Effect of gelatin/agar bilayer film incorporated with TiO2 nanoparticles as a UV absorbent on fish oil photooxidation

This research evaluated the effect of gelatin/agar bilayer film and nanocomposites containing different concentrations of TiO₂ nanoparticles (0.5%, 1% and 2%) as ultraviolet (UV) and oxygen barriers on the oxidative stability of fish oil. Samples of fish oil covered with the bilayer films were stored under UV light or in darkness and with or without lids at 18 °C for 12 days. Oil quality in terms of peroxide values (PV), thiobarbituric acid (TBA), conjugated diene (CD), fatty acids profile and colour change (?E) was monitored during storage. Fish oil photooxidation was hindered by increasing TiO₂ concentration, so that nanocomposite containing 2% of the nanoparticles could control photooxidation, similar to the samples stored in darkness. Furthermore, upon studying both photooxidation and autoxidation, the highest amounts of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), as well as the lowest amount of changes in PV, TBA, CD and ?E, were observed in oils covered with the nanocomposites.     

Influence of Surfactants on the Rheological Behavior of Starch/Gelatin Gels and Gel-Emulsions

Thixotropic behavior of mixed 8% starch/gelatin gels and gel-emulsions (8% of the sunflower oil dispersed in the starch/gelatin gel), prepared with the addition of different emulsifiers, by means of the rotational viscometer with coaxial cylinders, has been investigated. Different emulsifiers (Na-dodecyl sulfate, cetyl alcohol, mono- and diglycerides of fatty acids and alkyl polyglycolethers) were applied before (at 40°C) and after (at 96°C) gelatinization of the starch. Thixotropic properties, i.e. the coefficients of thixotropy of gels and emulsions were determined by the thixotropic loop method. Samples were taken in different time intervals (up to 72 h), in order to investigate the ageing effects. Very stable gels and gel emulsions (containing carbohydrate, protein and fatty component), with high aging stability can be obtained.     

Anthocyanin and colour changes during processing of pomegranate (Punica granatum L., cv. Hicaznar) juice from sacs and whole fruit

The effects of clarification and pasteurisation on anthocyanins (ACNs) and the colour of pomegranate juice (PJ) produced from sacs and whole fruits were investigated. Clarification caused a loss of 4% of ACNs in juice from sacs (JFS) and a loss of 19% in juice from whole fruit (JFWF). After pasteurisation, there was an 8–14% and 13–9% loss of ACNs from unclarified and clarified JFS and JFWF samples, respectively. Polymeric colour was very high even in unclarified samples (25–29%). Compared to JFS, higher polymeric colour was formed in JFWF. HPLC analyses of PJ revealed that cyanidin-3,5-diglucoside was the major ACN, followed by cyanidin-3-glucoside and delphinidin-3-glucoside. Cyanidin-3,5-diglucoside showed higher stability to clarification and pasteurisation than cyanidin-3-glucoside in both PJ samples. Cold clarification with only gelatin is recommended for PJ. To prevent excessive ACN loss and the formation of brown colouring, PJ should be subjected to minimal heating.     

Composition, sensory and shelf life stability analyses of Longissimus dorsi muscle from steers reared under organic and conventional production systems

In recent years the demand for organically grown food has increased. In this study, organic (O, n=6) and conventionally (C, n=6) reared steers aged between 18 and 24 months were slaughtered during the month of September 2002. Four days post-slaughter, the Longissimus dorsi (LD) muscle was excised from the left side of each carcass. All muscles were vacuum packed and aged in a chill for a further seven days. Steaks were cut from each sample, and from these, lean meat was removed, blended and compositional analysis was carried out. O samples were significantly higher (P>0.05) in fat content and therefore were significantly (P>0.05) lower in moisture content than C samples. No significant differences were observed between C and O samples for protein, ash, β-carotene, α-tocopherol or retinol. There was also no significant difference in fatty acid content between C and O samples. Colour stability and fat oxidative stability of samples were also measured, while stored under retail conditions. Samples were packed using both modified atmosphere packaging (MAP) and by overwrapping with cling film. MAP C samples had the best colour stability while overwrapped C samples had the best lipid stability. Therefore, colour and lipid stability of beef samples were influenced by sample composition and packaging format used, which resulted in C samples outperforming O samples with respect to shelf life stability.     

Fining of red wines with gluten or yeast extract protein

Due to a growing interest in alternatives to substitute gelatin as clarifying agent, this work investigates the use of yeast extracts and glutens. Physico‐chemical characteristics of proteins were analysed. Fining experiments were carried out on young red wines. Turbidity reduction, lees volume and effects on polyphenolic content and colour characteristics were determined. The results indicated that glutens and yeast extracts turbidity reduction is comparable to gelatin. Lees production was considerably reduced by non‐animal proteins: yeast extracts produced 44%, wheat glutens 60% and maize gluten 92% less than gelatin. Lees volume is highly correlated (R = ?0.720) with the absolute superficial charge density value (SCD) and with the pI (0.936) when clarifier was used in combination with bentonite. Treatments with glutens reduced less the polyphenolic content (between 0.6 and 8.7 units) than gelatin did. There were slight differences on the modification of colour intensity.     

Metmyoglobin reducing activity and colour stability of ovine longissimus muscle

Characteristics of metmyoglobin reducing activity in ovine longissimus were determined, and its effect on colour and colour stability of muscle was investigated in two experiments. In the first experiment vacuum packed ovine longissimus samples were incubated at 5–35°C during the first 16 h post mortem (n=8 per treatment). Metmyoglobin reducing activity was negatively affected by incubation temperatures above 30°C, but colour and colour stability were little affected at 24 h post mortem and after 2 weeks of vacuum storage at 2°C. In the second experiment the effects of pre-slaughter stress and electrical stimulation on metmyoglobin reducing activity, colour and colour stability of ovine longissimus (n=40) with an ultimate pH below 5.8 were investigated. Neither of the treatments had an effect on metmyoglobin reducing activity or colour parameters. The relatively large variation in metmyoglobin activity and colour parameters allowed correlation analysis. Metmyoglobin reducing activity was not correlated to colour or the colour stability parameters. The results of the present study indicate that metmyoglobin reducing activity is not the primary determinant of colour or colour stability of ovine longissimus muscle.     

The characteristics of gelatin extracted from sturgeon (Acipenser baeri) skin using various pretreatments

The physicochemical characteristics of gelatin obtained by different pretreatments of sturgeon (Acipenser baeri) skin with alkaline and/or acidic solutions have been studied. Visual appearance, pH, gel strength, viscosity and amino acid profile of the gelatins were evaluated. Pretreatment with alkaline solutions of Ca(OH)₂ and/or acetic acid (HAC) provided gelatin with a favourable colour. Pretreatment with alkali removed noncollagenous proteins effectively, whilst acid induced some loss of collagenous proteins. Gel strength and viscosity of gelatin pretreated with HAC or alkali followed by HAC were as high as gelatin extracted in the presence of protease inhibitors. Amino acid composition had no significant effect on the gelatin characteristics. The total acid concentration for the highest gel strength was inversely proportional to ionisation strength, and the preferred pH for extracting gelatin with the optimum gel strength was approximately 5.0. The results showed that any available protons, regardless of the type or concentration of the acid, inhibit protease activity, which significantly affects the gelatin characteristics.     

Functional stability of gelatin–lignosulphonate films and their feasibility to preserve sardine fillets during chilled storage in combination with high pressure treatment

The physico-chemical and functional stability of gelatin (G) and gelatin–lignosulphonate (GLS) films stored during 4 weeks at 21 °C, (i) in container or (ii) in contact with oil, was examined. Addition of lignosulphonate dramatically increased ABTS radical scavenging and ferric ion reducing capacities, which remained practically unaltered after the storage period. GLS films exhibited reduced elongation at break, irrespective of storage medium, and retained their water resistance. The feasibility of using GLS film to improve the quality of sardine fillets during chilled storage, alone or in combination with high pressure treatment (300 MPa/10 min/7 °C), was evaluated. The combined use of GLS film with high pressure reduced microbial growth, total volatile basic compounds (TVB) and thiobarbituric acid reactive substances (TBARS) during chilled storage. No noteworthy high pressure-induced colour changes were observed in the sardine muscle using this treatment alone, although an increase in yellowness due to the combined treatment was detected.Industrial RelevanceAddition of lignosulphonate dramatically increased antioxidant properties (ABTS radical scavenging and ferric ion reducing) of gelatin films, which remained practically unaltered during 4 weeks of storage at room temperature. Application of those films confers stability during storage of chilled sardine, especially in combination with high pressure treatment. These novel packaging was promising for fish preservation.     

柿子酒澄清方法的研究

用明胶、皂土、壳聚糖对柿子酒进行澄清处理,结果表明:明胶、壳聚糖的澄清效果优于皂土,其中明胶的澄清效果最佳,澄清后蛋白质、单宁含量有一定量的减少。明胶-壳聚糖联用效果优于单一的澄清剂,澄清后,酒体清亮透明,风味、色泽独特,稳定性强。     

Colour stability and lipid oxidation of fresh beef. Development of a response surface model for predicting the effects of temperature, storage time, and modified atmosphere composition

Samples of fresh beef muscles (Longissimus dorsi) were packed under varying modified atmosphere conditions (20-80% oxygen) and stored at 2-8°C for 10 days. At 2 day intervals meat samples were analysed for surface colour and extent of lipid oxidation (TBARS). Response surface models for predicting the effects of temperature, storage time and modified atmosphere composition on colour stability and lipid oxidation were developed. Temperature and time were found to be the most important factors for retaining meat colour and minimizing lipid oxidation. However, the oxygen content also had a significant effect on both quality parameters. A stable interval of maintaining a good meat colour was found between 55 and 80% O(2). Response surface modelling was found to be very promising for modelling of chemical quality changes in meat stored under different conditions, but the large biological differences between animals may complicate the development of generally valid models.     

Properties of bovine gelatin as affected by a cross-linking induced by horseradish peroxidase,glucose oxidase and glucose

Gelatin is an important protein-based hydrocolloid, providing excellent gelling properties in processed foods. Horseradish peroxidase (100 U/g protein), glucose oxidase (1 U/g protein), and glucose (0.025 mmol/g protein) were applied to cross-link bovine gelatin at 37 °C for 3 h, and the gelling properties of cross-linked gelatin were evaluated. Obviously, the cross-linking process did not change the composition of amino acids. The cross-linked gelatin had 39.2% increase in surface hydrophobicity, 54.7% increase in emulsion stability index, but 28.2% decrease in emulsifying activity index, in comparison with bovine gelatin. Laser scanning confocal microscopy observation indicated that cross-linked gelatin rather than bovine gelatin conferred better droplet stability on the generated emulsion after long-storage period of 48 h or 7 days. Moreover, cross-linked gelatin had decreased in vitro digestibility during pepsin hydrolysis (38.5%) and pepsin–trypsin hydrolysis (14.5%) than bovine gelatin. Finally, the gelling and melting temperatures of cross-linked gelatin were 2 °C higher than those of bovine gelatin. Overall, the cross-linking process of bovine gelatin led to easier gelation and improved heat resistance of the subsequently gels.     

The effects of residual oxygen concentration and temperature on the degradation of the colour of beef packaged under oxygen-depleted atmospheres

Samples of beef longissimus dorsi (LD), approximately 5 × 5 × 1 cm, were packaged in pairs under 10 litre volumes of N₂ or CO₂ containing O₂ at concentrations between 100 and 1000 ppm. The packaged samples were stored at temperatures of 5, 1, 0 or −1·5°C, for times between 4 and 48 h. Samples of beef psoas major (PM) were packaged under N₂ or CO₂ containing O₂ at between 100 and 600 ppm, and stored at −1·5°C for 24 or 48 h. After storage, each sample was assessed for colour deterioration and discoloration, and for the fraction of metmyoglobin in the surface pigment.

The results obtained with N₂ and CO₂ atmospheres were similar. The colours of all LD samples had deteriorated after 4 h storage at 5 or 1°C, although the degree of deterioration increased with increasing O₂ concentration. All LD samples stored for 12 h at 5 or 1°C were extensively discoloured, with metmyoglobin fractions generally exceeding 60%, but those stored at −1·5°C for 48 h or less, under O₂ concentrations ≤ 400 ppm had undergraded colours. The colours of some LD samples stored at −1·5°C under about 600 ppm of O₂ were also undergraded, but the colours of samples stored under 800 or 1000 ppm had deteriorated by 24 h. The colours of LD samples stored at 0°C under > 200 ppm had deteriorated after 24 h storage, and the colours of samples stored under 100 ppm O₂ had deteriorated after 48 h storage. All PM samples were wholly discoloured after storage at −1·5°C. Evidently, the colour of beef muscle of high colour stability is resistant to degradation by atmospheres containing < 600 ppm of O₂ when the meat is stored at sub-zero temperatures, but not when the storage temperature is at or above 0°C. Beef muscle of low colour stability, such as the PM, will discolour at all low concentrations of O₂ irrespective of the storage temperature.     

Efficacy of lactic acid salts and sodium acetate on ground beef colour stability and metmyoglobin-reducing activity

This study examined two concentrations (0.6 and 1.0mol) of three lactic acid salts (calcium lactate, CaL; potassium lactate, KL; and sodium lactate, NaL), with and without 0.01mol sodium acetate (n=3 replications), for effects on ground beef colour stability and metmyoglobin-reducing activity (MRA). Ground beef with CaL was least colour stable (P<0.05). Increasing CaL and NaL concentration decreased (P<0.05) colour stability. Ground beef with acetate only was most colour stable (P<0.05), but it did not result in more MRA (P>0.05) than control ground beef. Including both lactate and acetate was not as effective (P>0.05) in increasing colour stability as acetate alone. In general, both KL levels were equal (P>0.05) to the lower NaL concentration, and all three were superior in colour stability (P<0.05) to CaL and the higher NaL concentration. More MRA was generated by including lactates (P<0.05); KL and NaL had more MRA than CaL (P<0.05). However, these increases in MRA did not result in improved colour stability. Overall, adding KL to ground beef would not increase ground beef colour stability over adding nothing, but CaL and high levels of NaL would decrease colour stability. Using 0.01mol sodium acetate maximized ground beef colour stability.     

Dietary vitamin E supplementation, an ascorbic acid preparation, and packaging effects on colour stability and lipid oxidation in mince made from previously frozen lean beef

The effect of extra vitamin E (2025 International Units animal^-1 day^-1) in the diet of bulls on the colour stability and lipid oxidation of lean mince was studied. Control and enriched diets were provided for the last 136 days before slaughter. Minces were prepared from M. biceps femoris and M. semitendinosus that had been stored for 2 months at -40 °C. Samples of minces with and without an ascorbic acid preparation (AAP) from control (CON) and supplemented (SUP) beef were packaged, half on trays over-wrapped with an oxygen-permeable foil and half in modified atmosphere (MA) packs (gas mixture applied: O₂/CO₂/N₂, 75/20/5). Meats were displayed for 7days at 7 °C in an illuminated environment. The SUP meat was more resistant to lipid oxidation than the CON meat was. Also, the AAP consistently delayed lipid oxidation. A strong synergistic effect of both vitamins in this regard was demonstrated for the MA condition. MA packaging overall led to increased lipid oxidation. Colour measurements of SUP versus CON meats, without the AAP, generally failed to detect differences in redness values. The positive effect on the colour of freshly minced lean meats obtained by supplementation with vitamin E appeared to be almost nullified in minces made from previously stored frozen muscles. A sensory panel, however, still tended to judge the attractiveness of the colour of the SUP meat greater than that of CON meat. Addition of the AAP improved colour stability. Compared to the foil-overwrapped meat, colour was better retained in the MA packaged meat.     

Accelerated chilling and modified atmosphere packaging affect colour and colour stability of injection-enhanced beef round muscles

Beef knuckles were partially hot-boned within 1.5 h postmortem. Biceps femoris (BF), semimembranosus (SM), vastus lateralis (VL), and rectus femoris (RF) muscles were injection enhanced at 6% (experiment 1) or 10% (experiment 2) of non-injected weight and packaged in a high- (HiOx; 80% oxygen and 20% carbon dioxide) or ultra-low oxygen (LoOx; 80% nitrogen and 20% carbon dioxide) modified atmosphere. Hot boning accelerated chilling in all beef round muscles investigated. This resulted in a darker initial beef colour and darker visual colour during display for the BF, RF, and VL, as well as more uniform BF and knuckle steak colour. RF and VL, in experiments 1 and 2, respectively, had the most improved colour and colour stability. Steaks in HiOx MAP had longer colour life in display than steaks that had been in LoOx. Partially removing the beef knuckle early postmortem is a practical process that will improve colour and colour stability of beef round muscles.     

STABILITY OF OIL-IN-WATER EMULSIONS. 2. Effects of Oil Phase Volume, Stability Test, Viscosity, Type of Oil and Protein Additive

SUMMARY –Stability of oil-in-water emulsions stabilized in sodium caseinate, gelatin and soy sodium proteinate was found to be increased by either an increase in the aqueous phase protein concentration (0.5–2.5%) or oil phase volume (20–50%). Both factors were significantly interrelated. Emulsions stabilized by soy sodium proteinate were generally higher in stability as compared to those stabilized by gelatin or sodium caseinate. With emulsions containing gelatin, greater stability occurred when the stability testing temperature was increased from 37–70°C and when the time interval was decreased from 24 hr to 90 min. Maximum relative viscosities of emulsions stabilized by gelatin and sodium caseinate were 2.0 and 2.5, respectively. Emulsions stabilized by soy sodium proteinate were quite viscous, with relative viscosity from 1.5–30 depending on both protein concentration and oil phase volume. Interchanging the emulsified oil among corn, soybean, safflower and peanut oils did not alter emulsion stability when examined at three concentrations of soy sodium proteinate. Changing the oil to olive oil significantly increased emulsion stability at each soy sodium proteinate level with oil phase volumes of 30, 40 and 50%.     

散沫花提取物复合明胶膜对冷链运输及放置过程中牛肉品质的影响

本研究调查了以墨鱼皮明胶和散沫花提取物（HAE）作为天然保鲜剂制备出的功能性涂膜对模仿冷链运输及零售1、3、6和8 d牛肉贮藏损失、颜色、菌落总数、脂质氧化以及高铁血红蛋白、血红素铁和游离氨基酸含量的影响,综合评价了散沫花提取物复合明胶膜对牛肉冷藏保鲜效果的的影响。结果表明,与未涂膜样品相比,涂膜处理有效防止了水分的流失和高铁肌红蛋白的形成,保持了肉样的持水性和颜色特性（P<0.05）。随着放置期的延长,HAE+明胶膜通过在贮藏期减少脂质氧化程度、菌落总数和嗜冷菌数,显著延长了肉的货架期（P<0.05）。此外,根据游离氨基酸含量,涂膜处理可以显著降低蛋白水解过程的速率,而未涂膜处理的样品水解速率更快（P<0.05）。主成分分析表明,样品颜色的变化与pH、血红素铁含量、脂质氧化以及微生物繁殖存在高度相关性,而HAE+明胶涂膜良好地抑制了这些因素的发展。因此,HAE+明胶涂膜可以作为有效的活性保鲜方式,用于肉类的冷藏保鲜。     

Cryoprotectants improve physical and chemical properties of frozen blue crab meat (Callinectes sapidus)

The storage stability of cryogenically frozen crab meat treated with cryoprotectants was compared with pasteurised and water-treated frozen samples to determine changes in physical and chemical properties. Commercially processed, hand-picked blue crab meat was treated with solutions of polydextrose, sucrose + sorbitol/sodium tripolyphosphate or water, vacuum packaged, and cryogenically frozen prior to storage at ?29°C. All treatments were compared with an untreated reference control stored at ?65°C and a pasteurised sample stored at 1.1°C. Samples were evaluated for physical and chemical changes at 4-week intervals over 32 weeks of storage. Cryoprotectants improved oxidative stability, drip loss, expressible moisture, texture, and colour compared to untreated reference and pasteurised samples.     

Preparation and characterisation of chicken skin gelatin as an alternative to mammalian gelatin

The aims of this study were to report for the first time, the extraction and physico-chemical properties of chicken skin gelatin compared to bovine gelatin. Extracted chicken skin gelatin 6.67% (w/v) had a higher bloom value (355 ± 1.48 g) than bovine gelatin (259 ± 0.71 g). The dynamic viscoelastic profile of chicken gelatin exhibited higher viscous and elastic modulus values compared to bovine gelatin for a range of concentrations and frequencies. Thermal properties studied by differential scanning calorimetry (DSC) showed that the melting temperature of 6.67%, chicken skin gelatin was significantly greater (p < 0.05) than that of bovine gelatin, indicating lower stability of bovine gelatin compared to chicken skin gelatin. Results obtained in this study showed that Gly (33.70%), Pro (13.42%), H.Pro (12.13%) and Ala (10.08%) were the most dominant amino acids in chicken skin gelatin which contributed to the higher gel strength and stability. Raman spectra of chicken skin and bovine gelatin were similar and displayed typical protein spectra. Chicken gelatin showed strong hydrogen bonding compared to bovine gelatin as the tyrosine doublet ratio (I₈₅₅/I₈₃₀) of chicken gelatin was significantly lower than that of bovine gelatin. Significantly, the alpha helix and β-sheet type structures were higher for chicken skin gelatin compared with bovine gelatin. The average molecular weight of chicken gelatin was 285,000 Da. These findings, obtained for the first time for chicken skin gelatin, show that it has high potential for application as an alternative to commercial gelatin.