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Traceability of processed animal proteins with varying texture in feed: determination with microscopic and polymerase chain reaction methods

机译:饲料中具有不同质地的加工动物蛋白的可追溯性:显微和聚合酶链反应法测定

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To test the tiaceability of different animal components that could enter the feed chain two methods for the determination of processed animal proteins (PAPs) in feed - classical microscopy and polymerase chain reaction (PCR)-analysis - were applied inthe following study. To determine PAPs of varying but defined structure different animal meals were produced artificially and analysed after spiking to a set of 13 compound feed samples. The aims of the study were (i) to compare the capacity and the limits of both methods with respect to the determination of animal constituents of varying composition, (ii) to verify a correct interpretation of the results from each method and (iii) to determine an optimum application area for each method. Both methodscomplemented each other. The microscopic approach allowed a reproducible, high sensitive and quantitative determination of animal ingredients with morphological detectable structures, and in the presence of bone fragments a differentiation between fish and terrestrial animals was possible simultaneously. The PCR-analysis provided the detection of animal ingredients in feed even in absence of visible structures but fishmeal was not detected in a sufficient manner by the chosen screening setup. However, the PCR-method enabled to differentiate between animal groups or species and to identify animal species. The methods complemented each other not only in the analytical features but also regarding the results produced by the detection of two different analytical targets of PAPs, morphological structures and gene sequences, respectively. Suitable data regarding the presence of their analytical targets were produced by each method, but a combination of both methods enabled furthermore to report correct results regarding the presence of the artificially composed PAPs in the feed samples. It was concluded that a combination of microscopy and PCR-analysis is reasonable for special application purposes to determine PAPs in feed: while microscopy provides reliable results also in highly processed feed with well-preserved morphological animal structures even with highly degraded genomic material, PCR provides applicable results in feed samples with preserved genomic animal material even after the separation ofmorphological structures. These specialties have to be considered for the choice of capable analytical methods and even for a correct evaluation of the results obtained from these methods in highly processed feed. An interpretation scheme based on the results of the study was proposed.
机译:为了测试可能进入饲料链的不同动物成分的韧性,在以下研究中采用了两种测定饲料中加工的动物蛋白(PAP)的方法-经典显微镜和聚合酶链反应(PCR)分析。为了确定结构变化但结构明确的PAP,人工制作了不同的动物饲料,并在掺入一组13种复合饲料样品后进行了分析。该研究的目的是(i)比较两种方法在确定不同组成的动物成分方面的能力和局限性;(ii)验证每种方法的结果的正确解释;以及(iii)确定每种方法的最佳应用领域。两种方法相互补充。显微镜下的方法可以对具有形态学可检测结构的动物成分进行可重复,高灵敏度和定量测定,并且在存在骨碎片的情况下,可以同时区分鱼类和陆生动物。即使没有可见的结构,PCR分析也可以检测饲料中的动物成分,但是所选的筛选设置无法以足够的方式检测鱼粉。但是,PCR方法可以区分动物组或物种并识别动物物种。这些方法不仅在分析功能上相互补充,而且在通过检测PAP的两个不同分析目标(分别为形态结构和基因序列)产生的结果上也相互补充。每种方法均产生了有关其分析目标物存在的合适数据,但两种方法的组合还使报告了饲料样品中人工组成的PAP的存在的正确结果成为可能。结论是,显微镜和PCR分析的结合对于确定饲料中的PAP的特殊应用是合理的:尽管显微镜在经过高度加工的饲料中具有良好的形态动物结构,即使具有高度降解的基因组材料,也提供了可靠的结果,但是PCR提供了可靠的结果。即使在形态结构分离后,具有保留的基因组动物材料的饲料样品的适用结果。选择合适的分析方法,甚至正确评估在高度加工的饲料中从这些方法获得的结果时,都必须考虑这些专业。提出了基于研究结果的解释方案。

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