Allmann M, Candrian U, Höfelein C, Lüthy J
Department of Food Chemistry, University of Berne, Switzerland.
Z Lebensm Unters Forsch. 1993 Mar;196(3):248-51. doi: 10.1007/BF01202741.
A rapid, sensitive and specific analysis of food samples determining wheat contamination was established using polymerase chain reaction (PCR) technology. First, primers specific for highly conserved eukaryote DNA sequences were used to prove isolated nucleic acid substrate accessibility to PCR amplification. Subsequently, a highly repetitive and specific genomic wheat DNA segment was amplified by PCR for wheat detection. This assay was tested with 35 different food samples ranging from bakery additives to heated and processed food samples. In addition, the PCR method was compared to an immunochemical assay that detected the wheat protein component gliadin. Combination of both assays allowed a detailed characterization of wheat contamination. Hence, wheat flour contamination could be distinguished from gliadin used as a carrier for spices as well as from wheat starch addition.
利用聚合酶链反应(PCR)技术建立了一种快速、灵敏且特异的食品样本中小麦污染检测分析方法。首先,使用针对高度保守的真核生物DNA序列的引物来证明分离的核酸底物可用于PCR扩增。随后,通过PCR扩增一个高度重复且特异的小麦基因组DNA片段以检测小麦。该检测方法在35种不同的食品样本中进行了测试,这些样本涵盖了烘焙添加剂到加热和加工食品样本。此外,将PCR方法与检测小麦蛋白组分麦醇溶蛋白的免疫化学分析方法进行了比较。两种检测方法的结合能够对小麦污染进行详细表征。因此,可以区分小麦粉污染与用作香料载体的麦醇溶蛋白以及小麦淀粉添加。