首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
    
The present study focused on the isolation of individual caseins (α, β and κ) from defatted cow's milk using lactic acid‐mediated isoelectric precipitation coupled with cold extraction technique, followed by purification using sucrose‐based density gradient centrifugation method. In vitro characterisation of the isolated casein fractions confirmed preservation of micellar morphology throughout the experimental conditions with anionic surface charge and wider particle size range. The RP‐HPLC analysis showed a peak at retention time of 25.13 min and 27.84 min for α‐casein and β‐casein, respectively. Results confirmed isolation of pure casein fractions from cow's milk which could serve as a rich source of bioactive peptides for nutraceutical/pharmaceutical applications.  相似文献   

2.
    
Polymorphism of kappa‐casein (κ‐CN) gene in three Bos indicus cattle breeds was investigated using a polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) technique. Only genotypes AA and AB were observed, and no BB, AE, BE, EE, AC or BC genotypes were detected in the three cattle breeds. In the Sahiwal, Cholistani and Red Sindhi breeds, the frequencies of the allele A were 0.69, 0.90 and 0.86, and the frequencies of the allele B were 0.31, 0.10 and 0.14, respectively. The Sahiwal breed was found to have a higher frequency of the AB genotype as compared to the Cholistani and Red Sindhi breeds. The frequency of the κ‐CN alleles noted in the three cattle breeds was similar to those observed in other cattle breeds of B. indicus origin.  相似文献   

3.
    
A total of 259 cattle of four Turkish native cattle breeds, East Anatolian Red (EAR), South Anatolian Red (SAR), Turkish Grey (TG) and Anatolian Black (AB), Holstein and Brown Swiss (BS) breeds were genotyped for kappa‐casein (CSN3), bovine growth hormone (GH1) and prolactin (PRL) polymorphism by the polymerase chain reaction and restriction length polymorphism (PCR‐RFLP). The degree of genetic differentiation between populations FST was calculated as 0.053 and was found to be significant (P < 0.001). According to the genetic distance values (Nei), the highest genetic difference was found between SAR and EAR in four Turkish native cattle breeds and this difference was significant.  相似文献   

4.
    
In this study, prolactin gene polymorphism was investigated in Nili‐ Ravi buffaloes, Sahiwal and Achai cattle breeds, 100 per group, using polymerase chain reaction–restriction fragment length polymorphism (PCR‐RFLP) technique. Only genotype GG was observed in the case of Nili‐Ravi buffaloes. In Sahiwal and Achai cattle, three genotypes were found, AA, AG and GG: the frequency of these genotypes were 72%, 18% and 10% in Sahiwal cattle and 44%, 34% and 22% in Achai cattle, respectively. The frequency of genotype AA was found to be higher in both cattle breeds. Results of chi‐square test at P < 0.05 revealed that animals of Achai cattle were in Hardy–Weinberg equilibrium, whereas Sahiwal cattle were found to be deviating.  相似文献   

5.
LTQ-Orbitrap 液- 质联用技术对水牛奶酪蛋白的鉴定   总被引:1,自引:0,他引:1  
建立一种快速、高效的分析酪蛋白组分氨基酸序列的LTQ-Orbitrap质谱方法。为了研究水牛奶酪蛋白、乳牛奶酪蛋白和山羊奶酪蛋白的氨基酸序列组成及氨基酸的替换现象,采用LTQ-Orbitrap液-质联用技术分别对乳源酪蛋白的4种主要组分进行分析,搜索数据库获得4种组分的氨基酸全序列。与水牛奶4种酪蛋白组分进行比对。结果表明,乳牛奶的4种酪蛋白发生氨基酸替换的部位和比率明显小于山羊奶。这意味着与水牛奶酪蛋白相比,乳牛奶酪蛋白氨基酸的稳定性优于山羊奶酪蛋白。  相似文献   

6.
水牛奶中干物质含量较高,其综合营养价值高于普通牛奶,是多种生物活性成分的良好来源。因此,水牛奶及其相关制品受到越来越多的消费者的关注。本文根据水牛奶营养物质及其制品相关研究的前沿成果,介绍了水牛奶中蛋白质、脂肪、碳水化合物及其他营养物质的含量及其理化性质,同时针对水牛奶乳制品,如干酪、奶油、酸奶、冰淇淋等制备和相关研究进行了概述,最后针对水牛奶中的生物活性物质开发功能性食品的可能性提供了见解,为企业研发水牛奶相关产品提供参考。  相似文献   

7.
    
Kappa‐casein (κ‐CN) is the subtype of casein protein, an important constituent of bovine milk protein. The current study was undertaken to investigate the genetic polymorphism in κ‐CN gene of Nili‐ravi buffalo, Achai and Sahiwal cattle of Pakistan using polymerase chain reaction–restriction fragment length polymorphism (PCR‐RFLP) technique. The Nili‐ravi buffalo was found to be monomorphic (genotype BB only) for κ‐CN gene. Achai cattle were polymorphic for κ‐CN (having three genotypes AA, AB and BB) with a frequency of 0.70, 0.18 and 0.12, respectively, while in Sahiwal cattle, both the genotypes AA and AB were found with genotypic frequencies of 0.92 and 0.08, respectively. The presence of genotype BB in Achai cattle is surprising as it is absent in most of the cattle breeds worldwide.  相似文献   

8.
    
Microfiltration (MF) of milk was used to produce casein (CN) concentrates (80% protein) with reduced whey protein levels. By varying temperature of MF, we altered the proportion of β‐CN to αs‐CN in CN concentrates and compared them to milk protein concentrate (MPC). Casein content as a % of protein was approximately 90% for CN concentrates and approximately 80% for MPC. Smaller micelles and weaker rennet gels were observed for CN concentrates with low β‐CN level. Foam stability and yield stress values were higher for CN concentrates with a high β‐CN level. Modified CN concentrates can be produced by altering the proportions of individual CNs.  相似文献   

9.
The aim of this study was to assess the role of milk protein fractions in the coagulation, curd firming, and syneresis of bovine milk. Analyses were performed on 1,271 individual milk samples from Brown Swiss cows reared in 85 herds classified into 4 types of farming systems, from the very traditional (tied cows, feed manually distributed, summer highland pasture) to the most modern (loose cows, use of total mixed rations with or without silage). Fractions αS1-casein (CN), αS2-CN, β-CN, κ-CN, β-lactoglobulin (LG), and α-lactalbumin (LA) and genotypes at CSN2, CSN3, and BLG were obtained by reversed-phase HPLC. The following milk coagulation properties were measured with a lactodynamograph, with the testing time extended to 60 min: rennet coagulation time (RCT, min), curd firming time (min), and curd firmness at 30 and 45 min (mm). All the curd firmness measures recorded over time (total of 240 observations/sample) were used in a 4-parameter nonlinear model to obtain parameters of coagulation, curd firming, and syneresis: RCT estimated from the equation (min), asymptotic potential curd firmness (mm), the curd firming and syneresis instant rate constants (%/min), and the maximum curd firmness value (CFmax, mm) and the time taken to reach it (min). All the aforementioned traits were analyzed with 2 linear mixed models, which tested the effects of the protein fractions expressed in different ways: in the first, quantitative model, each protein fraction was expressed as content in milk; in the second, qualitative model, each protein fraction was expressed as a percentage of total casein content. Besides proteins, additional nuisance parameters were herd (included as a random effect), daily milk production (only for the quantitative model), casein content (only for the qualitative model), dairy system, parity, days in milk, the pendulum of the lactodynamograph, and the CSN2, CSN3, and BLG genotypes. Both αS1-CN and β-CN showed a clear and favorable effect on CFmax, where the former effect was almost double the latter. Milk coagulation ability was favorably affected by κ-CN, which reduced both the RCT and RCT estimated from the equation, increased the curd firming and syneresis instant rate constants, and allowed a higher CFmax to be reached. In contrast, αS2-CN delayed gelation time and β-LG worsened curd firming, both resulting in a low CFmax. The results of this study suggest that modification of the relative contents of specific protein fractions can have an enormous effect on the technological behavior of bovine milk.  相似文献   

10.
11.
12.
以未经热处理的水牛乳酪蛋白为对照,探究常见的4种热杀菌处理条件对水牛乳酪蛋白结构的影响,结果表明,加热产生大分子聚合物,大分子聚合物主要由二硫键联接形成;80 ℃时,水牛乳酪蛋白的起泡性和起泡稳定性最高,起泡性为137.33%,起泡稳定性为32.33%;超高温灭菌(135 ℃)条件下,水牛乳酪蛋白的平均粒径显著增加,粒径为516.2 nm;超高温灭菌乳的酪蛋白胶束被破坏,表面结构发生变化;热处理造成酪蛋白的二级结构发生变化,135 ℃条件下,α-螺旋结构和β-折叠含量显著下降,最小分别为13.76%和35.84%;酪蛋白的三级结构和表面疏水性发生改变,其中巴氏杀菌乳(80 ℃),荧光强度最高为582.44,超高温灭菌乳表面疏水性最大为258.96。基于上述结果,说明巴氏杀菌条件对酪蛋白的影响比较小,超高温条件容易造成蛋白聚集,从而影响产品的稳定性,80 ℃是较佳的热杀菌处理条件。从而为提升生产过程中水牛乳制品的稳定性提供理论基础。  相似文献   

13.
牛奶过敏原PCR检测方法的建立   总被引:1,自引:0,他引:1  
牛奶是主要的食品过敏原之一,其中β-乳球蛋白是引起牛奶过敏的主要成分。基于牛奶β-乳球蛋白基因序列设计一对PCR引物,经过反应条件的优化,建立了适合检测牛奶β-乳球蛋白过敏原的PCR方法。实验结果表明,当PCR反应体系中模板DNA量为25ng,引物浓度为4mmol/L时,检测效果最佳。所建立的方法不仅可用于不同保质期、不同来源牛奶β-乳球蛋白过敏原的测定,亦可用于牛、羊奶不同比例混合物中β-乳球蛋白过敏原的检测。  相似文献   

14.
利用双向电泳和基质辅助激光解吸电离飞行时间质谱(MALDI-MS)联用技术对水牛乳酪蛋白与其他乳源蛋白差异性进行了研究。根据Image Master 2D Platinum图像分析软件对不同乳源酪蛋白的双向电泳(2-DE)图谱进行蛋白斑点的匹配分析,获得21个存在于水牛奶中,主要分布在低丰度蛋白区的差异蛋白点,经质谱分析,得到4个属于水牛奶酪蛋白的主要组分,另外发现两个与水牛奶中的蛋白有较高同源性的新组分。  相似文献   

15.
    
Major allergen β‐lactoglobulin exists in many mammalian types of milk except human breast. Buffalo milk also contains this major allergen but the detailed information on its epitopes is not available. The aim of this work was to map and characterize its conformational antigenic epitopes. Sixty mimotopes of buffalo β‐lactoglobulin were produced by biopanning of phage display peptide library and then 2 mimotopes, specific for sera from rabbit 1 and 2, respectively, were predicted to be conformational epitope candidates by the use of DNAStar and web tool of MIMOX. On the basis of bioinformation analysis, 5 conserved amino acid residues PL‐ENK were identified in 2 conformational epitope sequences and 7 conformational epitopes were derived from 2 mimotopes by molecular modeling. The result showed that these conformational epitopes were located in the 2 regions on buffalo β‐lactoglobulin and composed of 5 hydrophilic and 2 hydrophobic amino acids.  相似文献   

16.
Proteolytic degradation and distribution of caseins and whey proteins between the soluble and colloidal phases were studied in six batches of commercial UHT milk (three skim and three whole milks) during storage at 25 ± 2 °C. For that purpose, at 30 day intervals, milk samples were ultracentrifuged and the pellets and supernatants analysed by capillary electrophoresis and SDS‐PAGE. Samples were also visually examined for signs of gelation. Extensive proteolytic degradation of the micellar fractions and severe changes in the electrophoretic pattern of the proteins present in the serum fractions were observed in all the batches. A higher proportion of denatured whey proteins not attached to the micelle surface was found in the skim milk samples as compared with the whole milk samples that could provide less resistance against gelation. In addition to β‐Lg, para‐κ‐casein was also found in the serum fraction. A high proteolytic activity against κ‐casein could be responsible for the hydrolysis of serum‐liberated κ‐casein or could have enhanced the liberation of β‐Lg–para‐κ‐casein complexes through proteolysis of micellar κ‐casein. © 1999 Society of Chemical Industry  相似文献   

17.
    
BACKGROUND: Identification of genotypes in Salvia is complicated owing to the morphological similarity and common occurrence of natural hybridisation within Salvia species. Species‐ and genotype‐specific DNA markers are very useful for plant identification, breeding and preservation programmes and can also provide a general overview on the prediction of plant essential oil yield. RESULTS: Polymerase chain reaction restriction fragment length polymorphism (PCR‐RFLP) was used for identification of species‐specific chloroplast and mitochondrial organelle DNA markers, and directed amplification of minisatellite DNA polymerase chain reaction (DAMD‐PCR) was used for genotyping of plant materials. Application of PCR‐RFLP resulted in species‐specific DNA markers, and use of DAMD‐PCR resulted in reproducible DNA patterns that are useful in Salvia genetic studies. Multivariate cluster analysis and principal coordinate analysis indicated that there were relationships between DNA marker patterns and essential oil yields at the species level. CONCLUSION: Results showed that genetic variations in Salvia are wide, and DNA patterns of relatedness among plant species appeared to correlate with essential oil yields. Further studies are required to confirm the application of PCR‐RFLP and DAMD‐PCR markers for selection of Salvia species with higher essential oil yield. Copyright © 2008 Society of Chemical Industry  相似文献   

18.
    
A total of 177 cattle of four breeds were genotyped for the bovine growth hormone (BGH)‐AluI polymorphism by polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP). The genotype and gene frequencies for each breed were determined and tested to be in Hardy–Weinberg equilibrium. According to breeds, frequencies of allele L gene were 0.905 for Brown Swiss, 0.898 for Holstein, 0.976 for East Anatolian Red and 0.893 for Turkish Grey Breeds. The allele L was predominant and variant VV was not detected in the breeds studied. BGH‐AluI genotypes were found to be in equilibrium within and among breeds.  相似文献   

19.
酶解水牛奶酪蛋白制备抗氧化活性肽工艺的研究   总被引:3,自引:0,他引:3       下载免费PDF全文
以水解度、还原能力和DPPH自由基清除率为检测指标,比较筛选碱性蛋白酶、中性蛋白酶、胰蛋白酶、木瓜蛋白酶和胃蛋白酶水解水牛奶酪蛋白制备抗氧化活性肽,筛选出中性蛋白酶是最适用酶。应用单因素和响应面法对酶解工艺进行优化。结果表明:中性蛋白酶酶解酪蛋白的最佳工艺参数:pH为6.9,温度为46℃,酶与底物浓度比为4.6%,酶解时间4.0h,此时10mg/mL酶解物的还原能力为0.457。实测结果与预测值符合性良好。   相似文献   

20.
    
A method for detection of the presence of pig derivatives in three types of food products—sausages and casings, bread and biscuits—using polymerase chain reaction–restriction fragment length polymorphism (PCR‐RFLP) analysis of a conserved region in the mitochondrial (mt) cytochrome b (cyt b) gene was developed. Genomic DNA of sausages and casings, bread and biscuits were extracted. The genomic DNA from the food products were found to be of good quality for the sausages and produced clear PCR products on the amplification of the mt cyt b gene of approximately 360 base pairs (bp). However, no genomic DNA was detected from the casing samples and poor quality of genomic DNA was extracted from bread and biscuits. No amplification of mt cyt b gene was produced from bread and biscuit samples. To differentiate between samples, the amplified PCR products were digested with restriction enzyme (RE) BsaJI, resulting in species‐specific RFLP. The cyt b PCR‐RFLP species identification assay gave excellent results for detection of pork adulteration in food products and is a potentially reliable technique to avoid species adulteration or fraudulent species substitution for halal authentication. Copyright © 2006 Society of Chemical Industry  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号