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trnL(UAA)-trnF(GAA) 基因间隔区是鉴定经济价值较高的开心果(Pistacia vera L.)中掺入绿豌豆(Pisum sativum L.)的有效标记。

The trnL (UAA)-trnF (GAA) intergenic spacer is a robust marker of green pea (Pisum sativum L.) adulteration in economically valuable pistachio nuts (Pistacia vera L.).

机构信息

Department of Biotechnology, Faculty of Science, Necmettin Erbakan University, Konya, Turkey.

Department of Molecular Biology and Genetics, Faculty of Science, Necmettin Erbakan University, Konya, Turkey.

出版信息

J Sci Food Agric. 2020 May;100(7):3056-3061. doi: 10.1002/jsfa.10336. Epub 2020 Feb 27.

Abstract

BACKGROUND

Pistachio (Pistacia vera L.) is an expensive culinary nut species; it is therefore susceptible to adulteration for economic profit. Green pea (Pisum sativum L.) kernels constitute the most common material used for adulterating chopped / ground pistachio nuts and pistachio paste. Food genomics enables the species composition of a food sample to be ascertained through DNA analysis. Accordingly, a barcode DNA genotyping approach was used to standardize a test method to identify green pea adulteration in pistachio nuts.

RESULTS

The trnL (UAA)-trnF (GAA) intergenic spacer in the plastid genome was the target analyte in the present study. The barcode locus displayed a significant, discriminatory size difference between pistachio and pea, with amplicon sizes of 449 and 179 bp, respectively. Polymerase chain reaction-capillary electrophoresis (PCR-CE) analysis of the intergenic spacer resulted in the successful identification of species composition in the in-house admixtures, which contained 5% to 30% of green pea.

CONCLUSION

The present work describes a fast and straightforward DNA test that identifies green pea adulteration in pistachio nuts without requiring a statistical data interpretation process. The plastid trnL (UAA)-trnF (GAA) intergenic spacer length widely varies among plant taxa, so the PCR-CE protocol that operates on the intergenic spacer holds the potential to reveal adulteration with a plethora of adulterants. The PCR-CE assay described in the present work can be adopted readily by food-quality laboratories in the public sector or the food industry as an easy and reliable method to analyze pistachio authenticity. © 2020 Society of Chemical Industry.

摘要

背景

开心果(Pistacia vera L.)是一种昂贵的食用坚果,因此容易为了经济利益而被掺假。青豆(Pisum sativum L.)仁是掺假碎/磨开心果和开心果酱最常用的材料。食品基因组学使通过 DNA 分析能够确定食品样品的物种组成。因此,采用条码 DNA 基因分型方法对识别开心果中青豆掺假的测试方法进行了标准化。

结果

本研究的靶标分析物是质体基因组中的 trnL(UAA)-trnF(GAA)基因间隔区。条码基因座在开心果和豌豆之间显示出显著的、可区分的大小差异,扩增子大小分别为 449bp 和 179bp。基因间隔区的聚合酶链反应-毛细管电泳(PCR-CE)分析导致能够成功识别内部混合物的物种组成,其中含有 5%至 30%的青豆。

结论

本工作描述了一种快速而直接的 DNA 测试方法,可识别开心果中的青豆掺假,而无需进行统计数据分析。叶绿体 trnL(UAA)-trnF(GAA)基因间隔区在植物分类群中广泛变化,因此基于基因间隔区操作的 PCR-CE 方案有可能揭示与多种掺杂物的掺假。本工作中描述的 PCR-CE 测定法可以被公共部门或食品工业的食品质量实验室容易地采用,作为分析开心果真实性的简单可靠方法。© 2020 化学工业协会。

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