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利用聚合酶链式反应(PCR)开发区分混合面粉中硬粒小麦/普通小麦和普通小麦的方法。

Development of methods to distinguish between durum/common wheat and common wheat in blended flour using PCR.

作者信息

Matsuoka Yasuyuki, Arami Shin-Ichiro, Sato Megumi, Haraguchi Hiroyuki, Kurimoto Youichi, Imai Shinjiro, Tanaka Keiko, Mano Junichi, Furui Satoshi, Kitta Kazumi

机构信息

Central Laboratory, Nippon Flour Mills Co., Ltd, Kanagawa, Japan.

出版信息

Shokuhin Eiseigaku Zasshi. 2012;53(5):195-202. doi: 10.3358/shokueishi.53.195.

Abstract

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.

摘要

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。

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