Effect of dry heat stabilisation on the functional properties of rice bran proteins

Rice bran was stabilised by dry heat method at 120 °C for 10–60 min, and then, protein was extracted from stabilised rice bran using weak alkali method. The storage characteristics of stabilised rice bran and the influences of dry heat pretreatment on the physicochemical properties of rice bran protein isolate were also evaluated. The results indicated that dry heat pretreatment could not only prevent rancidity of rice bran effectively, but also improve some functional properties of rice bran proteins, such as emulsifying properties, oil holding capacity, and water holding capacity. However, foaming properties and protein solubility were slightly destroyed because of heating. Rice bran was pretreated at 120 °C for 10 or 20 min and then extracted at pH 9.5, and the protein yields were 50.09% and 46.98%, respectively. Therefore, the dry heat treatment at 120 °C for 10 or 20 min was a suitable alternative process in stabilisation of rice bran.     

Production of functional substances from black rice bran by its treatment in subcritical water

Black rice bran was treated by water and subcritical water at temperatures ranging from 20 to 260 °C for 5 min and at 200 and 260 °C for 5-120 min. The bran extracts were analyzed for their radical scavenging activity, protein and carbohydrate contents, molecular-mass distribution, antioxidation activity, emulsifying activity, and emulsion-stabilizing activity. The radical scavenging activity and the protein content of the extract were higher at higher treatment temperature. The carbohydrate content also increased with increasing temperature up to 200 °C, then steeply decreased at the temperatures higher than 200 °C. The bran extracts treated at 260 °C for 5 min exhibited a suppressive activity toward autoxidation of linoleic acid with the increasing the weight ratio of the bran extract to linoleic acid. The bran extracts prepared at 40-200 °C for 5 min showed the emulsifying- and emulsion-stabilizing activities, while the extracts prepared at 220-260 °C were low in the activities.     

Design of a batch Ohmic heater and evaluating the influence of different treatment conditions on quality attributes of kinnow (Citrus nobilis × Citrus deliciosa) juice

A batch Ohmic heater (5 L) with a modified electrode arrangement was designed for quick and uniform heating of kinnow juice. A T-shaped arrangement and micro silver coating over stainless steel electrodes provided temperature variation of 0–2 °C across the system and a system performance coefficient of 0.96. The come-up time for 60–80 °C was 1.3–3 min at 180 V. Pectin methylesterase, the most resistant enzyme, was inactivated completely at (120 V/80 °C/1 min), (150 V/80 °C/30 s), (180 V/70 °C/10 s). No aerobic mesophiles, yeasts, and moulds were detected in these samples. Ohmic heating at 180 V did not influence the colour of the juice significantly; however, some samples showed a little elevation (by 0.2) in the pH. The reduction in vitamin C, antioxidants, and total phenols was 6–12% at 150 V/80 °C/30 s. The fuzzy analysis shows that the Ohmic pasteurized juice had the highest similarity score.Industrial relevancesA batch assembly (5 L capacity) of the Ohmic heater has been fabricated to make a shelf-stable kinnow juice. The produced juice is microbially safe, enzymatically stable, and retains maximum bioactive compared to conventional thermal treatment. Thus, Ohmic heated juice can fulfill the stakeholders' demand for microbial safety, enzymatic stability, and nutritional superiority. Industry can scale up the design of batch Ohmic heater for efficient and faster pasteurization of citrus juice like kinnow juice.     

5-Hydroxymethylfurfural (HMF) formation during subcritical water extraction

The aim of this study was to investigate the effect of material type (artichoke leave, lemon peel, flaxseed meal), extraction temperature (50, 100, 120, 140, 160, 180, 200 °C) and static extraction time (5, 15, 30, 45 min) on 5-hydroxymethylfurfural (5-HMF) formation during subcritical water extraction. 5-HMF content of artichoke leave and lemon peel extracts increased 7.2 and 26.1 times with the rise of extraction temperature from 160 to 180 °C for 5 min during subcritical water extraction, respectively. Besides, 5-HMF content of artichoke leave, lemon peel and flaxseed meal extracts increased 1.4, 2.0 and 4.5 times as static extraction time increased from 15 to 45 min at 180 °C during subcritical water extraction, respectively. The highest 5-HMF content of artichoke leave and lemon peel extracts were obtained as 58.83 and 231.21 mg/L at 180 °C and 45 min, respectively. However, for flaxseed meal, the highest 5-HMF content (222.94 mg/L) was obtained at 200 °C and 15 min during subcritical water extraction.     

Effect of microbial transglutaminase and setting condition on gel properties of blend fish protein isolate recovered by alkaline solubilisation/isoelectric precipitation

The effect of microbial transglutaminase (M-TGase) (0–0.6 units g⁻¹ sample) and setting condition (25 °C/180 min, 30 °C/120 min, 35 °C/60 min and 40 °C/30 min) on gel properties of blend protein isolate of gutted kilka and silver carp was studied. The protein isolate provided a good substrate for M-TGase activity so that a low amount of M-TGase (0.2 unit g⁻¹ sample) substantially improved textural properties and water holding capacity (WHC) of the gels. Breaking force of the gels was positively affected by M-TGase up to 0.6 unit g⁻¹ sample, but it negatively affected their WHC. Prior setting at 25–35 °C increased the breaking force of proteins compared to directly heated gel, resulting in maximum breaking force at 35 °C/60 min. However, the setting at 40 °C/30 min caused proteolysis, which was reflected in higher amounts of TCA-soluble peptides and gel weakening. Denser microstructure and higher myosin heavy chain polymerisation observed in the gels which experienced the setting was well correlated with improvement in textural properties.     

Frying oils with lower levels of saturated fatty acids induce less heterocyclic amine formation in meat floss (boiled,shredded and fried pork)

Heterocyclic amines (HAs) as potent mutagens are formed in meat floss which is a boiled, shredded and fried traditional meat product. In this study, effects of frying oils (lard, soybean oil and palm oil) on the formation of HAs in meat floss during frying have been investigated. The results showed that the contents of Norharman, Harman, AαC and MeAαC in meat floss that treated with lard and palm oil were higher than soybean oil which contained less saturated fatty acids (P < 0.05). The contents of total HAs in meat floss that treated with palm oil at 150 °C and 180 °C were significantly higher than that treated with soybean oil and lard (P < 0.05). In conclusion, meat floss treated with soybean oil at 120 °C, 150 °C and 180 °C contained lowest levels of HAs and soybean oil could be used as lard substitution to produce healthy meat floss.     

Compositions,flavour and antiradical properties of products from subcritical water treatment of raw Isada krill

Comparative analysis of subcritical water (SCW) treatment and ambient pressure boiling one of raw Isada krill was performed for the nutritive, flavour and antiradical properties of krill extracts and residues as well as the molecular mass and odour intensity of the extract. SCW treatment was performed for 10 min in a batch‐type vessel in the temperature range of 100–240 °C, using a 1:1 weight ratio of raw krill to water. Higher protein and lipid contents were obtained by SCW treatment relative to boiling. The lipid content of the SCW extracts increased with increasing treatment temperature. Protein was the main component in these extracts, and the highest protein content was achieved by SCW treatment at 200 °C. High‐molecular‐mass species decomposed under SCW treatment at high temperatures with consequent generation of smaller molecules. The antiradical activity of the SCW extract, determined by DPPH and ABTS assays, increased with increasing treatment temperature. The krill extracts and residues exhibited shrimp‐like flavour, and the most desirable flavour was obtained by SCW treatment at 140 °C or 160 °C for 10 min. The treatment would be applicable for the production of seasonings from Isada krill.     

Protective effect of rutin against ultraviolet b-induced cyclooxygenase-2 expression in mouse epidermal cells

Rice bran was heated at 120°C for 0 to 30 min to extend the oxidative stability. Also, effects of visible light irradiation on the crude rice bran oil (RBO) from rice bran heated at 120°C for 20 min were studied. As heat treatment time increased from 0 to 30 min, rice bran had significantly high oxidative stability at 40°C for 12 days (p<0.05). Headspace oxygen content in rice bran without heat treatment decreased significantly (p<0.05) whereas those in heat treated rice bran did not change significantly (p>0.05). Results of acid value and conjugated dienoic acid (CDA) confirmed the higher oxidative stability of heat treated rice bran. γ-Oryzanol content was not significantly different among crude RBO during heat treatment and storage (p>0.05). Visible light irradiation caused similar degree of lipid oxidation in crude RBOs from rice bran irrespective of heat stabilization for 48 h, which may be due to the presence of photosensitizers in crude RBO like chlorophylls. This study showed that heat treatment was not effective to enhance the oxidative stability of RBO under visible light irradiation and products containing rice bran should be stored in the dark conditions.     

Effect of high hydrostatic pressure and high-pressure homogenisation on <Emphasis Type="Italic">Lactobacillus plantarum</Emphasis> inactivation kinetics and quality parameters of mandarin juice

The inactivation kinetics of Lactobacillus plantarum in a mandarin juice treated by thermal treatment (45–90 °C), high-pressure homogenisation (HPH) (30–120 MPa at 15 and 30 °C) and high-pressure processing (HPP) (150–450 MPa at 15, 30 and 45 °C) were fitted to different Weibullian equations. A synergic effect between pressure and temperature was observed in HPH and HPP treatments achieving 2.38 log cycles after 120 MPa at 30 °C for 10 s (final T of 45 °C) and 6.12 log cycles after 400 MPa at 45 °C for 1 min (final T of 60 °C), respectively. A combined treatment of 100 MPa at 15 °C for 10 s and 300 MPa at 15–30 °C for 1 min in HPH and HPP, respectively, was needed to the first logarithm microbial population decline. Weibull model accurately predicted microorganism inactivation kinetics after HPH and HPP processing when displaying single shoulder or tail in the survivor curves, whereas when a more complex trend was observed after thermal treatment, the double-Weibull equation was found more appropriate to explain such behaviour. Equivalent treatments that achieved the same degree of microbial inactivation (77 °C–10 s in thermal processing, 120 MPa–10 s at 30 °C in HPH processing and 375 MPa–1 min at 30 °C in HPP) were selected to study the effects on quality parameters. The application of dynamic pressure led to a decrease in sedimentable pulp, transmittance and juice redness, thus stabilising the opaqueness and cloudiness of mandarin juice. Pectin methyl esterase (PME) was found to be highly baroresistant to static and dynamic pressure. Carotenoid content remained unaffected by any treatment. This study shows the potential of high-pressure homogenisation as an alternative for fruit-juice pasteurisation.     

Release of phenolic acids from defatted rice bran by subcritical water treatment

BACKGROUND: Oil production from rice bran, an undervalued by‐product of rice milling, produces defatted rice bran (DRB) as a waste material. Although it is considered a less valuable product, DRB still contains useful substances such as phenolic compounds with antioxidant, UV‐B‐protecting and anti‐tumour activities. In this study the phenolic acids in DRB were extracted with subcritical water at temperatures of 125, 150, 175 and 200 °C. RESULTS: Analysis of total phenolics using Folin–Ciocalteu reagent showed about 2–20 g gallic acid equivalent kg^?1 bran in the extracts. High‐performance liquid chromatography analysis showed low contents of phenolic acids (about 0.4–2 g kg^?1 bran). Ferulic, p‐coumaric, gallic and caffeic acids were the major phenolic acids identified in the extracts. Thermal analysis of the phenolic acids was also done. The thermogravimetric curves showed that p‐coumaric, caffeic and ferulic acids started to decompose at about 170 °C, while gallic acid did not start to decompose until about 200 °C. CONCLUSION: Subcritical water can be used to hydrolyse rice bran and release phenolic compounds, but the high temperatures used in the extraction can also cause the decomposition of phenolic acids. Copyright © 2010 Society of Chemical Industry     

Effects of deep‐fat frying temperature on antioxidant properties of whole wheat doughnuts

The total phenolic (TP) content, phenolic acid composition and in vitro antioxidant capacity of whole wheat doughnuts fried at 120–180 °C were determined to identify the effects of frying temperature. Significant differences (P < 0.05) in TP content were observed between doughnuts fried at different temperatures. The TP content of doughnuts decreased significantly when doughnuts were deep‐fat fried. The TP content of doughnuts increased with elevation with frying temperatures. These increases in TP content of doughnuts were also detected in the determination of individual phenolic compounds using HPLC. DPPH radical and iron‐chelating capacity of deep‐fat fried doughnuts exhibited increases with elevation of frying temperature from 120 to 180 °C. Deep‐fat frying at 120 °C lowered lipid peroxidation inhibition capacity of doughnuts prepared from both refined flour and whole‐grain meals and increased consistently with increased frying temperature from 120 to 180 °C. Moderate deep‐fat frying temperature would increase the content and activity of antioxidants of doughnuts.     

Survival of probiotic bacteria nanoencapsulated within biopolymers in a simulated gastrointestinal model

The objective of this work was to fabricate electrospun nanofiber mats (nano-scale in diameter) using a combination of corn starch (CS) and sodium alginate (SA) and encapsulate probiotic strains of lactobacilli (Lactobacillus acidophilus (LA5) and Lactobacillus rhamnosus 23,527 LGG) and bifidobacteria (Bifidobacterium bifidum and Bifidobacterium animalis) to improve their survival in simulated gastrointestinal fluids. The viability of the lactobacilli and bifidobacteria (determined using plate count method) after electrospinning was 94.1% and 89.4% of the initial population. Upon exposure to in vitro condition of gastric fluid (HCl and pepsin, at 37 °C), the population (starting level of 9 log CFU/mL) of nanoencapsulated lactobacilli and bifidobacteria decreased only by 1.58 and 1.03 log CFU at 120 min. Treated with in vitro prepared intestinal fluid (dipotassium hydrogen phosphate, sodium hydroxide, bovine bile salt, and trypsin) no cell was detected at 30 min and the number of coated lactobacilli and bifidobacteria decreased by 2.90 and 2.23 log CFU at 120 min in comparison to nonencapsulated control. After 180-min exposure to simulated gastrointestinal fluid, population of encapsulated lactobacilli and bifidobacteria decreased by 3.02 and 2.55 log CFU at 180 min. The viability of the probiotic bacteria in simulated gastrointestinal conditions was enhanced significantly (81–100% of the initial population) by nanoencapsulation within nanofiber mats of CS/SA.     

High-temperature air fluidization improves cooking and eating quality and storage stability of brown rice

Brown rice contains many valuable active ingredients; but due to its long cooking time, hard texture, heavy rice bran taste, and short shelf life, it is not widely accepted by consumers. Herein, we developed a novel processing technology so-called high-temperature air fluidization (HTAF) to treat brown rice. The effects of the HTAF treatment at 120 °C, 130 °C, and 140 °C for 60 s at a feed rate of 80 kg/h on the quality of brown rice were investigated. The results showed that the treatment with HTAF caused fissures to form on the surface and the interior of brown rice, and these fissures appeared to facilitate the penetration of water into the rice kernels during soaking. The optimal HTAF treatment temperature was 130 °C, the water adsorption of HTAF-treated brown rice at 130 °C (TBR-130) was increased to 25.3% after soaking for 160 min, which was higher than that of white rice and untreated brown rice (UBR; 13.7%). The optimal cooking time for TBR-130 was also 5 min shorter than that for UBR. The results further showed that TBR-130 had a larger degree of volume expansion compared to that of UBR, and cooked TBR-130 had softer texture than cooked UBR. The cohesiveness and sensory quality of TBR-130 were also higher than those of UBR, and the content of flavor compounds in TBR-130 was similar to that of white rice. HTAF caused no obvious damages to the main active components or nutritional components of TBR-130. Finally, TBR-130 had better chromaticity and higher storage stability than UBR. These results demonstrate that the HTAF treatment can improve cooking and eating quality and storage stability without causing obvious damages to nutritional quality of brown rice. This technology may play important roles in an attempt to promote the use of brown rice as staple foods.     

Effects of conjugated linoleic acid on the degradation and oxidation stability of model lipids during heating and illumination

The effects of methyl conjugated linoleate (MCLA) on the degradation and oxidative stability of model lipids, methyl linoleate (ML), methyl oleate (MO) and methyl stearate (MS), during heating at 100, 150 or 200°C for 3 h or illumination at 4000 lux for 14 days were studied. Results showed that under either temperature treatment or illumination, MCLA was the most susceptible to degradation, followed by ML, MO and MS. At 100°C, peroxide formation was the main reaction in each model lipid. However, at 150°C, peroxide formation was the main reaction in the initial period of heating, followed by degradation. At 200°C, the degradation was the major reaction. In contrast, peroxide formation was the main reaction for each model lipid during illumination. The addition of MCLA may slow degradation of each model lipid during heating. However, the oxidation stability of the whole system (model lipid plus MCLA) may also be decreased. Under light storage, the effect of MCLA was insignificant.     

Determination of celiac disease-specific peptidase activity of germinated cereals

A method to determine the celiac disease-specific peptidase activity of different germinated cereals was developed. Kernels of common wheat, spelt, emmer, einkorn, rye, and barley were germinated, lyophilized, and milled into flour and bran. The latter was extracted at pH 4.0 to obtain a solution enriched with peptidases. The synthetic α-gliadin peptide with the amino acid sequence PQPQLPYPQPQLPY (peptide IV), which has been shown to be toxic for celiac disease patients, was selected as substrate for bran peptidases. It was quantified by reversed-phase high-performance liquid chromatography on C₁₈ silica gel. For kinetic studies, rye bran extract was incubated with peptide IV at 50 °C and pH 6.5. The peptide was degraded continuously, and only 30.2% of the original peptide was detected after 90 min. Accordingly, the bran extracts of all cereals were investigated. The incubation time was set to 60 min at 50 °C, and the degradation of peptide IV was performed at pH 4.0 and 6.5, respectively. Except for rye, peptide degradation was faster at pH 4.0 than at pH 6.5. At pH 4.0, emmer extract was most active, followed by spelt, common wheat, and einkorn extracts. The activity of rye and barley extracts was significantly lower. In conclusion, the method is easy to perform, quick, and provides reproducible results. It can be applied to other peptidase sources such as bacterial or fungal cultures to optimize peptidase preparations suitable for detoxifying gluten-containing food or for drugs to treat celiac disease.     

Subcritical water extraction of phenolic compounds from flaxseed meal sticks using accelerated solvent extractor (ASE)

Subcritical water extraction (SWE) is a technique based on the use of water as an extractant, at temperatures between 100 and 374 °C and at a pressure high enough to maintain the liquid state. SWE provides higher selectivities, low cost, and shorter extraction times. In this study, phenolic compounds in flaxseed (Linum usitatissimum L.) meal sticks were extracted with subcritical water using accelerated solvent extractor. For this aim, the interactions between temperature (160, 170, and 180 °C) and extraction time (5, 15, 30, and 60 min) for subcritical water extraction of SDG lignan, total phenolics, and total flavonoids from flaxseed meal sticks were investigated. The highest extraction yield of SDG lignan (77.01 %) in subcritical water extracts was determined at 160 °C for 60 min. However, high extraction yields were obtained as 70.67 and 72.57 % at 170 and 180 °C for 15 min, respectively. Also, the highest extraction yield of total phenolics (70.82 %) and total flavonoids (267.14 %) were determined at 180 °C for 15 min. Besides, high correlations between SDG lignan–total phenolics, SDG lignan–total flavonoids, and total phenolics–total flavonoids were obtained from 0.86 to 1 in water extracts.     

Low‐field nuclear magnetic resonance analysis of the effects of heating temperature and time on braised beef

We investigated the characteristics of water mobility and distribution in Chinese braised beef after treatment at different temperatures for different times using low‐field nuclear magnetic resonance (LF‐NMR). The beef was heated at 45, 55, 65, 75, 85 or 95 °C for 30, 60, 90 and 120 min. Results showed that T₂ changed significantly with heating temperature. T₂₁ and A₂₁ decreased significantly with increasing temperature below 65 °C, with a steady phase from 75 to 95 °C, which agreed with cooking loss. Inversely, T₂₂ had no changes below 65 °C and changed apparently from 75 to 95 °C. The change in T₂₁ below 65 °C may be related to proteins denaturation and shrinkage and, above 65 °C, T₂₂ possibly induced by the dissolution of connective tissue. The characteristics of braised beef at 65 °C were different from those at other temperatures in T₂ distributions. The findings could provide a theoretical basis for the processing of Chinese braised beef.     

The effect of temperature on the development of browning of amorphous and crystalline lactose

When lactose crystals are dried in industrial driers the temperatures used can, when exposure time is too long, cause the crystals to undergo non-enzymatic browning. This leads to a defect in the final product. Understanding the kinetics allows driers to be designed to avoid this. To examine the non-enzymatic browning kinetics of amorphous and crystalline lactose, samples were heat treated for 2–120 min at 110 °C, 120 °C, 130 °C, 140 °C and 150 °C. The evolution of colour was followed by spectrophotometry at 420 nm and colorimetry (L* a* b*). The absorbance and the b* values increased while L* value decreased with time and temperature. A first order reaction model with Arrhenius temperature dependence provided a good fit to the data. A difference was seen between crystalline and amorphous lactose, with the latter having more intensive browning under the same conditions due to the increased surface area available.     

Physicochemical characteristics and gelation properties of collagen superfine powder from swine skin: the effects of preheating treatment

Following different preheating treatments (60 °C for 20 min; 80 °C for 20 min; or 120 °C for 10 min, referred as T₁, T₂ and T₃), edible collagen superfine powder (CSP) from swine skin was prepared by superfine grinding method. The CSPs showed a preheating‐dependent decrease in the D₅₀, with different degrees of hydrolysis (9.51–31.05%). A significant effect of preheating on rheological properties of the CSP aqueous dispersions at pH 4–9 was observed, wherein T₂ had the biggest viscosity and water holding capacity. All the 5% CSP dispersions were transformed into stable cold‐set gels after heating at 50–90 °C for 20 min, with insignificant differences in strength. These attributes were consistent with microstructures of the CSP gels detected by scanning electron microscope.     

Simultaneous rice bran oil stabilization and extraction using sub-critical water medium

Sub-critical water technique was used for simultaneous inactivation of lipase enzyme existing in rice bran and extraction of its oil in order to obtain the stabilized edible rice bran oil. Sub-critical water treatment was carried out in the temperature range between 120 and 240 °C for 10 and/or 20 min residence time in a batch reactor. The quality of the extracted oil was evaluated with respect to its total free fatty acids concentration over a 12 week period, and compared with the oil obtained by conventional extraction methods. Without sub-critical water treatment, the concentration of total free fatty acids in the rice bran significantly increased from 5.6% to 36.0%. In contrast, no increase was observed in the total free fatty acids concentration in the samples treated by sub-critical water. Experimental evidence showed that total free fatty acids concentration increased somewhat in the oils treated by conventional methods. Considering no change was observed in total free fatty acid concentration in the treated oils by sub-critical water, it was found that sub-critical water not only could efficiently extract oil from rice bran in a short residence time but also completely stabilized the extracted oil. Oil extraction yields generally increased with increases in sub-critical water treatment temperature and residence time. The highest extraction yield of oil was 249 (mg/g dry matter) obtained at 240 °C and 10 min residence time. Oil extraction by sub-critical water could be conducted in a very short residence time (10 and/or 20 min). Also, the kinetics of free fatty acids formation in untreated rice bran was investigated and developed which successfully describes the concentration of total free fatty acids in the course of rice bran storage.