# Identification and Characterization of a Putative Kaempferol Glucosyltransferase UGT78G3 in Medicago truncatula

## TL;DR

The study identifies and characterizes UGT78G3, a putative enzyme in Medicago truncatula that may glycosylate kaempferol but does not significantly impact its levels in plants.

## Contribution

The study identifies UGT78G3 as a putative kaempferol glucosyltransferase and explores its in vitro and in vivo roles.

## Key findings

- UGT78G3 catalyzes the formation of kaempferol 3-O-glucoside in vitro.
- Overexpression or mutagenesis of UGT78G3 does not significantly affect kaempferol 3-O-glucoside levels in vivo.
- UGT78G3 is a potential target for biocatalyst design for flavonoid glucoside synthesis.

## Abstract

UDP-glycosyltransferases (UGTs) represent a large multigene family that play a central role in glycosylating a highly diverse array of natural products, underscoring their critical importance in various biological processes. However, the functional roles of a substantial majority of UGTs remain to be elucidated. In the present study, we characterized the glycosyltransferase UGT78G3, a member of the UGT78 glycosyltransferase family in the model legume Medicago truncatula. Amino-acid sequence analysis revealed a conserved PSPG motif at the C-terminus of UGT78G3. Liquid chromatography-coupled tandem mass spectrometry (LC-MS/MS) analysis demonstrated that UGT78G3 catalyzes the formation of kaempferol 3-O-glucoside in vitro. However, neither UGT78G3 overexpression nor CRISPR/Cas9-mediated mutagenesis resulted in significant changes to the endogenous levels of kaempferol 3-O-glucoside, indicating that UGT78G3 does not play a predominant role in the biosynthesis of kaempferol 3-O-glucoside in vivo. Our findings identify a putative glycosyltransferase in M. truncatula and provide a target for biocatalyst design aimed at synthesizing flavonoid glucosides.