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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Simple and inexpensive method for the reliable determination of additions of soybean proteins in heat-processed meat products: an alternative to the AOAC official method
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Simple and inexpensive method for the reliable determination of additions of soybean proteins in heat-processed meat products: an alternative to the AOAC official method

机译:简单可靠的方法,可可靠地确定热加工肉制品中大豆蛋白的添加量:AOAC官方方法的替代方法

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摘要

Despite the existence of an AOAC official method based on an enzyme-linked immunosorbent assay (ELISA) for the determination of additions of soybean proteins in meat products, its use for quantitative assessment is limited. Accordingly, a simple and inexpensive method has been developed and validated in this work. The method involves defatting the meat samples with acetone, solubilization of soybean proteins in a 30 mM Tris-HCl buffer (pH 8) containing 0.5% (v/v) 2-mercaptoethanol, and the identification of two peaks from soybean proteins in the chromatogram obtained by perfusion reversed-phase chromatography and UV detection. Determination of soybean proteins by the proposed method did not suffer from matrix interferences, with a good linear correlation up to a concentration of 12.50 mg/mL soybean proteins being observed. The proposed method was proven to be specific, precise, accurate, robust, and sensitive, making possible the detection and the quantitation of additions of 0.07% (w/w) and 0.25% (w/w), respectively, of soybean proteins in meat products (related to 1 g of initial product). The method has been applied to the determination of the soybean protein content in commercial heat-processed meat products, obtaining results that were statistically similar to those obtained by the official ELISA method but with a higher reliability and simplicity and a lower cost and analysis time.
机译:尽管存在基于酶联免疫吸附测定(ELISA)的AOAC官方方法来确定肉制品中大豆蛋白的添加量,但其在定量评估中的应用受到限制。因此,已经开发并验证了一种简单且廉价的方法。该方法包括用丙酮使肉样品脱脂,将大豆蛋白溶解在含有0.5%(v / v)2-巯基乙醇的30 mM Tris-HCl缓冲液(pH 8)中,并从色谱图中的大豆蛋白中鉴定出两个峰通过灌注反相色谱和紫外检测获得。通过所提出的方法测定大豆蛋白不会受到基质干扰,在高达12.50 mg / mL的大豆蛋白浓度下,线性关系良好。实践证明,该方法具有特异性,精确性,准确性,鲁棒性和灵敏性,使得分别检测和定量分析大豆蛋白中0.07%(w / w)和0.25%(w / w)的添加量成为可能。肉类产品(与1克初始产品有关)。该方法已用于测定商品热加工肉制品中的大豆蛋白质含量,获得的结果与官方ELISA方法所获得的结果在统计学上相似,但具有更高的可靠性和简便性,并且成本和分析时间更低。

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