Life Science College, Anhui Agricultural University,Hefei 230036, China; State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei 230036, China.
Life Science College, Anhui Agricultural University,Hefei 230036, China.
Gene. 2019 Oct 30;717:144046. doi: 10.1016/j.gene.2019.144046. Epub 2019 Aug 18.
Flavonoids are major polyphenol compounds in plant secondary metabolism. The hydroxylation pattern of the B-ring of flavonoids is determined by the flavonoid 3'-hydroxylase (F3'H) and flavonoid 3',5'-hydroxylase (F3'5'H). In this paper, one CsF3'H and two CsF3'5'Hs (CsF3'5'Ha and CsF3'5'Hb) were isolated. The phylogenetic tree results showed that F3'H and F3'5'Hs belong to the CYP75B and CYP75A, respectively. The Expression pattern analysis showed that the expression of CsF3'5'Ha and CsF3'5'Hb in the bud and 1st leaf were higher than other tissues. However, the CsF3'H had the highest expression in the 4th and mature leaf. The correlation analysis showed that the expression of CsF3'5'Hs is positively associated with the concentration of B-trihydroxylated catechins, and the expression of CsF3'H is positively associated with the Q contentration. Heterologous expression of these genes in yeast showed that CsF3'H and CsF3'5'Ha can catalyze flavanones, flavonols and flavanonols to the corresponding 3', 4' or 3', 4', 5'-hydroxylated compounds, for which the optimum substrate is naringenin. The enzyme of CsF3'5'Hb can only catalyze flavonols (including K and Q) and flavanonols (DHK and DHQ), of which the highest activities in catalyzing are DHK. Interestingly, The experiment of site-directed mutagenesis suggested that two novel sites near the C-terminal were discovered impacting on the activity of the CsF3'5'H. These results provide a significantly molecular basis on the accumulation B-ring hydroxylation of flavonoids in tea plant.
类黄酮是植物次生代谢中主要的多酚化合物。类黄酮 B 环的羟化模式由类黄酮 3'-羟化酶(F3'H)和类黄酮 3',5'-羟化酶(F3'5'H)决定。本文分离得到一个 CsF3'H 和两个 CsF3'5'Hs(CsF3'5'Ha 和 CsF3'5'Hb)。系统进化树结果表明,F3'H 和 F3'5'Hs 分别属于 CYP75B 和 CYP75A。表达模式分析表明,CsF3'5'Ha 和 CsF3'5'Hb 在芽和第 1 叶中的表达高于其他组织。然而,CsF3'H 在第 4 叶和成熟叶中的表达最高。相关性分析表明,CsF3'5'Hs 的表达与 B-三羟基儿茶素浓度呈正相关,而 CsF3'H 的表达与 Q 浓度呈正相关。这些基因在酵母中的异源表达表明,CsF3'H 和 CsF3'5'Ha 可以催化黄烷酮、黄酮醇和黄烷醇转化为相应的 3',4' 或 3',4',5'-羟基化合物,其最适底物是柚皮素。CsF3'5'Hb 酶只能催化黄酮醇(包括 K 和 Q)和黄烷酮醇(DHK 和 DHQ),其中催化 DHK 的活性最高。有趣的是,定点突变实验表明,在 C 端附近发现了两个新的位点,影响 CsF3'5'H 的活性。这些结果为茶树中类黄酮 B 环羟化积累提供了重要的分子基础。