College of Agriculture and Bioresources, University of Saskatchewan, 51 Campus Drive, Saskatoon, SK, Canada, S7N 5A8.
Spectrochim Acta A Mol Biomol Spectrosc. 2011 Nov;82(1):1-7. doi: 10.1016/j.saa.2011.05.078. Epub 2011 Jun 29.
To date, there is no study on bioethanol processing-induced changes in molecular structural profiles mainly related to lipid biopolymer. The objectives of this study were to: (1) determine molecular structural changes of lipid related functional groups in the co-products that occurred during bioethanol processing; (2) relatively quantify the antisymmetric CH(3) and CH(2) (ca. 2959 and 2928 cm(-1), respectively), symmetric CH(3) and CH(2) (ca. 2871 and 2954 cm(-1), respectively) functional groups, carbonyl C=O ester (ca. 1745 cm(-1)) and unsaturated groups (CH attached to C=C) (ca. 3007 cm(-1)) spectral intensities as well as their ratios of antisymmetric CH(3) to antisymmetric CH(2), and (3) illustrate the molecular spectral analyses as a research tool to detect for the sensitivity of individual moleculars to the bioethanol processing in a complex plant-based feed and food system without spectral parameterization. The hypothesis of this study was that bioethanol processing changed the molecular structure profiles in the co-products as opposed to original cereal grains. These changes could be detected by infrared molecular spectroscopy and will be related to nutrient utilization. The results showed that bioethanol processing had effects on the functional groups spectral profiles in the co-products. It was found that the CH(3)-antisymmetric to CH(2)-antisymmetric stretching intensity ratio was changed. The spectral features of carbonyl C=O ester group and unsaturated group were also different. Since the different types of cereal grains (wheat vs. corn) had different sensitivity to the bioethanol processing, the spectral patterns and band component profiles differed between their co-products (wheat DDGS vs. corn DDGS). The multivariate molecular spectral analyses, cluster analysis and principal component analysis of original spectra (without spectral parameterization), distinguished the structural differences between the wheat and wheat DDGS and between the corn and corn DDGS in the antisymmetric and symmetric CH(3) and CH(2) spectral region (ca. 2994-2800 cm(-1)) and unsaturated group band region (3025-2996 cm(-1)). Further study is needed to quantify molecular structural changes in relation to nutrient utilization of lipid biopolymer.
迄今为止,尚无研究报道生物乙醇加工过程中主要与脂类生物聚合物相关的分子结构谱的变化。本研究的目的是:(1) 确定生物乙醇加工过程中发生在副产物中与脂质相关的功能基团的分子结构变化;(2) 相对定量分析约 2959 和 2928 cm(-1)(分别为不对称 CH(3) 和 CH(2))、约 2871 和 2954 cm(-1)(分别为对称 CH(3) 和 CH(2))、羰基 C=O 酯(约 1745 cm(-1)) 和不饱和基团(CH 与 C=C 相连)(约 3007 cm(-1)) 的光谱强度以及它们的不对称 CH(3)与不对称 CH(2)的比值;(3) 说明分子光谱分析作为一种研究工具,用于在无光谱参数化的复杂植物性饲料和食品系统中检测单个分子对生物乙醇加工的敏感性。本研究的假设是,生物乙醇加工改变了副产物中的分子结构谱,而不是原始谷物。这些变化可以通过红外分子光谱检测到,并与营养利用有关。结果表明,生物乙醇加工对副产物中功能基团的光谱谱图有影响。发现 CH(3)-不对称与 CH(2)-不对称伸缩强度比发生了变化。羰基 C=O 酯基团和不饱和基团的光谱特征也不同。由于不同类型的谷物(小麦与玉米)对生物乙醇加工的敏感性不同,因此它们的副产物(小麦 DDGS 与玉米 DDGS)之间的光谱模式和带成分谱也不同。原始光谱的多元分子光谱分析、聚类分析和主成分分析(无光谱参数化),区分了小麦和小麦 DDGS 以及玉米和玉米 DDGS 之间在不对称和对称 CH(3)和 CH(2)光谱区(约 2994-2800 cm(-1)) 和不饱和基团带区(3025-2996 cm(-1)) 的结构差异。需要进一步研究以量化与脂类生物聚合物的营养利用相关的分子结构变化。