Deng Cheng, Ku Xiuping, Cheng Lin-Lin, Pan Si-An, Fan Limao, Deng Wei-Wei, Zhao Jian, Zhang Zheng-Zhu
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei, China.
Front Plant Sci. 2020 Sep 9;11:551288. doi: 10.3389/fpls.2020.551288. eCollection 2020.
While caffeine is one of the most important bioactive metabolites for tea as the most consumed non-alcohol beverage, its biosynthesis and catabolism in tea plants are still not fully understood. Here, we integrated purine alkaloid profiling and transcriptome analysis on shoot tips and roots fed with caffeine, theophylline, or theobromine to gain further understanding of caffeine biosynthesis and degradation. Shoot tips and roots easily took up and accumulated high concentrations of alkaloids, but roots showed much faster caffeine and theophylline degradation rates than shoot tips, which only degraded theophylline significantly but almost did not degrade caffeine. Clearly feedback inhibition on caffeine synthesis or inter-conversion between caffeine, theophylline, and theobromine, and 3-methylxanthine had been observed in alkaloids-fed shoot tips and roots, and these were also evidenced by significant repression of and genes critical for caffeine biosynthesis. Among these responsively repressed genes, two highly expressed genes and were characterized for their enzyme activity. While we failed to detect TCS-4 activity, TCS-8 displayed -methyltransferase activities towards multiple substrates, supporting the complex metabolic network in caffeine biosynthesis in tea plants since at least 13 TCS-like -methyltransferase genes may function redundantly. This study provides new insight into complex metabolic networks of purine alkaloids in tea plants.
尽管咖啡因是茶叶中最重要的生物活性代谢产物之一,而茶作为消费最多的非酒精饮料,其在茶树中的生物合成和分解代谢仍未被完全了解。在此,我们对用咖啡因、茶碱或可可碱处理的茎尖和根进行了嘌呤生物碱谱分析和转录组分析,以进一步了解咖啡因的生物合成和降解。茎尖和根很容易吸收并积累高浓度的生物碱,但根显示出比茎尖更快的咖啡因和茶碱降解速率,茎尖仅能显著降解茶碱,但几乎不能降解咖啡因。在生物碱处理的茎尖和根中观察到了对咖啡因合成或咖啡因、茶碱、可可碱和3 - 甲基黄嘌呤之间相互转化的明显反馈抑制,对咖啡因生物合成至关重要的 和 基因的显著抑制也证明了这一点。在这些响应性抑制的基因中,对两个高表达基因 和 的酶活性进行了表征。虽然我们未能检测到TCS - 4的活性,但TCS - 8对多种底物表现出 - 甲基转移酶活性,这支持了茶树中咖啡因生物合成的复杂代谢网络,因为至少有13个TCS样 - 甲基转移酶基因可能功能冗余。本研究为茶树中嘌呤生物碱的复杂代谢网络提供了新的见解。