Distribution of fatty acids during germination of soybean seeds

Gas chromatographic determination of the fatty acids in the seeds of soybean (Glycine max) showed mainly linoleic, oleic and palmitic acids with linoleic acid being the major component. Changes in the distribution of fatty acids were measured during germination in the cotyledons and roots. A decrease in palmitic and oleic acids was observed in the cotyledons from 6 to 12 days, while linoleic acid increased during the same period. In roots also, the major fatty acid was linoleic acid, while palmitic and linolenic acids were higher in roots in comparison with the cotyledons. During the 3–12 days of germination period, no major changes in the distribution pattern of fatty acids were observed in the roots. The possible significance of these changes is discussed.     

Component fatty acids ofAspergillus terreus fat

The component fatty acids of the fat elaborated byAspergillus terreus Thom, which was found to be a promising mold for the production of fat, have been studied. The fat has, based on gas liquid chromatographic evidence, 0.1% lauric, 1.9% myristic, 23.4% palmitic, 0.1% palmitoleic, 0.3% stearic, 14.1% oleic, 39.4% linoleic and 20.7% linolenic acids. The presence of large proportions of linoleic and linolenic acids suggests technological interest for the fat.     

Fatty acid composition of oleaster pulp and pit oils

Fatty acid compositions of oleaster pulp and pit oils were determined by gas chromatography in 4 samples of different varieties. Pit oils were highly unsaturated, containing >90% linoleic, oleic, and linolenic acids, as well as traces of palmitoleic acid. Saturated fatty acids consisted of palmitic and stearic acids with traces of arachidic acid. Pulp oils showed fatty acid compositions entirely different from that of pit oils. They contained 9 saturated fatty acids, C₁₂ to C₂₄, some of them with high quantities, up to 34.9%, of the total fatty acids. Unsaturated fatty acids, mainly oleic and linoleic, with low quantities of palmitoleic and linolenic acids composed about one-third of the total fatty acids.     

Chemical composition and characteristics ofMoringa peregrina seeds and seeds oil

TheMoringa peregrina kernel contains 1.8% moisture, 54.3% oil, 22.1% protein, 3.6% fiber, 15.3% carbohydrate and 2.5% ash. The composition and characteristics of the extracted oil were determined. Gas liquid chromatography of methyl esters of the fatty acids shows the presence of 14.7% saturated fatty acids and 84.7% unsaturated fatty acids. The fatty acid composition is as follows: palmitic 9.3%, palmitoleic 2.4%, stearic 3.5%, oleic 78.0%, linoleic 0.6%, linolenic 1.6%, arachidic 1.8% and behenic 2.6%.     

Fatty acid composition of rice lipids by gas-liquid chromatography

Gas-liquid Chromatographic analysis of the methyl ester of lipids of four rice varieties showed that bran lipids had significantly higher mean contents of linoleic and linolenic acids, but lower contents of myristic, palmitic, palmitoleic, and stearic acids than milled rice lipids. Nine fatty acids were detected. The principal components were oleic, linoleic, and palmitic, which also was confirmed by thin-layer chromatography of the esters. Issued as I.R.R.I. Journal Series No. 12     

Fatty acid composition of lymphocytes and macrophages from rats fed fiber-rich diets: A comparison between oat bran- and wheat bran-enriched diets

The effect of oat bran-(OBD) and wheat bran-enriched diets (WBD) on fatty acid composition of neutral lipids and phospholipids of rat lymphocytes and macrophages was investigated. In neutral lipids of lymphocytes, OBD reduced the proportion of palmitoleic acid (48%), whereas WBD reduced by 43% palmitoleic acid and raised oleic (18%), linoleic (52%), and arachidonic (2.5-fold) acids. In neutral lipids of macrophages, OBD increased palmitic (16%) and linoleic (29%) acids and slightly decreased oleic acid (15%). The effect of WBD, however, was more pronounced: It reduced myristic (60%), stearic (24%) and arachidonic (63%) acids, and it raised palmitic (30%) and linoleic (2.3-fold) acids. Neither OBD nor WBD modified the composition of fatty acids in phospholipids of lymphocytes. In contrast, both diets had a marked effect on composition of fatty acids in macrophage phospholipids. OBD raised the proportion of myristic (42%) and linoleic (2,4-fold) acids and decreased that of lauric (31%), palmitoleic (43%), and arachidonic (29%) acids. WBD increased palmitic (18%) and stearic (23%) acids and lowered palmitoleic (35%) and arachidonic (78%) acids. Of both cells, macrophages were more responsive to the effect of the fiber-rich diets on fatty aicd composition of phospholipids. The high turnover of fatty acids in macrophage membranes may explain the differences between both cells. The modifications observed due to the effects of both diets were similar in few cases: an increase in palmitic and linoleic acids of total neutral lipids occurred and a decrease in palmitoleic and arachidonic acids of phospholipid. Therefore, the mechanism involved in the effect of both diets might be different.     

Cyclopropenoid fatty acids in abutilon ramosum seed oil

Seed oil of Abutilon ramosum was found to contain the following fatty acids (wt.%): malvalic (2.48%), sterculic (1.29%), myristic (1.0%), C₁₅:0 (1.78%), palmitic (19.1%), palmitoleic (0.51%), stearic (6.53%), oleic (23.72%), linoleic (42.55%) and linolenic (0.91%). The qualitative and quantitative analysis of the fatty acids were carried out by HBr-titration and the gas-liquid chromatography of the silver nitrate-methanol-treated esters using the fatty acid esters of the oil of sterculia foetida as reference standard.     

Oxidative stability of natural and randomized high-palmitic-and high-stearic-acid oils from genetically modified soybean varieties

The oxidative stability of soybean oil triacylglycerols (TAG) obtained from genetically modified soybeans was determined before and after chemical randomization. Soybean oil oxidative studies were carried out under static oxygen headspace at 60°C in the dark and oxidative deterioration was monitored by peroxide value, monometric and oligomeric oxidation products, and volatile compounds. Randomization of the soybean oil TAG improved the oxidative stability compared to the natural soybean oil TAG. Oxidative stability was improved by three factors. Factor one was the genetic modification of the fatty acid composition in which polyunsaturated acids (such as linolenic and linoleic acids) were decreased and in which monounsaturated fatty acids (such as oleic) and saturated acids (palmitic and stearic) were increased. Factor two was the TAG compositional modification with a decrease in linolenic and linoleic-containing TAG and an increase in TAG with stearic and palmitic acids in combination with oleic acid. Factor three was the TAG structure modification accomplished by an increase in saturated fatty acids and a decrease in linoleic and linolenic acids at the glycerol moiety carbon 2. Presented at the AOCS Annual Meeting & Expo, Chicago, IL, May 10–13, 1998.     

Composition of the lipids in cabbage

Cabbage leaves contain 0.16% total lipids of which 51.02% are neutral lipids, 40.78% glycolipids, and 8.18% phospholipids. The predominant fatty acids in the total lipid analysis are linolenic, linoleic, oleic, palmitic, and stearic acids. Linolenic, palmitic, tridecanoic, and oleic are the principal components in the neutral lipid fraction while glycolipids are composed mainly of linolenic, palmitic, lauric, myristic, and tricosanoic acids. Phospholipids are high in palmitic, linolenic, and linoleic acids. Both glucose and galactose were observed in the glycolipid fraction.     

Oviposition response ofLobesia botrana females to long-chain free fatty acids and esters from its eggs

Avoidance of occupied ovisposition sites supposes that females perceive information related to their own progency. Fatty acids identified from egg extracts have been reevaluated using a different extraction method, and we have investigated the dose-dependent oviposition response of European grape vine moths (Lobesia botrana) to myristic acid, palmitic acid, palmitoleic acid, stearic acid, oleic acid, linoleic acid, methyl palmitate, methyl oleate, and ethyl palmitate; all except ethyl palmitate have been identified from eggs ofL. botrana. A methylene dichloride extract of eggs fromL. botrana revealed the presence of saturated free fatty acids (myristic, palmitic, and stearic) and unsaturated acids (palmitoleic, oleic, linoleic, and linolenic) in amounts ranging from 3.9 ng/egg equivalent for myristic acid to 30 ng/egg equivalent for palmitic and oleic acids. The extract also contained traces of methyl palmitate and methyl stearate. The greatest avoidance indexes were observed in response to palmitic, palmitoleic, and oleic acids. All the other compounds tested caused weaker responses. A reduction in the number of eggs laid was observed when moths were exposed to each of the esters applied at 0.3 µg per application spot. Reduction in eggs laid was also observed at a 10-fold higher dose of oleic acid. The present results confirm that general and simple molecules can be involved in the regulation of oviposition site selection and that they may participate in chemical marking of the eggs.     

The lipids of the common house cricket,Acheta domesticus L. I. Lipid classes and fatty acid distribution

The lipids of the common house cricket,Acheta domesticus L., have been examined with the following results. The fatty acids associated with the lipid extracts do not change significantly from the third through the eleventh week of the crickets' postembryonic life. The major fatty acids are linoleic (30–40%), oleic (23–27%), palmitic (24–30%), and stearic acids (7–11%). There are smaller amounts of palmitoleic (3–4%), myristic (∼1%), and linolenic acids (<1%). The fatty acid composition of the cricket lipids reflects but is not identical to the fatty acids of the dietary lipids: linoleic (53%), oleic (24%), palmitic (15%), stearic (3%), myristic (2%), and linolenic acid (2%). The amount of triglycerides present in the crickets increases steadily from the second through the seventh or eighth week of postembryonic life, then drops sharply. Other lipid classes, such as hydrocarbons, simple esters, diglycerides, monoglycerides, sterols, and free fatty acids remain about constant. The composition of the fatty acids associated with the tri-, di-, and monoglycerides and the free fatty acid fraction are all about the same. The fatty acids associated with the simple esters are high in stearic acid. Postdoctoral Research Associate, Department of Chemistry, University of Michigan, 1965–1967.     

Fatty acid composition of Iranian citrus seed oils

Fatty acid compositions of seed oils from eight Iranian citrus fruits were determined. The ranges of values for major fatty acids were 21.8–29.4% palmitic, 3.1–7.60% stearic, 0.3–1.3% palmitoleic, 23.5–32.3% oleic, 33.5–39.8% linoleic, and 3.1–7.6% linolenic. Low amounts (up to 0.1%) of myristic and arachidic acids and traces of a few unidentified ones constituted minor fatty acids.     

Oil characteristics of sweet and sour cherry kernels

Oil content and oil characteristics of sweet and sour cherry kernels from 8 Iranian cultivars were examined. The ranges of values were: 20.5–37.9% for the oil content of the kernels; 0.77–1.19% for unsaponfiable matter; 188.2–191.5 for saponification value; 123.1–127.8 for iodine value (Hanus); and 1.4692–1.4721 for refractive index at 40 C. As to fatty acid composition of the samples, traces of myristic, 6.7–9.9% palmitic, 0.9–4.2% stearic, 0.3–1.1% arachidic, 0.3–0.7% palmitoleic, 38.6–53.2% oleic, 33.9–51.9% linoleic, and 0.2–0.8% linolenic acids were determined by gas chromatographic analysis.     

Composition and biosynthesis of fatty acids inPyramimonas grossii

The green algaPyramimonas grossii orginating in the coastal waters of the Atlantic Ocean Argentina was subcultured until a monoalgal culture was obtained. The fatty acid composition of the alga grown in a mineral medium at 12 C was determined by gas liquid chromatography (GLC) on 2 columns. The major fatty acids were oleic, linoleic, palmitic and α-linolenic acids, but the 20-carbon polyunsaturated acids, 20∶4ω6 and 20∶5ω3, respectively, belonging to the linoleic and α-linolenic series, were also found. Incubation with [¹⁴C] oleate, [¹⁴C] acetate, [¹⁴C] linoleate and [¹⁴C] α-linolenate suggests that linoleate is not directly converted to α-linolenate. [¹⁴C] Acetate was easily converted to palmitic, palmitoleic and oleic acids. However, after 48 hr of incubation, only traces of radioactivity were detected in linoleic acid and no label was found in α-linolenic acid.     

Chemical Composition and Characteristics of <Emphasis Type="Italic">Commiphora wightii</Emphasis> (Arnott) Bhandari Seed Oil

The seeds of Commiphora wightii (Arnott) Bhandari contain 9.8 ± 0.7% oil. The fatty acid composition and chemical properties of the extracted oil were determined. Gas liquid chromatography of the methyl esters of the fatty acids shows the presence of 46.62% saturated fatty acids and 51.40% unsaturated fatty acids. The fatty acid composition is as follows: capric acid 3.50%, myristic acid 14.51%, palmitic acid 6.68%, stearic acid 4.70%, arachidic acid 3.18%, behenic acid 14.05%, myristoleic acid 1.34%, palmitoleic acid 12.07%, oleic acid 14.15%, eicosenoic acid 0.11%, linoleic acid 22.34% and alpha linoleic acid 1.37%.     

两种不同酯化方法分析樱桃仁中的脂肪酸成分

以乙醚为溶剂,采用索氏抽提法提取樱桃仁粗脂肪油,分别用氢氧化钾/甲醇碱催化甲酯化法和N,O-二(三甲基硅烷)乙酰胺硅酯化法进行衍生化处理,通过气相色谱/质谱联用技术分析脂肪酸的组成。结果显示,粗脂肪油提取量24.6%,主要成分为亚油酸、油酸、棕榈酸、硬脂酸、亚麻酸以及二十碳二烯酸等,其中多不饱和脂肪酸占大部分,两种衍生化方法测得其总含量分别为79.21%和64.25%,三甲基硅酯化法是一种更全面的分析测定樱桃仁脂肪酸组成的衍生化方法。     

Fatty acids,carbohydrates and crude protein in twenty cassava cultivars(Manihot esculenta Crantz)

Twenty cassava cultivars (Manihot esculenta Crantz) were analyzed for fatty acids, nonstructural carbohydrates and crude protein contents. The main constituent fatty acids were myristic, palmitic, stearic, oleic, linoleic and linolenic. Trace amounts of lauric, myristoleic and palmitoleic acids were detected. Saturated acids ranged from 26.58 to 58.05%. Acid-digestible carbohydrates ranged from 11.82 to 40.70% of the green matter. Reducing and non-reducing soluble oligosaccharides also were determined. Crude protein ranged from 1.39 to 4.70% of the dry matter. Linear regression analyses were made, but no significant correlations were found. Some possible genetic relationships are proposed for certain cultivars.     

黄须菜籽成分分析

黄须菜籽经有机溶剂抽提出油率为 38% ,气相色谱法测定脂肪酸的组成为 :w(棕榈酸 ) =6 .11%、w(棕榈油酸 ) =1.18%、w(硬脂酸 ) =1.47%、w(油酸 ) =13.19%、w(亚油酸 ) =71.99%、w(亚麻酸 ) =5 .45 % ,不饱和脂肪酸含量较高 ,占脂肪酸总质量的 92 .8%。毛油中w(β +γ VE) =0 .0 2 % ,w(磷脂 ) =0 .5 5 7%。饼粕中w(灰分 ) =8.95 7% ,w(总氮 ) =2 .794%。黄须菜籽油可以作为医疗保健、食品工业等的油源加以开发利用     

Determination of the fatty acid profile by 1H‐NMR spectroscopy

The common unsaturated fatty acids present in many vegetable oils (oleic, linoleic and linolenic acids) can be quantitated by ¹H‐nuclear magnetic resonance spectroscopy (¹H‐NMR). A key feature is that the signals of the terminal methyl group of linolenic acid are shifted downfield from the corresponding signals in the other fatty acids, permitting their separate integration and quantitation of linolenic acid. Then, using the integration values of the signals of the allylic and bis‐allylic protons, oleic and linoleic acids can be quantitated. The procedure was verified for mixtures of triacylglycerols (vegetable oils) and methyl esters of oleic, linoleic and linolenic acids as well as palmitic and stearic acids. Generally, the NMR (400 MHz) results were in good agreement with gas chromatographic (GC) analyses. As the present ¹H‐NMR‐based procedure can be applied to neat vegetable oils, the preparation of derivatives for GC would be unnecessary. The present method is extended to quantitating saturated (palmitic and stearic) acids, although in this case the results deviate more strongly from actual values and GC analyses. Alternatives to the iodine value (allylic position equivalents and bis‐allylic position equivalents) can be derived directly from the integration values of the allylic and bis‐allylic protons.     

Estimation of cetane index for esters of fatty acids

Cetane indexes have been calculated for the esters of the individual saturated fatty acids in the C₈-C₂₄ range plus palmitoleic, oleic, linoleic, and linolenic acids. Two methods were used for these calculations: ASTM 976 and a method involving simultaneous equations relating the experimentally determined cetane numbers for several transesterified oils and the fatty acid compositions of the oils. Cetane indexes calculated according to ASTM 976 produced values which were too low for ester mixtures high in saturated acids and low in polyunsaturated acids, and were somewhat high for ester mixtures high in polyunsaturated acids. When cetane indexes calculated according to the simultaneous equation method were applied to the fatty acid mixtures, the agreement with those experimentally determined was approximately the error of determination of the cetane number.