Gene clone and functional identification of sterol glycosyltransferases from Paris polyphylla var. yunnanensis.
10.19540/j.cnki.cjcmm.20230413.101
- Author:
Min HE
1
;
Si-Yuan GUO
2
;
Yan YIN
3
;
Chi ZHANG
1
;
Xia-Nan ZHANG
1
Author Information
1. School of Traditional Chinese Medicine, Capital Medical University Beijing 100069, China.
2. Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences Beijing 100700, China.
3. Hunan Academy of Chinese Medicine Changsha 410600, China.
- Publication Type:Journal Article
- Keywords:
biosynthetic pathway;
polyphyllin;
sterol glycosyltransferases
- MeSH:
Ligands;
Glycosyltransferases/genetics*;
Sterols;
Phylogeny;
Ascomycota;
Liliaceae/chemistry*;
Melanthiaceae;
Diosgenin;
Sugars;
Glucose;
Uridine Diphosphate
- From:
China Journal of Chinese Materia Medica
2023;48(14):3774-3785
- CountryChina
- Language:Chinese
-
Abstract:
In this study, the authors cloned a glycosyltransferase gene PpUGT2 from Paris polyphylla var. yunnanensis with the ORF length of 1 773 bp and encoding 590 amino acids. The phylogenetic tree revealed that PpUGT2 belonged to the UGT80A subfamily and was named as UGT80A49 by the UDP-glycosyltransferase(UGT) Nomenclature Committee. The expression vector pET28a-PpUGT2 was constructed, and enzyme catalytic reaction in vitro was conducted via inducing protein expression and extraction. With UDP-glucose as sugar donor and diosgenin and pennogenin as substrates, the protein was found with the ability to catalyze the C-3 hydroxyl β-glycosylation of diosgenin and pennogenin. To further explore its catalytic characteristic, 15 substrates including steroids and triterpenes were selected and PpUGT2 showed its activity towards the C-17 position of sterol testosterone with UDP-glucose as sugar donor. Homology modelling and molecule docking of PpUGT2 with substrates predicted the key residues interacting with ligands. The re-levant residues of PpUGT2-ligand binding model were scanned to calculate the corresponding mutants, and the optimized mutants were obtained according to the changes in binding affinity of the ligand with protein and the surrounding residues within 5.0 Å of ligands, which had reference value for design of the mutants. This study laid a foundation for further exploring the biosynthetic pathway of polyphyllin as well as the structure of sterol glycosyltransferases.
