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SCAR markers for adulterant detection in ground chilli

机译:SCAR标记用于地辣椒中的掺假检测

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摘要

Purpose - This study aims to treat the development and application of sequence characterised amplified region (SCAR) markers for the detection of plant based adulterants (dried red beet pulp and powdered Ziziphus nummularia fruits) in traded ground chilli. Design/methodology/approach - Adulterant-specific DNA fragments (red beet pulp specific -"Beet 01" and Z. nummularia specific - "Ziz 01") identified by random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) analysis were cloned and sequenced for SCAR marker development. Red beet pulp specific SCAR primer pair, Bl, and Z. nummularia specific SCAR primer pair, Zl, were designed from the corresponding RAPD marker sequences to amplify SCAR markers of 320 bp and 389 bp, respectively. The utility of the SCAR markers for adulterant detection was verified in model blends of chilli powder with the adulterants. Six commercial samples of ground chilli powder were analysed using the SCAR markers. Findings - SCAR markers could detect the adulterants at a concentration as low as 10 g adulterant kg~(-1) of blended sample. The Z. nummularia SCAR marker could detect the presence of Z. nummularia fruit adulteration in one of the commercial samples. All the market samples tested were free from red beet pulp adulteration. Practical implications - The PCR-based method developed in the study is simple, rapid, and sensitive and has the potential to be developed into a quantitative analytical method and for commercial PCR kits for the large-scale screening of ground chilli to detect and prevent plant-based adulterants. The work has public health significance too, as ground chilli is one of the major spices consumed worldwide. Originality/value - The study is the first report on the development of SCAR markers for adulterant detection in ground chilli. This work has relevance, as adulteration is a major concern of the sanitary and phytosanitary issues of the World Trade Organization (WTO) agreement.
机译:目的-这项研究旨在治疗序列特征扩增区(SCAR)标记物的开发和应用,以检测交易地面辣椒中基于植物的掺假物(干红甜菜果肉和西葫芦粉)。设计/方法/方法-通过随机扩增多态性DNA聚合酶链反应(RAPD-PCR)分析鉴定出掺假体特异的DNA片段(红甜菜浆特异的-“甜菜01”和num。zumnumaria特异的“ Ziz 01”),并克隆用于SCAR标记开发的序列。从相应的RAPD标记序列设计了红甜菜浆特异性的SCAR引物对B1和N.nummularia特异性的SCAR引物对Z1,分别扩增了320 bp和389 bp的SCAR标记。 SCAR标记物在掺假物检测中的效用已在辣椒粉与掺假物的模型混合物中得到验证。使用SCAR标记分析了六个商用辣椒粉的商业样品。研究结果-SCAR标记物可在低至10 g掺混物kg〜(-1)的混合样品中检测掺入物。 Z. nummularia SCAR标记可以检测其中一种商业样品中Z. nummularia水果掺假的存在。测试的所有市场样品均不含红甜菜浆掺假。实际意义-研究中开发的基于PCR的方法简单,快速,灵敏,并且有可能发展为定量分析方法,并可以用于商业PCR试剂盒,用于大规模筛选地面辣椒以检测和预防植物的掺假者。这项工作也具有公共卫生意义,因为辣椒粉是全世界消费的主要香料之一。原创性/价值-这项研究是关于用于地面辣椒掺假检测的SCAR标记开发的第一份报告。这项工作具有相关性,因为掺假是世界贸易组织(WTO)协议中有关卫生和植物检疫问题的主要问题。

著录项

  • 来源
    《British Food Journal》 |2011年第5期|p.656-668|共13页
  • 作者单位

    Crop Improvement and Biotechnology Division,Indian Institute of Spices Research, Calicut, India;

    Crop Improvement and Biotechnology Division,Indian Institute of Spices Research, Calicut, India;

    Crop Improvement and Biotechnology Division,Indian Institute of Spices Research, Calicut, India;

    Crop Improvement and Biotechnology Division,Indian Institute of Spices Research, Calicut, India;

  • 收录信息 美国《科学引文索引》(SCI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    food products; food additives; food testing; chemical analysis and testing;

    机译:食物产品;食品添加剂;食品检测;化学分析测试;

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