Antioxidant capacity of the striped sunflower seed (Helianthus annuus L.) aqueous extract

The aim of this work was to study the aqueous extract of cotyledons derived from the striped sunflower seeds, with regard to the kinetics of its antioxidant capacity and its phenolic composition. The results showed that, among the phenolic compounds of this extract which were identified by gas chromatography, chlorogenic acid (12.88%) was the prevailing compound. The effectiveness of the aqueous extract in the β‐carotene/linoleate model system was estimated on the basis of the oxidation induction period, which was determined by the method of tangents to the two parts of this extract's kinetic curve, and the study showed that the extract antioxidants may be effective in blocking radical chain reactions and may also interfere with the reactions that produce the secondary products that speed up the system's oxidative process when present in higher concentrations (233.2 µg/mL). The result found by the Rancimat® method showed that the aqueous extract at 300 µg/mL (15.2% IP) was comparable to the BHA standard at 100 µg/mL (16.0 ± 0.86%) in a lipidic system.     

Effects of Microbial Utilization of Phenolic Acids and their Phenolic Acid Breakdown Products on Allelopathic Interactions

Reversible sorption of phenolic acids by soils may provide some protection to phenolic acids from microbial degradation. In the absence of microbes, reversible sorption 35 days after addition of 0.5–3 mol/g of ferulic acid or p-coumaric acid was 8–14% in Cecil A_p horizon and 31–38% in Cecil B_t, horizon soil materials. The reversibly sorbed/solution ratios (r/s) for ferulic acid or p-coumaric acid ranged from 0.12 to 0.25 in A_p and 0.65 to 0.85 in B_t horizon soil materials. When microbes were introduced, the r/s ratio for both the A_p and B_t horizon soil materials increased over time up to 5 and 2, respectively, thereby indicating a more rapid utilization of solution phenolic acids over reversibly sorbed phenolic acids. The increase in r/s ratio and the overall microbial utilization of ferulic acid and/or p-coumaric acid were much more rapid in A_p than in B_t horizon soil materials. Reversible sorption, however, provided protection of phenolic acids from microbial utilization for only very short periods of time. Differential soil fixation, microbial production of benzoic acids (e.g., vanillic acid and p-hydroxybenzoic acid) from cinnamic acids (e.g., ferulic acid and p-coumaric acid, respectively), and the subsequent differential utilization of cinnamic and benzoic acids by soil microbes indicated that these processes can substantially influence the magnitude and duration of the phytoxicity of individual phenolic acids.     

Effect of roasting on the physico-chemical properties,fatty acids,polyphenols and mineral contents of tobacco (Nicotiana tabacum L.) seed and oils

The physico-chemical properties, phytochemicals, mineral contents of tobacco (Nicotiana tabacum L.) seeds grown at Samsun province in Turkey were evaluated. The oil contents of tobacco seeds ranged from 20.6% (control) to 29.0% (microwave-roasted). L*, a* and b* values of tobacco seeds ranged from 32.38 to 35.61; from 6.32 to 6.78; from 13.72 to 14.27, respectively. Total phenolic contents of tobacco seed extract and oils were reported between 31.02 (oven-roasted) and 34.42 mg GAE/100 g (microwave-roasted) to 4.60 (microwave-roasted) and 6.45 mg GAE/100 g (oven-roasted), respectively. Total flavonoid values of raw and roasted tobacco seed extract and oils were determined between 26.62 (oven) and 67.10 mg/100 g (control) to 21.57 (control) and 44.71 mg/100 g (microwave-roasted), respectively. Gallic acid, 3,4-dihydroxybenzoic acid and catechin are the predominant phenolic components of raw and roasted tobacco seed oils. The amounts of oleic and linoleic acid in raw and roasted tobacco seed oils ranged from 10.23% (oven-roasted) to 12.48% (control) and 73.72% (control) to 76.63% (oven-roasted), respectively. The abundant elements found in seeds were K, P, Ca, Mg, S and Fe. The mineral amounts of the roasted seeds were found higher than that of the control. The highest increase was detected in oven roasted tobacco seeds.     

Kariya (Hildegardia barteri) seed oil extraction: comparative evaluation of solvents,modeling, and optimization techniques

In this work, the effects of solid/solvent ratio (0.10–0.25?g/ml), extraction time (3–8?h), and solvent type (n-hexane, ethyl acetate, and acetone) together with their shared interactions on Kariya seed oil (KSO) yield were investigated. The oil extraction process was modeled via response surface methodology (RSM), artificial neural network (ANN) and adaptive neuro-fuzzy inference system (ANFIS) while the optimization of the three input variables essential to the oil extraction process was carried out by genetic algorithm (GA) and RSM methods. The low mean relative percent deviation (MRPD) of 0.94–4.69% and high coefficient of determination (R²) > 0.98 for the models developed demonstrate that they describe the solvent extraction process with high accuracy in this order: ANFIS, ANN, and RSM. The best operating condition (solid/solvent ratio of 0.1?g/ml, extraction time of 8?h, and acetone as solvent of extraction) that gave the highest KSO yield (32.52?wt.%) was obtained using GA-ANFIS and GA-ANN. Solvent extraction efficiency evaluation showed that ethyl acetate, n-hexane, and acetone gave maximum experimental oil yields of 19.20?±?0.28, 25.11?±?0.01, and 32.33?±?0.04?wt.%, respectively. Properties of the KSO varied based on the type of solvent used. The results of this work showed that KSO could function as raw material in both food and chemical industries.     

Influence of the dilute‐solution properties of cellulose acetate in solvent mixtures on the morphology and pervaporation performance of their membranes

The pervaporation performance of cellulose acetate (CA) membranes prepared from acetone (AC), acetone/tetrahydrofuran (AC/THF), acetone/chloroform (AC/CF), and acetone/cyclohexane (AC/CYH) was studied for separating MeOH/MTBE (methyl tert‐butyl ether) mixture with 5 (wt) % MeOH. The dilute‐solution properties and Huggins constant (K_H) of CA dissolved in AC and AC/solvent mixtures with 15 vol % of the second solvent (tetrahydrofuran, chloroform, or cyclohexane) were examined. J and α of the CA membranes were affected by the types of solvent mixtures used to prepare the casting solutions. Under the same conditions, the membrane with AC/CYH had the highest J value and the lowest α value, and it was followed by the membranes with AC/CF, AC/THF, and AC. The increasing value of J and decreasing value of α for the CA membranes from different solvent mixtures were in good agreement with the increasing value of K_H of CA in corresponding solvent mixtures. Furthermore, differences in the morphology from scanning electron microscopy images of the cross sections or from atomic force microscopy photographs of the surfaces of the membranes existed, and they provided proof of the different pervaporation performances of the CA membranes prepared from AC and AC/solvent mixtures. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97:1891–1898, 2005     

Silica/mullite fiber composite membrane with double-layer structure for efficient sub-micrometer dust removal

Here, we developed silica/mullite fiber composite membranes with double-layer structure by a simple vacuum procedure for the removal of sub-micrometer dust. The support with three-dimensional skeleton structure exhibited high porosity (higher than 90%), low density (lower than 0.25?g/cm³) and high compressive strength (higher than 0.55?MPa) at 1000?°C. By controlling the mass ratio of silica sol to mullite fiber, we can obtain uniform and complete filtering layers with different thicknesses. The composite membranes exhibited high PM filtration efficiency with 99% for 1–10?µm, 97% for 0.5?µm and 90% for 0.3?µm. These samples had high air flow with very low pressure drop (lower than 600?Pa when airflow velocity reached 1?m/s). These results indicated that the silica/mullite fiber composite membranes were very promising for PM pollution control in the field of hot gas filtration.     

Screening the Antioxidant and Antimicrobial Properties of the Extracts from Plantain (Plantago Major L.) Leaves

Abstract

Antioxidant and antimicrobial activities of the extracts obtained by classical (maceration) and ultrasonic (40 kHz) extraction from dry Plantago major leaves were compared. The antioxidant activities of extracts obtained by ultrasonic and classical extraction were 0.87±0.02 and 0.85±0.02 µg/µg DPPH, respectively. Ultrasound positively affected the extractive substance yield and the kinetics of extraction, but the extract obtained by classical extraction contained higher total contents of phenolic compounds and flavonoids than that obtained by ultrasonic extraction. Extracts of P. major showed better antimicrobial activity against the yeasts than against the bacteria.     

Production of eicosapentaenoic acid bySaprolegnia sp. 28YTF-1

Saprolegnia sp. 28YTF-1, isolated from a freshwater sample, is a potent producer of 5,8,11,14,17-cis-eicosapentaenoic acid (EPA). The fungus used various kinds of carbon sources, such as starch, dextrin, sucrose, glucose, and olive oil for growth, and olive oil was the best carbon source for EPA production. The EPA content reached 17 mg/g dry mycelium (0.25 mg/L) when the fungus was grown in a medium that contained 2.5% olive oil and 0.5% yeast extract, at pH 6.0 and 28°C for 6 d with shaking. Accompanying production of arachidonic acid (AA; 3.2 mg/g dry mycelia, EPA/AA = 5.1) and other ω6 polyunsaturated fatty acids was low. Both EPA content and EPA/AA ratio increased in parallel by lowering growth temperature. Triglyceride was the major mycelial lipid (ca. 84%), but EPA comprised only 2.2% of the total fatty acids of this lipid. About 40% of the EPA produced was found in polar lipids, such as phosphatidylethanolamine (EPA content, 28.2%), phosphatidylcholine (13.6%), and phosphatidylserine (21.2%).     

Synthesis of a Cocoa Butter Equivalent by Enzymatic Interesterification of Illipe Butter and Palm Midfraction

This study aims to synthesize a cocoa butter equivalent (CBE)‐structured lipid from a blend of illipe butter (IB) and palm midfraction (PMF) by means of enzymatic interesterification using Rhizomucor miehei sn‐1,3 specific lipase, Lipozyme^® RM IM (Novozymes North America, Inc., Franklinton, NC, USA) as the biocatalyst. Physical and chemical attributes of the CBE and cocoa butter (CB) were analyzed. The synthesized CBE matched the triacylglycerol (TAG) profile range of a commercial CB and is therefore hypothesized to show similar physical and chemical characteristics to CB. The TAG profile, fatty‐acid constituents, melting and cooling behavior, polymorphism, and crystal morphology were determined using high‐performance liquid chromatography, gas chromatography, differential scanning calorimetry, X‐ray diffraction (XRD), and polarized light microscopy, respectively. Four enzymatically interesterified blends of IB:PMF at different weight ratios were analyzed for their TAG profiles, and a ratio of IB:PMF 10:3 (%, w/w) at 5% enzyme load and a reaction time of 30 min gave similar TAG results to CB. The TAG values of the IB:PMF 10:3 interesterified product (IP) were 1,3‐dipalmitoyl‐2‐oleoylglycerol at 19.1 ± 1.0%, 1‐palmitoyl‐2‐oleoyl‐3‐stearoylglycerol at 42.7 ± 1.0%, and 1,3‐distearoyl‐2‐oleoylglycerol at 29.9 ± 0.3%. The melting and the cooling profile of IP and CB showed no significant difference. XRD of IP and CB displayed similar dominant peaks at 4.6 Å, representing a β polymorph. Both CB and IP have similar granular spherulitic crystals.     

Chemical Characterization of the Seed and Antioxidant Activity of Various Parts of <Emphasis Type="Italic">Salvadora persica</Emphasis>

This study investigated the fatty acid, tocopherol, sterol and total phenolic compounds of Salvadora percica seeds as well as the potential antioxidant activity of the leaves, bark and seedcake extracts. Two samples of S. persica seed collected from Kordofan (sandy soil) and Gezira (heavy clay soil) states in Sudan were used. The predominant fatty acids were 14:0, 16:0 and 18:1 representing 45.50, 35.12 and 10.20% for Kordofan and 45.20, 34.49 and 10.66% for Gezira samples. Gamma-tocopherol was the predominant tocopherol in both samples representing 61.3 and 61.7% of the total tocopherols, respectively, followed by α-tocopherol at 21.1 and 20.2%, respectively. Total sterol content was 3399.6 and 3385.3 mg/kg for Kordofan and Gezira samples, respectively. Beta-sitosterol, campesterol, stigmasterol and Δ5-avenasterol were predominant. The content of total phenolic compounds was determined in S. persica bark (SPB), S. persica leaves (SPL), and S. persica seedcake (SPC) extracts of each sample according to the Folin–Ciocalteau method as 111.70, 132.60, and 66.10 mg GAE/g extract for the Kordofan sample. They were found to be 105.90, 129.10 and 62.90 mg GAE/g extract in the Gezira sample, respectively. The two samples were significantly (P < 0.05) different in total phenolic content with SPL as the highest in both samples. The methanolic extracts of SPL, SPB, and SPC in both samples were markedly effective in inhibiting the oxidation of linoleic acid and subsequent bleaching of β-carotene in comparison with the control. But they were less effective than butylated hydroxyanisole.     

Characterization of a Partially Purified Extract from Flax (Linumusitatissimum L.) Seed

A water‐soluble partially purified extract from defatted flax seed was obtained and characterized; it contained proteins (828.8 g/Kg), as well as water‐soluble carbohydrates (101.4 g/Kg) and phenolic compounds (22.2 g/Kg), essentially secoisolariciresinol diglucoside (SDG, 18.40 g/Kg) and ferulic acid (1.45 g/Kg) and p–coumaric acid (2.07 mg/kg) mainly in their glycoside forms. Proteins of 23–24 kDa were the main protein fractions found in the extract. In an emulsion model system, the flax extract was able to inhibit the production of oxidation products (conjugated diene, peroxides and aldehydes) as well as the degradation of flax oil carotenoids. The antioxidant effects of the flax extract were concentration dependent. Oxidation kinetics of the emulsion supplemented with 0.10 % flax extract were similar to the oxidation kinetics of the control blank, whereas, oxidation parameters of the emulsion supplemented with 0.48 % (and higher) flax extract were equal to or better than the oxidation parameters obtained with the test control emulsion containing 0.01 % BHT. These results suggested that flax seed phenolic compounds (SDG) and low molecular weight proteins, both found in the studied extract, might have very strong antioxidant properties. This is paper number 1089 of the Canadian Grain Commission.     

Antioxidant Activity of Rambutan (Nephelium lappaceum L.) Peel Extract in Soybean Oil during Storage and Deep Frying

Rambutan (Nephelium lappaceum L.) peel (RBP) is discarded as the main by‐product during processing of the fruit. Increasing attention is now paid to the valorization of RBP for the recovery of valuable compounds. Geraniin, ellagic acid, quercetin, and rutin are the main phenolic compounds found in methanolic RBP extract. Extracted rambutan peel powder (ERPP) is used to evaluate the oxidative stability of soybean oil stored at 4 and 30 °C in the dark and light and deep fried with potatoes at 160 °C. Tert‐butylhydroquinone (100 µg g^?1 oil, TBHQ) serves as positive control. Oil supplemented with ERPP of 1000 µg gallic acid equivalents (GAE) g^?1 of oil shows positive effects on the retardation of the oxidation process during storage in comparison with oil without addition. During deep frying, either ERPP (1000 µg GAE g^?1) or TBHQ retards the lipid oxidation of oil. Levels of thiobarbituric acid reactive substances of potatoes fried in oil fortified with the extract and TBHQ (0.4–0.59 µg g^?1) are much lower than those without the extract (1.31 ± 0.10 µg g^?1) (p < 0.05). Therefore, RBP extract exhibits favorable antioxidant effects and can be used for effectively inhibiting lipid oxidation in oil during storage and deep frying. Practical Applications: An extract from rambutan fruit peel containing phenolic compounds, that is, geraniin, ellagic acid, rutin, and quercetin showed promising results to be used as potential antioxidants in soybean oil during deep frying. Both oxidation of the frying oil as well as the oxidation of the food product, that is, potatoes were inhibited. These results demonstrated that rambutan fruit peel extract can be used as a natural antioxidant in frying oil to replace synthetic antioxidants, that is, TBHQ.     

Chemical Analysis of Polyphenols with Antioxidant Capacity from Pinus durangensis Bark

The most active phenolics in Pinus durangensis residual bark were identified and evaluated following a chromatographic fractionation. Bark powder was defatted with hexane, and a crude extract (CE) was obtained by extraction with aqueous acetone (67%). A liquid partition with ethyl acetate was performed to produce an organic extract (OE), which was subsequently purified by column chromatography (Toyopearl HW-40F, methanol), resulting in ten fractions (MF1 to MF10) and an oligomeric fraction eluted with acetone 67% (OLF). Subfraction MF6-1 was obtained by a second chromatographic purification of MF6. Extraction yields, total phenolics, flavonoids, and flavanols contents were determined in CE and OE. The antioxidant activity of bark extracts was measured by DPPH and ABTS assays at 100 µg/mL, expressed in percentage, median effective concentration (IC₅₀), and TEAC (mM). Also the low density lipoprotein inhibition was evaluated. Identification of major phenolics was carried out by HPLCESI–MS and HPLC–DAD instruments. Bioactive taxifolin (dihydroquercetin), dihydromyricetin, myricetin, quercetin, pinomyricetin (myricetin-methoxy), pinoquercetin (quercetin-methoxy), trimeric, and tetrameric procyanidins were detected and identified in P. durangensis bark extracts. Polyphenols found are similar to those contained in Pycnogenol and other Pinus species.     

Induction and/or Selection of Phenolic Acid-Utilizing Bulk-Soil and Rhizosphere Bacteria and Their Influence on Phenolic Acid Phytotoxicity

Bulk-soil and rhizosphere bacteria are thought to exert considerable influence over the types and concentrations of phytotoxins, including phenolic acids, that reach a root surface. Induction and/or selection of phenolic acid-utilizing (PAU) bacteria within the bulk-soil and rhizosphere have been observed when soils are enriched with individual phenolic acids at concentrations 0.25 mol/g soil. However, since field soils frequently contain individual phenolic acids at concentrations well below 0.1 mol/g soil, the actual importance of such induction and/or selection remains uncertain. Common bacteriological techniques (e.g., isolation on selective media, and plate dilution frequency technique) were used to demonstrate in Cecil A_p soil systems: (1) that PAU bacterial communities in the bulk soil and the rhizosphere of cucumber seedlings were induced and/or selected by mixtures composed of individual phenolic acids at concentrations well below 0.25 mol/g soil; (2) that readily available carbon sources other than phenolic acids, such as glucose, did not modify induction and/or selection of PAU bacteria; (3) that the resulting bacterial communities readily utilize mixtures of phenolic acids as a carbon source; and (4) that depending on conditions (e.g., initial PAU bacterial populations, and phenolic acid concentration) there were significant inverse relationships between PAU bacteria in the rhizosphere of cucumber seedlings and absolute rates of leaf expansion and/or shoot biomass. The decline in seedling growth could not be attributed to resource competition (e.g., nitrogen) between the seedlings and the PAU bacteria in these studies. The induced and/or selected rhizosphere PAU bacteria, however, reduced the magnitude of growth inhibition by phenolic acid mixtures. For a 0.6 mol/g soil equimolar phenolic acid mixture composed of p-coumaric acid, ferulic acid, p-hydroxybenzoic acid, and vanillic acid, modeling indicated that an increase of 500% in rhizosphere PAU bacteria would lead to an approximate 5% decrease (e.g., 20–25%) in inhibition of absolute rates of leaf expansion. As far as we know, this is the first time that such a relationship has been quantified.     

Effect of Operating Parameters on Oil and Phenolic Extraction Using Supercritical CO<Subscript>2</Subscript>

Supercritical fluid extraction (SFE) with carbon dioxide was used to extract oil from canola press cake. Different operating conditions, e.g. pressure, temperature, and co-solvent % were investigated to optimize extraction parameters to yield canola meal with <4% oil. The residual oil content in the extracted canola meal reduced to 2.1–2.9% in our experimental trials. Residues of the optimum conditions based on oil yield were compared for the total phenolic content and the main phenolic compounds. Sinapine (the choline ester of sinapic acid) was the major phenolic constituent in both the SFE and n-hexane extracted canola meals and press cakes. n-Hexane extracted residues showed the retention of the highest sinapic acid, sinapine, sinapoyl glucose and total phenolic contents (mg/g) while the SF-extracted residues showed the lowest values for these compounds.     

Fungistatic Activity of Ruta graveolens Extract and Its Allelochemicals

The biological activity of an extract of Ruta graveolens and its allelochemicals [8-methoxypsoralen (8-MOP), 5-methoxypsoralen (5-MOP) and 4-hydroxycoumarin] (previously isolated) was evaluated gainst pathogenic fungi: Fusarium solani, Pyrenochaeta lycopersici, and Trichoderma viride. In addition a rue lyophilized extract was also tested against Penicillium sp., Thielaviopsis basicola, and Verticillium dahliae. We determined that 5 g rue lyophilized extract/liter, the lowest concentration tested, inhibited the mycelial growth of P. lycopersici and V. dahliae by 63.6% and 47%, respectively, with IC₅₀ (the concentration required to inhibit growth 50%) values of 4.16 and 6.5 g/liter, respectively. Moreover, the rue lyophilized extract was shown to reduce radial growth of all six fungal species significantly at concentrations ranging from 5.0 to 40.0 g/liter. Mycelial growth of Penicillium sp. was promoted at 5.0 g lyophilized rue extract/liter and inhibited at higher concentrations. 4-OH coumarin had no effect on the growth of these fungi at concentrations ranging from 0.32 to 2.60 mg/liter, whereas 8-MOP and 5-MOP inhibited the mycelial growth of F. solani and T. viride with IC₅₀ values of 6 mg/liter (5-MOP) and 27 mg/liter (8-MOP) for both fungi, respectively. A mixture of 5-MOP and 8-MOP, tested at 64.8 mg/liter (as they naturally occur in the crude rue extract) significantly inhibited the growth of all tested fungal species. These results suggest potential role for the rue extract and its allelochemicals in controlling pathogenic fungal infections.     

Effects of mixtures of four phenolic acids on leaf area expansion of cucumber seedlings grown in Portsmouth B1 soil materials

Cucumber seedlings growing in a 12 mixture of soil (Portsmouth B₁) and sand adjusted to pH 5.2 were treated every other day five times with 0, 0.0625, 0.125, 0.25, or 0.5 mol/g soil of ferulic, caffeic,p-coumaric,p-hydroxybenzoic, protocatechuic, sinapic, syringic, or vanillic acids. Treatments began when seedlings were 8 days old. The effects on mean absolute rates of leaf expansion were used to estimate the relative potencies of these phenolic acids to ferulic acid. Based on the results of this experiment, ferulic,p-coumaric,p-hydroxybenzoic, and vanillic acids were chosen for further study. Materials and procedures were identical in the second study, but treatments consisted of mixtures of the four phenolic acids at concentration combinations designed to achieve 40 % or 60 % inhibition of absolute rates of leaf expansion. Using joint action analysis, a model describing the action of the phenolic acid mixtures was developed. A model involving only two factor terms was sufficient to describe the observed responses of cucumber leaf area to the phenolic acid mixtures. The action ofp-hydroxybenzoic acid on absolute rates of leaf expansion was inhibited by the presence of the other three phenolic acids. No other antagonisms or synergisms existed among the four compounds.This research was partially supported by the North Carolina Agricultural Research Service, Raleigh, North Carolina 27695-7643 and by the US-Spain Joint Committee for Scientific and Technological Cooperation project CCA-8309/166.     

Temperature stability of vitamin D2 and color changes during drying of UVB-treated mushrooms

The study investigates the effect of drying temperature on vitamin D₂ content and color changes of UVB-treated shiitake (Lentinula edodes), oyster (Pleurotus ostreatus), and white and brown button mushrooms (Agaricus bisporus). Fresh samples were UVB treated up to 1.5?J/cm² for 20?min at 25°C and either dried in a high precision dryer (temperatures: 40, 60, 80°C, specific humidity: 10?g/kg, air velocity: 0.6?m/s) or frozen at ?25°C, and then freeze-dried (pressure: 0.28?mbar). Vitamin D₂ content was not negatively affected by the increased temperatures of the drying air. The highest content of vitamin D₂ was detected in freeze-dried (171.84?µg/g) and hot-air dried shiitake at 60°C (169?µg/g), followed by oyster (121.96?µg/g), whereas the lowest amount was observed in brown button mushrooms at 40°C (34.65?µg/g). Although vitamin D₂ indicated a remarkable stability even at 80°C, the dried samples were characterized by intensive tissue darkening.     

Influence of number of puffing times on physicochemical,color, texture,and microstructure of explosion puffing dried apple chips

The impact of number of puffing times during explosion puffing drying (EPD) on drying characteristics and qualities of apple chips was studied. Physicochemical characteristics, antioxidant capacity, color, texture, expansion ratio, rehydration ratio, hydroscopicity, and microstructure of apple chips dried by EPD with 0 (vacuum drying, VD), 1, 3, 5, 7, and 9 puffing times were analyzed. The apple chips dried by EPD with 3 and 5 puffing times exhibited better color (ΔE 7.27–7.70) and texture (hardness 40.5–40.8 N, crispness 8.8–9.3 N/mm), as well as higher expansion ratio (104.4–109.7%) compared to VD and EPD with fewer or more puffing times. The samples dried with 3 and 5 puffing times also showed relatively higher rehydration ratio and hygroscopicity, and acceptable retention of total phenolic content (0.32–0.37 mg/g) and ascorbic acid content (1.66–1.89 mg/100 g), as well as considerable antioxidant abilities (DPPH 79.45–81.17 AEAC µM/g, FRAP 66.54–68.25 TEAC µM/g, ABTS 73.36–79.21 TEAC µM/g) compared to VD dried samples. In conclusion, experiments with apple chips indicated that EPD drying with 3 to 5 puffing times yielded superior overall quality than that with more or fewer puffing times.     

Antioxidant properties of polyphenol‐containing extract from soybean fermented with Saccharomyces cerevisiae

The antioxidant properties and total phenolic compounds of soybean extract fermented with Saccharomyces cerevisiae during 24 h were evaluated. Total polyphenolic compounds extracted in ethanol/water (1:1) solution were 789.54 mg/g dry extract, and flavonoids were 169.47 mg quercetin equivalents/g of dry extract. Reducing power (91.18%) and DPPH scavenging (79.30% at 4‐times diluted) were excellent, and so high as BHA, 92.17% and 73.8% respectively, while superoxide anion scavenging showed poor inhibition (4876 equivalent SOD U/g). Antioxidant activity in linoleic acid/water emulsion system of fermented extract measured as peroxide formation inhibition at 37 °C was the strongest (95.62%), while it exerted a moderate inhibition for conjugated dienes and thiobarbituric acid reactive substances (64.77% and 54.33%). At 80 °C the antioxidant activity assayed at a higher concentration was less effective (29.35% on CD; 74.58% on PV and 35.04% on TBARS).