Fatty Acid Profiles of Oil Obtained from Mid-Oleic Sunflowers Grown in Tropical Region

This study aimed to verify whether the fatty acid profiles of mid-oleic genotypes grown in the tropical region of Brazil fit the Codex Alimentarius and to examine the possibility of using traditional inbred lines to produce high-oleic hybrids. For this purpose, we assessed the fatty acid profile of six mid-oleic hybrids grown in environments with different minimum temperatures during oil formation in the achenes. The tests were conducted between 2015 and 2017 in an experimentally randomized complete block design with four replications. The oleic, linoleic, palmitic, and stearic acid contents were determined using gas chromatography. The mid-oleic hybrids presented varying levels of fatty acids, with oleic acid ranging between 43.6% and 84.6%, linoleic acid between 8.5% and 45.6%, palmitic acid between 3.9% and 5.7%, and stearic acid between 2.2% and 6.2%. Some of the fatty acid values were outside the ranges established by the CODEX STAN 210-1999 and were characteristic of high-oleic type sunflowers. This finding shows that we can take advantage of the potential of combining traditional inbred lines to produce high-oleic hybrids for faster and more economical breeding programs in these environments.     

Fatty Acid Profiles in Sunflower Grains During Storage in Different Environments

This study aimed to evaluate the fatty acid profiles of sunflower oil extracted from hybrid grains produced and stored in different environments. The trials were conducted in Teresina (Piauí), Vilhena (Rondônia), and Jaguariúna (São Paulo) in randomized complete block design with 4 replicates. After harvesting, grains from 1 high oleic and 3 traditional hybrids were packed in kraft paper bags and stored in a covered shed and in a cold chamber up to 12 months. The fatty acid profiles were determined by gas chromatography after 0, 4, 8, and 12 months of storage. Analyses of variance were conducted in a split‐plot design, with hybrids being considered as whole plots and storage times as subplots. Tukey's test was performed to compare hybrids and regression analyses for storage times. The initial fatty acid profile of the grains of the same hybrid varied depending on the production location. The grain storage of high oleic and traditional sunflower hybrids during 12 months in covered shed and in cold chamber resulted in little changes in oil fatty acid profiles, regardless of the initial contents. These changes occurred only for linoleic and palmitic acids.     

Influence of Temperature on the Fatty Acid Composition of the Oil From Sunflower Genotypes Grown in Tropical Regions

The influence of temperature on the fatty acid composition of the oils from conventional and high oleic sunflower genotypes grown in tropical regions was evaluated under various environmental conditions in Brazil (from 0° S to 23° S). The amounts of the oleic, linoleic, palmitic and stearic fatty acids from the sunflower oil were determined using gas chromatography (GC). The environment exhibited little influence on the amounts of oleic and linoleic fatty acids in high oleic genotypes of sunflower. In conventional genotypes, there was broad variation in the average amounts of these two fatty acids, mainly as a function of the minimum temperature. Depending on the temperature, especially during the maturation of the seeds, the amount of oleic acid in the oil of conventional sunflower genotypes could exceed 70 %. Higher temperatures led to average increases of up to 35 % for this fatty acid. Although the minimum temperature had the strongest effect on the fatty acid composition, locations at the same latitude with different minimum temperatures displayed similar values for both oleic acid and linoleic acid. Furthermore, minimum temperature had little influence on the amounts of palmitic and stearic fatty acids in the oil.     

Comparison of Fatty Acid Profile of Specialty Maize to Normal Maize

Increasing utilization of specialty maize prompted us to evaluate its fatty acid profile. For this purpose maize germplasm, classified as low oil normal maize (group 1), high oil normal maize (group 2), quality protein maize (QPM) (group 3) and sweet corn (group 4) was evaluated for oil, starch, protein and fatty acid composition mainly palmitic, stearic, oleic and linoleic acid. High oil content was observed in sweet corn samples which might be result of shriveled grain texture because of an increased embryo to kernel ratio. Individual fatty acids showed wide differences among different groups. A slightly higher amount of palmitic acid was reported in specialty maize as compared to normal maize. In contrast, stearic acid content was significantly low in high oil normal maize (56 %), QPM (36.2 %) and sweet corn (28.4 %) in comparison to low oil normal maize. Although no significant differences were observed for oleic acid between low oil normal and high oil normal maize, but sweet corn samples showed significantly reduced oleic acid compared to low oil normal maize. However, the most important observation was the higher content of linoleic acid in specialty maize (groups 2, 3 and 4) as compared to low oil normal maize. Further, the ratio of MUFA/PUFA was also discussed. It was concluded that specialty maize possesses a better oil quality in comparison to low oil normal maize.     

Combination of the Elevated Stearic Acid Trait with Other Fatty Acid Traits in Soybean

Stearic acid is one of five major fatty acids found in soybean oil. It is a fully saturated lipid and is known for neutral or positive effects on LDL cholesterol when consumed by humans. Unfortunately, stearic acid only accounts for about 4% of the total seed oil produced in commodity soybean. Previous work has shown that stearic acid can reach levels as high as 28% of the total oil fraction when the SACPD-C gene, encoding the delta-9-stearoyl-acyl carrier protein desaturase responsible for most of the stearic acid variation in soybean seed, is ablated in combination with other loci. In order to increase stearic acid content and create soybeans with improved utility based on fatty acid composition, we combined mutations in SACPD-C with other mutations in the fatty acid biosynthetic pathway. Soybean plants carrying mutant alleles of both SACPD-C and FAD2-1A produce seed with stearic acid levels from 14% to 21%, and with elevated levels of oleic acid. Soybeans carrying mutations in both SACPD-C and FAD3A or FAD3C have both statistically significantly elevated levels of stearic acid (from 15–21%) and statistically reduced linolenic acid levels. Neither mutant combination appears to affect other agronomic properties such as plant morphology or seed protein levels making this a potentially viable trait.     

Optimizing Conditions for the Purification of Linoleic Acid from Sunflower Oil by Urea Complex Fractionation

The separation and purification of linoleic acid (LA) from sunflower seed oil by urea complex fractionation was studied. Crystallization reaction conditions of urea inclusion were optimized using the response surface method, and the optimal model was developed. Using the linear weighting method of the fitting model for optimization, the optimal balance between the purity and the recovery of LA was obtained. Under optimal conditions, the purity of LA was 87.8%, and the recovery was 83.4% at a urea-to-fatty acids ratio (w/w) of 0.94, 95% ethanol-to-urea (v/w) of 5.00, a crystallization temperature of 18.0 °C, and a crystallization time of 5.0 h. Verification results revealed that the predicted values from these models were reasonably close to the experimentally observed values.     

Commercial Runner peanut cultivars in the USA: Fatty acid composition

Though peanuts are classified as a high‐fat food, they possess good proportions of fatty acids deemed as heart healthy. The fatty acid compositions of Runner peanuts were determined for commercially grown cultivars over two recent crop years. GC‐FID analyses revealed that the fatty acid levels for Runner peanuts were significantly (p <0.05) different among the normal, mid‐, and high‐oleic peanuts investigated. Oleic acid‐to‐linoleic acid (O/L) ratios were found to be 1.93 ± 0.30, 5.25 ± 1.12, and 16.9 ± 5.20 for normal, mid‐, and high‐oleic peanut lipids, respectively. Tamrun OL01 possessed a fatty acid profile characteristic of a mid‐oleic cultivar. From the sample set (n = 151), mean % weights for oleic acid and linoleic acid were 52.09 ± 2.84 and 27.38 ± 2.60 in normal, 69.33 ± 3.18 and 13.66 ± 2.35 in mid‐oleic, and 78.45 ± 2.05 and 5.11 ± 1.67 in high‐oleic peanuts, respectively. Cluster analysis segregated cultivars based on fatty acids into normal, mid‐, and high‐oleic groups. Factorial analysis revealed that cultivar effects were significant (p <0.01) for all fatty acids, except for lignoceric acid. Cultivar effects were also highly significant (p <0.001) for O/L, IV, unsaturated/saturated fatty acid (U/S) ratio, and % saturation. Significant crop year effects were shown for palmitic, oleic, arachidic, gondoic, and lignoceric acids, as well as U/S ratio and % saturation. Healthy unsaturated fats accounted for ?80% in all crop years and cultivars.     

Discrimination of Origin of Sesame Oils Using Fatty Acid and Lignan Profiles in Combination with Canonical Discriminant Analysis

The aims of this study were to investigate total fatty acid composition and lignan contents of Korean, Chinese and Indian roasted sesame oils and to differentiate the geographic origins of the oils using analytical data in combination with canonical discriminant analysis. The analytical data were obtained from 84 oil samples that were prepared from 51 Korean, 19 Chinese, and 14 Indian white sesame seeds harvested during 2010 and 2011 and distributed in Korea during the same period. Six variables selected for the discriminant analysis were the contents of three fatty acids (linoleic, oleic, and palmitic) and three lignans (sesamin, sesamolin, and sesamol). A good discrimination between sesame oils from Korea, China, and India was achieved by applying two canonical discriminant functions, with 97.6 % of the samples correctly classified into the geographic origin. When the origins of five commercial oil samples (one was prepared from Korean sesame seeds and the other four were made from imported sesame seeds) were predicted using discriminant functions, the Korean sesame oil was accurately distinguished from the others.     

Combined Fish Oil and High Oleic Sunflower Oil Supplements Neutralize their Individual Effects on the Lipid Profile of Healthy Men

Both n-3 and n-9 fatty acids share a common metabolic pathway and can potentially and individually improve cardiovascular disease risk factors. Dietary n-6 is known to weaken the efficacy of n-3 fatty acids due to competition for the same enzymes. Still unclear is whether a similar competition exists between n-3 and n-9 fatty acids. Thus, a 12-week intervention study was conducted to investigate the effect of different combinations of fish oil and high-oleic sunflower oil (OSO) on healthy subjects. Included were five groups (98 subjects): three groups received a fixed amount of n-9 (8 g/day) with varying amounts of n-3 (1, 2 or 4 g/day), one group was given n-3 fatty acids only (2 g/day) and another was given n-9 only (8 g/day). We found that fish oil supplement (2 g/day) was able to decrease TAG by about 13 %, this effect was diminished with the co-ingestion of n-9 (OSO). Intake of OSO (8 g/day) reduced both total and LDL cholesterol by about 10 %, this effect was reduced by the addition of fish oil. Both fish oil and OSO failed to have any significant effect on both glycemic and blood pressure parameters. In conclusion; the impact of oleic acid (n-9) on total and LDL cholesterol was altered by the addition fish oil (n-3). These effects may have been the result of enzymatic competition between the two types of fatty acids.     

Bioactive Compounds in Virgin Olive Oil of the PDO Montoro-Adamuz

Virgin olive oil (VOO) is generally recognized as a healthy fat because of its fatty acid composition and content in minor compounds but a wide range of these substances can be found in commercial oils. The concentration of compounds with attributed health benefits were analyzed in VOO of the PDO Montoro‐Adamuz. Oleic acid represented around 79 % of the total fatty acids, and the mean squalene and tocopherols concentrations were 5800 and 247 mg/kg respectively. Despite the changes found in polyphenols concentration in the oils analyzed for six consecutive crops, these substances accounted for more than 700 mg/kg. Moreover, the effect of irrigation regime and sun radiation on the content in bioactive substances of these oils was also assessed. No significant differences were detected between oils from trees irrigated ad libitum or rain‐feed. In contrast, the level of tree radiation exerted a great effect on the concentration of bioactive substances in oils. Oils from trees cultivated in a sunny area (south orientation) had a higher percentage of oleic acid and concentration in phenolic compounds than those from shady areas (north orientation). The opposite was detected for tocopherols and squalene which were more concentrated in oils from olives of the shady area. The results obtained in this study point out VOO of the PDO Montoro‐Adamuz as a very healthy fat due to their composition in bioactive substances, in particular their richness in phenolic compounds.     

Comparison of the Frying Performance of High Oleic Oils Subjected to Discontinuous and Prolonged Thermal Treatment

Frying is a popular practice because of its unique sensory characteristics and low cost. The high temperature reached with this cooking method alters molecules present in the oil. The deterioration of the oil depends primarily on its chemical composition. The aim of this study was to evaluate the thermal stability of high oleic sunflower oil (HOSO), sunflower oil (SO) and mixed oil (MIX) during deep frying of French fries. Octanoic acid and unsaturated fatty acid (UFA)/saturated fatty acid (SFA) ratio showed a good correlation with total polar compounds (TPC) for all frying samples analyzed. HOSO and MIX were characterized by reduced levels of thermal degradation, while SO resulted in the highest values of oxidation products (highest TPC values). SO was also the oil more retained by the food matrix, whereas MIX was the least absorbed. HOSO and MIX, having a high oleic acid content (77.58 and 59.92 %, respectively) and a low linoleic acid content (13.42 and 25.70 %, respectively), showed the best characteristics for the frying process.     

Dynamic Features of the Rumen Metabolism of Linoleic Acid,Linolenic Acid and Linseed Oil Measured in Vitro

The lipid quality of ruminant products is largely determined by the extent of rumen microbial biohydrogenation (BH) of polyunsaturated fatty acids (FAs) and the substances formed thereby. In vitro batch incubations with mixed rumen bacteria were tracked over 24 h to characterize the profiles and kinetics of the BH products from three lipid sources: pure linoleic acid (c9,c12–18:2), pure linolenic acid (c9,c12,c15–18:3) and linseed oil (mainly c9,c12,c15–18:3 in triacylglycerols). After 24 h of incubation biohydrogenation was more complete for c9,c12–18:2, which gave mainly stearic acid (18:0), than for c9,c12,c15–18:3, which yielded mainly trans-18:1 FAs. This suggests inhibition of the final BH step (18:1 to 18:0). Incubations of c9,c12–18:2 resulted in high levels of carbon 10- and 12-desaturated 18:1, t10,c12- and c9,t11-CLAs. Incubations of c9,c12,c15–18:3 resulted in high levels of t11–18:1, carbon 13- and 15-desaturated 18:1 as well as t11,c15–18:2 and 11,13-CLAs. A comparative study of linolenic acid and linseed oil kinetics revealed that the BH process was not significantly slowed by the esterification of polyunsaturated FAs, but may have been limited by the isomerization step in which the cis12 double bond goes to the trans11 position. The disappearance rates of c9,c12–18:2 and c9,c12,c15–18:3 ranged from 23.6 to 44.6%/h. The wide variety of BH intermediates found here underlines the large number of possible BH pathways. These data help provide a basis for dynamic approaches to BH processes.     

Mechanism Controlling High-Temperature Degradation of Sunflower Oil Triacylglycerols in the Absence of Oxygen

The aim of the present study is to describe the mechanism controlling heat-induced formation of sunflower oil triacylglycerol and fatty acid methyl ester oligomers. The unique combination of high-performance size-exclusion chromatography with hyphenated electrospray ionization mass spectrometry (MS), atmospheric pressure chemical ionization-MS, and high-temperature gas chromatography-MS techniques allows differentiating between radical coupling species and Diels–Alder cycloadducts. Targeted analysis of thermally degraded sunflower oils confirms the exact structures of various acyclic oligomers accompanied by less-abundant products of pericyclic transformations. A series of model experiments simulate the impact of dienophile nature on the course of Diels–Alder reactions. Thus, α-tocopherylquinone, δ-tocopherylquinone, and methyl-(E)-11-oxoundec-9-enoate are synthesized as naturally occurring dienophiles bearing electron-withdrawing groups. The geometry of poor dienophiles does not affect concerted cyclization, while the structure of electron deficient dienophiles can overcome low reactivity. Practical Application: In the absence of oxygen, heat-induced degradation of polyunsaturated triacylglycerols proceed predominantly via a radical pathway, whereas concerted reactions represent minor mechanisms. Sunflower oil triacylglycerol molecules in the system without propagation stage can be effectively protected by natural and/or synthetic antioxidants. Application of chelates is also recommended. However, antioxidant-derived quinones, such as α-tocopherylquinone, can enter the Diels–Alder reaction even more easily than dienophiles without electron-withdrawing groups. Unsaturated core aldehydes possess the same reactivity. Examination of the mechanism controlling high-temperature degradation of triacylglycerols is especially important for processing engineers in edible oil refineries and food technologists. New perspective may help them to minimize undesirable changes in polyunsaturated species.     

Natural Abundance Carbon Isotopic Analysis Indicates the Equal Contribution of Local Synthesis and Plasma Uptake to Palmitate Levels in the Mouse Brain

Saturated fatty acids are the most abundant fatty acids in the brain, however, there has been some debate regarding the ability of intact dietary saturated fatty acids to be incorporated into the brain. In the present study, we use compound specific isotope analysis to measure the natural abundance carbon isotopic signature of brain, liver, and blood palmitic acid (PAM) and compare it to the dietary PAM and sugar isotopic signatures to calculate the relative contribution of both the incorporation of intact and endogenously synthesized PAM to these pools. Mice were equilibrated to the study diet, and extracted fatty acids were analyzed with gas chromatography isotope ratio mass spectrometry to determine the carbon isotopic signature of PAM (δ¹³C_PAM). Liver, serum total, and serum unesterified fatty acid δ¹³C_PAM ranged between ?20.6 and ?21.1 mUr and were approximately 8.5 mUr more enriched in ¹³C when compared to the dietary PAM signature. Brain δ¹³C_PAM was found to be more enriched than liver or blood pools (?16.7 ± 0.2 mUr, mean ± SD). Two end‐member‐mixed modeling using the carbon isotopic signature of dietary PAM and dietary sugars determined the contribution of synthesis to the total tissue PAM pool to range between 44% and 48%. This suggests that endogenous synthesis and dietary PAM are near equal contributors to brain, liver, and blood PAM pools. In conclusion, our data provide evidence that brain PAM levels are maintained by both local endogenous synthesis and through the uptake of intact PAM from the blood.     

From Aquatic to Terrestrial Food Webs: Decrease of the Docosahexaenoic Acid/Linoleic Acid Ratio

Fatty acid composition of the adipose tissue of six carnivorous mammalian species (European otter Lutra lutra, American mink Mustela vison, European Mink Mustela lutreola, European polecat Mustela putorius, stone marten Martes foina and European wild cat Felis silvestris) was studied. These species forage to differing degrees in aquatic and terrestrial food webs. Fatty acid analysis revealed significant differences in polyunsaturated fatty acid composition between species. More specifically, our results underline a gradual significant decrease in the docosahexaenoic acid (DHA)/linoleic acid (LNA) ratio of carnivore species as their dependence on aquatic food webs decreases. In conclusion, the use of the DHA/LNA ratio in long-term studies is proposed as a potential proxy of changes in foraging behaviour of semi-aquatic mammals.     

On the Determination of the Diffusivity of CO 2 in Aqueous and NonAqueous Solvents: Investigations with Laminar Jets and Wetted Wall Columns

The diffusivity of CO 2 in ethanol, n-heptane and methyl tertiary butyl ether (MTBE) has been determined using a laminar jet reactor and a wetted wall column at two temperatures (293 K and 298 K). The reactors have been operated in the laminar and transition regime. In the transition regime, the effective diffusivity of CO 2 was found to increase with Reynolds number, which could be explained by the increasing contribution of eddy diffusivity to the overall mass transfer. However, even in the laminar regime, the molecular diffusivity of CO 2 was found to vary with experimental conditions, i.e., the Reynolds number. It has been observed that the value of D CO 2 reduces with increasing Re in the case of ethanol, while the opposite trend is observed for n-heptane. These effects can be (partially) explained by accounting for combined molecular and eddy diffusivity within the laminar regime as proposed by the mass transfer model of King (1966). To the knowledge of the authors, these effects of gas absorption in nonaqueous/organic solvents have not been reported earlier. The present findings indicate that data on gas absorption in these types of systems should be used with caution.     

确保2250热轧粗轧机主轴螺栓的紧固质量的研究

2250热轧R1、R2轧机中间轴与主电机之间采用以双头螺栓连接的连接方式,双头螺栓的螺杆部分与连接孔之间采用间隙配合形式。基于工作经验,改进制备了典型形态的铝系混凝剂,进行了混凝剂投加量对混凝去除有机物效果的研究。     

Transparent Polysilsesquioxane Films Obtained from Bridged Ureasil Precursors: Tunable Photoluminescence Emission in the Visible Region and Filtering of UV‐Radiation

Bridged ureasil precursors were synthesized by the reaction of either ethylenediamine (1 mol) or m‐xylylenediamine (1 mol) with isocyanatepropyltriethoxysilane (2 mol). Transparent polysilsesquioxane films were obtained by the hydrolytic condensation of the pure precursors or their co‐condensation in a 50:50 molar ratio. Films based on pure ureasil precursors showed a blue photoluminescent emission band assigned to the photoinduced proton‐transfer among H‐bonded urea groups and the subsequent radiative recombination of ionized groups. Films synthesized by the co‐condensation of both precursors exhibited a significant red‐shift of their absorption, excitation, and emission spectra, associated to de‐localization of H‐bonds, and a high absorption of UV‐radiation.

     

Application of Taguchi Method in the Enzymatic Modification of Menhaden Oil to Incorporate Capric Acid

Structured lipids (SL) were produced using menhaden oil and capric acid or ethyl caprate as the substrate. Enzymatic reaction conditions were optimized using the Taguchi method L9 orthogonal array with three substrate molar ratio levels of capric acid or ethyl caprate to menhaden oil (1:1, 2:1, and 3:1), three enzyme load levels (5, 10, and 15% [w/w]), three temperature levels (40, 50, and 60 °C), and three reaction times (12, 24, 36 hours). Recombinant lipase from Candida antarctica, Lipozyme^® 435, and sn‐1,3 specific Rhizomucor miehei lipase, Lipozyme^® RM IM (Novozymes North America, Inc., Franklinton, NC, USA), were used as biocatalysts in both acidolysis and interesterification reactions. Total and sn‐2 fatty acid compositions, triacylglycerol (TAG) molecular species, thermal behavior, and oxidative stability were compared. Optimal conditions for all reactions were 3:1 substrate molar ratio, 10% [w/w] enzyme load, 60 °C, and 16 hours reaction time. Reactions with ethyl caprate incorporated significantly more C10:0, at 30.76 ± 1.15 and 28.63 ± 2.37 mol% versus 19.50 ± 1.06 and 9.81 ± 1.51 mol%, respectively, for both Lipozyme^® 435 and Lipozyme^® RM IM, respectively. Reactions with ethyl caprate as substrate and Lipozyme^® 435 as biocatalyst produced more of the desired medium‐long‐medium (MLM)‐type TAGs with polyunsaturated fatty acids (PUFA) at sn‐2 and C10:0 at sn‐1,3 positions.     

Impact of Canolol‐Enriched Extract from Heat‐Treated Canola Meal to Enhance Oil Quality Parameters in Deep‐Frying: a Comparison with Rosemary Extract and TBHQ‐Fortified Oil Systems

Canolol‐enriched extracts obtained from the extraction of fluidized bed treated canola meal with supercritical carbon dioxide were added to high‐oleic canola oil in different concentrations (200, 500 and 750 mg/kg). After 30 h of deep‐fat frying, oils fortified with canolol‐enriched extracts showed a two to three times better frying performance in comparison to the commonly used antioxidants (TBHQ, 200 mg/kg; rosemary extract, 40 and 200 mg/kg) and a control without antioxidants with regards to the formation of di‐ and polymer triacylglycerols, total polar compounds, secondary degradation products (anisidine value) and the iodine value. The canolol‐enriched extracts were also able to slow down the degradation of α‐ and γ‐tocopherol during frying resulting in significant amounts of tocopherols after 30 h of frying in comparison to the other oils. The influence of the canolol‐enriched extracts indicated strongly concentration‐dependent performance. With increasing concentration of the extract, the thermal stability of the fortified oil was improved. The only disadvantage of the addition of the extracts was an increase in the initial acid value, but within the frying time, only oil fortified with 750 mg canolol‐enriched extract/kg reached the limit given in different countries.