Matsuoka Yasuyuki, Arami Shin-Ichiro, Sato Megumi, Haraguchi Hiroyuki, Kurimoto Youichi, Imai Shinjiro, Tanaka Keiko, Mano Junichi, Furui Satoshi, Kitta Kazumi
Central Laboratory, Nippon Flour Mills Co., Ltd, Kanagawa, Japan.
Shokuhin Eiseigaku Zasshi. 2012;53(5):195-202. doi: 10.3358/shokueishi.53.195.
A PCR-based method was developed to distinguish between durum/common wheat and common wheat by leveraging slight differences of DNA sequence in Starch Synthase II (SS II) coded on wheat A, B and D genomes. A primer pair, SS II ex7-U/L, was designed to hybridize with a conserved DNA sequence region found in SS II-A, B and D genes. Another primer pair, SS II-D 1769U/1889L, was constructed to recognize a unique sequence in the SS II-D gene. The target region of SS II ex7-U/L with the size of 114 bp was amplified from durum and common wheat DNA, while no amplification was observed from any cereals other than those in the wheat genus. A DNA fragment with the size of 121 bp was specifically amplified from common wheat with SS II-D 1769U/1889L. In blended flour prepared from wheat and other cereals, the developed PCR system composed of two primer pairs effectively detected durum/common wheat and common wheat. These results suggested that PCR using two primer pairs is useful for detecting common and/or durum wheat in blended flour and could be utilized to ensure accurate food labeling.
通过利用小麦A、B和D基因组编码的淀粉合酶II(SS II)中DNA序列的细微差异,开发了一种基于PCR的方法来区分硬粒小麦/普通小麦和普通小麦。设计了一对引物SS II ex7-U/L,使其与在SS II-A、B和D基因中发现的保守DNA序列区域杂交。构建了另一对引物SS II-D 1769U/1889L,以识别SS II-D基因中的独特序列。从硬粒小麦和普通小麦DNA中扩增出大小为114 bp的SS II ex7-U/L目标区域,而从小麦属以外的任何谷物中均未观察到扩增。用SS II-D 1769U/1889L从普通小麦中特异性扩增出大小为121 bp的DNA片段。在由小麦和其他谷物制成的混合面粉中,由两对引物组成的已开发PCR系统有效地检测到了硬粒小麦/普通小麦和普通小麦。这些结果表明,使用两对引物的PCR可用于检测混合面粉中的普通小麦和/或硬粒小麦,并可用于确保准确的食品标签。