Bioactive properties of enzymatic hydrolysates from abdominal skin gelatin of yellowfin tuna (Thunnus albacares)

Gelatin (90.6 ± 0.1%) was optimally prepared by response surface methodology from yellowfin tuna (Thunnus albacares, YT) abdominal skin. To investigate bioactive properties of enzymatic hydrolysates from the abdominal skin gelatin (ASG), ASG was hydrolysed with alcalase, protamex, neutrase and flavourzyme as affected by hydrolysis time. Antioxidant, nitrite scavenging and angiotensin‐I converting enzyme (ACE) inhibitory activities of the hydrolysates were determined. Antioxidant activities of the hydrolysates were found through linoleic acid peroxidation inhibitory effects. Alcalase‐derived hydrolysates (AHs) were more effective than others in metal ions chelating, superoxide anion scavenging and hydroxyl radical scavenging activities (P < 0.05). AHs showed significantly stronger nitrite scavenging activities (44.4–60.7%) than others (P < 0.05). Fraction A from AH showed strong ACE inhibitory activity (IC₅₀ of 0.75 mg mL^?1). These results suggest that YT ASG and its enzymatic hydrolysates could be functional food and/or pharmaceutical ingredients with potent antioxidant, anticarcinogenic and antihypertensive benefits.     

PTR-TOF-MS Analysis for Influence of Milk Base Supplementation on Texture and Headspace Concentration of Endogenous Volatile Compounds in Yogurt

In the present study, the effects of milk fat (0.3% and 3.5% w/w), solids non-fat (8.4% and 13% w/w), and modified tapioca starch (0%, 0.5%, 1.0%, 1.5%, and 2.0% w/w) concentrations on the textural and physicochemical properties as well as the concentration of several endogenous flavor compounds in the headspace of set and stirred yogurts were investigated. The novel proton transfer reaction time-of-flight mass spectrometry technique was implemented for the non-invasive determination of the amounts of volatile organic compounds in the samples headspace. Milk fat and skim milk powder supplementation of the milk samples increased significantly the firmness and adhesiveness of yogurts (p < 0.001) and improved the stability of the formed gels by increasing their water holding capacity and reducing the amounts of expulsed whey (3.94 and 5.1 g for the milk fat and SNF-fortified samples). Acetaldehyde was significantly (p < 0.001) higher in the low fat-unfortified systems (6.15 ± 0.48 and 5.6 ± 0.60 ppmv, respectively). A similar trend was also reported in the case of 2-propanone (0.91 ± 0.11 and 1.13 ± 0.07 ppmv), diacetyl (334 ± 37 and 350 ± 34 ppbv), 2,3-pentanedione (54 ± 6 and 55 ± 6 ppbv), and 2-butanone (56 ± 7 and 68 ± 5 ppbv) for the same systems. In contrast, the concentration of flavor compounds in the headspace with hydroxyl groups (ethanol and acetoin) increased (p < 0.001) by solid non-fat fortification of milk base (350 ± 32 and 206 ± 7 ppbv, respectively, for the systems fortified with skim milk powder). Modified tapioca starch addition improved the textural properties and gel stability of yogurts whereas affected only the ethanol concentration (222 ± 16 and 322 ± 55 for the control and 2.0% w/w containing systems, respectively). Our data suggested that the reinforcement of textural and structural properties combined with the protein binding affinity of the flavor compounds seemed to be responsible for the aforementioned observations. In the case of stirred yogurts, the gel breakdown did not provoke significant changes in the headspace concentration of the most compounds, with the exception of ethanol, acetoin, and 2,3-pentanedione being significantly (p < 0.05) higher in the stirred yogurts (267 ± 29, 153 ± 11, and 38 ± 1 ppbv, respectively) than set style ones (232 ± 19, 134 ± 9, and 45 ± 3 ppbv, respectively).     

Effects of Lactic and Acetic Acid on Survival of Salmonella enteritidis During Refrigerated and Frozen Storage of Chicken Meats

Chicken leg and breast meat samples inoculated with Salmonella enteritidis [4–5 log most probable number (MPN)/cm²] were dipped into lactic acid (LA; 1% and 3%) and acetic acid (AA; 1% and 2%) solutions for 10 min. After packaging, samples were stored at 4 °C (10 days) or −18 °C (6 months). Immediately after dipping into 1% LA, 3% LA, 1% AA, and 2% AA solutions, S. enteritidis counts on leg meat samples were reduced by 0.75, 1.21, 0.85, and 0.95 log MPN/cm², while the reductions were 0.97, 1.72, 0.92, and 1.58 log MPN/cm² on breast meat samples, respectively. The differences between the water-washed control and the acid-treated groups for Salmonella counts were statistically significant (P < 0.05). Salmonella counts on leg meat samples treated with 1% LA, 1% AA, and 2% AA were reduced by 0.54–1.52 log MPN/cm² (P < 0.05) during storage at 4 °C. However, for the breast meat samples, only Salmonella counts of water-washed controls were significantly reduced during refrigerated storage (P < 0.05). S. enteritidis counts on organic acid-treated samples were reduced by 0.13–0.55 log MPN/cm² during storage at −18 °C for 6 months, while the reduction on the water-washed controls was 0.64 log MPN/cm². It can be concluded that lactic or acetic acid treatment could be useful especially for reducing the initial Salmonella contamination. On the other hand, this pathogen could survive on poultry meats during refrigerated and frozen storage even following lactic or acetic acid decontamination.     

Evaluation of free radical‐scavenging activities of sweet potato protein and its hydrolysates as affected by single and combination of enzyme systems

To evaluate the free radical‐scavenging activities of sweet potato protein (SPP) and its hydrolysates, single enzymes alone (alcalase, neutrase, protamex) or in combination with flavourzyme were employed. Compared with SPP, free radical‐scavenging activities of the resulting hydrolysates were all significantly increased (P < 0.05). Alcalase (ALC) hydrolysates exhibited the highest superoxide, hydroxyl and 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical‐scavenging activities (P < 0.05), which was 18.71 ± 0.22, 27.13 ± 0.24 and 90.10 ± 0.15% respectively. Compared with SPP hydrolysates by single enzymes, the hydrolysates obtained by combination of enzyme systems exhibited higher degree of hydrolysis, but lower free radicals scavenging activities. In addition, the content of several antioxidant amino acid residues, such as His, Met, Tyr and Phe, in ALC hydrolysates was much higher compared with SPP and other hydrolysates using amino acids composition assay. The results suggested that peptides with free radical‐scavenging activity could be released from entire SPP chain via moderate enzymatic hydrolysis.     

Effects of Soy and Corn Flour Addition on Batter Rheology and Quality of Deep Fat-Fried Shrimp Nuggets

In this paper, the effects of soy and corn flour (5 and 10% w/w) addition to the batter formulation on the quality of deep fat-fried shrimp nuggets were evaluated. Rheological properties of batters, coating pick-up, moisture content, and oil content of the samples were determined. Shrimp nuggets were fried at 150 °C, 170 °C, 190 °C, for 1, 2, 3, 4, and 5 min. The coating pick-up, oil and moisture content were found to be directly proportional to batter viscosity. All batters were found to show shear thinning behavior by exhibiting flow behavior index ≤ 1. The batters were modeled as power law fluids. Batter formulation, frying time, and temperature significantly (p < 0.01) affected moisture and oil content of shrimp nuggets. Soy flour added batters provided the highest consistency index, 7.595 and 10.635 Pa.sⁿ for 5% and 10% soy flour added, respectively. Soy flour was found to be an effective ingredient in decreasing oil content of fried nuggets. Batters containing 5% corn flour showed the lowest moisture content and the highest oil content among all the formulations. The mean moisture and fat content of shrimp nuggets coated with batter contained 10% soy and 5% corn flour, fried at 190 °C, for 5 min were 0.59 ± 0.022, 0.480 ± 0.029 and 0.149 ± 0.035, 0.346 ± 0.024 (g/g db), respectively.     

Co-production of Lactic Acid and <Emphasis Type="Italic">Lactobacillus rhamnosus</Emphasis> Cells from Whey Permeate with Nutrient Supplements

Lactic acid and cell production from whey permeate by Lactobacillus rhamnosus with different nutrient supplements were investigated in this study. Yeast extract was identified as the most effective nutrient affecting lactic acid production. Increase in inoculum size from 0.05% to 1% (v/v) resulted in a substantial increase in lactic acid productivity from 0.66 to 0.83 g L⁻¹ h⁻¹ (P < 0.001). The optimal temperature for lactic acid production was 37 °C, while the highest cell production was obtained at 42 °C. When whey permeate and yeast extract concentrations were 6.8% (w/v) and 3 g L⁻¹, respectively, lactic acid productivity reached 0.85 g L⁻¹ h⁻¹ after 48-h cultivation, which is 3.40 times of those without nutrient supplements.     

Comparison of Physicochemical and Antioxidant Properties of Egg-White Proteins and Fructose and Inulin Maillard Reaction Products

The Maillard reaction (MR), involving the condensation of a carbonyl group of reducing sugar and an amino group of protein, can change functional properties of proteins. In this study, chemical characteristics and functional properties of glycosylated albumin, ovomucoid, and lysozyme (egg proteins) and casein with fructose or inulin through the MR were evaluated. The protein and sugar mixtures were heated at 60 °C and 79% relative humidity for 3 days. Chemical characteristics of the egg protein–sugar Maillard reaction product (MRP) mixtures were evaluated by fluorescence development, absorbance intensity (at 420 nm), and color change. Functional properties of the protein–sugar MRP mixtures were also evaluated, including emulsifying activity, emulsion stability, and antioxidant activity. The protein–sugar conjugates were found to have significant (p < 0.05) changes compared to the controls (unheated protein–sugar samples) in color, fluorescence, and absorbance intensity. All protein–sugar MR models exhibited a change in emulsifying activity, with Csn–Fru MRP displaying the greatest significant (p < 0.05) improvement. In addition, all protein–sugar MR models exhibited changes in emulsion stability, with Ovo/Inu MRP displaying the greatest significant (p < 0.05) change. All protein–sugar MR models exhibited great scavenging activity towards 1,1-diphenyl-2-picryl-hydrazyl radical at MRP concentrations of 0.2, 0.5, and 1.0 mg/mL. With the exception of the 0.2 mg/mL MRP concentration, there was a significant difference (p < 0.05) between the heated protein–fructose and the heated protein–inulin MRPs.     

双酶水解菜籽粕及水解物的抗氧化活性研究

中性蛋白酶分别与alcalase,protamex,flavourzyme,木瓜蛋白酶及胰蛋白酶相结合,用双酶相继水解菜籽粕,得到5组菜籽粕的双酶水解物。双酶水解物抗氧化活性试验结果表明,所有水解物都具有一定清除DPPH自由基活性的能力、还原能力和抑制亚油酸氧化活性的能力,但以中性蛋白酶和胰蛋白酶组合的水解物最强。该水解物的凝胶层析分离结果表明,4组分离物中分子量为6500-1050Da的组分清除DPPH自由基的活性最高,显示菜籽粕双酶水解物的抗氧化活性取决于水解物的分子结构,即不仅与酶的种类有关,还与水解条件和水解度有关。     

Antilisterial Peptides Released by Enzymatic Hydrolysis from Grass Carp Proteins and Activity on Controlling L. monocytogenes Inoculated in Surimi Noodle

The primary objective of this study was to prepare the antilisterial peptides by enzymatic (pepsin, trypsin, protamex, neutrase, flavourzyme, papain, alcalase, and acid protease) hydrolysis of grass carp proteins with various degree of hydrolysis. The second objective was to evaluate the antilisterial activity of grass carp proteins hydrolysates (GCPH) at differnet levels in the surimi noodle samples with or without boiling treatment inoculated with 10⁴ CFU/g of Listeria monocytogenes for storage at 4 and 25 °C up to 20 d. These results revealed that GCPH, obtained by treatment with the neutrase hydrolysates at degree of hydrolysis of 19% (NSH19), showed the highest antilisterial activity reaching up to 64.8% inhibition of bacterial growth. The antilisterial activity of NSH19 in the raw surimi noodle was stronger than that of the boiled group, and the samples treated by NSH19 at 10 g/100 g level had no‐detectable numbers of L. monocytogenes for both raw and boiled noodle samples within 20 d of storage at 4 and 25 °C. The results of this study indicated that antilisterial peptides generated via neutrase from grass carp proteins can efficiently inhibit the growth of L. monocytogenes in surimi noodle, which was useful as natural preservatives for storage and distribution of meat based products.     

Kinetics Modeling of Mass Transfer Using Peleg’s Equation During Osmotic Dehydration of Seedless Guava (<Emphasis Type="Italic">Psidium guajava</Emphasis> L.): Effect of Process Parameters

Peleg’s equation was used to study the effect of process parameters on kinetics of mass transfer in terms of solids gain and water loss during osmotic dehydration using 30–50% (w/w) sucrose solution at 30, 40 and 50 °C. The experimental data were successfully fitted employing Peleg’s equation with the coefficient of determination (R ²) higher than 0.88, the root mean square error, and the mean relative percentage deviation modulus (E) of less than 0.003% and 6.40% for all treatments, respectively. In all cases, initial mass transfer rate parameter (K ₁) decreased significantly (p < 0.05) as the solution concentration and solution temperature increased suggesting a corresponding increase in the initial mass transfer rate. Initial mass transfer rate followed an Arrhenius relationship which showed that solids gain had the highest temperature sensitivity (E _a = 21.93–33.84 kJ mol⁻¹) during osmotic dehydration. Equilibrium mass transfer parameter (K ₂) decreased significantly (p < 0.05) as solution concentration increased demonstrating that the equilibrium solid and water contents increased with increase in solution concentration. The equilibrium solid and water contents were also estimated adequately using Peleg’s equation (R ² > 0.78). The results of this work allow estimating the kinetics of mass transfer during osmotic dehydration in order to obtain products with determined solid and water contents.     

Microencapsulation of enzymes for potential application in acceleration of cheese ripening

An encapsulation efficiency of 70% was achieved when flavourzyme was encapsulated in selected polymers and gelled in 0.1 m CaCl₂ containing 0.1% (w/v) chitosan. Enzyme retention in capsules did not increase with alginate concentration or with coating of capsules with 0.15% (w/v) alginate or 0.05% (w/v) poly l-lysine. Gelling duration of 10 min was found to be optimum, while 2.0% trisodium citrate was necessary for efficient release of encapsulated flavourzyme. During 10-week storage after freeze-drying and freezing, about 80% retention of enzyme activity was noted in flavourzyme capsules with or without poly l-lysine coating, while air-dried capsules retained about 53% activity and 32% on coating with poly l-lysine over 10 weeks. Flavourzyme leakage from capsules increased with an increase in the duration of the simulated cheese press from 4 to 16 h. Capsule addition before rennetting resulted in an even distribution compared with capsule addition before salting.     

Quality Evaluation of an Ohmically Cooked Ham Product

Selected parameters (cooking loss, instrumental colour and texture and sensory quality) of a brine-injected pork muscle cooked by a novel and rapid ohmic cooking protocol were examined and compared with those obtained in conventionally cooked samples. Ohmic samples were cooked using either a low-temperature long-time (LTLT) protocol (2 min equilibration, 5 min ohmic heating to 70 °C, 8 min holding) or a high-temperature short-time (HTST) procedure (2 min equilibration, 6 min ohmic heating to 95 °C) performed within a hot air cabinet set at 80 °C (LTLT) and 100 °C (HTST). Conventional cooking (steam oven at 80 °C for 120 min) was conducted to a core temperature of 70 °C. The LTLT treatment gave a much lower cooking loss value (4–5% lower, p < 0.05) than the other treatments, though the full magnitude of this difference was not completely reflected in the proximate composition of the cooked products. Ohmically cooked ham showed a significantly (p < 0.05) lighter surface colour with Hunter L values of 65.3 (LTLT) and 63.5 (HTST) relative to the control (61.4). Texture profile analysis (TPA) indicated a significant difference (p < 0.05) in hardness (N) especially between the HTST surface (82.1 N) and the conventional centre (58.8 N). Although the ohmic cooking protocols yielded products with quite acceptable eating qualities, sensory evaluation found the overall quality of the conventionally cooked ham to be significantly (p < 0.05) superior, indicating that further optimisation of the ohmic cooking protocols would be required prior to any commercial adoption.     

Optimization of supercritical CO2 extraction of phytosterol-enriched oil from Kalahari melon seeds

Supercritical carbon dioxide (SC-CO₂) extraction of oil from Kalahari melon seeds was investigated in this study. Response surface methodology was applied to model and optimize the extraction, namely pressure (200–400 bar), temperature (40–80 °C), and supercritical fluid flow rate (10–20 mL/min). Well-fitting models were successfully established for oil recovery (R ² = 0.9672) and phytosterol concentration (milligrams per 100 g; R ² = 0.8150) through multiple linear regressions with backward elimination. The effect of supercritical fluid flow rate was the most significant (P < 0.05) factor that affected oil recovery but this factor had no significant (P > 0.05) effect on phytosterol concentration. The optimal processing conditions for oil recovery and phytosterol concentration were pressure of 300 bar, temperature at 40 °C, and supercritical fluid flow rate of 12 mL/min. These optimal conditions yielded a 76.3% oil recovery and 836.5 mg/100 g of phytosterol concentration. The oil content in the Kalahari melon seeds as estimated by Soxhlet extraction was around 30.5/100 g. The phytosterol concentration in the oil extracted with SC-CO₂ extraction was 94% higher than that obtained with solvent extraction.     

Optimization of Conditions for Enzymatic Production of ACE Inhibitory Peptides from Collagen

Enzymatic condition for producing angiotensin I-converting enzyme (ACE) inhibitory peptides from collagen was optimized with the aid of response surface methodology, which also derived a statistical model for experimental validation. The results showed that the optimal condition for the hydrolysis by pepsin was at pH 2, temperature 37 °C, and in enzyme to substrate ratio (E/S) of 2 when 8.23% collagen (w/v) and 3.82 h of hydrolysis time were applied. Through the single-enzyme hydrolysis, the ACE inhibitory activity could reach an average of 78.06%. In contrast, when a combination of pepsin and trypsin was used for a multiple-proteases hydrolysis, the ACE inhibitory activity could be significantly improved to an average of 88.25%. Furthermore, the IC₅₀ (μg/mL) value of the enzyme combination by pepsin and trypsin (141.64 ± 22.11) was significantly lower than that of the combinations of pepsin and papain (438.59 ± 84.37) or pepsin and protease M (336.76 ± 87.88; p<0.05). Our results have shown that collagen can be used for enzyme-mediated production of ACE inhibitory peptides.     

Direct Determination of Molybdenum in Milk and Infant Food Samples Using Slurry Sampling and Graphite Furnace Atomic Absorption Spectrometry

A fast and efficient method to determine molybdenum, Mo, in milk and other infant food by atomic absorption spectrometry with electrothermal atomization employing slurry sampling was developed. Slurries were prepared in ultrapure water with 5 to 20 min of sonication in concentrations of 10% w/v. The injection of 5.0 μL of a 0.1% (v/v) cetyl trimethyl ammonium chloride solution before the temperature program reduced the effect of build-up of carbonaceous residues within the atomizer. Europium (chemical modifier) and niobium (permanent modifier) were chosen for use from several potential modifiers. The parameters of merit were obtained in the optimized conditions T _a  =  2,700 oC, T _p  = 2,000 oC, tp = 20 s, and Eu 5.0 μg + permanent Nb 500.0 μg. These parameters were linear working range up to 100.0 μg/L, limit of detection (1.1 ± 0.1) μg/L, aqueous calibration, and standard addition curves with r ² > 0.9900 and relative standard deviation of 0.6% to 8.7%. The accuracy was evaluated by recovery tests and by certified material analysis; the agreement among these numbers validated the method. The powdered sample concentrations were between 39 and 1,570 μg/kg.     

Structural Relaxation of Salmon Gelatin Films in the Glassy State

Mechanical relaxation of glassy carbohydrates has been reported extensively in the literature; however, little work is available on protein-based systems. This study deals with the structural relaxation of salmon (Salmo salar) gelatin in the glassy state. Skin gelatin was obtained by an acid–alkaline extraction method. Molecular weight (M _w) was determined by capillary viscometry. Films prepared by casting (7% w/v) were equilibrated to a moisture content of ~18.4% (db). The glass transition temperature (T _g) and enthalpic relaxation were determined by differential scanning calorimetry (DSC). Mechanical properties were assessed using a texture analyzer at constant temperature and moisture content. DSC showed a T _g ~34°C, and the selected storage temperature (T _a ) was 29°C (T _g − T _a = 5°C). The films were aged for 0, 4, 8, 16, and 40 h. Viscometry produced values of M _w ~90.2 kDa. The stress relaxation was modeled by the Kohlrausch–Wlliams–Watts (KWW) equation, reporting an increase in relaxation time (τ ₀) as the ageing time increased (τ ₀ ~6.41E + 03 s for 0 h; τ ₀ ~9.01E + 05 s for 40 h). β parameter was smaller for the aged films, indicating a spread of relaxation times. The derivative of KWW equation (dφ/dt) indicated a more rapid relaxation in a fresh sample compared with aged films. DSC showed an excess in enthalpy (ΔH) on the aged samples due to the non-equilibrium state of the matrix. ΔH increased with ageing time with values of ΔH ~2.42 J/g for the films aged for 40 h. This work demonstrated molecular relaxation process of gelatin in the glassy state, which must be taken into account if this material is used as a structure forming matrix.     

Physicochemical Properties of Caribbean Sweet Potato (Ipomoea batatas (L) Lam) Starches

The proximate compositions and physicochemical properties of 21 Caribbean sweet potato (Ipomoea batatas (L) Lam) starches were investigated. Proximate composition, amylose, reducing and non-reducing sugars were determined using standard methods. Swelling power and solubility were evaluated and pasting properties of the starches were determined using Rapid Visco Analyzer. Moisture (8.0–12.4%), protein (0.0–0.2%), ash (0.1–0.5%), and reducing (0.3–2.3%) and non-reducing sugar (0.1–0.2%) contents of starches were significantly different (P < 0.05) among the cultivars. Amylose content varied significantly between 12.8–21.3%. Swelling power and solubility ranged between 7.8–31.1% and 1.5–9.6%, respectively. Pasting properties such as peak viscosity measured in Rapid Visco Units (143.2–288.8 RVU), breakdown viscosity (29.4–162.6 RVU), and setback viscosity (15.0–78.8 RVU), pasting temperature (73.5–87.7 °C) and time to pasting temperature (3.6–4.5 min) varied significantly among the cultivars. Breakdown viscosity was poorly correlated with final viscosity attained (r = − 0.0507, P < 0.05); however, pasting temperature was correlated (r = 0.479, P < 0.05) with setback viscosity. The variability observed in the physicochemical properties of the starches was related to specific requirements for use in the production of noodles, pasta, and inclusion in bread and weaning food formulations.     

Detection of Raw Pork Targeting Porcine-Specific Mitochondrial Cytochrome B Gene by Molecular Beacon Probe Real-Time Polymerase Chain Reaction

Pork identification in raw meat using real-time polymerase chain reaction (PCR) was developed. Total DNA from meat samples were successfully extracted and found to be of high quality and produced clear PCR products. Porcine-specific molecular beacon probe and primers that amplifies 119 bp of the cytochrome b gene fragment of swine (Sus scrofa domestica) was used. Analysis of data showed that the C _q (quantification cycle) from 10 ng/μl porcine DNA is (18.70 ± 0.12 to 19.08 ± 0.06). Meanwhile, the other samples exhibited negative result, which confirmed the specificity of the primers. The method also showed that the limit of detection of pork was 0.0001 ng. Based on the regression analysis of the standard curve, the 96% efficiency of real-time PCR was achieved with high correlation coefficient (r ² = 0.9989). Sensitivity of the assay in discriminating pork as low as 0.1% (w/w) pork in pork–beef mixtures was also obtained. Reproducibility of the assay was successfully validated by applying sample and experimental replicates in every assay being conducted. Thus, this methodology could serve as a fast and sensitive method for detection of pork for meat species verification.     

Effect of salting processes on chemical composition,textural properties and microstructure of duck egg

BACKGROUND: Salted eggs have been produced in Thailand and consumed nationwide. Salted egg can be made by brining eggs in saturated saline or by coating the egg with soil paste mixed with salt. The achievement of salting is generally indicated by the textural development of egg yolk. Yolk property is therefore a prime factor governing consumer acceptability and market demand. The objective of this study was to determine chemical composition, textural properties and microstructure of duck egg obtained from the coating and immersing methods at different salting times. RESULTS: Decreases in moisture content with coincidental increases in salt content in both egg white and yolk were observed during salting, regardless of salting process. However, no difference in salt content was noticeable in yolks (P > 0.05). The paste coating method tended to yield greater oil exudation of egg yolk than the immersing method. Maximum transition temperature (T_max) of egg proteins and thiobarbituric acid‐reactive substance (TBARS) value in yolk increased with increasing salting time. A similar hardening ratio of yolk was observed in both processes. Higher hardness and adhesiveness were found in yolk with the paste coating method, whereas greater fracturability, springiness, gumminess and chewiness were observed with the immersing method. Nevertheless, both processes rendered the yolk with similar cohesiveness. Yolk granules were aligned closely when salting proceeded, irrespective of salting process. CONCLUSION: Dehydration and release of lipids in egg yolk increased with increasing salting time and were more pronounced with the paste coating method. Therefore salting processes affected the properties of salted eggs. Copyright © 2009 Society of Chemical Industry