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首页> 外文期刊>Food analytical methods >A Method to Check and Discover Adulteration of Nebbiolo-Based Monovarietal Musts: Detection of Barbera and Dolcetto cv via SSR Analysis Coupled with Lab-On-Chip~R Microcapillary Electrophoresis
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A Method to Check and Discover Adulteration of Nebbiolo-Based Monovarietal Musts: Detection of Barbera and Dolcetto cv via SSR Analysis Coupled with Lab-On-Chip~R Microcapillary Electrophoresis

机译:一种检查和发现基于内比奥罗的单种野菜掺假的方法:通过SSR分析结合Lab-On-Chip〜R微毛细管电泳技术检测Barbera和Dolcetto cv

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摘要

The process of wine traceability/authentication is a key target for Italy, the world’s first largest wine producer (around 4.6 million tons in 2010 according to FAOSTAT). Several European countries developed appellation systems, with their own uniquelabels and seals, trying to fight label fraud that misrepresented the true origins of the wine. Advancements on this topic were provided by Council Regulation (EC) No. 479/2008 on the common organisation of the market in wine. As reported by experts, itis suspected that as much as 5 % of the wine sold in secondary markets worldwide could be counterfeit. Despite the high number of traceability methods, commonly based on the use of time consuming and expensive techniques (SNIF-NMR and stable isotope-ratio mass spectrometry), few applications report the use of polymerase chain reaction directly in musts or in bottled wine. Information on genetic polymorphism given by simple sequence repeats (SSR; microsatellite markers) proved helpful when applied to grape and musts analysis. The limited quantity of amplifiable grape genomic DNA in wine represents the main issue for the application of such analytical approach. Musts are the first intermediate product to be checked, in order to exclude the unintentionalor fraudulent contamination with foreign grape varieties. The aims of this work are (1) the selection of performing SSR markers able to discriminate ‘Barbera’ and ‘Dolcetto’ from ‘Nebbiolo’ and (2) the hyphenated use of capillary micro-electrophoresis (lab-on-chip technology) for polymorphisms detection, to highlight the presence of foreign grape in ‘Nebbiolo’ musts produced in purity, as required by the designation disciplinary. Finally, we suggest using this approach by exploiting VVS2 markerin order to detect Barbera and Dolcetto grapes in Nebbiolo musts, waiting for more robust and powerful method to extract and amplify specific DNA from bottled wine.
机译:对于全球第一大葡萄酒生产国意大利(根据FAOSTAT统计,2010年约为460万吨),葡萄酒的可追溯性/认证过程是其主要目标。几个欧洲国家开发了具有自己独特标签和印章的商标制度,试图与错误地陈述葡萄酒真实来源的标签欺诈作斗争。关于葡萄酒市场共同组织的第479/2008号理事会条例(EC)提供了有关此主题的进展。据专家报道,艾迪斯怀疑全世界二级市场上出售的葡萄酒中有多达5%是假冒的。尽管有大量的可追溯方法,通常基于使用费时且昂贵的技术(SNIF-NMR和稳定同位素比质谱法),但很少有应用报告直接在芥末或瓶装葡萄酒中使用聚合酶链反应。简单序列重复(SSR;微卫星标记)给出的遗传多态性信息在应用于葡萄和葡萄汁分析时被证明是有用的。葡萄酒中可扩增的葡萄基因组DNA数量有限,代表了这种分析方法的主要应用问题。必需品是要检查的第一个中间产品,以排除外来葡萄品种的无意或欺诈性污染。这项工作的目的是(1)选择能够区分'Barbera'和'Dolcetto'与'Nebbiolo'的SSR标记,以及(2)毛细管微电泳(芯片实验室技术)的联用多态性检测,以突出指定名称要求的纯净生产的'Nebbiolo'葡萄汁中外来葡萄的存在。最后,我们建议通过利用VVS2标记物来使用这种方法,以检测内比奥洛葡萄汁中的巴贝拉和多尔切托葡萄,等待更健壮和强大的方法从瓶装葡萄酒中提取和扩增特定的DNA。

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