首页> 外文期刊>Journal of dairy research >Proteolytic patterns and plasmin activity in ewes' milk as affected by somatic cell count and stage of lactation.
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Proteolytic patterns and plasmin activity in ewes' milk as affected by somatic cell count and stage of lactation.

机译:受体细胞计数和泌乳阶段影响的母羊牛奶中的蛋白水解模式和纤溶酶活性。

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A total of 120 milk samples were collected from Comisana ewes throughout lactation. The ewes were ranked into two somatic cell count (SCC) categories: normal milk (N Milk) with SCC lower than 5.00x105/ml and high somatic cell milk (HSC Milk) with SCC higher than 1.00x106/ml. Milk samples were analysed in triplicate for pH, fat and protein contents, renneting parameters, and plasmin and plasminogen activities. The peptide profile due to total proteolytic activity (endogenous and exogenous enzymes) on alpha - and beta -CNs were determined using urea-PAGE on sodium caseinate (pH 8.0 and pH 5.0) incubated at 37 degrees C for 4 d after sampling. The peptide profile due to non-plasmin enzyme activities at pH 5.0 was also determined using urea-PAGE. Plasmin activity was higher in the HSC milk than in the N milk throughout the study period. A decrease in plasmin activity was observed in the N milk during mid-lactation, which was probably related to decrease in pH, and in the HSC milk during late lactation, which may be ascribed to an enhanced influx of plasmin inhibitors from the blood stream. Proteolytic patterns in Comisana ewe milk were mainly affected by plasmin activity that increased with the SCC in milk. Also non-plasmin proteolytic activity was strongly enhanced by elevated SCC and resulted in a higher degradation of alpha -casein than of beta -casein. In general, plasmin activity did not increase with the advancement of lactation and exhibited a different trend in HSC and N milk, suggesting that physiological factors did not play a key role in regulating the plasminogen-plasmin system in ewes' milk. Plasmin activity, detected with the colorimetric assay was consistent with proteolytic activity on sodium caseinate shown in urea-PAGE electrophoregram.
机译:整个泌乳期共从Comisana母羊中收集了120个牛奶样品。将母羊分为两类体细胞计数:SCC低于5.00x105 / ml的普通牛奶(N Milk)和SCC高于1.00x106 / ml的高体细胞奶(HSC Milk)。一式三份分析牛奶样品的pH,脂肪和蛋白质含量,凝乳酶参数以及纤溶酶和纤溶酶原活性。使用酪蛋白酸钠(pH 8.0和pH 5.0)在37℃下孵育4 d后的尿素-聚丙烯酰胺凝胶电泳测定因对α-和β-CN的总蛋白水解活性(内源和外源酶)而产生的肽谱。还使用尿素-PAGE测定了在pH 5.0时由于非纤溶酶活性引起的肽谱。在整个研究期间,HSC牛奶中的血浆纤溶酶活性均高于N牛奶。泌乳中期,N乳中的纤溶酶活性降低,这可能与pH降低有关;泌乳后期,HSC乳中,纤溶酶活性下降,这可能归因于来自血流的纤溶酶抑制剂的流入增加。 Comisana母羊牛奶中的蛋白水解模式主要受纤溶酶活性的影响,纤溶酶活性随牛奶中SCC的增加而增加。非纤溶酶的蛋白水解活性也通过升高的SCC而大大增强,并导致α-酪蛋白的降解程度高于β-酪蛋白。通常,纤溶酶活性不会随着泌乳的进行而增加,并且在HSC和N牛奶中呈现出不同的趋势,这表明生理因素在调节母乳中的纤溶酶原-纤溶酶系统中没有关键作用。用比色法检测到的纤溶酶活性与尿素-PAGE电泳图中显示的酪蛋白酸钠的蛋白水解活性一致。

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