共查询到19条相似文献,搜索用时 62 毫秒
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通过提高乳清蛋白粉水解产物(Whey protein powder hydrolysate,WPPH)的抗氧化活性,对乳清蛋白粉的酶解工艺进行优化。首先以WPPH水解度及抗氧化活性(1,1-二苯基-2-三硝基苯肼(1,1-diphenyl-2-picrylhydrazyl,DPPH)自由基清除率、羟自由基清除率、总抗氧化能力)为指标,从4种蛋白酶中筛选得到酶解效果较好的胰蛋白酶和菠萝蛋白酶。然后通过单因素与正交试验确定双酶协同水解乳清蛋白粉的最适酶解条件。结果表明:复合酶最优酶解条件为菠萝蛋白酶和胰蛋白酶以1:1的比例同时添加,pH6.0、温度50℃、酶底比0.3%、底物浓度3 g/100 mL、酶解时间2.5 h,在此条件下WPPH水解度达到34.24%,分子量低于1000 Da的肽段占比在50%以上,DPPH自由基清除率91.42%±0.51%、羟自由基清除率80.85%±0.47%、总抗氧化能力(46±0.65)μmol/L。在本研究确定的酶解工艺条件下,乳清蛋白粉水解产物具有较强的抗氧化活性,在天然抗氧化剂和保健食品领域有一定的开发利用价值。 相似文献
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花生蛋白酶水解产物抗氧化活性研究 总被引:9,自引:0,他引:9
利用蛋白酶水解花生蛋白并对水解产物的抗氧化活性进行研究.采用中性蛋白酶AS1.398和低温高碱性蛋白酶水解花生蛋白,AS1.398的水解条件为:温度55℃,pH6.5,底物浓度5.0%,酶用量1.0%,水解时间6 h;碱性蛋白酶的水解条件为:温度40℃,pH7.5,底物浓度5.0%,酶用量2.0%,水解时间6 h.在此条件下进行水解、灭酶、离心除去不溶性的成分,水解产物冷冻干燥.酶水解产物的抗氧化活性用油脂的过氧化值进行评价.产物添加到猪油中,65℃恒温保存30 d,每隔一定时间取样测定其过氧化值.Rancimat也用于评价花生蛋白酶水解产物的抗氧化活性,添加不同的酶水解产物后测定样品的氧化诱导期,用诱导期作为花生蛋白酶水解产物的抗氧化活性的评价指标.研究结果表明,花生蛋白酶水解产物具有一定的抗氧化性能. 相似文献
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乳清蛋白抗氧化肽的制备及体外抗氧化活性研究 总被引:1,自引:0,他引:1
采用酶解法制备乳清蛋白抗氧化肽并研究其体外抗氧化活性。结果表明:以羟自由基清除率和多肽含量为指标,筛选出中性蛋白酶为最优酶;在单因素试验的基础上,通过响应面试验确定最佳酶解条件为pH 5. 50、酶解温度65℃、酶解时间1. 65 h、底物质量分数5%、加酶量5 000 U/g,此条件下乳清蛋白抗氧化肽对羟自由基清除率为74. 54%;乳清蛋白抗氧化肽对羟自由基、ABTS+自由基、DPPH自由基和超氧阴离子自由基都具有较好的清除能力,IC50值分别为2. 174、0. 709、2. 813mg/m L和4. 579 mg/m L。表明乳清蛋白抗氧化肽具有较强的体外抗氧化活性,具有一定的开发利用价值。 相似文献
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研究干酪乳清酶解产物对小鼠抗氧化活性产生的影响。给小鼠灌胃干酪乳清酶解产物样品后,通过测定小鼠肝脏和血清中超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)和丙二醛(MDA)三种指标,研究其抗氧化功能。干酪乳清的木瓜蛋白酶和碱性蛋白酶水解产物可以提高小鼠肝脏和血清中的SOD的含量,与假衰老组差异不显著。乳清的碱性蛋白酶水解产物提高小鼠肝脏和血清中的GSH-PX的含量,差异性显著。乳清的木瓜蛋白酶和碱性蛋白酶水解产物对雄性小鼠的肝脏和血清中MDA含量影响不著性。用干酪乳清酶解产物喂养小鼠,能明显增强抗氧化活性,效果明显优于乳清。 相似文献
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干酪乳清Alcalase 2.4L酶解的最优条件,即酶解时间为2 h、pH 9.5、酶与底物比为4%、酶解温度为50 ℃。利用超滤、葡聚糖凝胶层析和三羟甲基氨基甘氨酸-十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(tricine-sodiumdodecyl sulfate-polyacrylamide gelelectrophoresis,tricine SDS-PAGE)等方法从干酪乳清中提取抗氧化性蛋白肽。分别考察操作压力、料液温度、料液pH值、操作时间对超滤膜膜通量的影响。乳清酶解物超滤的最佳条件为:压力0.25 MPa、温度30 ℃、时间120 min、初始pH 9.0。分子质量4 000~6 000 D肽的水解液脂质过氧化抑制率最高,达到47.28%。利用Sephadex G-50型葡聚糖凝胶进行纯化,将分离的组分进行Tricine-SDS-PAGE分析和脂质过氧化抑制率的测定。第34管洗脱液的脂质过氧化抑制率最高,分子质量范围为4 000~4 100 D。 相似文献
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Hyun Soo Shin Sang Bum Kim Soo Cheol Kang Muhammad Ajmal Khan Hyeon Shup Kim Hyun Jung Shin Chi Hoon Chang 《Journal of the science of food and agriculture》2007,87(11):2055-2060
This study examined the effect of different proteolytic enzymes on the production of cheese whey protein (CWP) hydrolysates with low antigenicity. Four enzyme combinations (1:1) trypsin + papain W‐40 (TP), trypsin + neutrase 1.5 (TN), papain W‐40 + protease S (PP) and papain W‐40 + neutrase 1.5 (PN) were added at the rate of 1% of the CWP and it was incubated for 15, 30, 60, 90, 120 and 180 min at 50 °C. CWP hydrolysis and its non‐protein nitrogen concentrations were higher with TP and TN compared with PP and PN at all incubation times. The SDS‐PAGE revealed complete removal of α‐lactalbumin (α‐LA) and β‐lactoglobulin (β‐LG) from hydrolysates produced by trypsin‐containing enzyme mixtures. Reverse‐phase HPLC analysis ascertained the CWP hydrolysis and SDS‐PAGE results. The lowest antigenicity in CWP hydrolysates was observed with the use of trypsin‐containing enzyme mixtures compared with other enzyme combinations. Present results suggested that TP and TN combinations were the most effective for CWP hydrolysis for the removal of β‐LG from CWP. Further research is warranted to identify the peptides in CWP hydrolysates produced with these enzyme combinations that may help enhance the utilisation of whey protein in human food. Copyright © 2007 Society of Chemical Industry 相似文献
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Xueming Xu Ruyan Cao Liu He Na Yang 《Journal of the science of food and agriculture》2009,89(11):1897-1903
BACKGROUND: In China alone, more than 400 million pigs are slaughtered each year to provide meat. Porcine blood is rich in proteins but is usually discarded, which can cause environmental contamination. Recovering porcine blood and converting it to high‐value products is therefore economically and environmentally desirable. However, very little information on antioxidant peptides from porcine blood by‐products is currently available. In this study the antioxidant properties of porcine plasma hydrolysates PPE and PPA prepared with pepsin and papain respectively were investigated. RESULTS: Both PPE and PPA showed excellent antioxidant activity in a linoleic acid system (AL) compared with α‐tocopherol (VE) at the same concentration (P < 0.01). Their activities were respectively 3.33 and 1.83 times stronger than that of VE at a concentration of 10 µg mL?1 and 5.4 and 5.6 times stronger at 100 µg mL?1. The 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical‐scavenging activity (DRSA) reached 48.4 and 43.1% for PPE and PPA respectively at 500 µg mL?1. The ferrous ion‐chelating power (FICP) of PPE at 100 µg mL?1 was about 1.5 times stronger than that of 10 µmol L?1 ethylene diamine tetraacetic acid (EDTA) in a 50 µmol L?1 Fe2+ system, whereas the FICP of PPA at 100 µg mL?1 was 61% that of 10 µmol L?1 EDTA. Furthermore, PPE was separated on Resource 15RPC and Superdex peptide 10/300GL columns, and the antioxidant activity of the peptides and its relationship to their polarity and molecular weight (MW) were analysed. The hydrolysate was divided into four groups (R1–R4) with hydrophobicities ranging from weak to strong by Resource 15RPC, while it was divided into three groups (S1, MW 7–12 kDa; S2, MW 3–7 kDa; S3, MW 1–3 kDa) by Superdex peptide 10/300GL. CONCLUSION: The results showed that AL was significantly and positively correlated with the relative amounts of R1, S2 and S3 and that DRSA was dependent on R3 and S1. The fractions of PPE were not responsible for FICP. Copyright © 2009 Society of Chemical Industry 相似文献
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酶解对乳清蛋白抗原性影响的研究 总被引:6,自引:0,他引:6
研究了酶解对乳清蛋白抗原性的影响。选择了7种常见蛋白酶在同一水解模式下水解乳清蛋白,用竞争ELISA法测定水解物的残留抗原性,从而间接测定其过敏性变化。结果表明,酶解能有效降低乳蛋白抗原性,但水解物仍能与特异抗体反应,保留一部分抗原性。不同酶对乳清蛋白过敏原的影响不同,酶的特异性对乳清蛋白水解物的抗原性有较大的影响,碱性蛋白酶降低乳蛋白抗原性的效果最佳,对抗β-乳球蛋白(β-LG)和抗α-乳白蛋白(α-LA)抗体的抗原性分别降低了50.02%和99.72%。 相似文献