Transglutaminase effects on gelation capacity of thermally induced beef protein gels

Transglutaminase (TG) is an enzyme that catalyzes an acyl-transfer reaction between the γ-carboxyamide group of peptide or protein-bound glutaminyl residues, and primary amines. TG action on protein molecules, causes a cross-linking and polymerizing effect of these latter, through ε-(γ-glutamyl)lysine bonds. This TG-mediated protein cross-linking creates drastic physical changes in protein-rich foods.     

冷冻鱼糜制品中大肠杆菌生长动力学模型的构建

以冷冻鱼糜制品为原料将大肠杆菌接种到鱼糜制品中,托盘包装后分别在5、10、15、20、25和85℃贮藏。并应用Curve Expert1.3软件拟合不同温度下大肠杆菌的生长情况。结果表明,修正的Gompertz方程能较好地描述不同温度下大肠杆菌在鱼糜制品中的生长动态,温度对大肠杆菌生长参数μmax(最大比生长速率)和λ(延滞时间)的影响,采用平方根模(Belehradek)描述呈良好线性关系。85℃用失活模型Linear的拟合较好。通过13℃和18℃下大肠杆菌的生长对构建的Gompertz模型进行了验证,并经数学检验参数偏差值和准确值计算,偏差度分别为0.938、0.956,准确度为1.034、1.083,表明所建立模型是有效的。      

Effect of oxidised phenolic compounds on the gel property of mackerel (Rastrelliger kanagurta) surimi

The effects of different oxidised phenolic compounds (ferulic acid, OFA; tannic acid, OTA; catechin, OCT and caffeic acid, OCF) at different levels (0-0.60% of protein content) on the properties of gels from mackerel (Rastrelliger kanagurta) surimi were investigated. Gels with addition of 0.40% OFA, 0.50% OTA, 0.50% OCF or 0.10% OCT had increases in breaking force by 45%, 115%, 46.1% and 70.3% and in deformation by 12.2, 27.5, 28.1 and 28.4%, respectively, compared with the control (without addition of oxidised phenolics). Lowered expressible moisture content without any change in the whiteness of resulting gels was found. Slightly lower myosin heavy chain (MHC) band intensity of gels added with oxidised phenolics at the optimal level was noticeable compared with that of the control. A sensory evaluation study indicated that addition of oxidised phenolic compounds had no negative impact on the colour and taste of the resulting gels (P > 0.05). Gels with addition of all oxidised phenolics had a finer matrix with smaller strands.     

Oxidation of lipid and protein in horse mackerel (Trachurus trachurus) mince and washed minces during processing and storage

Protein and lipid oxidation was followed during processing and storage of mince and washed minces prepared from horse mackerel (Trachurus trachurus). Briefly horse mackerel mince (M0) was washed with three volumes of water, mimicking the surimi production and different washed products were obtained: M1, M2 and M3, with one, two and three washing steps, respectively. The different products were characterised (i.e. lipid content, protein, water, iron, fatty acid profile and tocopherol content) and analysed for protein and lipid oxidation in order to investigate the impact of the washing steps on oxidation. Subsequently the different products were stored for up to 96 h at 5 °C and samples were taken out regularly for analysis. Lipid oxidation was investigated by measuring primary oxidation products (lipid hydroperoxides) and secondary oxidation products (volatiles). Protein oxidation was followed by determination of protein solubility, protein thiol groups and protein carbonyl groups using colorimetric methods as well as western blotting for protein carbonyl groups. Lipid and protein oxidation markers indicated that both lipid and protein oxidation took place during processing and the ranking for oxidation was as follows M0 < M1 < M2 ? M3 with M0 being significantly less oxidised than M3. Results indicated that washing creates an imbalance in the initial prooxidant-antioxidant equilibrium in the muscle tissue and contributes to the observed differences in the oxidative status of the four products obtained. In contrast, during storage of different products, lipid oxidation development was faster in M0 and the ranking was as follows M0 > M1 > M2 ? M3. Lipid and protein oxidation developed simultaneously in different minces during storage, but it was not possible to determine at which level these two reactions were coupled.     

甘露醇/山梨醇共结晶体性质及在鱼糜中的应用优势

甘露醇和山梨醇是一对同分异构体,在化学合成法生产甘露醇时,所产生的山梨醇母液,不可避免的含有部分甘露醇。论述甘露醇/山梨醇共晶体的性质,说明该产品在鱼糜产品的应用优势。     

Comparison of Atlantic menhaden gels from surimi processed by acid or alkaline solubilization

Heat-induced gelling abilities of surimis prepared by pH shifting (isoelectric precipitation following acid (AC) or alkaline (AL) solubilization) were compared to that of conventionally washed (CW) surimi. Greater endogenous transglutaminase activity (evidenced as enhanced strength of cooked gels subjected to 30–40 °C preincubation) was measured for CW and AL surimi than for AC surimi (all at pH 7). Upon addition of microbial transglutaminase (MTGase), increased crosslinking of myosin heavy chain and gel strengthening during 30–40 °C preincubation were apparent for all three types of surimi, most markedly in CW and AL surimi. Salt addition improved CW gels most, but seemed to adversely affect MTGase activity in AC and AL surimi. AC and AL surimi gels were of lower whiteness than were CW surimi gels.     

Interactions of dietary fibre and omega-3-rich oil with protein in surimi gels developed with salt substitute

Most Western populations have insufficient intake of fibre and ω-3 polyunsaturated fatty acids (PUFAs), while sodium intake greatly exceeds the recommended maximum. Surimi seafood is not currently fortified with these nutraceutical ingredients. Alaska pollock surimi seafood was developed with salt substitute and fortified with either 6 g/100 g of fibre or 10 g/100 g of ω-3 oil (flax:algae:menhaden, 8:1:1) or fibre + ω-3 oil (6 g/100 g of fibre + 10 g/100 g of ω-3 oil). The objective was to determine effects of the dietary fortification on physicochemical properties of surimi. Fortification with either dietary fibre or ω-3 oil alone or in combination enhanced (P < 0.05) rheological and textural characteristics. The combined fortification had a synergistic effect on rheological properties. This indicates greater gelation of surimi in the presence of fibre + ω-3 oil, suggesting their interaction with surimi myofibrillar proteins. Fibre results in protein dehydration increasing protein concentration; while oil is immobilised by protein filling void spaces in the gel matrix. Differential scanning calorimetry showed that fibre and ω-3 oil did not interfere with normal denaturation of surimi proteins. Colour properties were only slightly affected (P < 0.05). Fortification of surimi with fibre and ω-3 oil resulted in a quality product that could be useful in developing surimi products with nutritional benefits.     

Chemical Interactions and Protein Conformation Changes During Silver Carp (Hypophthalmichthys Molitrix) Surimi Gel Formation

Chemical interactions and protein conformations changes during the formation of silver carp surimi gel were studied by textural analysis, chemical methods, laser Raman spectroscopy, and circular dichrosim. The optimum setting time at 40°C was 60 min. During surimi gel formation, ionic bonds and hydrogen bonds decreased significantly (P ≤ 0.05), while hydrophobic interactions, disulfide bonds, and non-disulfide covalent bonds increased significantly (P ≤ 0.05). Hydrophobic interactions, disulfide bonds, and non-disulfide covalent bonds were the main chemical interactions maintaining the stable structure of surimi gel. Secondary structural analysis of surimi protein showed that 94.11% α-helix existed in native myosin and it partly changed into β-turn and random coil during heating. Myosin gel was made up of 33.70% α-helix, 12.40% β-turn and 53.90% random coil. These three kinds of secondary structures were the main protein conformations in surimi gel.     

钙与热处理对鱼糜凝胶强度的影响

探讨了ＣａＣｌ２、ＥＤＴＡ及不同热处理对鱼糜凝胶强度的影响。结果表明,Ｃａ＾２＋对鱼糜凝胶强度有重要作用,ＣａＣｌ２在４０℃下可明显提高鱼糜凝胶强度,而在９０℃和６０℃下效果均不明显。当ＣａＣｌ２浓度增至１２０ｍｍｏｌ／ｋｇ时,效果与６０ｍｍｏｌ／ｋｇ时相比无显著提高,加入ＥＤＴＡ会导致鱼糜凝胶强度的下降。     

Impact of microbial transglutaminase on gelling properties of Indian mackerel fish protein isolates

Impacts of microbial transglutaminase (MTGase) (0–0.6 units/g sample) on gel properties of Indian mackerel unwashed mince, surimi and protein isolates with and without prewashing were studied. Generally, lower myoglobin and lipid contents were found in protein isolate with and without prewashing, compared to those of unwashed mince and surimi (P < 0.05). Protein isolate had the decreased Ca²⁺-ATPase and protein solubility, indicating protein denaturation. When MTGase was incorporated, breaking force and deformation of all gels markedly increased, especially as MTGase levels increased (P < 0.05). At the same MTGase level, gel from protein isolate with prewashing exhibited the highest breaking force and deformation (P < 0.05). The addition of MTGase could lower the expressible moisture content of most gels. No change in whiteness of gel was observed with the addition of MTGase (P > 0.05), but gel from protein isolate gels had decreased whiteness as MTGase at high level was added. The microstructure of protein isolate gels without prewashing showed a similar network to unwashed mince gels, whilst a similar network was observed between surimi gel and gel from protein isolate with prewashing. Nevertheless, a larger void was noticeable in gels from protein isolates. All gels incorporated with MTGase (0.6 units/g) showed a slightly denser network than those without MTGase. Thus, gel with improved properties could be obtained from protein isolate from Indian mackerel with added MTGase.