Harnly James, Chen Pei, Sun Jianghao, Huang Huilian, Colson Kimberly L, Yuk Jimmy, McCoy Joe-Ann H, Reynaud Danica T Harbaugh, Harrington Peter B, Fletcher Edward J
Food Composition and Methods Development Laboratory, Beltsville Human Nutrition Research Center, Agricultural Research Service, U. S. Department of Agriculture, Beltsville, MD, USA.
Bruker BioSpin, Billerica, MA, USA.
Planta Med. 2016 Feb;82(3):250-62. doi: 10.1055/s-0035-1558113. Epub 2015 Dec 21.
Flow injection mass spectrometry and proton nuclear magnetic resonance spectrometry, two metabolic fingerprinting methods, and DNA sequencing were used to identify and authenticate Actaea species. Initially, samples of Actaea racemosa from a single source were distinguished from other Actaea species based on principal component analysis and soft independent modeling of class analogies of flow injection mass spectrometry and proton nuclear magnetic resonance spectrometry metabolic fingerprints. The chemometric results for flow injection mass spectrometry and proton nuclear magnetic resonance spectrometry agreed well and showed similar agreement throughout the study. DNA sequencing using DNA sequence data from two independent gene regions confirmed the metabolic fingerprinting results. Differences were observed between A. racemosa samples from four different sources, although the variance within species was still significantly less than the variance between species. A model based on the combined A. racemosa samples from the four sources consistently permitted distinction between species. Additionally, the combined A. racemosa samples were distinguishable from commercial root samples and from commercial supplements in tablet, capsule, or liquid form. DNA sequencing verified the lack of authenticity of the commercial roots but was unsuccessful in characterizing many of the supplements due to the lack of available DNA.
流动注射质谱法和质子核磁共振光谱法这两种代谢指纹分析方法以及DNA测序被用于鉴定和认证类叶升麻属物种。最初,基于主成分分析以及流动注射质谱法和质子核磁共振光谱法代谢指纹的类类比软独立建模,来自单一来源的总状升麻样本与其他类叶升麻属物种得以区分。流动注射质谱法和质子核磁共振光谱法的化学计量学结果吻合良好,且在整个研究过程中都呈现出类似的一致性。使用来自两个独立基因区域的DNA序列数据进行的DNA测序证实了代谢指纹分析结果。虽然观察到来自四个不同来源的总状升麻样本之间存在差异,但物种内部的变异仍明显小于物种之间的变异。基于来自四个来源的总状升麻样本组合构建的模型始终能够区分不同物种。此外,组合的总状升麻样本可与商业根样本以及片剂、胶囊或液体形式的商业补充剂区分开来。DNA测序证实了商业根的真实性存疑,但由于缺乏可用的DNA,未能成功鉴定许多补充剂的特征。