Abstract Soybeans are one of the most important crops in terms of volume and applications of the products obtained from them. Grown for oil and protein production, soybeans are feedstock for food, feed, fuel, and biobased products. Today, soybean oil can be found in most food products, as a result of its availability and positive nutritional and functional properties. The extensive scientific research and development conducted by both industry and academia on soybean oil is a main contributor to its important positioning among oils. This article provides a comprehensive review of this work, including information on the composition of soybeans, soybean oil, and other soybean lipids, especially as affected by environment, variety, and genetic modification; the physical properties of soybean oil, grading of soybeans, oil extraction, and the effect of various extraction techniques on oil quality and the various soy protein ingredients; basic refining and processing of soybean oil and soybean refinery co‐products; the major uses of soybean oil; trading rules for soybean oil; and the oxidative quality of soybean oil along with its health aspects.

An in vitro semi-continuous long-term (3 wk) anaerobic incubation system simulating lower gut fermentation was used to determine variability in gut microbial metabolism between 4 predigested high amylose-resistant starch residues (SR): SRV, SRVI, SRVII, and SRGEMS in human fecal samples. Subjects participated twice, 5 mo apart: 30 in Phase I (15 lean, 9 overweight and 6 obese), 29 in Phase II (15 lean, 9 overweight, 5 obese); 13 of 15 lean subjects participated in both phases. Of the 4 SRs, SRV displayed the highest gelatinization temperature, peak temperature, enthalpy changes, and the least digestibility compared with the other SRs. In both phases, compared with blank controls, all SRs increased butyrate ∼2-fold which stabilized at week 2 and only SRV caused greater propionate concentration (∼30%) after 3 wk which might have been partly mediated by its lesser digestibility. Fecal samples from lean and overweight/obese subjects incubated with SRs showed similar short-chain fatty acid production across both time points, which suggests that resistant starch may benefit individuals across BMIs.

Fibers important in the human diet are referred to as total dietary fiber, composed of soluble (SF) and insoluble dietary fiber components. "Dietary fiber" also refers to the supporting structures of plant cell walls and the substances intimately associated with them. Fruit, oat,barley, and legumes are the best natural food sources of SF. The chapter aims to identify crops targeted for genetic alteration of one or more of their fiber components, to indicate strategies for attaining the goals, and to characterize progress. As with the other grains mentioned, high SF has been a major impediment to a broader acceptance of rye as an animal feed. The SF from yellow mustard is known as mucilage, generally defined as polysaccharides containing galactose, galacturonic acid residues, and often xylose and arabinose. Flax, one of the oldest crops known to humans, traditionally was cultivated for its fiber and oil.

ABSTRACTOats (Avena sativa L.) have received significant attention for their positive and consistent health benefits when consumed as a whole grain food, attributed in part to mixed‐linkage (1‐3,1‐4)‐β‐d‐glucan (referred to as β‐glucan). Unfortunately, the standard enzymatic method of measurement for oat β‐glucan is costly and does not provide the high‐throughput capability needed for plant breeding in which thousands of samples are measured over a short period of time. The objective of this research was to test a microenzymatic approach for high‐throughput phenotyping of oat β‐glucan. Fifty North American elite lines were chosen to span the range of possible values encountered in elite oats. Pearson and Spearman correlations (r) ranged from 0.81 to 0.86 between the two methods. Although the microenzymatic method did contain bias compared with the results for the standard streamlined method, this bias did not substantially decrease its ability to determine β‐glucan content. In addition to a substantial decrease in cost, the microenzymatic approach took as little as 6% of the time compared with the streamlined method. Therefore, the microenzymatic method for β‐glucan evaluation is an alternative method that can enhance high‐throughput phenotyping in oat breeding programs.

The amounts of soybeans and total vegetable oil crops have been rising for a number of years. World production of soybeans in 2003 was estimated to be 184.49 million MT out of 317.89 million MT total for vegetable oil crops, making soybeans the world’s largest oilseed crop, rivaled only by palm oil (1). The 2003 crop of soybeans was expected to yield 29.85 million MT of soybean oil out of a total of 91.79 million MT of vegetable oil worldwide. The U.S. production of soybean oil was estimated at 8.59 million MT for 2002, of which 7.86 million MT was consumed domestically. During 2002–2003, Brazil produced 4.90 million MT and Argentina 4.12 million MT of soybean oil (2). The U.S. price of crude soybean oil has varied from $0.24/kg to $0.62/kg over the past 5 years with the lower prices being more recent (1). Soybeans owe their dominance of the oilseed market to the value of their protein, which is much greater than that of other oilseeds. Of the oilseed meals produced in 2003, 129.58 million MT out of a total of 185.69 milllion MT was soybean meal (1). Of the money made on extracting soybeans, the meal accounted for between 51% and 76% of the total in the last 10 years. Soybean oil of typical composition performs well as a salad oil, but it is usually hydrogenated for use as a margarine stock or frying oil. Soybean oil’s stability to oxidation also is limited by its content

The impacts of the molecular weight (MW), viscosity, and solubility of β-glucan on the rate of in vitro starch digestion and estimated glycemic index (GI) were evaluated. Extracted oat starch and β-glucan suspensions with high, medium, and low MW were heated to gelatinize the starch. The viscosity increased and the solubility decreased with an increase in the MW of β-glucan. The in vitro starch hydrolysis of the mixtures and a control, white bread, increased as the digestion time increased. As the MW of β-glucan increased, the starch hydrolysis decreased during in vitro digestion. The in vitro estimated GI of the mixture without β-glucan, determined from the starch hydrolysis rate, was 88.3 for Jim and 80.0 for N979, which decreased to 68.4 and 66.8, respectively, with the inclusion of high-MW β-glucan. The estimated GI values were negatively correlated with the β-glucan peak and final viscosities (r = -0.81 and -0.82). These results illustrated the importance of viscosity attributed to the β-glucan MW on starch hydrolysis during in vitro digestion. These findings will help to develop new food products with a low GI by using oat β-glucan.

The in vitro starch digestion rate and estimated glycemic index (GI) of oat flours and oat starches from typical and high β-glucan oat lines were evaluated along with the impact of heating on starch digestion. Flour from oat lines ('Jim', 'Paul', IA95, and N979 containing 4.0, 5.3, 7.4, and 7.7% β-glucan, respectively) was digested by pepsin and porcine pancreatin. To determine the impact of heating on starch digestion, oat slurries were prepared by mixing oat flour and water (1:8 ratio) and heating for 10 min prior to digestion. Viscosity, as measured on a Rapid Visco Analyzer, increased with increases in concentration and molecular weight of β-glucan. The in vitro starch digestion of oat flours and a control, white bread made from wheat flour, increased as the digestion time increased. Starch digestion of oat flour was slower than that of the control (p < 0.05). Heat treatment of oat-flour slurries increased the starch digestion from a range of 31–39% to a range of 52–64% measured after 180 min of in vitro digestion. There were no differences in starch digestibility among oat starches extracted from the different oat lines. The GI, estimated by starch hydrolysis of oat flours, ranged from 61 to 67, which increased to a range of 77–86 after heating. Oat-flour slurries prepared from IA95 and N979 lines with high β-glucan concentrations had lower GI values than did slurries made from Jim and Paul lines. Starch digestion was negatively correlated with β-glucan concentrations in heated oat-flour slurries (R2 = 0.92). These results illustrate that the oat soluble fiber, β-glucan, slowed the rate of starch digestion. This finding will help to develop new food products with low GI by using oat β-glucan.

Three major oat components, β-glucan, starch, and protein, and their interactions were evaluated for the impact on viscosity of heated oat slurries and in vitro bile acid binding. Oat flour from the experimental oat line "N979" (7.45% β-glucan) was mixed with water and heated to make oat slurry. Heated oat slurries were treated with α-amylase, lichenase, and/or proteinase to remove starch, β-glucan, and/or protein. Oat slurries treated with lichenase or lichenase combined with α-amylase and/or proteinase reduced the molecular weight of β-glucan. Heat and enzymatic treatment of oat slurries reduced the peak and final viscosities compared with the control. The control bound the least amount of bile acids (p < 0.05); heating of oat flour improved the binding. Heated oat slurries treated with lichenase or lichenase combined with α-amylase and/or proteinase bound the least amount of bile acid, indicating the contribution of β-glucan to binding. Oat slurries treated with proteinase or proteinase and α-amylase together improved the bile acid binding, indicating the possible contribution of protein to binding. These results illustrate that β-glucan was the major contributor to viscosity and in vitro bile acid binding in heated oat slurries; however, interactions with other components, such as protein and starch, indicate the importance of evaluating oat components as whole system.

Detection of quantitative trait loci (QTL) controlling complex traits followed by selection has become a common approach for selection in crop plants. The QTL are most often identified by linkage mapping using experimental F(2), backcross, advanced inbred, or doubled haploid families. An alternative approach for QTL detection are genome-wide association studies (GWAS) that use pre-existing lines such as those found in breeding programs. We explored the implementation of GWAS in oat (Avena sativa L.) to identify QTL affecting β-glucan concentration, a soluble dietary fiber with several human health benefits when consumed as a whole grain. A total of 431 lines of worldwide origin were tested over 2 years and genotyped using Diversity Array Technology (DArT) markers. A mixed model approach was used where both population structure fixed effects and pair-wise kinship random effects were included. Various mixed models that differed with respect to population structure and kinship were tested for their ability to control for false positives. As expected, given the level of population structure previously described in oat, population structure did not play a large role in controlling for false positives. Three independent markers were significantly associated with β-glucan concentration. Significant marker sequences were compared with rice and one of the three showed sequence homology to genes localized on rice chromosome seven adjacent to the CslF gene family, known to have β-glucan synthase function. Results indicate that GWAS in oat can be a successful option for QTL detection, more so with future development of higher-density markers.

For whole grains, the most sensitive components to the environmental changes are the lipids. In the current study, the effects of drying temperature (27 and 93 °C) and storage temperature (4 and 27 °C) on the fatty acid (FA) levels and lipid classes of endosperm lipids on four selected corn genotypes were investigated during a 12-month storage period. Storage temperature indicated greater impact on the FA composition than did the drying temperature. The ratio of saturated to unsaturated fatty acids, which was around 0.20–0.22 levels in the free lipid (FL) fractions of all corn types studied here, did not change significantly due to the drying and storage temperatures. However, in the bound lipid (BL) fractions, it was changed by a change in the drying and storage temperature in some of the corn types. Some changes were also found in the lipid classes within the FL and BL fractions of the studied corn samples. No lysophosphatidylcholine (LPC) was found in the FL fractions. In the BL fractions of two of the corn samples, the level of free fatty acids (FFA) increased more likely due to the deterioration of LPC. The results of the current study indicated a possible migration of triglycerides and FFA between the FL and BL fractions due to drying and storage at higher temperatures.

ABSTRACTPorridge and muffins were made from oat bran of two publicly available line, “Paul” and “Jim,” two experimental lines N979‐5‐2–4 (N979) and IA95111 (IA95) and a retail oat bran, to represent wet and dry food systems. N979 and IA95 had greater % β‐glucan and protein, less starch, greater water solubility index than other brans. Slurries of ground N979 bran had the greatest peak viscosity among all bran types. The adhesiveness of porridge was positively correlated and the firmness of fresh muffins was negatively correlated with % β‐glucan. No relationship was found between % β‐glucan and mouth coating of porridge during sensory evaluation. IA95 and N979 muffins were rated to have greater dome shape and coarser surface texture than Jim and Paul muffins. Although β‐glucan could increase the adhesiveness of a wet oat food and make a dry oat food less firm, the impact of β‐glucan on the sensory properties was minimal.PRACTICAL APPLICATIONSPorridge and muffins made with oat bran are popular foods among health‐conscientious people. In this study, porridge was made entirely with oat bran and water, thus delivering a high concentration of the soluble fiber. Porridges made with oat bran having different β‐glucan concentrations also differed in sensory and physical properties, perhaps providing guidance in labeling oat brans according to their functional characteristics. Muffins contained only 25.6% of oat bran; however, the impact of β‐glucan on the appearance, mouthfeel and taste of muffins was great. Thus, understanding these impacts may help producers choose appropriate food systems for delivery of high amounts of β‐glucan.

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ABSTRACT Muffins containing different amounts and molecular weights (MW) of β‐glucan were evaluated for the effect of β‐glucan on the physical characteristics of the muffins and on in vitro bile acid binding and fermentation with human fecal flora. Wheat flour muffins were prepared with the addition of β‐glucan extracts with high‐, medium‐, or low‐MW. For oat flour muffins, the native oat flour contained high‐MW β‐glucan; the oat flours were treated to create medium‐ and low‐MW β‐glucan within the prepared muffin treatments. For each 60‐g muffin, the amounts of β‐glucan were 0.52, 0.57, and 0.59 g for high‐, medium‐, and low‐MW β‐glucan wheat flour muffins, and 2.38, 2.18, and 2.23 g for high‐, medium‐, and low‐MW β‐glucan oat flour muffins, respectively. The lower the MW of the β‐glucan in muffins, the lower the height and volume of the muffins. The oat flour muffins were less firm and springy than the wheat flour muffins as measured on a texture analyzer; however, MW had no effect on muffin texture. The oat flour muffins bound more bile acid than did the wheat flour muffins. The muffins with high‐MW β‐glucan bound more bile acid than did those with low‐ and medium‐MW β‐glucan. Muffin treatment affected the formation of gas and total short‐chain fatty acids (SCFA) compared with the blank without substrate during in vitro fermentation. There were no differences in pH changes and total gas production among muffin treatments. The high‐MW β‐glucan wheat flour muffins produced greater amounts of SCFA than did the wheat flour muffin without β‐glucan and the oat flour muffins; however, there were no differences in SCFA production among muffins with different MW. In general, the β‐glucan MW affected the physical qualities of muffins and some potential biological functions in humans.

A previous study showed β-glucan with low molecular weight (MW, 1.56×10(5) g/mol) bound more bile acid and produced greater amounts of short-chain fatty acids (SCFA) than did β-glucan with high MW (Mn=6.87×10(5) g/mol). In the current study, β-glucan extracted from oat flour was fractionated into six different MW levels (high MW, 7.09×10(5); low level 1 (L1), 3.48×10(5); L2, 2.42×10(5); L3, 1.61×10(5); L4, 0.87×10(5); and L5, 0.46×10(5) g/mol) and evaluated to find the optimum MW affecting in vitro bile acid binding and fermentation. The β-glucan fractions with 2.42×10(5)-1.61×10(5) g/mol (L2 and L3) bound the greatest amounts of bile acid. After 24 h of fermentation, no differences were found in total SCFA formation among L1, L2, L3, and L4 fractions; however, the high MW and L5 MW fractions produced lower amounts of total SCFA. Thus, the optimum MW of β-glucan to affect both hypocholesterolemic and antitumorigenic in vitro effects was in the range of 2.42×10(5)-1.61×10(5) g/mol. This MW range also was the most water-soluble among the MWs evaluated.

Seven experimental oat lines with high (5.9% to 7.2%), medium (5.3% to 5.5%), and low (4.4%) β-glucan concentrations were evaluated for the effects of β-glucan molecular weight (MW) and structure on viscosities of oat-flour slurries. The MW of β-glucans was determined by size-exclusion high-performance liquid chromatography. The structural features of β-glucans were measured by using fluorophore-assisted capillary-electrophoresis after complete hydrolysis with lichenase. The oat-slurry viscosities were measured on a Rapid Visco Analyser under 4 conditions: (1) without starch (amylolysis, removal of starch by α-amylase); (2) without β-glucan (removal of β-glucan by lichenase); (3) natural action of enzymes (autolysis, in sodium buffer); and (4) inhibition of enzymes (in silver nitrate solution). Excluding one line (regression outlier), significant correlations (P < 0.05) between peak MW of β-glucan and viscosities of oat slurries were obtained under inhibition. The ratio of degree of polymerization (DP) 3/DP4 negatively correlated with viscosity under amylolysis, autolysis, and inhibition (P < 0.05). The amount of DP ≥ 5 negatively correlated with pasting final viscosity after β-glucan removal by lichenase (P < 0.05). Positive correlations (P < 0.05) between the ratio of β-(1→4)/β-(1→3) linkages and viscosities under autolysis and inhibition were found. Overall, these findings demonstrated that the peak MW, ratio of DP3/DP4, amount of DP ≥ 5, and ratio of β-(1→4)/β-(1→3) linkages of β-glucans impacted pasting properties of oat-flour slurries.

The effect of temperature on the oil oxygen concentration, tested in both soybean and olive oils with no added polydimethylsiloxane (PDMS), showed that the oxygen concentration increased with temperature to approximately 100 °C. Above 100 °C, the oxygen concentration abruptly decreased. This change was attributed to the balance between the rates of oxygen uptake and consumption by oil oxidation, which favored oxygen consumption over uptake at temperatures above 100 °C. The addition of 100 ppb PDMS to soybean oil, enough to form a continuous layer over the surface of the oil, reduced the oxygen concentration when compared to a soybean oil control containing no added PDMS at temperatures ranging from 93 to 180 °C; thus suggesting an oxygen barrier effect of PDMS. The accumulation of PDMS at the air–oil interface in soybean oil held at 180 °C was determined by comparing the oil’s internal temperature and the apparent surface temperature. A decrease in the apparent surface temperature while the oil was held at a constant internal temperature was attributed to a change in the emissivity of the surface as a consequence of the accumulation of PDMS in the air–oil interface. The presence of PDMS at the air–oil interface was confirmed for 100 ppm of PDMS, a concentration greater than the concentration necessary to form a monolayer of PDMS on the oil surface.

ABSTRACT Water‐soluble β‐glucan (BG) extracted from a high‐BG oat line was treated with different amounts of lichenase (1→3)(1→4)‐β‐ d ‐glucanase) enzyme to yield three different molecular weight (MW) BG extracts. Low (LMW‐BG, 157,000), medium (MMW‐BG, 277,000), and high (HMW‐BG, 560,000) MW BG extracts were added to plain muffin formulations at a level of 0.52% (0.42% in the batter, 0.52% in the resultant muffins) to investigate the effect of MW of BG on textural and bile acid (BA) binding properties of the muffins. In addition, treatments were prepared containing LMW‐BG, MMW‐BG, and HMW‐BG extracts in amounts providing equivalent batter firmness as determined on a texture analyzer. Resultant BG concentrations (and per serving amounts) of these muffins were 1.36% (0.81 g/60 g muffin), 1.05% (0.63 g/60 g muffin), and 0.52% (0.31 g/60 g muffin), respectively; thus, the LMW treatment complied with a U.S. Food and Drug Administration health claim requiring 0.75 g of BG per serving. The firmness, springiness, and BA‐binding capacity of the muffins were unaffected by the MW of BG. However, when added at the maximum limit for equivalent batter firmness, the LMW treatment was more firm and less springy than the HMW treatment. Furthermore, BA‐binding capacities of LMW and MMW fractions tended to be greater than that of the HMW fraction when added at the maximum limit. These results add further evidence to the importance of fine‐tuning BG structure to provide maximum health benefits while maintaining high product quality.

Soybean oils treated with 5, 10, 25, 50, and 100 ppb polydimethylsiloxane (PDMS) and a control soybean oil (no PDMS) were heated at 180 °C for 48 h. The decomposition of linoleate (18:2) and tocopherols was monitored. The degradation of 18:2 and both γ- and δ-tocopherols followed pseudo first-order kinetics. For 25 ppb PDMS (the concentration necessary to form a PDMS monolayer on the air-oil interface) and greater concentrations, 18:2 degradation decreased at a rate comparable to the control. However, for the samples with 25 ppb or more PDMS, there was a subsequent increase in the rate of 18:2 degradation during the 48 h of heating period. The same trend seen for 18:2 degradation also was observed for the rates of degradation of both γ- and δ-tocopherols; but, for the tocopherols the treatment with 10 ppb PDMS also decreased the rate of degradation. For those PDMS treatments in which a subsequent increase in degradation rates were observed, the rates of degradation after the change were similar to the rate of degradation in the control oil. In general, the time that the changes in rates occurred increased with the PDMS concentrations. The occurrence of these changes was attributed to decreases in the concentrations of tocopherols or PDMS such that the protective effects were lost.

SummaryWhole oat flour, N979‐5‐2‐4 (N979), IA95111 (IA95), ‘Jim’ and ‘Paul’ with β‐glucan concentration of 8.6%, 7.6%, 5.3%, and 5.9%, respectively, was made into extruded breakfast cereal (EBC). EBC β‐glucan had greater peak molecular weight than corresponding whole oat flour. Both whole oat flour and EBC from N979 and IA95 had greater peak viscosity (PV), as measured using a Rapid ViscoAnalyser, than that from Jim or Paul. Bile acid binding of EBC, correlated with total β‐glucan concentrations and PV, was either similar or greater than that of corresponding whole oat flour. Jim EBC had the least expansion ratio, lowest brown colour and cereal aroma but greatest tooth packing values. Paul and N979 EBC, although different from each other in a few sensory attributes, had similar acceptability as judged from a consumer test, suggesting that oats with elevated β‐glucan concentrations can be successfully incorporated into EBC with minimal processing alterations.