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荧光假单胞菌耐热蛋白酶对凝乳酶凝固特性和牛奶蛋白质水解的影响。

Effect of thermoresistant protease of Pseudomonas fluorescens on rennet coagulation properties and proteolysis of milk.

机构信息

Teagasc, Animal and Grassland Research and Innovation Centre, Moorepark, Fermoy, County Cork P61 C996, Ireland; School of Food and Nutritional Sciences, University College Cork, County Cork T12 K8AF, Ireland.

School of Food and Nutritional Sciences, University College Cork, County Cork T12 K8AF, Ireland.

出版信息

J Dairy Sci. 2020 May;103(5):4043-4055. doi: 10.3168/jds.2019-17771. Epub 2020 Mar 5.

Abstract

This study aimed to investigate the effect of different activity levels of a thermoresistant protease, produced by Pseudomonas fluorescens (ATCC 17556), on the cheesemaking properties of milk and proteolysis levels. Sterilized reconstituted skim milk powder was inoculated with the bacteria, and after incubation, centrifuged to obtain a supernatant-containing protease. Raw milk was collected and inoculated to obtain a protease activity of 0.15, 0.60, and 1.5 U/L of milk (treatments P1, P4, and P10, respectively). One sample was not inoculated (control) and noninoculated supernatant was added to a fifth sample to be used as a negative control. Samples were stored at 4°C for 72 h. After 0, 48, and 72 h, the rennet coagulation properties and proteolysis levels were assessed. The protease produced was thermoresistant, as no significant differences were observed in the activity in the pasteurized (72°C for 15 s) and nonpasteurized supernatants. The chromatograms and electrophoretograms indicated that the protease preferably hydrolyzed κ-casein and β-casein, and levels of proteolysis increased with added protease activity over storage time. The hydrolysis of α-caseins and major whey proteins increased considerably in P10 milk samples. At 0 h, the increase in the level of protease activity decreased the rennet coagulation time (RCT, min) of the samples, possibly due to synergistic proteolysis of κ-casein into para-κ-casein. However, over prolonged storage, hydrolysis of β-casein and α-casein increased in P4 and P10 samples. The RCT of P4 samples increased over time and the coagulum became softer, whereas P10 samples did not coagulate after 48 h of storage. In contrast, the RCT of P1 samples decreased over time and a firmer coagulum was obtained, possibly due to a lower rate of hydrolysis of β-casein and α-casein. Increased levels of protease could result in further hydrolysis of caseins, affecting the processability of milk over storage time.

摘要

本研究旨在探究荧光假单胞菌(ATCC 17556)产生的一种耐热蛋白酶的不同活性水平对牛奶的干酪制作特性和蛋白水解水平的影响。将细菌接种到消毒的再制脱脂奶粉中,孵育后离心获得含有蛋白酶的上清液。采集生奶,接种后使蛋白酶的活力分别达到 0.15、0.60 和 1.5 U/L 的牛奶(分别为处理 P1、P4 和 P10)。一个样本未接种(对照),并向第五个样本中添加非接种上清液作为阴性对照。样品在 4°C 下储存 72 h。在 0、48 和 72 h 后,评估凝乳酶凝固特性和蛋白水解水平。所产生的蛋白酶具有耐热性,因为巴氏杀菌(72°C 下 15 s)和未经巴氏杀菌的上清液中的酶活性没有显著差异。色谱图和电泳图表明,该蛋白酶优先水解κ-酪蛋白和β-酪蛋白,并且随着储存时间的增加和添加的蛋白酶活性的增加,蛋白水解水平增加。α-酪蛋白和主要乳清蛋白的水解在 P10 奶样中大大增加。在 0 h,样品中蛋白酶活性的增加降低了凝乳酶凝固时间(RCT,min),这可能是由于κ-酪蛋白协同水解成副κ-酪蛋白。然而,在长时间储存过程中,P4 和 P10 样品中β-酪蛋白和α-酪蛋白的水解增加。P4 样品的 RCT 随时间增加而增加,凝块变得更软,而 P10 样品在储存 48 h 后不再凝结。相比之下,P1 样品的 RCT 随时间降低,获得更坚实的凝块,这可能是由于β-酪蛋白和α-酪蛋白的水解速率较低。蛋白酶水平的增加可能导致乳蛋白进一步水解,影响牛奶在储存过程中的加工性能。

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