食品科学 ›› 2025, Vol. 46 ›› Issue (13): 214-180.doi: 10.7506/spkx1002-6630-20250108-055

• 成分分析 • 上一篇    

L-茶氨酸与单糖模拟热反应挥发性成分分析

郭向阳,宛晓春   

  1. (1.信阳师范大学茶学与食品学院,河南 信阳 464000;2.深圳大学化学与环境工程学院,广东 深圳 518060;3.安徽农业大学 茶树种质创新与资源利用全国重点实验室,安徽 合肥 230036)
  • 发布日期:2025-06-13
  • 基金资助:
    国家自然科学基金面上项目(32072634);茶树种质创新与资源利用全国重点实验室开放课题(NKLTOF20240116); 河南省科技攻关项目(252102110093)

Composition of Volatile Compounds Generated from Simulated Thermal Reaction of L-Theanine with Monosaccharides

GUO Xiangyang, WAN Xiaochun   

  1. (1. College of Tea and Food Science, Xinyang Normal University, Xinyang 464000, China; 2. College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, China; 3. National Key Laboratory for Tea Plant Germplasm Innovation and Resource Utilization, Anhui Agricultural University, Hefei 230036, China)
  • Published:2025-06-13

摘要: 为深入探究茶氨酸作为香气前体的潜力,借鉴美拉德反应原理,利用气相色谱-质谱联用技术对L-茶氨酸与单糖在加热条件下的模拟反应生成的挥发性成分进行分析。在120 ℃加热2 h的条件下,L-茶氨酸与4 种茶叶中常见单糖(D-葡萄糖、D-半乳糖、D-阿拉伯糖及D-木糖)均能够反应并生成挥发性成分。L-茶氨酸与D-葡萄糖、D-半乳糖模拟反应中产生较多的挥发性成分,分别鉴定出32 个和21 个化合物,其中含氮的化合物分别有17 个和12 个,且以含吡咯和酰胺类结构的杂环化合物为主,包括具烘烤香的4-乙基-2-甲基吡咯、4-乙基-2,3-二甲基-1H-吡咯、2-乙酰基吡咯及N-乙基琥珀酰胺。相比之下,L-茶氨酸与D-阿拉伯糖、D-木糖模拟反应中鉴定出的挥发性成分数量较少,分别为6 个和9 个。L-茶氨酸与D-阿拉伯糖模拟反应中含吡咯结构的杂环化合物含量较高,如具烘烤香的2,3-二甲基-1H-吡咯;而D-木糖与L-茶氨酸模拟反应中主要生成含呋喃结构的杂环化合物。此外,L-茶氨酸单独加热到120 ℃时也能产生挥发性成分。在这些鉴定的挥发性成分中,含嘧啶结构的杂环化合物及烷烃类化合物含量较高。同时,对模拟反应中产生的部分化合物的香气生成机理进行推测,即加热条件下,以L-茶氨酸和糖作为反应底物,可能通过美拉德反应或斯特勒克降解反应生成挥发性成分。主成分分析能够较好地将不同模拟反应进行区分,表明L-茶氨酸与不同单糖之间的热反应特性不同。本研究不仅为茶叶香气生成机理提供了数据支持,也为茶叶加工工艺优化及品质控制奠定了理论基础。

关键词: L-茶氨酸;茶叶单糖;挥发性成分;美拉德反应;茶叶香气生成机理

Abstract: To investigate the potential of L-theanine (Thea) as an aroma precursor, the composition of volatile compounds generated from the thermal reaction between Thea and monosaccharides, simulating the Maillard reaction, was analyzed by gas chromatography-mass spectrometry (GC-MS). Thea reacted with four common monosaccharide in tea, D-glucose (Glc), D-galactose (Gal), D-arabinose (Arab) and D-xylose (Xyl) at 120 ℃ for 2 h, generating volatile compounds. The reaction with Glc and Gal generated larger numbers of volatile compounds (32 and 21, respectively), and 17 and 12 nitrogen-containing compounds were found in the reaction products, respectively, heterocyclic compounds with pyrrole and amide structures being the major ones, including four compounds contributing to roasted aroma, 4-ethyl-2-methylpyrrole, 4-ethyl-2,3-dimethyl-1H-pyrrole, 2-acetylpyrrole and N-ethyl succinimide. In contrast, only 6 and 9 volatile compounds were identified in the reaction products of Thea with Arab and Xyl, respectively. The reaction with Arab produced larger amounts of heterocyclic compounds with pyrrole structure such as 2,3-dimethyl-1H-pyrrole, responsible for roasted aroma, whereas the reaction with Xyl mainly produced heterocyclic compounds with furan structure. Additionally, Thea was transformed into volatile components when heated to 120 ℃. Among the identified volatile compounds, those with pyrimidine structure and alkane compounds were present in higher amounts. Furthermore, it was speculated that some volatile components might be formed by the Maillard reaction or the Strecker degradation. Principal component analysis (PCA) could effectively distinguish different thermal reactions, indicating that the reaction characteristics of Thea with different monosaccharides varied. This study not only provides data support for understanding the formation mechanism of tea aroma but also lays a theoretical foundation for the processing optimization and quality control of tea.

Key words: L-theanine; tea monosaccharides; volatile compounds; Maillard reaction; formation mechanism of tea aroma

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