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烘烤过程中变黄期湿球温度对翠碧一号烟叶品质与代谢物转化的影响

The effect of wet-bulb temperature during the yellowing period on the curing quality and metabolite transformation of Cuibi-1 tobacco leaves

  • 摘要: 为揭示烘烤过程中变黄期湿球温度对烟叶品质及代谢物转化的影响机制,以翠碧1号(CB-1)中部烟叶为材料,设置烟叶变黄中前期、变黄中后期和变黄后期的湿球温度分别为37~37.5、 36~37、36~37 ℃(T1,低温低湿),37.5~38、38~39、38 ℃(T2,中温中湿),38、39~40、36~37 ℃(T3,高温高湿)3种烘烤工艺,分析烤后烟叶的化学成分与感官质量,并通过非靶向代谢组学技术检测烟叶在变黄期与定色期的差异代谢物。结果显示:①相较于T1和T3烘烤工艺,T2烘烤工艺烤后烟叶烟碱、总糖、还原糖、氯离子含量以及糖碱比和钾氯比等指标更为适宜,风格特征与品质特征指标得分更高,香型风格突出,清甜感、甜度与香气质好,感官评吸质量最佳。②代谢组学分析结果表明,共鉴定出4 327种代谢物,3种烘烤工艺在烟叶变黄中后期至定色中期的差异代谢物均超过2 000种。其中,烟叶变黄后期的差异代谢物最多,表明该阶段是湿球温度影响烟叶品质形成的关键时期。3种烘烤工艺烟叶中有机含氮物、碳水化合物、黄酮类、生物碱、萜类和脂类物质等差异代谢物在烘烤过程中发生明显变化。③相较于T1和T3烘烤工艺,T2烘烤工艺在烟叶定色后期有机含氮化合物转化更彻底,碳水化合物分解生成更多蜜二糖、梓醇、半乳糖二酸、L–古洛糖和甘露三糖等香甜物质,赋予烟叶清甜蜜甜香型风格。T2烘烤工艺定色期烟叶草黄酮、甜菜苷、乌头原碱和乙酰戊烯酸相对丰度较高,香型风格与香气特征更为独特。T2烘烤工艺变黄后期烟叶的蛇根碱、罂粟碱、赝靛叶碱、麦角胺碱和α–那可丁碱相对丰度较高。

     

    Abstract: To investigate the effects of wet-bulb temperature during the yellowing stage on the curing quality and metabolite changes of tobacco leaves, this study used the middle leaves of Cuibi-1 (CB-1) as experimental materials and set the wet-bulb temperatures of 37~37.5℃ - 36~37℃ - 36~37℃ (T1 treatment), 37.5~38℃ - 38~39℃ - 38℃ (T2 treatment), and 38℃ - 39~40℃ - 36~37℃ (T3 treatment) during the early, middle, and late stages of yellowing. The chemical composition and taste quality of the cured tobacco leaves were evaluated, and differential metabolites between the three curing treatments were identified throughout the yellowing and color-fixing stages using non-targeted metabolomics technology. The results showed that, compared with the T1 and T3 treatments, the T2 treatment yielded the most balanced chemical composition, including nicotine, total sugar, reducing sugar, chloride ions, sugar-alkali ratio, chlor-alkali ratio, and potassium-chloride ratio. It also achieved the highest scores for style and quality characteristics, with a more pronounced aromatic style and superior sweetness, aroma quality, and overall sensory evaluation. Metabolomics analysis identified 4327 metabolites in CB-1 tobacco leaves across the three curing treatments. From the mid-late yellowing stage S4 to the mid color-fixing stage S6, more than 2000 metabolites differed among the three treatments. The greatest number of differential metabolites was observed in the late yellowing stage S5, indicating that this stage is critical for the formation of quality differences caused by variations in wet-bulb temperatures. Significant changes were observed in key metabolites, including organic nitrogen compounds, carbohydrates, flavonoids, alkaloids, terpenes, and lipids, during the curing process. Compared with T1 and T3, the T2 treatment exhibited more complete conversion of organic nitrogen compounds in the late stage of color-fixing. Carbohydrate decomposition produces more sweet substances such as melibiose, catalpol, galacturonic acid, L-gulose, and mannotriose, contributing to its clear and sweet style under the T2 curing treatment. T2 treatment generates greater amounts of glabridin, betanin, aconine, and acetylvalerenolic acid, which underlie its aroma classification and aroma characteristics. Furthermore, the accumulation of reserpine, oripavine, baptifoline, ergotamine, and alpha-narcotine during the late yellowing stage under T2 treatment was associated with enhanced smoking vigor.

     

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