Brezná Barbara, Dudásová Hana, Kuchta Tomás
Food Research Institute, Department of Microbiology and Molecular Biology, Priemyselná 4, P.O. Box 25, 824 75 Bratislava 26, Slovakia.
J AOAC Int. 2010 Jan-Feb;93(1):197-201.
A qualitative real-time PCR-based method for the detection of the Brazil nut (Bertholletia excelsa) component in food is described. The method consists of DNA isolation by chaotropic SPE and the subsequent PCR with Brazil nut-specific primers and a TaqMan fluorescent probe. The primers and the probe are targeted to the gene encoding for the 11s globulin of the Brazil nut. The method was positive for eight Brazil nut samples from the market and negative for all other tested plant and meat materials used in the food industry (36 samples). The intrinsic LOD of the method was 10 pg Brazil nut DNA. Using a series of model nut paste mixtures with defined Brazil nut contents, a practical detection limit of 0.1% (w/w) Brazil nut was estimated. Practical applicability of the entire method was tested by qualitative analysis of nine food samples; no discrepancies between the declared and detected Brazil nut contents were found. The presented PCR-based method is useful for sensitive and selective detection of Brazil nut in food samples.
描述了一种基于定性实时PCR的食品中巴西坚果(巴西栗)成分检测方法。该方法包括通过离液剂固相萃取法分离DNA,随后使用巴西坚果特异性引物和TaqMan荧光探针进行PCR。引物和探针靶向巴西坚果11S球蛋白的编码基因。该方法对市场上的8个巴西坚果样品呈阳性,对食品工业中使用的所有其他测试植物和肉类材料(36个样品)呈阴性。该方法的内在检测限为10 pg巴西坚果DNA。使用一系列具有确定巴西坚果含量的模型坚果酱混合物,估计实际检测限为0.1%(w/w)巴西坚果。通过对9个食品样品的定性分析测试了整个方法的实际适用性;未发现申报的和检测到的巴西坚果含量之间存在差异。所提出的基于PCR的方法可用于食品样品中巴西坚果的灵敏和选择性检测。