Willd. is recognized to be an excellent nutrient with high nutritional content. However, few genotypes of quinoa were analyzed, so we found a knowledge gap in the comparison of quinoa seeds of ...different genotypes. This study aims to compare the physicochemical, antioxidant, and anticancer properties of seed oil from three
genotypes. Seeds of three genotypes (white, red, and black) were extracted with hexane and compared in this study. The oil yields of these quinoa seeds were 5.68-6.19% which contained predominantly polyunsaturated fatty acids (82.78-85.52%). The total tocopherol content ranged from 117.29 to 156.67 mg/kg and mainly consisted of γ-tocopherol. Total phytosterols in the three oils ranged from 9.4 to 12.2 g/kg. Black quinoa seed oil had the highest phytosterols followed by red and white quinoas. The chemical profile of quinoa seed oils paralleled by their antioxidant and anticancer activities in vitro was positively correlated with the seed coat color. Black quinoa seed oil had the best antioxidant and anti-proliferation effect on HCT 116 cells by the induction of apoptosis in a dose-dependent manner, which may play more significant roles in the chemoprevention of cancer and other diseases related to oxidative stress as a source of functional foods.
Color reversion has long been a major problem for the vegetable oil industry, and the enzymatic oxidation of γ-tocopherol is thought to trigger this phenomenon. In this study, first, the extraction, ...purification, and detailed characterization of tocopherol oxidase from fresh corn germs were performed. Then, the relationship between the enzyme reaction of γ-tocopherol and oil color reversion was verified. The results showed that the membrane-free extracts of raw corn germ performed specific catalysis of tocopherol in the presence of lecithin. In terms of the oxidation product, tocored (the precursor of color reversion) was detected in the mixture after the catalytic reactions, indicating that this anticipated enzyme reaction was probably correlated with the color reversion. Furthermore, the optimal pH and temperature for the tocopherol oxidase enzyme were 4.6 and 20 °C, respectively. In addition, ascorbic acid at 1.0 mM completely inhibited the enzymatic reaction.
•2-Methylpentane based isohexane exhibited higher polarity than industrial hexane.•sn-SOS was selectively crystallized from mango kernel fat (MKF) using the isohexane.•MKF stearin rich in sn-SOS ...showed higher thermostability compared to cocoa butter.•MKF stearin rich in sn-SOS exhibited accepted compatibility with cocoa butter.•The thermostability and compatibility could be improved by further tempering.
High-purity isohexane containing 88.12% 2-methylpentane, which has a higher polarity than industrial hexane, was selected to selectively fractionate mango kernel fat to produce 1,3-distearoyl-2-oleoyl-glycerol (SOS)-rich fat. The three-stage fractionation process was optimized by considering the stearin yield and its SOS content to obtain a third stearin (TS). This fat contained a high percentage of SOS (69.2%) with only 0.8% diacylglycerol. Mass spectra and sn-2 fatty acid analyses further revealed that the TS was mainly composed of symmetrical monounsaturated triacylglycerols. Compared with cocoa butter (CB), the unique composition of the TS improved its thermal properties (35.6% and 0% solid fat content at 35°C for the TS and CB, respectively). In particular, tempered binary fat blends, which were composed of 20–50% TS and 50–80% CB, showed acceptable compatibility at 20–28°C. The TS could be utilized by chocolate manufacturers to make products suitable for sale and consumption in tropical conditions.
Refinement is usually used to remove undesired components to improve coconut oil quality. In the present study, crude coconut oil (CCO) was refined in four stages: conventional degumming, ...neutralization, bleaching, and deodorization. Physiochemical indices during the refinement were evaluated: peroxide value (PV), free fatty acid (FFA), fatty acid composition; fat composition; triacylglycerol profile, micronutrient (e.g., tocopherols and sterols) and contaminant (e.g., 3-monochloropropane-1,2-diol esters (3-MCPD esters), and glycidyl esters (GEs) levels. Compared to CCO, the quality of refined oil was improved by reducing PV and FFA levels. No significant changes in triacylglycerol compositions were found during refinement. However, unsaturated fatty acids like oleic and linoleic acids were decreased after refinement. Also, some micronutrients like tocopherol and sterol were decreased from 12.39 to 0.10 mg/kg and from 679.69 to 426.50 mg/kg, respectively. The undesired contaminants, i.e., 3-MCPD esters and GEs, increased markedly during refinement.
Three palm mid-fraction (PMF) groups produced from different fractionation paths were analyzed in terms of the fat, triacylglycerol and sn-2 fatty acid compositions, thermal properties (melting and ...crystallization behaviors, and solid fat contents (SFCs)), micronutrient levels and oxidative stability indexes (OSIs) to achieve their sufficient utilization. PMF-A (iodine value (IV), 48.4 g/100 g) fractionated from palm olein contained 43.8% 1,3-dipalmitoyl-2-oleoyl-glycerol (POP) and 16.7% 1-palmitoyl-2,3-dioleoyl-glycerol, showing soften properties (slip melting point (SMP), 27.6°C; SFC at 30°C, 2.2%) at hot weather. PMF-B (IV, 42.3 g/100g) obtained from palm stearin showed similar fat and triacylglycerol compositions as PMF-A, but the high 1,2,3-tripalmitoyl-glycerol level (6.2%) improves its thermal behaviors (SMP, 34.9°C; SFC at 30°C, 13.8%). The SFC profiles of PMF-A and PMF-B were comparable to those found in frozen and puff margarine shortenings. Furthermore, both of the PMF groups exhibited excellent OSIs (13.2 and 11.2 h, respectively) because of their high micronutrient levels (especially γ-tocopherol and campesterol). In general, γ-tocopherol and campesterol contribute to preventing lipids from oxidation under frying conditions. Therefore, PMF-A and PMF-B are recommended for manufacturing margarine shortenings and frying fasts. PMF-C (IV, 33.0 g/100g) produced from the additional fractionation of PMF-A or PMF-B contained the highest POP percentage (67.1%) and showed heat-resistant property (SMP, 31.8°C; SFC at 30°C, 22.4%). Its steep SFC profile was superior to that of cocoa butter, suggesting the fat is preferred in producing hard chocolate fats.
Celotno besedilo
Dostopno za:
DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, UILJ, UKNU, UL, UM, UPUK
To overcome the disadvantages of severe emulsification and difficulty in obtaining free oil during aqueous extraction of peanut oil, the effect of roasting assisted aqueous ethanol extraction on free ...oil recovery was investigated. When peanut kernels were roasted at 180 °C for 10 min, free oil recovery increased from 57% to 96%, and the acid and peroxide values of the peanut oil met the requirements of good quality. The degree of hydration swelling of proteins in the extract increased, and soluble solids were easier to aggregate, resulting in reduced emulsification and significantly higher free oil recovery. The roasting conditions selected were found to significantly promote protein hydrophilicity, aggregation and fusion of oil bodies, as well as cell rupture, which facilitated the release of free oil but with a lower degree of protein denaturation. This study may promote the practical application of aqueous extraction technology for peanut oil.
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•Free oil recovery of peanut oil exceeded 95% without demulsification.•Peanut proteins were more hydrophilic but were less denatured.•Roasting caused separated oil bodies to aggregate and fuse, as well as cell rupture.•Roasting reduced emulsification but had no effect on oil quality.
•There are some errors when applying ACT in food science mainly during 2014–2019.•An elementary step is required to apply the ACT.•Units used in ACT should be consistent.•Choose proper temperatures ...to effectively analyze the thermodynamic parameters.
Activated complex theory (ACT), apart from Van 't Hoff equation, has long been applying as an alternative tool to connect the kinetics (reaction rate constant, k) and thermodynamics parameters (including standard enthalpy of activation, △H++; standard entropy of activation, △S++; standard Gibbs free energy of activation, △G++). The study mainly focuses on ACT application in food systems, especially oil and fruit juice processing. Considering there are several improper calculations or mistakes often found in papers published recently in 2014–2019, three considerations are presented when applying the ACT, including 1) Understand that the reaction should be a single chemical elementary step; 2) Ensure that the units used should be consistent; 3) Effectively analyze the kinetics and thermodynamic parameters by choosing proper temperatures. This study is expected to further improve the understanding and correct application of this well-known theory in future work.
•Oleoyl chloride succeed efficiently esterifying 4,4-dimethylsterols.•The 4,4-dimethylsterol conversion of 99.27% was obtained.•A kinetic model was successfully developed to depict acyl chloride ...esterification.
In this study, the 4,4-dimethylsterol oleates were efficiently synthesized through esterification of 4,4-dimethylsterols and oleoyl chloride. The impact of reaction parameters on the 4,4-dimethylsterol conversion were investigated. The 4,4-dimethylsterol conversion increased with pyridine dosage, molar ratio of oleoyl chloride to 4,4-dimethylsterols, and temperature. The highest conversion of 99.27% was obtained with molar ratio of 1.1:1 at 313 K for 60 min. A second-order kinetic model describing acyl chloride esterification featuring high correlation coefficients was established. Arrhenius-Van't Hoff plot suggested activation energy and pre-exponential factor were 15.54 kJ mol−1 and 1.78 × 103 L mol−1 min−1, respectively. The molecular structure of 4,4-dimethylsterol oleates were finally identified by attenuated total reflection fourier transform infrared spectroscopy (ATR-FTIR), ultra-performance liquid chromatography system coupled with quadrupole time of flight mass spectrometry (UPLC-Q-TOF-MS), and nuclear magnetic resonance (NMR).
•Substrate molar ratio and lipase type are key factors affecting SOS yield.•NS40086 had a higher catalytic activity and lower selectivity than Lipozyme RM IM.•Acetone fractionation is an effective ...method for the purification of SOS.•Purified SOS product can be used as a cocoa butter improver in chocolate industry.
1,3-Distearoyl-2-oleoylglycerol (SOS) is widely used as a cocoa butter improver and an anti-blooming agent in the chocolate industry. In this study, an effective process was developed to prepare SOS by enzymatic acidolysis. Under optimal reaction conditions (substrate molar ratio of 12, NS40086 loading of 10%, a solvent-free system, 75°C for 4h), a SOS yield of 70.2% was obtained. Subsequently, two-step purification was applied to purify the crude SOS product. Free fatty acids were completely removed after molecular distillation. After acetone fractionation, the purity of SOS reached 92.2% with an 85.1% recovery. Comparison of various physicochemical properties of purified SOS and a commercial cocoa butter improver showed their properties to be similar. This study provides an effective and sustainable process for the synthesis of SOS product, which is expected to be used as a high-quality cocoa butter improver or an anti-blooming agent in the chocolate industry.
Inhibition of α-glucosidase activity is closely related to the treatment of type 2 diabetes. However, the potential mechanism by which 4,4-dimethylsterols inhibit α-glucosidase has not been ...elucidated. In this work, the inhibitory activity and mechanism of 4,4-dimethylsterols against α-glucosidase were studied through kinetic analysis, fluorescence spectroscopy, ultraviolet spectroscopy, circular dichroism, and molecular docking. 4,4-Dimethylsterols showed higher inhibition activity against α-glucosidase than acarbose with an IC50 value of 0.71 mg/mL and a noncompetitive inhibition type. They could bind to α-glucosidase through van der Waals forces and hydrogen bonds and quench its endofluorescence with a static quenching mechanism. Changes in the secondary structure of α-glucosidase were induced by its binding interaction with 4,4-dimethylsterols. Molecular docking further indicated that a hydrogen bond was generated between OH at the C-3 position of 4,4-dimethylsterols and the α-glucosidase residue Arg-442. This study provides new insights into the potential utilization of 4,4-dimethylsterols as antidiabetic phytochemicals in dietary supplements.
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