Department of Chemistry, University of California, Davis, CA, USA.
Department of Chemistry, University of California, Davis, CA, USA; Agricultural and Environmental Chemistry Graduate Group, University of California, Davis, CA, USA.
Carbohydr Polym. 2021 Apr 1;257:117570. doi: 10.1016/j.carbpol.2020.117570. Epub 2021 Jan 5.
The identification of polysaccharide structures in complex samples remains a unique challenge complicated by the lack of specific tools for polymeric mixtures. In this work, we present a method that depolymerizes polysaccharides to generate diagnostic oligosaccharide markers that are then analyzed by high performance liquid chromatography-quadrupole time-of-flight mass spectrometry (HPLC-QTOF MS). Rapid identification of food polysaccharides was performed by aligning the identified oligosaccharides with a library of oligosaccharide markers generated from standard polysaccharides. Measurements of standard and food polysaccharides were performed to obtain the contributions of the identified polysaccharides using percent peak coverage and angle cosine methods. The method was validated using a synthetic mixture of standard polysaccharides while the reproducibility was confirmed with experimental triplicates of butternut squash samples, where standard deviation was less than 3% for the relative abundance of oligosaccharides. The method was further employed to examine diverse set of food samples.
在缺乏用于聚合混合物的特定工具的情况下,鉴定复杂样品中的多糖结构仍然是一项独特的挑战。在这项工作中,我们提出了一种方法,可将多糖解聚生成诊断性寡糖标记物,然后通过高效液相色谱-四极杆飞行时间质谱法(HPLC-QTOF MS)进行分析。通过将鉴定出的寡糖与从标准多糖生成的寡糖标记物库进行比对,可快速鉴定食品多糖。使用峰面积覆盖率和角余弦法对标准和食品多糖进行了测量,以获得鉴定出的多糖的贡献。该方法使用标准多糖的合成混合物进行了验证,并且通过南瓜样本的实验重复三次确认了重现性,其中寡糖的相对丰度的标准偏差小于 3%。该方法进一步用于检查各种食品样本。