PcUGT84A82 catalyzes a key step in the biosynthesis of galloylated macrocyclic polyphenols in Penthorum chinense Pursh

Penthorum chinense Pursh has been used for centuries as an herbal medicine and food in East Asia. The main active substances in P. chinense are galloylated macrocyclic polyphenolic compounds, which have excellent medicinal properties. Galloylation and glycosylation are key steps in the formation of polyphenolic compounds, as the glycosylation of flavonoids is required for the acylation of flavonoid glycosides, and the glycosylation of gallic acid is necessary for its role as an acyl donor. Therefore, glycosylation to generate the acyl donor or acceptor is a core step in the biosynthesis of polyphenolic compounds. However, how this glycosylation occurs in P. chinense is unknown. In this study, we determined that the UDP-glucose transferase PcUGT84A82 mediates the glycosylation of gallic acid and pinocembrin to produce 1- O -Galloyl-β-D-glucose and pinocembroside, respectively. Metabolic profiling of polyphenolic compounds using UHPLC-ESI–Q-TOF/MS revealed high levels of polyphenols in flowers, leaves, and roots, and low levels in stems of P. chinense . We performed isoform-sequencing (Iso-seq) to assemble a full-length transcriptome of P. chinense , from which we identified 58 UGT family members. PcUGT84A82 is highly similar to functional UGTs in other plant species, and PcUGT84A82 transcript levels were positively correlated with the levels of various polyphenolic compounds. We validated the function of PcUGT84A82 via in vitro enzyme assays and transient expression in Nicotiana benthamiana leaves. Subcellular localization tests showed that PcUGT84A82 localizes to the nucleus and cytoplasm. In summary, PcUGT84A82 catalyzes the conversion of gallic acid to 1- O -Galloyl-β-D-glucose as the acyl donor and pinocembrin to pinocembroside as the acyl acceptor, mediating the biosynthesis of galloylated macrocyclic polyphenolic compounds in P. chinense. These findings lay the foundation for elucidating the entire biosynthetic pathway of active polyphenols in this important herbal plant species.

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Publication Details

Journal
The Crop Journal
Published
2025-12-13
DOI
https://doi.org/10.1016/j.cj.2025.12.001
Primary Topic
Plant Gene Expression Analysis
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article
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article

PcUGT84A82 catalyzes a key step in the biosynthesis of galloylated macrocyclic polyphenols in Penthorum chinense Pursh

Doudou Huang, Wansheng Chen, Yinan Zou, Yang Xu et al.
The Crop Journal
Plant Gene Expression Analysis
article

PcUGT84A82 catalyzes a key step in the biosynthesis of galloylated macrocyclic polyphenols in Penthorum chinense Pursh

Doudou Huang, Wansheng Chen, Yinan Zou, Yang Xu, Y. Liu, Ke Zhang, Yun Wang, Junfeng Chen, Yajing Li, Jiajia Cao, Ying Xiao, Minghui Lu, Lianna Sun, Xiao Li
article en

Abstract

Penthorum chinense Pursh has been used for centuries as an herbal medicine and food in East Asia. The main active substances in P. chinense are galloylated macrocyclic polyphenolic compounds, which have excellent medicinal properties. Galloylation and glycosylation are key steps in the formation of polyphenolic compounds, as the glycosylation of flavonoids is required for the acylation of flavonoid glycosides, and the glycosylation of gallic acid is necessary for its role as an acyl donor. Therefore, glycosylation to generate the acyl donor or acceptor is a core step in the biosynthesis of polyphenolic compounds. However, how this glycosylation occurs in P. chinense is unknown. In this study, we determined that the UDP-glucose transferase PcUGT84A82 mediates the glycosylation of gallic acid and pinocembrin to produce 1- O -Galloyl-β-D-glucose and pinocembroside, respectively. Metabolic profiling of polyphenolic compounds using UHPLC-ESI–Q-TOF/MS revealed high levels of polyphenols in flowers, leaves, and roots, and low levels in stems of P. chinense . We performed isoform-sequencing (Iso-seq) to assemble a full-length transcriptome of P. chinense , from which we identified 58 UGT family members. PcUGT84A82 is highly similar to functional UGTs in other plant species, and PcUGT84A82 transcript levels were positively correlated with the levels of various polyphenolic compounds. We validated the function of PcUGT84A82 via in vitro enzyme assays and transient expression in Nicotiana benthamiana leaves. Subcellular localization tests showed that PcUGT84A82 localizes to the nucleus and cytoplasm. In summary, PcUGT84A82 catalyzes the conversion of gallic acid to 1- O -Galloyl-β-D-glucose as the acyl donor and pinocembrin to pinocembroside as the acyl acceptor, mediating the biosynthesis of galloylated macrocyclic polyphenolic compounds in P. chinense. These findings lay the foundation for elucidating the entire biosynthetic pathway of active polyphenols in this important herbal plant species.

The Crop JournalVol. 14(1)
Openalex Percentile: Top 63%
Plant Gene Expression Analysis
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