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Bioassay for Nisin in Milk Processed Cheese Salad Dressings Canned Tomatoes and Liquid Egg Products

机译:牛奶加工奶酪色拉调味品番茄罐头和蛋液产品中乳链菌肽的生物测定

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摘要

A sensitive nisin quantification bioassay was constructed, based on Lactococcus lactis chromosomally encoding the nisin regulatory proteins NisK and NisR and a plasmid with a green fluorescent protein (GFP) variant gfpuv gene under the control of the nisin-inducible nisA promoter. This strain, LAC275, was capable of transducing the signal from extracellular nisin into measurable GFPuv fluorescence through the NisRK signal transduction system. The LAC275 cells detected nisin concentrations of 10 pg/ml in culture supernatant, 0.2 ng/ml in milk, 3.6 ng/g in processed cheese, 1 ng/g in salad dressings and crushed, canned tomatoes, and 2 ng/g in liquid egg. This method was up to 1,000 times more sensitive than a previously described GFP-based nisin bioassay. This new assay made it possible to detect significantly smaller amounts of nisin than the presently most sensitive published nisin bioassay based on nisin-induced bioluminescence. The major advantage of this sensitivity was that foods could be extensively diluted prior to the assay, avoiding potential inhibitory and interfering substances present in most food products.
机译:基于乳酸乳球菌的染色体编码乳酸链球菌素调节蛋白NisK和NisR,以及在乳酸链球菌素可诱导的nisA启动子的控制下,带有绿色荧光蛋白(GFP)变体gfpuv基因的质粒,构建了敏感的乳酸链球菌素定量生物测定法。该菌株LAC275能够通过NisRK信号转导系统将细胞外乳链菌肽的信号转导至可测量的GFPuv荧光。 LAC275细胞在培养上清液中检测到的乳链菌肽浓度为10 pg / ml,在牛奶中检测到的乳链菌肽浓度为0.2 ng / ml,在加工奶酪中检测到的乳链菌肽浓度为3.6 ng / g,在色拉调味料和番茄酱中的1 ng / g压碎,罐装番茄,液体中的浓度为2 ng / g蛋。该方法的灵敏度比以前描述的基于GFP的乳链菌肽生物测定高1000倍。与目前基于乳链菌肽诱导的生物发光的最敏感的乳链菌肽生物检测法相比,这种新的检测方法可以检测到显着更少的乳链菌肽。这种敏感性的主要优点是可以在检测前将食品充分稀释,避免了大多数食品中存在的潜在抑制和干扰物质。

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