» Articles » PMID: 32647038

Complete Biosynthesis of the Anti-Diabetic Plant Metabolite Montbretin A

Overview
Journal Plant Physiol
Specialty Physiology
Date 2020 Jul 11
PMID 32647038
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Diabetes and obesity are affecting human health worldwide. Their occurrence is increasing with lifestyle choices, globalization of food systems, and economic development. The specialized plant metabolite montbretin A (MbA) is being developed as an antidiabetes and antiobesity treatment due to its potent and specific inhibition of the human pancreatic α-amylase. MbA is a complex acylated flavonol glycoside formed in small amounts in montbretia ( × ) corms during the early summer. The spatial and temporal patterns of MbA accumulation limit its supply for drug development and application. We are exploring MbA biosynthesis to enable metabolic engineering of this rare and valuable compound. Genes and enzymes for the first four steps of MbA biosynthesis, starting from the flavonol precursor myricetin, have recently been identified. Here, we describe the gene discovery and functional characterization of the final two enzymes of MbA biosynthesis. The UDP-glycosyltransferases, CcUGT4 and CcUGT5, catalyze consecutive reactions in the formation of the disaccharide moiety at the 4'-hydroxy position of the MbA flavonol core. CcUGT4 is a flavonol glycoside 4'--xylosyltransferase that acts on the second to last intermediate (MbA-XR) in the pathway. CcUGT5 is a flavonol glycoside 1,4-rhamnosyltransferase that converts the final intermediate (MbA-R) to complete the MbA molecule. Both enzymes belong to the UGT family d-clade and are specific for flavonol glycosides and their respective sugar donors. This study concludes the discovery of the MbA biosynthetic pathway and provides the complete set of genes to engineer MbA biosynthesis. We demonstrate successful reconstruction of MbA biosynthesis in .

Citing Articles

Compositional Analysis of Grape Berries: Mapping the Global Metabolism of Grapes.

Hou H, Li Y, Zhou S, Zhang R, Wang Y, Lei L Foods. 2024; 13(23).

PMID: 39682788 PMC: 11639774. DOI: 10.3390/foods13233716.


A metabolomics study in citrus provides insight into bioactive phenylpropanoid metabolism.

Wang S, Shen S, Wang C, Wang X, Yang C, Zhou S Hortic Res. 2024; 11(1):uhad267.

PMID: 38304332 PMC: 10831325. DOI: 10.1093/hr/uhad267.


The parallel biosynthesis routes of hyperoside from naringenin in .

Wang Y, Cui Z, Li Q, Zhang S, Li Y, Li X Hortic Res. 2023; 10(9):uhad166.

PMID: 37727703 PMC: 10506691. DOI: 10.1093/hr/uhad166.


Medicinal plant genomics.

Siadjeu C, Pucker B BMC Genomics. 2023; 24(1):429.

PMID: 37528364 PMC: 10391748. DOI: 10.1186/s12864-023-09542-8.


Dehydrogenase MnGutB1 catalyzes 1-deoxynojirimycin biosynthesis in mulberry.

Yang Z, Luo Y, Xia X, He J, Zhang J, Zeng Q Plant Physiol. 2023; 192(2):1307-1320.

PMID: 36800200 PMC: 10231399. DOI: 10.1093/plphys/kiad065.


References
1.
Irmisch S, Ruebsam H, Jancsik S, Yuen M, Madilao L, Bohlmann J . Flavonol Biosynthesis Genes and Their Use in Engineering the Plant Antidiabetic Metabolite Montbretin A. Plant Physiol. 2019; 180(3):1277-1290. PMC: 6752896. DOI: 10.1104/pp.19.00254. View

2.
Ogata J, Kanno Y, Itoh Y, Tsugawa H, Suzuki M . Plant biochemistry: anthocyanin biosynthesis in roses. Nature. 2005; 435(7043):757-8. DOI: 10.1038/nature435757a. View

3.
Jung S, Kim W, Park S, Jeong J, Park M, Lim S . Two ginseng UDP-glycosyltransferases synthesize ginsenoside Rg3 and Rd. Plant Cell Physiol. 2014; 55(12):2177-88. DOI: 10.1093/pcp/pcu147. View

4.
Scheen A . Is there a role for alpha-glucosidase inhibitors in the prevention of type 2 diabetes mellitus?. Drugs. 2003; 63(10):933-51. DOI: 10.2165/00003495-200363100-00002. View

5.
Osmani S, Bak S, Moller B . Substrate specificity of plant UDP-dependent glycosyltransferases predicted from crystal structures and homology modeling. Phytochemistry. 2009; 70(3):325-47. DOI: 10.1016/j.phytochem.2008.12.009. View