首页|期刊导航|食品科学技术学报|咖啡酸对葡萄酒中萜烯类物质挥发性影响的作用机制

咖啡酸对葡萄酒中萜烯类物质挥发性影响的作用机制OA

Mechanism of Effect of Caffeic Acid on Terpene Volatility in Wine

中文摘要英文摘要

萜烯类物质是葡萄酒中典型的品种香气化合物,其挥发呈香受到酒体中酚类物质的基质效应影响;咖啡酸是葡萄酒中酚类物质——酚酸的代表性化合物,能影响葡萄酒贮藏期间萜烯类风味物质的挥发损失.为解析萜烯类化合物与咖啡酸之间的分子互作机制,以配制的模拟葡萄酒(含 7 种萜烯类化合物)为研究体系,添加不同质量浓度的咖啡酸(0、62.5、125、250、500、750 mg/L),采用顶空固相微萃取-气相色谱-质谱联用技术(SPME-GC-MS),分析模拟酒在室温(25℃)贮藏90 d过程中萜烯类化合物的含量变化;随后通过感官分析,评价咖啡酸对葡萄酒中萜烯类化合物嗅觉感知的影响;采用热力学测定和量子化学计算从实验和理论两个方面揭示萜烯-咖啡酸分子互作机制;最后通过化学键断裂实验验证互作机制.结果表明,咖啡酸可以抑制萜烯类化合物的挥发,酒体中咖啡酸为500 mg/L及以上时效果较佳;且在贮藏 90 d后,750 mg/L咖啡酸处理组的总萜烯含量是对照组的 113.42%,显著降低了萜烯的挥发损失.感官分析结果进一步表明,与未添加咖啡酸的酒体相比,750 mg/L咖啡酸处理组引发的酒体中 7 种萜烯类化合物的香气感知变化识别率均为高度显著(P<0.01).紫外-可见光谱法测定的萜烯-咖啡酸分子热力学结果表明,ΔH°与ΔS°均大于零;疏水作用是萜烯-咖啡酸分子非共价相互作用的主要驱动力.量子化学计算结果表明,ΔH°与ΔS°均为负值,氢键是稳定萜烯-咖啡酸分子的关键因素.化学键断裂实验结果也证实了疏水作用与氢键在萜烯-咖啡酸分子中协同存在.研究得出,在葡萄酒贮藏期间,添加500 mg/L及以上咖啡酸可以减缓萜烯类物质的挥发损失,咖啡酸与萜烯类物质可通过疏水作用与氢键结合形成稳定复合物.希望研究可为葡萄酒中萜烯类物质挥发呈香的调控和多酚基质效应的评价提供技术支撑和理论依据.

Terpenes are typical varietal aroma compounds in wine,and their volatilization and aroma expression are influenced by the matrix effect of phenolic compounds present in wine.Caffeic acid is a representative phenolic acid in wine and can affect the volatilization loss of terpene flavor compounds during wine storage.To elucidate the molecular interaction mechanism between terpenes and caffeic acid,a model wine system containing seven terpenes was prepared.Different concentrations of caffeic acid(0,62.5,125,250,500,and 750 mg/L)were added,and headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was employed to monitor the changes in terpene concentrations during 90 days of storage at room temperature(25℃).Subsequently,sensory analysis was conducted to evaluate the effect of caffeic acid on the olfactory perception of terpenes in wine.Thermodynamic analysis and quantum chemical calculations were performed to investigate the terpene-caffeic acid interaction mechanism from both experimental and theoretical perspectives.Finally,chemical bond disruption experiments were carried out to validate the proposed interaction mechanism.The results showed that caffeic acid suppressed the volatilization of terpenes,with concentrations of 500 mg/L or higher exhibiting the most pronounced effect.After 90 days of storage,the total terpene content in the 750 mg/L caffeic acid treatment group was 113.42%of that in the control group,indicating a significant reduction in volatilization loss.Sensory analysis further corroborated these findings:compared with the control,the 750 mg/L caffeic acid treatment group induced highly significant differences(P<0.01)in the recognition rates of aroma perception changes for all seven terpenes.Thermodynamic parameters determined by ultraviolet-visible spectroscopy revealed that both ΔH° and ΔS° were positive,indicating that hydrophobic interactions constituted the primary driving force for the non-covalent interaction between terpenes and caffeic acid.In contrast,quantum chemical calculations yielded negative values for ΔH° and ΔS°,suggesting that hydrogen bonding was the key stabilizing factor in terpene-caffeic acid complexes.The chemical bond disruption experiments confirmed the synergistic presence of both hydrophobic interactions and hydrogen bonding in the terpene-caffeic acid system.It was concluded that the addition of caffeic acid at concentrations of 500 mg/L or higher during wine storage could mitigate the volatilization loss of terpenes,and that caffeic acid and terpenes could form stable complexes through hydrophobic interactions and hydrogen bonding.This study was expected to provide technical support and a theoretical basis for the regulation of terpene volatilization and aroma expression in wine,as well as the evaluation of the polyphenolic matrix effect.

宋鸿聪;王一清;冯林;李爱华;汪兴杰;陶永胜

西北农林科技大学 葡萄酒学院,陕西 杨凌 712100西北农林科技大学 葡萄酒学院,陕西 杨凌 712100西北农林科技大学 葡萄酒学院,陕西 杨凌 712100西北农林科技大学 食品科学与技术学院,陕西 杨凌 712100西北农林科技大学 葡萄酒学院,陕西 杨凌 712100西北农林科技大学 葡萄酒学院,陕西 杨凌 712100||陕西省葡萄与葡萄酒重点实验室,陕西 杨凌 712100

轻工纺织

葡萄酒萜烯类物质咖啡酸量子化学计算分子互作

wineterpenecaffeic acidquantum chemical calculationmolecular interaction

《食品科学技术学报》 2026 (2)

54-66,13

国家自然科学联合基金重点项目(U25A20736). Key Project of Joint Fund of National Natural Science Foundation of China(NSFC)(U25A20736).

10.12301/spxb202600059

评论