首页> 美国卫生研究院文献>Journal of Experimental Botany >Identification of UDP-glycosyltransferases involved in the biosynthesis of astringent taste compounds in tea (Camellia sinensis)
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Identification of UDP-glycosyltransferases involved in the biosynthesis of astringent taste compounds in tea (Camellia sinensis)

机译:茶中涩味化合物生物合成中涉及的UDP-糖基转移酶的鉴定

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摘要

Galloylated catechins and flavonol 3-O-glycosides are characteristic astringent taste compounds in tea (Camellia sinensis). The mechanism involved in the formation of these metabolites remains unknown in tea plants. In this paper, 178 UGT genes (CsUGTs) were identified in C. sinensis based on an analysis of tea transcriptome data. Phylogenetic analysis revealed that 132 of these genes were clustered into 15 previously established phylogenetic groups (A to M, O and P) and a newly identified group R. Three of the 11 recombinant UGT proteins tested were found to be involved in the in vitro biosynthesis of β-glucogallin and glycosylated flavonols. CsUGT84A22 exhibited catalytic activity toward phenolic acids, in particular gallic acid, to produce β-glucogallin, which is the immediate precursor of galloylated catechin biosynthesis in tea plants. CsUGT78A14 and CsUGT78A15 were found to be responsible for the biosynthesis of flavonol 3-O-glucosides and flavonol 3-O-galactosides, respectively. Site-directed mutagenesis of the Q373H substitution for CsUGT78A14 indicated that the Q (Gln) residue played a catalytically crucial role for flavonoid 3-O-glucosyltransferase activity. The expression profiles of the CsUGT84A22, CsUGT78A14, and CsUGT78A15 genes were correlated with the accumulation patterns of β-glucogallin and the glycosylated flavonols which indicated that these three CsUGT genes were involved in the biosynthesis of astringent compounds in C. sinensis.
机译:镀锌的儿茶素和黄酮醇3-O-糖苷是茶中的特征性涩味化合物。这些代谢产物形成的机制在茶树中仍然未知。本文通过对茶转录组数据的分析,确定了178个UGT基因(CsUGTs)。系统发育分析表明,这些基因中的132个被分为15个先前建立的系统发育组(A至M,O和P)和一个新鉴定的R组。测试的11种重组UGT蛋白中有3种参与体外生物合成β-葡萄糖gallin和糖基化黄酮醇。 CsUGT84A22对酚酸(特别是没食子酸)表现出催化活性,可产生β-葡糖醇,这是茶树中没食子儿茶素生物合成的直接前体。发现CsUGT78A14和CsUGT78A15分别负责黄酮醇3-O-糖苷和黄酮醇3-O-半乳糖苷的生物合成。 Q373H取代CsUGT78A14的定点诱变表明,Q(Gln)残基对类黄酮3-O-葡萄糖基转移酶活性起催化关键作用。 CsUGT84A22,CsUGT78A14和CsUGT78A15基因的表达谱与β-葡萄糖醇和糖基化黄酮醇的积累模式相关,表明这三个CsUGT基因参与中华绒螯蟹中涩味化合物的生物合成。

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