Escola de Veterinária da Universidade Federal de Minas Gerais, Avenida Antônio Carlos, 6627, Belo Horizonte, 30123-970, Brazil.
Instituto Mineiro de Agropecuária, Rodovia Américo Gianetti, 4001, Belo Horizonte, 31630-901, Brazil.
Poult Sci. 2017 Sep 1;96(9):3375-3381. doi: 10.3382/ps/pex108.
In order to evaluate the efficiency of the pasteurization process in liquid whole eggs, an UV/visible spectrophotometric method was developed and validated for the assessment of alpha-amylase activity. Samples were collected from 30 lots of raw eggs (n = 30) and divided into three groups: one was reserved for analysis of the raw eggs, the second group was pasteurized at 61.1°C for 3.5 minutes (n = 30), and the third group was pasteurized at 64.4°C for 2.5 minutes (n = 30). In addition to assessing alpha-amylase activity, the microbiological quality of the samples was also evaluated by counting total and thermotolerant coliforms, mesophilic aerobic microorganisms, Staphylococcus spp., and Salmonella spp. The validated spectrophotometric method demonstrated linearity, with a coefficient of determination (R2) greater than 0.99, limits of detection (LOD) and quantification (LOQ) of 0.48 mg kg-1 and 1.16 mg kg-1, respectively, and acceptable precision and accuracy with relative standard deviation (RSD) values of less than 10% and recovery rates between 98.81% and 105.40%. The results for alpha-amylase activity in the raw egg samples showed high enzyme activity due to near-complete hydrolysis of the starch, while in the eggs pasteurized at 61.1°C, partial inactivation of the enzyme was observed. In the samples of whole eggs pasteurized at 64.4°C, starch hydrolysis did not occur due to enzyme inactivation. The results of the microbiological analyses showed a decrease (P < 0.0001) in the counts for all the studied microorganisms and in the frequency of Salmonella spp. in the pasteurized egg samples according to the two binomials under investigation, compared to the raw egg samples, which showed high rates of contamination (P < 0.0001). After pasteurization, only one sample (3.33%) was positive for Salmonella spp., indicating failure in the pasteurization process, which was confirmed by the alpha-amylase test. It was concluded that the validated methodology for testing alpha-amylase activity is adequate for assessing the efficiency of the pasteurization process, and that the time-temperature binomial used in this study is suitable to produce pasteurized eggs with high microbiological quality.
为了评估液态全蛋液巴氏消毒过程的效率,建立并验证了一种用于评估α-淀粉酶活性的 UV/可见分光光度法。从 30 批生鸡蛋(n=30)中采集样本,并将其分为三组:一组用于分析生鸡蛋,第二组在 61.1°C 下巴氏消毒 3.5 分钟(n=30),第三组在 64.4°C 下巴氏消毒 2.5 分钟(n=30)。除了评估α-淀粉酶活性外,还通过计数总耐热大肠菌群、需氧嗜温微生物、金黄色葡萄球菌和沙门氏菌来评估样品的微生物质量。验证后的分光光度法表现出良好的线性,决定系数(R2)大于 0.99,检测限(LOD)和定量限(LOQ)分别为 0.48 mg kg-1和 1.16 mg kg-1,具有可接受的精密度和准确度,相对标准偏差(RSD)值小于 10%,回收率在 98.81%至 105.40%之间。生鸡蛋样本中α-淀粉酶活性的结果显示,由于淀粉几乎完全水解,酶活性很高,而在 61.1°C 巴氏消毒的鸡蛋中,观察到酶的部分失活。在 64.4°C 巴氏消毒的全蛋液样本中,由于酶失活,淀粉水解未发生。微生物分析的结果表明,与生鸡蛋样本相比,在所研究的所有微生物的数量以及沙门氏菌的频率均显著降低(P<0.0001),这表明巴氏消毒鸡蛋样本的污染率很高(P<0.0001)。巴氏消毒后,只有一个样本(3.33%)呈沙门氏菌阳性,表明巴氏消毒过程失败,这通过α-淀粉酶测试得到了证实。研究得出结论,所建立的用于检测α-淀粉酶活性的方法适用于评估巴氏消毒过程的效率,并且本研究中使用的时间-温度组合适用于生产具有高微生物质量的巴氏消毒鸡蛋。