Cloning, prokaryotic expression, and functional validation of flavonoid 3-O-glycosyltransferase gene (Rh3GT) from Rhododendron hybridum Hort.
- Author:
Yicheng YAN
1
;
Zehang WU
1
;
Yuhang JIANG
1
;
Gaoyuan HU
1
;
Yujie YANG
1
;
Xiaohong XIE
1
;
Yueyan WU
1
;
Yonghong JIA
1
Author Information
- Publication Type:Journal Article
- Keywords: Rhododendron hybridum Hort; expression analysis; flavonoid 3-O-glycosyltransferase (3GT); prokaryotic expression; transient overexpression
- MeSH: Rhododendron/classification*; Glucosyltransferases/metabolism*; Cloning, Molecular; Escherichia coli/metabolism*; Recombinant Proteins/biosynthesis*; Anthocyanins/biosynthesis*; Phylogeny; Plant Proteins/metabolism*; Amino Acid Sequence
- From: Chinese Journal of Biotechnology 2025;41(2):881-895
- CountryChina
- Language:Chinese
- Abstract: Flavonoid 3-O-glucosyltransferase (3GT) is a key enzyme in the glucosidation of anthocyanins. To investigate the 3GT gene in rhododendron, we cloned an open reading frame (ORF) of 3GT gene (named Rh3GT) from Rhododendron hybridum Hort (Red cultivar) and then characterized this gene and the deduced protein in terms of the biochemical characteristics, expression level, and enzymatic function. The results showed that Rh3GT had a full length of 993 bp and encoded 330 amino acid residues. The deduced protein was hydrophilic, stable, weak acid, belonging to the glycosyltransferase family (GT-B type), with glutamine (Q) at position 44 in the PSPG box. The phylogenetic analysis showed that Rh3GT was most closely related to Vc3GT from Vaccinium corymbosum and Vm3GT from Vaccinium myrtillus. Rh3GT was expressed in the stems, leaves, and flowers and almost not expressed in the roots, with the highest expression level in petals during full blooming stage. Introduction of pCAMBIAL1302-Rh3GT into petals significantly up-regulated the expression level of Rh3GT and increased the total anthocyanin accumulation. Rh3GT was successfully expressed in Escherichia coli BL21 in the form of inclusion bodies with a size of about 36 kDa. The results of HPLC showed that the recombinant Rh3GT after denaturation, purification, and dilution could catalyze the synthesis of cyanidin and UDP-glucose to synthesize cyanidin 3-O-glucoside, indicating that the expressed protein had 3GT activity. This study provides basic data for further studying the molecular regulation mechanism of anthocyanin biosynthesis and theoretical support for molecular breeding of rhododendron.
