statistical analysis was performed with partial least squares (PLS). For the husked samples, C18:3, C18:1 and C18:2 showed the highest correlation coefficient of validation (R_v; = 0.9756, 0.9467 and 0.8485, respectively) and the ratio of performance to deviation (RPD; = 3.58, 1.91 and 2.17, respectively); however, C16:0 did not reach expectations (R_v = 0.7783, RPD = 1.32). For intact samples, C18:3 showed the best prediction (R_v = 0.9096, RPD = 3.14), followed by C18:2 (R_v = 0.8479, RPD = 1.96). The results for C18:1 were poor (R_v = 0.7237, RPD = 1.70). For single seeds, only the results for C18:3 (R = 0.9150, RPD = 1.73) were good in the husked seed samples. It was concluded that NIRS can be used to rapidly assess the content of the major fatty acids in small samples.     

Tomato Seed Oil I Fatty Acid Composition,Stability and Hydrogenation of the Oil

Tomato seed oil was investigated to study their components of fatty acids, stability and hydrogenation conditions. The estimation of the fatty acids of tomato seed oil from Ace variety and tomato seed oil extracted from local waste in comparison with cotton seed oil (the most familiar edible oil in Egypt) - Giza 69 variety - extracted by n-hexane and oil obtained by pressing shows that more than 50% of the total fatty acids are linoleic. Palmitic acid was found in a range between 20% to 29% and oleic acid was in a range between 13% to 18%. Other fatty acids like stearic, arachidic, and linolenic acid were less than 3%. The induction periods (at 100°C) for oils of fresh, roasted and stored tomato seeds were found to be 7, 10, and 5 hours respectively. The hydrogenation conditions of crude tomato seed oil were 180°C, 3 kg/cm² and 0.2% nickel catalyst for three hours of hydrogenation to reach a melting point of 50.7°C and an iodine value of 42.     

Activation and specificity ofcrambe abyssinica seed lipase

The lipase ofCrambe abyssinica seed is not ac-tive in crushed seeds stored at 5-7% moisture at room temp. Lipase activity is very low even at 10-15% moisture: free acids in the crambe oil increased 1.6% to a total of 4% in 6 weeks. At higher moisture levels the lipase is active, hy-drolyzing the oil in 5-7 weeks. Oil in whole seed is resistant to lipolysis when stored air-dry. These results indicate good stability of the oil during seed storage and the usual steps in seed processing. Crambe lipase hydrolyzes triglycerides in a nearly random fashion. The hydrolysis pattern indicates a small preference for the shorter chain acids (C₁₆ and C₁₈), but no specificity for position within the triglyceride is apparent. A laboratory of the No. Utiliz. Ees. & Dev. Div., ARS, USDA.     

Fatty acid composition of oil from soybean leaves grown at extreme temperatures

Leaves from soybean (Glycine max (L.) Merr.) plants were assayed to determine if the relationship between temperature and relative fatty acid composition observed in the seed oil also existed for the triglycerides in the leaf oil. Leaf samples were harvested from eight soybean lines (A5, A6, C1640, Century, Maple Arrow, N78-2245, PI 123440 and PI 361088B) grown at 40/30,28/22 and 15/ 12°C day/night. At 40/30 and 28/22°C, seven fatty acids were observed at a level greater than 1.0%. These included the five major fatty acids found in the seed oil: palmitic (16:0), stearic (18:0), oleic (18:1), linoleic (18:2) and linolenic (18:3) acid; plus two fatty acids that had retention times the same as palmitoleic (16:1) and γ-linolenic (18:3 g) acid. In addition, an eighth fatty acid that had a retention time the same as behenic (22:0) acid was found in the leaves of all lines at 15/12°C. Palmitic, palmitoleic and stearic acid content did not differ significantly over temperatures. The oleic and linoleic acid content were each highest at 15/12°C, while the γ-linolenic and the linolenic acid content were each highest at 40/30°C. The fatty acid composition of the triglyceride portion of the leaf oil did not display the same pattern over temperatures as that observed for seed oil.     

NMR,GC–MS and ESI-FTICR-MS Profiling of Fatty Acids and Triacylglycerols in Some Botswana Seed Oils

In the search for non-traditional seed oils, physicochemical parameters, fatty acid (FA) and triacylglycerol (TAG) profiles for five Botswana seed oils, obtained by Soxhlet extraction, were determined. GC–MS and ¹H-NMR analyses showed the FA profiles for mkukubuyo, Sterculia africana, and manketti, Ricinodendron rautanenii, seed oils dominated by linoleic and oleic acids, 26.1, 16.7 and 51.9, 24.4%, respectively, with S. africana containing significant amounts of cyclic FAs (19.9%). Mokolwane, Hyphaene petersiana, seed oil was typically lauric; 12:0 and 14:0 acids were 25.9 and 13.4%, respectively. Morama, Tylosema esculentum, seed oil resembled olive oil; 18:1 (47.3%) and 18:2 (23.4%) acids dominated. Moretologa-kgomo, Ximenia caffra, seed oil had 45.8% of 18:1 FA, plus significant amounts of very long chain FAs: 26:1 (5.8%), 28:1 (13.9%), 30:1 (3.9%), and acetylenic acids, 9a-18:1 (1.5%) and 9a, 11t-18:2 (16.0%). TAG classes and regiochemistry were determined with ESI-FTICR-MS, and ¹³C-NMR spectra, respectively. Morama showed seven major TAG classes with C54:4 and C54:3 dominating; mokolwane had 16 major classes with C32:0, C38:0 and C42:2 dominating; manketti had 11 major classes with C54:7, C54:6 and C54:4 dominating; mkukubuyo had 12 major classes with C52:4, C52:3 and C54:4 dominating; moretologa-kgomo had 30 major TAG classes with C64:5, C64:3 and C62:3 dominating. Saturated FAs were generally distributed over the sn-1(3) position for morama, manketti, and moretologa-kgomo but at the sn-2 position for mokolwane and mkukubuyo. These findings indicate that morama and manketti seed oils can be developed for food uses, whilst moretologa-kgomo and mkukubuyo seed oils only for nonfood uses.     

Co-occurrence of Coronaric and Vernolic Acids in Compositae Seed Oils

Seed oils of Lactuca scariola Linn., L. sativa Linn. and Siegesbeckia orientalis Linn., were found to contain epoxy acids in 10.0% (6.0% coronaric + 4.0% vernolic), 27.4% (16.9% coronaric + 10.5% vernolic) and 20.0% (16% coronaric + 4.0% vernolic) amount, respectively, alongwith normal fatty acids. The co-occurrence of the two epoxy acids was confirmed by chromatographic (TLC, GLC), spectroscopic and chemical methods. Further, this was confirmed by mass spectral study of methyl ester and its methoxy hydroxy derivative in the case of S. orientalis seed oil.The seed oils of Chrysanthemum coronariumand Vernonia anthelmintica were used as reference standard.     

Jojoba—Variability in oil content and composition in a collection of 1156 native plants

Data are presented on the oil content and composition in the seeds of 1156 native jojoba plants harvested individually from inland and coastal areas of California and Arizona in the U.S. and from Sonora and Baja California in Mexico. The mean oil content of these samples was 53.2%; 34.2% of the samples exceeded 53%. The mean single seed weight was 0.56 g. A significant correlation between single seed weight and oil content was found but there was no correlation between oil content of the seed and seed yield per plant. Analysis of the oil for fatty acids and fatty alcohols showed very little variability among samples. This compositional uniformity is a major asset in terms of industrial application of this oil. Half the seeds studied in 144 samples had a mean oil content of 49.5% and mean single seed weight of 0.39 g. Simple correlations between fatty acids and oil content were similar to those reported earlier.     

Peanut oil: Compositional data

The major fatty acids of peanut oil acylglycerols are palmitic (C16:0), oleic (C18:1), and linoleic (C18:2) acids, and only a trace amount of linolenic fatty acid (C18:3) is present. Thus they have a very convenient oxidative stability and have been considered premium cooking and frying oils. This paper provides information about compositional data of peanut oil taking into account major (triacylglycerols and their fatty acids) and minor (free fatty acids, diacylglycerols, phospholipids, sterols, tocopherols, tocotrienols, triterpenic and aliphatic alcohols, waxes, pigments, phenolic compounds, volatiles, and metals) compounds. Moreover, the influence of genotype, seed maturity, climatic conditions, and growth location on peanut oil chemical composition is considered in the present report. In addition, peanut oils from wild species found in South America as well as from peanut lines developed through conventional breeding are also compared.     

Component Fatty Acids of Some Indian Seed Oils

The seed oil Chrysalidocarpus (Areca) lutescens, Terminalia paniculata, Roth, Combretum ovalifolium, Roxb., Dioscorea oppositifolia, Linn, Dioscorea anguina, Roxb., Stachytarpheta indica, Vahl, Aristolochia indica, Sanseveria cylindrica, Sanseveria zeylanica and Basella alba have been examined for their component fatty acids.     

Determination of seed oil content and fatty acid composition in sunflower through the analysis of intact seeds, husked seeds, meal and oil by near-infrared reflectance spectroscopy

A methodological study was conducted to test the potential of near-infrared reflectance spectroscopy (NIRS) to estimate the oil content and fatty acid composition of sunflower seeds. A set of 387 intact-seed samples, each from a single plant, were scanned by NIRS, and 120 of them were selected and further scanned as husked seed, meal, and oil. All samples were analyzed for oil content (nuclear magnetic resonance) and fatty acid composition (gas chromatography), and calibration equations for oil content and individual fatty acids (C_16:0, C_16:1, C_18:0, C_18:1, and C_18:2) were developed for intact seed, husked seed, meal, and oil. For intact seed, the performance of the calibration equations was evaluated through both cross- and external validation, while cross-validation was used in the rest. The results showed that NIRS is a reliable and accurate technique to estimate these traits in sunflower oil (validation r ² ranged from 0.97 to 0.99), meal (r ² from 0.92 to 0.98), and husked seeds (r ² from 0.90 to 0.97). According to these results, there is no need to grind the seeds to scan the meal; similarly accurate results are obtained by analyzing husked seeds. The analysis of intact seeds was less accurate (r ² from 0.76 to 0.85), although it is reliable enough to use for pre-screening purposes to identify variants with significantly different fatty acid compositions from standard phenotypes. Screening of intact sunflower seeds by NIRS represents a rapid, simple, and cost-effective alternative that may be of great utility for users who need to analyze a large number of samples.     

Chemical Composition and Fatty Acid Profile of Khat (Catha edulis) Seed Oil

The proximate, physicochemical, and fatty acid compositions of seed oil extracted from khat (Catha edulis) were determined. The oil, moisture, crude protein, crude fiber, crude carbohydrate, and ash content in seeds were 35.54, 6.63, 24, 1.01, 30.4 %, and 1.32 g/100 g DW respectively. The free fatty acids, peroxide value, saponification value, and iodine value were 2.98 %, 12.65 meq O₂/kg, 190.60 mg KOH/g, and 145 g/100 g oil, respectively. Linolenic acid (C_18:3, 50.80 %) and oleic (C_18:1, 16.96 %) along with palmitic acid (C_16:0, 14.60 %) were the dominant fatty acids. The seed oil of khat can be used in industry for the preparation of liquid soaps and shampoos. Furthermore, high levels of unsaturated fatty acids make it an important source of nutrition especially as an animal product substitute for omega‐3 fatty acids owing to the high content of linolenic acid.