Hasenkopf K, Ubel B, Bordiehn T, Pischetsrieder M
Friedrich-Alexander-University Erlangen, Institute of Pharmacy and Food Chemistry, Schuhstrasse 19, D-91052 Erlangen, Germany.
Nahrung. 2001 Jun;45(3):206-9. doi: 10.1002/1521-3803(20010601)45:3<206::AID-FOOD206>3.0.CO;2-1.
Oxalic acid monolysinylamide (OMA), a Maillard product which had initially been identified as a reaction product of L-ascorbic acid, was formed, dependent on the reaction conditions, also from other carbohydrate sources. At elevated temperatures and in the presence of oxygen, the reaction of lactose with proteins resulted in the formation of relatively high amounts of OMA. Using a polyclonal antibody, which bound with high specificity and affinity to OMA-modified proteins, a competitive enzyme linked immunosorbent assay (ELISA) was developed to measure OMA formation in heat-treated milk products. The assay performance was characterized for OMA-modified beta-lactoglobulin diluted in buffer or pasteurized milk. For the latter, the least detectable dose was determined as 1.4 ng/ml with a linear range for quantification between 2 ng/ml and 200 ng/ml. For some samples intra- and interassay variation were determined. The ELISA was used to measure OMA-formation in heated milk and commercially available infant formula.
草酸单赖氨酰胺(OMA)是一种美拉德产物,最初被鉴定为L - 抗坏血酸的反应产物,根据反应条件,它也可由其他碳水化合物来源生成。在高温和有氧条件下,乳糖与蛋白质的反应会生成相对大量的OMA。利用一种与OMA修饰蛋白具有高特异性和亲和力的多克隆抗体,开发了一种竞争性酶联免疫吸附测定法(ELISA)来测量热处理乳制品中OMA的生成。该测定法针对在缓冲液或巴氏杀菌牛奶中稀释的OMA修饰的β - 乳球蛋白进行了性能表征。对于后者,最低检测剂量确定为1.4 ng/ml,定量线性范围为2 ng/ml至200 ng/ml。测定了一些样品的批内和批间变异。ELISA用于测量加热牛奶和市售婴儿配方奶粉中OMA的生成。