大豆分离蛋白对涂抹型再制干酪质构的影响

添加大豆蛋白可降低涂抹型再制干酪的成本，但也会对再制干酪的质构产生一定的影响。设计4因素3水平正交实验．应用TA—XT2i型物性分析仪考察添加了大豆蛋白后的再制干酪产品的质构变化，使用Statistix 8.0统计分析软件对实验结果进行统计分析并作出比较和对正交试验作极差分析。结果表明，4个因素在水平不同的9组正交实验的结果的差异性显著（p〈0.05），在极差分析中，4个因素对硬度的影响排序为D〉C〉A〉B；4个因素对剪切功的影响排序为D〉A〉B〉C；4个因素对粘着性的影响排序为A〉B〉D〉C；4个因素对感官评价的影响排序为A〉D〉C〉B。最后重做不同的最优组并再次测定各项指标，得到最好的组合为大豆蛋白添加量6％．黄油添加量10％，乳化盐添加量1、5％，加水量50％（均为质量分数，下同）。     

含大豆分离蛋白的干酪在成熟过程中化学组成和感官特性的变化

分析了不同大豆分离蛋白含量的干酪在成熟期化学组成（水分、蛋白质、脂肪、灰分）的变化，评价了其感官特性。结果表明，质量分数为5%大豆分离蛋白的干酪与纯牛乳干酪相比，其感官特性最佳。     

大豆品种对双蛋白干酪得率和品质特性的影响

用8种不同品种大豆制作的豆乳与牛奶混合,按照切达干酪生产工艺制作双蛋白切达干酪,以同批次纯牛奶制作的干酪为对照组,对产品的得率、色泽、质构和感官特性等指标进行了分析和比较。实验结果表明,各组双蛋白干酪均比纯牛奶干酪的得率高,各组双蛋白干酪之间得率存在较大差异。质构测定结果表明,不同大豆品种生产的双蛋白干酪在硬度、弹性和粘聚性等指标方面具有较大差异。感官评价中,除添加小粒豆8号豆乳的双蛋白干酪带有较浓豆腥味外,其余组与对照组相差不大。相关性分析结果表明,大豆蛋白中球蛋白和β-伴球蛋白的比值(11S/7S)与双蛋白干酪的硬度和粘聚性显著相关,而大豆的蛋白含量、脂肪含量和植酸含量等指标与双蛋白干酪的品质指标无显著相关性。     

Thermal behavior of emulsions manufactured with soy protein ingredients

The conformation, denaturation and aggregation behavior of proteins are important factors which dictate their ingredient functions and applications in formulated food products. The effect of variation in pre-treatment temperature (70–90 °C × 30 s), pH (6.4–7.5) and calcium supplementation (450 and 850 mg/L) on heat coagulation time (HCT at 140 °C) of model emulsions (3.6% (w/v) protein) stabilized with soy protein isolate (SPI) and soy protein hydrolysate (SPH) ingredients was determined. Generally, HCT of emulsions was not significantly affected by alteration of constituent pre-heating temperatures. Model emulsions displayed higher HCTs with increasing pH and lower levels of intrinsic ash content. At both supplementation levels, calcium addition led to decreased HCTs. Supplementation with chloride salts caused a greater decrease in HCT compared to supplementation with citrate salts. Furthermore, soy protein hydrolysis was associated with lower emulsion thermal stability. Results demonstrate that modification of ingredient and manufacturing parameters may be a useful approach for enhancing thermal stability properties of soy protein stabilized emulsions.     

Influence of temperature,pH and ionic strength on the production of isoflavone-rich soy protein isolates

Soy protein isolates (SPI) may present different isoflavone profiles and contents, depending on processing conditions. In the present work, seven different SPI, resulting from changes in the processing steps, were obtained. The best parameters for obtaining isoflavone-richer SPI were: extraction at pH 9 and temperature of 55 °C, acid precipitation performed at pH 4.5, acid-washing of the precipitate and mild centrifugation conditions for the separation of acid-precipitated proteins. Isoflavones were soluble in aqueous solution in the pH range 2–10 (73–93% of the amount solubilized in 80% methanol). The profile of isoflavones was dependent on the temperature used for the aqueous extraction. Temperatures below 50 °C caused hydrolysis of β-glucosides with increase of aglucones, by endogenous β-glucosidase activity.     

Thermal stability of soy protein isolate and hydrolysate ingredients

The objective of this study was to characterize the effects of pH, protein concentration and calcium supplementation on thermal stability, at 140 °C, of soy protein isolate (SPI) and soy protein hydrolysate (SPH) ingredients. Increasing pH between 6.4 and 7.5 led to significantly (p < 0.05) higher mean heat coagulation times (HCTs) at 140 °C, for all soy protein ingredients at 1.8, and 3.6% (w/v) protein. Increasing protein concentration from 1.8 to 7.2% (w/v) led to shorter HCTs for protein dispersions. Calcium supplementation up to 850 mg/L, except in the case of supplementation of SPI 1 with calcium citrate (CaCit), decreased HCT for soy protein ingredient dispersions, at pH 6.4 – 7.5. No significant differences (p < 0.05) were found in mean HCT for dispersions supplemented with calcium chloride (CaCl₂) and those supplemented with CaCit at 450, 650 and 850 mg/L Ca²⁺, in the pH range 6.4–7.5.     

大豆降胆固醇活性肽的初步分离纯化

研究了大豆降胆固醇活性肽的初步分离纯化,用Alcalase碱性蛋白酶水解大豆分离蛋白得到的酶水解物经过大孔吸附树脂脱盐,并用不同浓度的乙醇以疏水性大小洗脱,得出浓度为75%的乙醇洗脱物具有最高的降胆固醇活性,将此洗脱物再经过SephadexG15凝胶过滤色谱进行分子量分级,得到了部分纯化的大豆降胆固醇肽,其最高降胆固醇活性肽是分子量大多在1000以下的小肽,抑制率为81.26%。     

Electrophoretic ripening index for the evaluation of proteolysis and the deduction of the age of Parmesan cheese

We have established an electrophoretic method to evaluate proteolysis in Parmesan cheese by means of an objective ripening index. The separation of caseins by alkaline polyacrylamide gel electrophoresis (PAGE) (12% T, 2.6% C, pH 8.9, 5 M urea) is followed by the densitometric analysis of the- and-casein fractions. The relationship between the resulting coefficients (-Cn/-Cn) and the age of reference samples of Original Italian Grana Padano (6–22 months) was linear up to 15 months, allowing an evaluation of the extent of proteolysis and therefore a deduction of the age of the Parmesan samples analysed. Based on this calibration we propose to use a threshold level of 1.3 (-Cn/-Cn) to verify the required age, i.e. 12 months, of Parmesan cheese, retailed as a loaf or prepacked slices. Commercially grated Parmesan samples may contain 20% cheese rind, which has a very low degree of casein breakdown. So a threshold level of 0.8 (-Cn/-Cn) is proposed for all grated Parmesan products. The preparation of reference solutions with defined coefficients (-Cn/-Cn), corresponding to the proteolysis indices of reference samples of different aged Grana Padano is described. The coefficients (-Cn/-Cn) as well as the-casein content of two additional series of reference samples and of 49 commercial Parmesan samples taken from retail outlets in Austria and Italy are presented.     

pH spatial distribution model during ripening of Camembert cheese

During ripening of Camembert cheese, a soft cheese, the pH values continually change, which impacts the growth of Listeria monocytogenes. In this study, a pH distribution model suitable for the ripening phase of Camembert cheese was developed and verified. An experimental trend-based statistical model for pH using normalized time and normalized pH as variables was developed to determine the evolution of pH. The pH model showed good agreement with the mean pH measured values, i.e., the pH model was able to capture the magnitudes and trends sufficiently. The R² values for top surface, center, inner-outer side surface, and bottom surface regions’ mean measured and pH model-predicted values were 0.97, 0.95, 0.99, and 0.99, respectively.     

Probiotic Cheddar cheese: Influence of ripening temperatures on survival of probiotic microorganisms, cheese composition and organic acid profiles

Bifidobacterium longum 1941, Bifidobacterium animalis subsp. lactis LAFTI^®B94 (B94), Lactobacillus casei 279, Lb. casei LAFTI^®L26 (L26), Lactobacillus acidophilus 4962 or Lb. acidophilus LAFTI^®L10 (L10) were used as an adjunct in the production of Cheddar cheeses which were ripened for 24 wk at 4 and 8 °C. Effects of ripening temperatures on survival of starter lactococci and probiotic microorganisms, pH and composition of cheeses and production of organic acids were examined. The counts of starter lactococci in cheeses produced with B. animalis B94, Lb. casei L26 or Lb. acidophilus 4962 ripened at 8 °C were significantly lower than those ripened at 4 °C (P < 0.05) at 24 wk. Probiotic microorganisms remained viable (>7.50 log₁₀ CFU/g) at the end of 24 wk and their viability was not affected by the ripening temperatures. There were significant effects of the type of probiotic microorganisms used, ripening time, ripening temperatures and their interactions on the concentration of lactic and acetic acids in the cheeses (P < 0.05). The acetic acid concentration in cheeses made with Bifidobacterium sp. or Lb. casei sp. was significantly higher than that of the control cheese (P < 0.05). Citric, propionic and succinic acids contents of the cheeses were not significantly affected by the type of probiotic microorganisms or ripening temperatures (P > 0.05).     

The effect of mendi (Chaerophyllum sp.) on ripening of vacuum-packed herby cheese

The composition, biochemical and sensory parameters of control cheese (without herbs) and four herby cheeses at 0.5, 1, 2 and 3% herb levels (mendi, Chaerophyllum sp.) ripened at 4 ± 1°C for 90 days were compared. As herb levels increased from 0.5 to 3%, dry matter and pH value decreased significantly. However, dry matter of all cheeses showed similar changes during ripening. The salt content of samples changed from 3.44 to 5.47% during ripening. There was a tendency toward slightly higher titratable acidity in cheeses with more added herbs. Ripening index, trichloroacetic acid-soluble nitrogen/total nitrogen, phosphotungstic acid-soluble nitrogen/total nitrogen, and lipolysis values of the cheese samples were affected by adding herbs and by ripening time. The most acceptable sensory score was obtained with 1% added herbs.     

Effect of ripening on total conjugated linoleic acid and its isomers in buffalo Cheddar cheese

Cheese is a biologically and biochemically dynamic product in which a series of sequential changes take place throughout its manufacture and subsequent ripening. These changes improve nutritional value, body and texture and enrich the flavour. Conjugated linoleic acids (CLA), a group of naturally occurring geometrical and positional isomers of linoleic acid, are present in high concentration in dairy products and fat from ruminant animals. Six isomers of CLA have been separated and identified by gas liquid chromatography (GLC) analysis. Buffalo milk had higher 9c,11t-18:2 isomer (86.14%). Total CLA concentration of CLA isomers was increased significantly ( P <  0.05) on conversion of milk into cheese and subsequent storage. The concentration of the 9c,11t-18:2 isomer was decreased significantly ( P <  0.05), whereas that of trans , trans -isomers (12,14-; 11,13-; 10,12-; 9,11-) increased significantly ( P <  0.05).     

Effect of some technological parameters on microbiological, chemical and sensory qualities of Civil cheese during ripening

The objective of this research was to determine the effects of different ripening methods [brine salting, dry salting, incorporating with Lor cheese (LR) and vacuum packaging] of Civil cheeses on its microbiological, chemical and sensory properties. Civil cheeses were analysed on the 2nd, 30th, 60th and 90th day of ripening. Chemical compositions of the cheeses were significantly different. While the highest dry matter and titratable acidity values were determined on dry salted cheeses, the highest fat and fat in dry matter contents were found in Civil cheese ripened together with LR. The water-soluble nitrogen and ripening index values were lower in cheese ripened incorporating with LR. Excessive proteolysis was not seen in any of cheese samples. The ripening in different methods affected microbiological and sensory properties of Civil cheese. Panellists preferred vacuum packaging and dry-salting cheeses compared to the other samples on the 90th day of ripening.     

黑豆豆乳添加量对Mozzarella奶酪成熟过程中品质的影响

在牛乳中添加不同的黑豆豆乳,研究不同的黑豆豆乳添加量对Mozzarella奶酪在成熟0 d、30 d、60 d、90 d时的水分活度、pH、质构、色泽、蛋白质降解等品质指标变化的影响。结果显示,随着黑豆豆乳添加量在2%～6%范围内的增大,奶酪的水分活度不断增大,pH不断降低,奶酪的硬度、弹性、粘附性、咀嚼性增加,奶酪的明亮度（L*值）下降,红度（a*值）和黄度（b*值）增加,而加入黑豆豆乳的奶酪在成熟过程中蛋白质降解与对照奶酪相似。综合各个指标,在牛乳中加入4%黑豆豆乳条件下制作的黑豆豆乳牛乳奶酪,既有独特的风味,同时奶酪具有较好的色度、质构、蛋白降解等指标特性。     

Volatile aroma components of soy protein isolate and acid-hydrolysed vegetable protein

The volatile aroma components of soy protein isolate (SPI) and acid-hydrolysed vegetable protein (aHVP) were compared by gas chromatography–mass spectrometry (GC–MS) and gas chromatography olfactometry (GCO). Major differences were found between the two soy-based products. Aliphatic aldehydes and ketones were mainly found in SPI, whereas pyrazines and sulphur-containing compounds were dominant in aHVP. Analyses of the non-volatile components showed that SPI was mainly protein (82.5%) with some lipid (3.5%), whereas aHVP contained no protein, only free amino acids (18.4%) and a trace quantity of lipid (0.4%). Polyunsaturates (47.8%), followed by saturates (24.9%) and monounsaturates (14.8%) dominated the fatty acid profile of the SPI lipid fraction. Both SPI and aHVP had a free fatty acid content <0.1%. Sensory analyses of aqueous suspensions of SPI and aHVP demonstrated significant differences in the odours of the two products. Compounds responsible for some of these differences were identified by GCO and GC–MS analyses of aqueous suspensions. The possible role of SPI and aHVP in the development of aroma in extrudates containing these soy products is discussed.     

Effect of supplementation of brine with calcium on the Feta cheese ripening

Feta blocks ripened in plain or calcium‐supplemented brine were analysed with respect to biochemical characteristics, proteolysis and inorganic fractions; moreover, the inorganic and N content of the respective brines was estimated. The acidification of Feta in supplemented brine was faster, the moisture content was lower, secondary proteolysis was more extended, and the organoleptic scores were higher compared to control Feta ripened in plain brine. The TCASN fraction of cheeses contributed more than that of WSN to the N enrichment of brine. It was concluded that calcium supplementation of the brine retarded the diffusion of cheese N and Ca into the brine.     

Effect of sesame protein isolate in partial replacement of milk protein on the rheological,textural and microstructural characteristics of fresh cheese

Soft cheeses were manufactured from bovine milk with the addition of 0–12% sesame protein isolate (SPI) were utilised to investigate rheology, texture and microstructure at different stages of cheese making. SPI addition reduced the speed of milk fermentation, kappa‐casein proteolysis of rennet and elongated the time of cheese curd formation. Renneted milk storage modulus G′_60min was decreased and coagulation time increased with increasing SPI content. Low SPI supplements (4% and 8%) enhanced the hardness, cohesiveness, adhesiveness and gumminess of the soft cheese, while high SPI addition (12%) deteriorated the texture. In the cheese curd gel matrix, SPI distributed as specific SPI‐gel clusters on the surface of curd fractures, stacked or fused with ball‐shaped casein micelles and wrapped up to casein gel strands. In summary, SPI actively interacted with casein colloid throughout the cheese making process.     

Microwave improvement of soy protein isolate–saccharide graft reactions

Soy protein isolate (SPI) was mixed with lactose, maltose, dextran or soluble starch (SS) and heated (temperature ?90 °C) by microwave irradiation. Compared to the classical heating, the microwave heating (MH) speeded up the graft reactions of SPI with sugars. From the results calculated, the rate constants of free amino groups in the grafts of SPI with lactose, maltose, dextran and SS by MH were, respectively, 6, 7, 57 and 12.3 times of those by classical heating. After heating by microwave, the lysine and arginine decreased and from, the FTIR spectroscopy of SPI and its grafts by MH, the absorbance of –C–O stretching and –OH deformation vibrations (1050–1150 cm⁻¹) and free –OH form (3643–3630 cm⁻¹) in SPI grafts increased compared to SPI. The temporal development of the graft reactions of SPI with sugars by MH was also shown by SDS–PAGE.     

The effect of refrigerated storage of raw milk on the physicochemical and microbiological quality of Tunisian semihard Gouda‐type cheese during ripening

A Tunisian semihard Gouda‐type cheese made from milk kept at 4 °C for 24, 48, 72 and 96 h was monitored during 45 days of ripening. The effect of milk refrigeration on the evolution of physicochemical parameters in relation to the quantitative variation of the microbial population during ripening of Gouda‐type cheese was investigated. Microbiological and physicochemical analyses were performed on raw milk and cheese samples after curding, 2, 9, 16, 23, 30, 37 and 45 days of ripening time. The raw milk kept under refrigeration at 4 °C for 96 h showed the highest microbial count and proteolysis level. The duration of storage significantly reduced the cheese yield as a result of important solubilisation casein in proteoses‐peptones. Results of different nitrogenous fractions by Kjeldahl method showed enzymatic hydrolysis products of casein whose intensity depended on the maturing stage as well as the refrigeration time. Besides the evident action of the plasmin, original milk protease, on the hydrolysis of casein in soluble fractions, the proteolysis of cheese caseins is also initiated by proteolytic action of the chymosin and extracellular heat‐resistant proteases notably produced by the same psychrotrophic microflora. Lactic acid bacteria starters that constitute the dominant microflora of this type of cheese are also considered as aroma precursors.     

Changes in the rheological properties of Iranian UF-Feta cheese during ripening

The frequency sweep test was used to evaluate storage modulus (G′), loss modulus (G′′) and loss tangent [tan (δ)] of Iranian UF-Feta cheese during ripening period (3, 20, 40 and 60 days). With development of ripening, storage and loss moduli increased at varying rates. The rate of increase in G′ was greater than that in G′′ resulting in a reduction in tan (δ). That is, storage modulus was dominant to loss modulus and as a result the elasticity nature was greater than the viscous nature of cheese samples. Due to the disruption of fat globules and proteolysis, protein matrix rearranged and formed a more compact texture containing aggregates of casein. Ripening did not influence the pH level and also the concentrations of dry matter, fat, salt, and total nitrogen in dry matter. However, water soluble nitrogen increased significantly (P < 0.05).