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首页> 外文期刊>Dairy science & technology >Effect of rennet on the composition, proteolysis and microstructure of reduced-fat Cheddar cheese during ripening
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Effect of rennet on the composition, proteolysis and microstructure of reduced-fat Cheddar cheese during ripening

机译:凝乳酶对成熟过程中低脂切达干酪的组成,蛋白水解和微观结构的影响

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摘要

Rennet is an important ingredient in Cheddar cheese manufacturing and both the type used and the concentration applied can affect the ripening process. In this work, reduced-fat Cheddar cheese was produced using different concentrations of microbial rennet (Hannilase; 0.026, 0.052 and 0.150 international milk clotting units (IMCU).g(-1) of milk) as well as recombinant camel chymosin (0.052 IMCU.g(-1) of milk). The composition of the resulting cheeses was not statistically different, but the ratio of pH 4.6 soluble nitrogen/total nitrogen (pH 4.6-SN/TN) increased significantly with increasing Hannilase rennet concentration. This ratio was also significantly lower in the cheese made with recombinant camel chymosin at a similar rennet concentration. Microstructural, biochemical and textural changes in the cheese were also monitored during ripening. The gel made with a high rennet concentration was qualitatively more porous but these changes in porosity were not reflected in the freshly pressed cheese. After 31 weeks of ripening, the cheese made with recombinant camel chymosin had a thicker protein network compared to the cheese made with microbial rennet (Hannilase), possibly due to lower proteolysis. Most of the Hannilase rennet was lost to the whey when the rennet was increased above the concentration of 0.052 IMCU.g(-1) of milk. A lower concentration of Hannilase rennet may prove beneficial, as the texture was not significantly affected at the end of the observed ripening period. Recombinant camel chymosin may potentially be used as a substitute for products requiring lower proteolysis during ripening. However, the texture of this cheese was harder than the cheese made with Hannilase rennet at the end of the ripening period.
机译:凝乳酶是切达干酪生产中的重要成分,所用类型和所用浓度均会影响成熟过程。在这项工作中,使用不同浓度的微生物凝乳酶(Hannilase; 0.026、0.052和0.150国际牛奶凝块单位(IMCU).g(-1)牛奶)以及重组骆驼凝乳酶(0.052 IMCU)生产了低脂切达干酪.g(-1)牛奶)。所得干酪的组成没有统计学差异,但是随着Hannilase凝乳酶含量的增加,pH 4.6可溶性氮/总氮的比率(pH 4.6-SN / TN)显着增加。用重组骆驼凝乳酶在类似凝乳酶浓度下制成的奶酪中,该比例也显着降低。在成熟过程中,还对奶酪的微观结构,生化和质地变化进行了监测。凝乳酶含量高的凝胶定性上更多孔,但孔隙率的这些变化未在新鲜压制的奶酪中反映出来。成熟31周后,与使用微生物凝乳酶(Hannilase)制成的奶酪相比,重组骆驼凝乳酶制成的奶酪具有较厚的蛋白质网络,这可能是由于较低的蛋白水解作用所致。当将凝乳酶增加到0.052 IMCU.g(-1)的牛奶浓度以上时,大多数汉尼酵母酶凝乳酶就会丢失给乳清。较低浓度的Hannilase凝乳酶可能被证明是有益的,因为在观察到的成熟期结束时质地并未受到明显影响。重组骆驼凝乳酶可以潜在地替代成熟期间需要较低蛋白水解的产品。但是,在成熟期结束时,这种奶酪的质地比用Hannilase凝乳酶制成的奶酪要硬。

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