Research Group "Analytical Chemistry of Contaminants", Department of Chemistry and Physics, Research Centre for Mediterranean Intensive Agrosystems and Agrifood Biotechnology (CIAIMBITAL), Agrifood Campus of International Excellence (ceiA3), University of Almeria, E-04120 Almeria, Spain.
Food Res Int. 2021 Dec;150(Pt A):110722. doi: 10.1016/j.foodres.2021.110722. Epub 2021 Sep 27.
An untargeted metabolomics approach based on ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS) fingerprinting was applied to investigate the metabolic differences of black pepper among three geographical origins (Sri Lanka, Vietnam, and Brazil) and two post-harvest processing (sterilized and non-sterilized spice). Principal component analysis (PCA) was employed to assess the overall clustering of samples, whereas supervised orthogonal partial least squares discriminant analysis (OPLS-DA) was effectively used for discrimination purposes. OPLS-DA models were fully validated (RY and Q values > 0.5) and the variable importance in projection (VIP) approach was employed to provide valuable data about differential metabolites with high discrimination potential (8 markers were putatively identified). For origin differentiation, three markers were highlighted with VIP values > 1.5 (i.e. reynosin, artabsinolide D, and tatridin B). Fatty acid derivates were the most frequent markers within the metabolites annotated for processing discrimination (e.g. 10,16-dihydroxyhexadecanoic acid and 9-hydroperoxy-10E-octadecenoic acid). Additionally, different combinations of mid-level data fusion of chromatographic-mass spectrometric techniques (UHPLC and gas chromatography coupled to HRMS) and proton nuclear magnetic resonance spectroscopy (H NMR) were evaluated for the first time for geographical and processing discrimination of black pepper. The NMR-UHPLC-GC mid-level fused model was preferred among the tested fusion approaches since good sample clustering and no misclassification were achieved. Enhanced correct classification rate was achieved by mid-level data fusion compared with the findings obtained for one of the individual techniques (H NMR fingerprinting) (from 92% to 100% of samples correctly classified). This study opens the path to new metabolomics approaches for black pepper authentication and quality control.
本研究采用基于超高效液相色谱-高分辨质谱联用技术(UHPLC-HRMS)指纹图谱的非靶向代谢组学方法,研究了三个产地(斯里兰卡、越南和巴西)和两种收获后加工(灭菌和未灭菌香料)的黑胡椒的代谢差异。主成分分析(PCA)用于评估样品的整体聚类,而正交偏最小二乘判别分析(OPLS-DA)则用于有效判别。OPLS-DA 模型得到了充分验证(RY 和 Q 值>0.5),并采用变量重要性投影(VIP)方法提供了具有高判别潜力的差异代谢物的有价值数据(鉴定出 8 个标记物)。对于产地鉴别,有 3 个标记物的 VIP 值>1.5(即雷索辛、阿塔比醇 D 和塔特里丁 B)。脂肪酸衍生物是代谢物中注释为加工鉴别最常见的标记物(如 10,16-二羟基十六烷酸和 9-过氧-10E-十八烯酸)。此外,还首次评估了中层次数据融合的不同组合,包括色谱-质谱技术(UHPLC 和气相色谱与 HRMS)和质子核磁共振波谱(H NMR),用于黑胡椒的地理和加工鉴别。在测试的融合方法中,UHPLC-GC-NMR 中层次融合模型是首选,因为它实现了良好的样品聚类且没有误分类。与单一技术(H NMR 指纹图谱)的发现相比,中层次数据融合实现了更高的正确分类率(从 92%提高到 100%的样品正确分类)。这项研究为黑胡椒的鉴定和质量控制开辟了新的代谢组学方法的道路。