Effect of xanthan gum on enhancing the foaming properties of whey protein isolate

The foaming properties of whey protein isolate (WPI) in the presence of xanthan gum (XG) were investigated. XG dispersion did not exhibit any foaming properties. The optimal foaming overrun (FO), or the amount of air incorporated into the dispersion, was obtained from the dispersion of 5% WPI and 0.05% XG at 949%. This WPI-XG dispersion had a significantly higher overrun than that of WPI (868%) or egg white (879%) (P<0.05). Optimal foam stability (FS) of 216 min was obtained at 5% WPI and 0.2% XG; however, the overrun was reduced slightly (844%). XG increased stability to 15 times that of WPI alone. The overrun of 5% WPI plus 0.05% XG was further increased to 1343% when 1 M NaCl was added (P<0.05). However, FS (51 min) was significantly reduced. A significant increase in the FO of 5% WPI plus 0.05% XG (1081%) was observed when pH was adjusted to 5.0 with no significant change in FS (56 min) (P<0.05). The FO (1457%) was significantly increased (P<0.05) when the WPI-XG was heat treated (55°C for 5 min). WPI-XG dispersions at acidic pH and temperatures below 85°C have a variety of potential applications in products such as protein beverages, angel food cake, and unique infant formulas.     

Soy protein biopolymers cross-linked with glutaraldehyde

Biopolymers from soy protein isolate (SPI) crosslinked with glutaraldehyde (GA) were prepared. Surface hydrophobicities of SPI-GA biopolymers and SPI were 4.4 and 11.5, respectively. The solubility profile of SPI was slightly higher than that of SPI-GA biopolymers. Foaming capacities of SPI-GA biopolymers (23 mL) were higher than that of SPI (19 mL), but similar to egg white (22 mL). Foaming stabilities of SPI-GA biopolymers (120 min) were significantly higher than those of SPI (40 min) and egg white (98 min). The emulsifying properties of SPI-GA biopolymers were lower than those of SPI and bovine serum albumin (P>0.05). Tensile strength (TS) and elongation at break (ETB) of SPI-GA biopolymer films were significantly higher than those of glycerol-plasticized soy protein films. TS and ETB of SPI-GA biopolymer films increased with increasing GA concentrations. GA treatment intensified yellowness of SPI-GA biopolymer films. SPI-GA biopolymers may have potential use for biodegradable packaging materials.     

Foam-Mat Freeze Drying of Egg White—Mathematical Modeling Part II: Freeze Drying and Modeling

Foam-mat freeze drying is one of the promising methods of drying, which utilizes advantages of both freeze drying and foam-mat drying. Egg white with its excellent foaming properties makes a suitable candidate for foam-mat freeze drying. Experiments were conducted to study foam-mat freeze drying of egg white, in an effort to determine the suitability of this method. Xanthan gum (XG) at 0.125% concentration was used as stabilizer for foaming. The results showed that the addition of xanthan gum during foaming has a positive impact in reducing the total drying time and also produces excellent quality egg white powder. The addition of stabilizer also plays an important role in improving drying. Simple models were applied for determining drying time and diffusion coefficients during freeze drying.     

Foam Mat Drying of Alphonso Mango Pulp

The foam mat drying of Alphonso mango pulp using various food foaming agents, namely soy protein (0.25, 0.5, 1.0, and 1.5%) with methyl cellulose (0.5%), glycerol mono stearate (0.5, 1.0, 2.0 and 3.0%), and egg albumen (2.5, 5.0, 10 and 15%) with methyl cellulose (0.5%), was studied. Drying was carried out in a batch type thin layer dryer at four drying temperatures (60, 65, 70, and 75°C) on 1-, 2-, or 3-mm thickness foamed samples. The optimum concentrations of each foaming agent were determined to be 1% soy protein, 2% glycerol mono stearate, and 10% egg albumen. All were obtained after 25 min whipping time. The drying time was lower for foamed mango pulps as compared to non-foamed pulp at all drying temperatures. Biochemical analysis showed that the foam mat dried powder at 60°C retained a significantly higher (P < 0.05) content of biochemical compounds than at higher temperatures. The treatment of mango pulp with 10% egg albumen and 0.5% methyl cellulose and drying at 60°C (1-mm foam thickness), retained the highest nutritional quality characteristics than the other treatments.     

Dietary CLA alters yolk and tissue FA composition and hepatic histopathology of laying hens

The effect of dietary CLA along with n-3 PUFA on yolk FA profile and hepatic lipid accumulation was investigated. Laying hens (n=40) were randomly assigned to four experimental diets containing 0, 0.5, 1.0, or 2.0% CLA. Menhaden oil was used as the source of n-3 PUFA. Dietary CLA did not affect the total lipid content of egg yolk (P>0.05). The amounts of CLA isomers (cis-9 trans-11, trans-10 cis-12) in the egg yolk were proportional to the levels of CLA in the diet (P<0.05). The total CLA content in the egg yolk was 0, 0.97, 2.4, and 5.3 wt%, respectively (P<0.05). Addition of CLA resulted in an increase in saturated FA (P<0.05) with a concomitant reduction in monounsaturated FA (P<0.05) in the yolk, liver, abdominal fat, breast, and thigh muscle. No difference in saturated and monounsaturated FA content in heart and spleen tissue was noted. Dietary CLA at all concentrations resulted in an increase (P<0.05) in the total number of fat vacuoles and lipid infiltration in hepatocytes. The number of cells with 75% or higher lipid vacuolation in the cytoplasm was also increased (P<0.05) by 2.0% CLA. Dietary CLA at 0.5% levels resulted in an increase (P<0.05) in the total lipid content of hepatic tissue. The total lipid content in leg muscle was lower (P<0.05) in CLA-fed birds. However, no effect of CLA on lipid content of breast muscle, heart, spleen and adipose tissue was observed (P>0.05). The current study used CLA in a FFA form. The effects of using CLA in other form such as TG on avian hepatic tissue need to be investigated.     

Maternal dietary conjugated linoleic acid alters hepatic triacylglycerol and tissue fatty acids in hatched chicks

The effects of feeding CLA to hens on newly hatched chick hepatic and carcass lipid content, liver TAG accumulation, and FA incorporation in chick tissues such as liver, heart, brain, and adipose were studied. These tissues were selected owing to their respective roles in lipid assimilation (liver), as a major oxidation site (heart), as a site enriched with long-chain polyunsaturates for function (brain), and as a storage depot (adipose). Eggs with no, low, or high levels of CLA were produced by feeding hens a corn-soybean meal-basal diet containing 3% (w/w) corn oil (Control), 2.5% corn oil +0.5% CLA oil (CLA1), or 2% corn oil +1.0% CLA oil (CLA2). The egg yolk content of total CLA was 0.0, 1.0, and 2.6% for Control, CLA1, and CLA2, respectively (P<0.05). Maternal dietary CLA resulted in a decrease in chick carcass total fat (P<0.05). Liver tissue of CLA2 chicks had the lowest fat content (P<0.05). The liver TAG content was 8.2, 5.8, and 5.1 mg/g for Control, CLA1, and CLA2 chicks, respectively (P<0.05). The chicks hatched from CLA1 and CLA2 incorporated higher levels of cis-9,trans-11 CLA in the liver, plasma, adipose, and brain than Control (P<0.05). The content of 18∶0 was higher in the liver, plasma adipose, and brain of CLA1 and CLA2 than Control (P<0.05), but no difference was observed in the 18∶0 content of heart tissue. A significant reduction in 18∶1 was observed in the liver, plasma, adipose, heart, and brain of CLA1 and CLA2 chicks (P<0.05). DHA (22∶6n−3) was reduced in the heart and brain of CLA1 and CLA2 chicks (P<0.05). No difference was observed in carcass weight, dry matter, or ash content of chicks (P>0.05). The hatchabilities of fertile eggs were 78, 34, and 38% for Control, CLA1, and CLA2, respectively (P<0.05). The early dead chicks were higher in CLA1 and CLA2 than Control (18 and 32% compared with 9% for Control), and alive but not hatched chicks were 15 and 19% for CLA1 and CLA2, compared with 8% for Control (P<0.05). Maternal supplementation with CLA leads to a reduction in hatchability, liver TAG, and carcass total fat in newly hatched chicks.     

Compositional characteristics of protein ingredients prepared from high-sucrose/low-stachyose soybeans

High-sucrose/low-stachyose (HS/LS) soybeans contained lower total concentrations of free sugars (13.3%), less stachyose (0.7%), and more galactinol (0.7%) (galactopyranosylmyo-inositol) than the control normal soybeans (14.9, 5.1, and 0.2%, respectively). A low-fiber soybean protein concentrate (LFSPC) process was developed, which is especially suited to HS/LS soybeans, by which defatted soy flour is merely extracted with alkali to remove fiber and then neutralized and dried to produce the protein-rich soluble fraction. Two different pH values (7.5 and 8.5) were used in extracting protein, and these LFSPC were compared with traditional ethanol-washed soy protein concentrate (EWSPC) and soy protein isolate (SPI) prepared from both normal and HS/LS soybeans. The LFSPC had slightly lower yields of solids and protein (∼70 and ∼81%, respectively) than conventional FWSPC (∼77 and ∼93%, respectively) but much higher than conventional SPI (∼42 and ∼70%, respectively). The LFSPC prepared from HS/LS soybeans contained significantly (P<0.05) more protein (∼66% protein content) than LFSPC prepared from normal soybeans (∼63%). Total isoflavone contents of the LFSPC (∼12 μmol/g) were significantly higher than for EWSPC (∼1.5 ìmol/g) or SPI (∼10 μmol/g). The LFSPC prepared from HS/LS soybeans contained higher sugar contents (∼15%) than either traditional EWSPC (∼2.5%) or SPI (∼1.5%); but the sums of stachyose and raffinose were only ∼1% for the LFSPC compared with ∼1% for EWSPC and 0.5% for SPI prepared from normal soybeans.     

Proteins from Crambe abyssinica oilseed. II. Biochemical and functional properties

Little information is available concerning the properties of proteins that constitute a major component of the seed of Crambe abyssinica. Therefore, a method was developed to isolate these proteins. This procedure resulted in two fractions, an isoelectric precipitate (Fraction 1) and a retentate after ultrafiltration (Fraction 2). Biochemical and functional properties of both fractions were studied. Gel permeation chromatography revealed that high-molecular-weight proteins (>669,000 Da) are present only in Fraction 1, whereas Fraction 2 consists of proteins with lower molecular weights (<200,000 Da). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis, in the presence of mercaptoethanol, showed that both fractions consist of proteins that range mainly from 40,000 to less than 14,400 Da. Fraction 1 was highly soluble only at acid and alkaline pH values, while the solubility of Fraction 2 remained high (>80%) over the whole pH range tested. Addition of NaCl did not have any profound effect on the solubility of Fraction 2, but it increased significantly that of Fraction 1 in the isoelectric range. Foaming properties of Fraction 1 were better than those of chicken egg white only at pH 9, whereas those of Fraction 2 were superior at almost every pH value studied. Addition of NaCl improved significantly the foaming properties of Fraction 1 at all pH values tested but did not have a profound effect on the foaming properties of Fraction 2. Both fractions had good emulsifying properties only at alkaline pH values.     

Long-chain polyunsaturated fatty acids in plasma lipids of obese children

Fatty acid composition of plasma phospholipids (PL), triglycerides (TG), and sterol esters (STE) was determined by high-resolution capillary gas-liquid chromatography in 22 obese children (age: 13.7±1.4 y, body weight relative to normal weight for height: 170±24%, mean ±SD) and compared with data obtained in 25 age-matched healthy controls. There were no differences in the levels of linoleic acid (LA, C_18∶2n-6) in any of the plasma fractions from the obese children and the controls. Obese children exhibited significantly higher values of arachidonic acid (AA, C_20∶4n-6) than controls both in PL (12.6 [2.4] vs. 8.3 [1.4], % wt/wt, [median (interquartile range)],P<0.001) and STE (7.3 [1.8] vs. 6.0 [1.1],P<0.05). Similarly, obese children showed higher values than controls for dihomo-γ-linolenic acid (DHGLA, C_20∶3n-6) in PL (4.0 [0.5] vs. 3.0 [0.6],P<0.001), TG (0.4 [0.1] vs. 0.2 [0.1],P<0.001), and STE (0.9 [0.1] vs. 0.7 [0.1],P<0.01), and for γ-linolenic acid (C_18∶3n-6) in STE (1.1 [0.2] vs. 0.8 [0.2],P<0.001). The AA/LA ratios were higher in obese children than in controls in PL (0.68 [0.16] vs. 0.42 [0.09],P<0.0005) and STE (0.16 [0.04] vs. 0.12 [0.02],P<0.05), whereas the AA/DHGLA ratios were lower in TG of obese children than in controls (3.40 [0.64] vs. 5.10 [1.75],P<0.005). Plasma glucose concentrations were inversely related to AA in TG (r=0.53,P<0.05), and plasma TG concentrations were inversely related to AA in PL and STE (r=−0.49,P<0.05 andr=−0.48,P<0.05) and to the AA/DHGLA ratios in PL (r=−0.57,P<0.01),TG (r=−0.56,P<0.01) and STE (r=−0.56,P<0.01). We conclude that the significantly higher values of n-6 long-chain polyunsaturated fatty acids (LCP) in plasma lipids of obese children than in age-matched controls may be caused by an enhanced activity of Δ6-desaturation, and we speculate that elevated fasting immunoreactive insulin seen in obese children (19.4±8.0 μU/mL) may stimulate synthesis of n-6 LCP fatty acids.     

Foaming and emulsifying properties of soy protein isolate and hydrolysates in skin and hair care products

There is a growing market for formulating proteins into a wide variety of products including laundry detergents, bath products, shampoos, and skin cleansers. Soy protein isolate (SPI), soy protein hydrolysate A (SPHA) from papainmodified SPI, and hydrolysate B from papain- and proteasemodified SPI were used in blends with three major detergents, sodium dodecyl sulfate (SDS), sodium laureth sulfate (SLS), and disodium lauryl sulfosuccinate (DSLSS). SPHA was used to partially replace these detergents in bath soap, conditioning shampoo, and cream hand cleanser. The effectiveness of SPI, SPHA, or SPHB blends with the three detergents and their influence in prototype products on foaming and emulsifying properties were investigated. At a blending ratio of 75% detergents and 25% proteins (75∶25), the foaming capacities (FC) were the same as detergents alone without adding proteins (100∶0); at 50∶50 blending ratio, FC values were not significantly reduced for blends with SDS and SLS; and at 25∶75 ratio the FC values were significantly lower, especially for blends with DSLSS. When replacing up to 100% of the major detergents in the skin and hair care products with SPHA, FC values remained almost unchanged except for hand cleanser FC values, which were lower at higher protein content (75 and 100%). In contrast with FC performance, emulsion stability (ES) values for all products increased with increasing soy protein content. Furthermore, FC and ES values for detergents blended with SPHA or SPHB were not significantly different from each other, but these values were always higher than those for detergents blended with SPI. Products in which soy protein or soy protein hydrolysates were used to partially replace detergents not only retained excellent foaming properties but also exhibited enhanced emulsifying properties. These results indicate that modified soy proteins may be used in laundry and cosmetic products to fulfill market demand.     

Influence of sorghum wax,glycerin, and sorbitol on physical properties of soy protein isolate films

Sorghum wax, sorbitol, glycerin, and soy protein isolate (SPI) composite films were prepared. Effects of sorghum wax, sorbitol, and glycerin concentrations on various films were evaluated using response surface methodology. All independent variables significantly (P<0.05) affected film water vapor permeability (WVP), tensile strength (TS), elongation at break (E), total color difference, and total soluble matter (TSM). Increasing the sorghum wax concentration decreased WVP and E. As sorbitol content increased in the composite films, WVP and TS increased. Sorbitol had a critical point of 2–5 g/5 g SPI for low values of TSM. The addition of sorbitol contributed more to the properties of the film than did glycerin.     

Functional properties of protein ingredients prepared from high-sucrose/low-stachyose soybeans

High-sucrose/low-stachyose (HS/LS) soybeans were used to prepare ethanol-washed soy protein concentrate (EWSPC), soy protein isolate (SPI), and a new low-fiber soy protein concentrate (LFSPC) in which the protein was extracted with alkali to remove fiber and the protein extract was neutralized and freeze-dired. LFSPC prepared from HS/LS soybeans contained significantly higher ratios of β-conglycinin to glycinin (1∶1.32) than did EWSPC (1∶1.75) or SPI (1∶1.69), which may have affected functional properties. The LFSPC were also high in soluble sugars (14.7%) and low in fiber (0.3%) compared with traditional EWSPC (2.9 and 3.4%, respectively) and SPI (1.8 and 0.3%, respectively). For both normal and HS/LS soybean varieties, the LFSPC, especially when extracted at pH 7.5 as opposed to pH 8.5, had higher denaturation enthalpies than did EWSPC and SPI, indicating less denaturation had occurred. Water solubilities, surface hydrophobicities, and emulsification properties were highest for the LFSPC and lowest for EWSPC. The LFSPC also had good foaming properties and low viscosities. These desirable functional properties of the LFSPC make them unique among alternative soy protein ingredients and highly suitable for industrial applications as food additives and ingredients.     

Controlling water permeability of composite films of polylactide acid,cellulose, and xyloglucan

To test the hypothesis that the introduction of a hydrophilic hemicellulose would affect viscoelastic properties and increase water permeability, xyloglucan (XG) was adsorbed onto the surface of microcrystalline cellulose (MCC) in water dispersion prior to the extrusion of 79–80 wt % polylactide acid (PLA), 20 wt % MCC, and 0–1 wt % XG. For comparison, composites of PLA, MCC, and non‐absorbed XG were produced. Analysis of thermal properties showed no differences for glass‐transition or melting temperatures, but the crystallinity of the films increased with the addition of MCC and XG. Storage modulus of the composite materials increased with XG content; however, at higher humidities storage modulus decreased, probably because of lower interfacial adhesion. Water permeability through the films increased more with the addition of XG adsorbed to the MCC than with the MCC and XG simply mixed in the same amounts. © 2014 The Authors. Journal of Applied Polymer Science Published by Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41219.     

Evaluation of Variation in Protein Composition on Solubility,Emulsifying and Gelling Properties of Soybean Genotypes Synthesizing β' Subunit

The effects of subunit composition of two major proteins of soybean: glycinin (11S) and β‐conglycinin (7S) in nine different genotypes, on solubility and emulsifying and gelling properties at different pH (3, 5, 6, and 8) were examined. High‐protein genotypes (more than 40%) contained low amounts of the β′ subunit. The main factors influencing solubility at pH 6 were the content of α′, α (r = 0.89 and r = 0.91 at P < 0.05, respectively) and β′ subunit contents (r = ?0.71 at P < 0.05) of β‐conglycinin, while at pH 3 acidic subunits in glycinin had a positive correlation with solubility (r = 0.69 at P < 0.05). Emulsion activity at pH 6 was higher for genotypes synthesizing β′ subunit (r = 0.57 at P < 0.05). Genotypes synthesizing higher amounts of α′ and α subunit had higher emulsion stability at pH 6 (r = 0.85 and r = 0.92 at P < 0.05, respectively) and pH 8 (r = 0.91 and r = 0.97 at P < 0.05, respectively). The rheological measurements showed that genotypes with 11S/7S ratio higher than 2.2 formed gels with enhanced storage moduli. This influence was largely due to the high content of SH groups in glycinin acidic polypeptides resulting in stabilization of gels via disulfide bonding. Gels prepared from genotypes containing higher amounts of β′ subunit of β‐conglycinin exhibited reduced elastic properties. Genotypes showing better solubility also had higher emulsion stability, but formed weaker gels and had lower emulsion activity near neutral pH.     

Hydrophobicity, solubility, and emulsifying properties of soy protein peptides prepared by papain modification and ultrafiltration

Peptide size control is important for obtaining desirable functional properties so that these peptides can be better utilized. Proteolytic enzymatic modification of soy protein isolates (SPI), followed by ultrafiltration, is an effective way to fractionate these proteins into peptides with controlled molecular size. SPI was predenatured by mild alkali at pH 10 and heated at 50°C for 1 h prior to partial hydrolysis by papain at pH 7.0 and 38°C for 10, 30, and 60 min (PMSPI10, PMSPI30, and PMSPI60). The hydrolysate PMSPI60 was further fractionated by ultrafiltration with a stirred cell and disc membranes (100-, 50-, and 20-kDa molecular weight cut-off) into one retentate (R100) and three permeates (P100, P50, and P20). Molecular weight distribution, surface hydrophobicity (S ₀), protein solubility (PS), emulsifying activity index (EAI), and emulsion stability index (ESI) of the control SPI (without added papain), hydrolysates, and ultrafiltrates were investigated. Significant increases (P<0.001) in S ₀, PS, EAI, and ESI were observed in the hydrolysates. Peptides in the permeates had higher PS and EAI but lower S ₀ than the peptides in the retentate and hydrolysate. Soy protein peptides that were prepared from SPI by papain modification and ultrafiltration had lower molecular weight, higher solubility, and higher emulsifying properties. They could find use in products that require these properties, especially in the cosmetic and health food industries.     

Textural properties of cheese analogs containing proteolytic enzyme-modified soy protein isolates

Cheese analogs were prepared from untreated or proteolytically modified soy protein isolates (SPIs), replacing 60% of casein, to explore their potential to replace higher-priced milk proteins. Quality attributes of cheese analogs were evaluated by texture profile analysis with the Instron and melting spread. Compared with commercial milk-based cheeses, ranging from hard-type (Cheddar) to soft-type products (Mozzarella), textural properties of cheese analogs were markedly different; they were harder and more fracturable with no measurable adhesiveness. The use of enzyme-modified SPI significantly (P < 0.05) lowered both hardness and fracturability of cheese analogs and also brought about adhesiveness, all of which fell within the range observed for dairy cheeses. Although melting spread of cheese analogs was improved by the use of enzyme-modified SPI, it was still inferior to those of dairy cheeses and needed further improvement. Treatments of SPI with alcalase and trypsin were more influential in modifying textural properties of the resulting cheese analogs than those with other proteases studied.     

Effects of Extraction Temperature and Preservation Method on Functionality of Soy Protein

The effects of extraction temperature and preservation method on the functional properties of soy protein isolate (SPI) were determined. Four extraction temperatures (25, 40, 60, and 80 °C) were used to produce SPI and yields of solids and protein contents were determined. Three preservation methods were also tested (spray-drying, freeze-drying, and freezing–thawing) and compared to fresh (undried) samples for each extraction temperature. No differences in yields of solids and protein were observed among SPIs extracted at 25, 40, and 60 °C; however, SPI extracted at 80 °C yielded significantly less solids and protein. Extraction temperature significantly affected SPI functionality. As extraction temperature increased, solubility and emulsification capacity decreased; surface hydrophobicities, emulsification activities and stabilities, and dynamic viscosities increased; and foaming properties improved. Preservation method also significantly affected SPI functionality. Drying method did not affect the denaturation enthalpies of SPIs, but spray-dried SPIs had higher solubilities, surface hydrophobicities, and emulsification stabilities, and lower viscosities, emulsification activities and rates of foaming than freeze-dried SPI exhibited. Emulsification and foaming capacities and foaming stabilities were similar for both methods of drying. There was significant interaction between extraction temperature and preservation method for all functional properties except emulsification capacity.     

Protein/glycerol blends and injection‐molded bioplastic matrices: Soybean versus egg albumen

Two well‐known proteins have been selected in order to produce bioplastics through injection molding: a soy protein isolate (SPI) and an egg white albumen concentrate (EW). Each of them has been thoroughly mixed with glycerol (40 wt %) and the blend then obtained have been characterized by means of rheological and thermomechanical techniques, which allowed the optimization of the processing moulding conditions (cylinder temperature, 60°C–65°C; mould temperature, 120°C; post‐injection pressure, 500–600 bars). Once bioplastics were obtained, their thermomechanical and tensile properties, as well as their water uptake capacity and transparency were evaluated. Bioplastics containing EW showed higher values in the elastic and loss moduli, E′ and E″, from ?30°C to 130°C, than the corresponding SPI bioplastic. However, they both showed qualitatively the same evolution with temperature, where E′ and E″ decreased up to a plateau at high temperatures. When examining their tensile and water uptake properties is found that SPI bioplastics are more ductile and present enhanced water uptake behavior over EW bioplastics, which on the other hand possess higher Young's modulus. SPI seems to provide tougher bioplastics, being an excellent option for potential superabsorbent applications, whereas EW would suit for those applications requiring higher mechanical properties. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42980.     

Hepatic lipid characteristics and histopathology of laying hens fed CLA or n−3 fatty acids

The effect of dietary CLA and n−3 PUFA on hepatic TAG accumulation, histopathology, and FA incorporation in lipid classes by laying chickens was investigated. One hundred twenty 30-wk-old single-comb white leghorn laying hens were distributed randomly to four treatments (3 replications of 10 birds) and were fed diets containing CLA and animal fat (Diet I), 18∶3n−3 (Diet II), or long-chain n−3 FA (Diet III). A sunflower oil (n−6 FA)-based diet was the control. Feeding Diet I resulted in an increase in hepatic total lipids (P<0.05). The liver TAG content was 32.2, 18.9, 29.4, and 18.7 mg/g for hens fed Diet I, Diet II, Diet III, and the control diet, respectively (P<0.05). The serum TAG was lowest in bilds fed Diet II (P<0.05). Diet I resulted in an increase in the total number of fat vacuoles and lipid infiltration in hepatocytes (P<0.05). The number of cells with 75% or higher lipid vacuolation was observed only in birds fed Diet I. Feeding diets containing CLA resulted in an increase in the content of the c9,t11 CLA isomer in liver TAG and PC (P<0.05). No difference was observed in the CLA concentration of hepatic PE fractions. The content of DHA (22∶6n−3) was higher in the TAG, PC, and PE of hens fed Diet II and Diet III than Diet I and the control (P<0.05). Feeding CLA resulted in an increase in total saturated FA in the TAG and PC fractions (P<0.05). Long-term feeding of CLA in laying birds leads to an increase in liver TAG and may predispose birds to fatty liver hemorrhagic syndrome.     

Preparation of soy protein concentrate and isolate from extruded-expelled soybean meals

Soy protein concentrates (SPC) and soy protein isolates (SPI) were produced from hexane-defatted soy white flakes and from two extruded-expelled (EE) soy protein meals with different degrees of protein denaturation. Processing characteristics, such as yield and protein content, and the key protein functional properties of the products were investigated. Both acid-and alcohol-washed SPC from the two EE meals had higher yields but lower protein contents than that from white flakes. Generally, SPC from an acid wash had much better functional properties than those from an alcohol wash. The SPI yield was highly proportional to the protein dispersibility index (PDI) of the starting material, so the EE meal with lower PDI had lower SPI recovery. The protein content in SPI prepared from EE meals was about 80%, which was lower than from white flakes. Nevertheless, SPI from EE meals showed functional properties similar to or better than those from white flakes. The low protein contents in SPC and SPI made from EE meals were mainly due to the presence of residual oil in the final products. SPI made from EE meals had higher concentration of glycinin relative to β-conglycinin than that from white flakes.