Overexpression of SrUGT76G1 in Stevia alters major steviol glycosides composition towards improved quality.


Journal

Plant biotechnology journal
ISSN: 1467-7652
Titre abrégé: Plant Biotechnol J
Pays: England
ID NLM: 101201889

Informations de publication

Date de publication:
06 2019
Historique:
received: 20 08 2018
revised: 12 10 2018
accepted: 28 10 2018
pubmed: 21 12 2018
medline: 26 2 2020
entrez: 21 12 2018
Statut: ppublish

Résumé

Steviol glycosides (SGs) are extracted from Stevia leaves for use as a natural sweetener. Among SGs, stevioside is most abundant in leaf extracts followed by rebaudioside A (Reb A). However, Reb A is of particular interest because of its sweeter and more pleasant taste compared to stevioside. Therefore, the development of new Stevia varieties with a higher Reb A to stevioside ratio would be desirable for the production of higher quality natural sweeteners. Here, we generated transgenic Stevia plants overexpressing Stevia UDP-glycosyltransferase 76G1 (SrUGT76G1) that is known to convert stevioside to Reb A through 1,3-β-d-glucosylation in vitro. Interestingly, by overexpressing SrUGT76G1, the Reb A to stevioside ratio was drastically increased from 0.30 in wild-type (WT) plants up to 1.55 in transgenic lines without any significant changes in total SGs content. This was contributed by a concurrent increase in Reb A content and a decrease in stevioside content. Additionally, we were able to find an increase in the Reb C to dulcoside A ratio in transgenic lines. Using the glutathione S-transferase-tagged SrUGT76G1 recombinant protein for an in vitro glucosyltransferase assay, we further demonstrated that Reb C can be produced from the glucosylation of dulcoside A by SrUGT76G1. Transgenic Stevia plants having higher Reb A to stevioside ratio were visually indistinguishable from WT plants. Taken together, our results demonstrate that the overexpression of SrUGT76G1 in Stevia is an effective way to generate new Stevia varieties with higher proportion of the more preferred Reb A without compromising on plant development.

Identifiants

pubmed: 30569490
doi: 10.1111/pbi.13035
pmc: PMC6523589
doi:

Substances chimiques

Diterpenes, Kaurane 0
Glucosides 0
stevioside 0YON5MXJ9P
Uridine Diphosphate 58-98-0
Glycosyltransferases EC 2.4.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1037-1047

Informations de copyright

© 2018 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

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Auteurs

Mi Jung Kim (MJ)

Temasek Life Sciences Laboratory, National University of Singapore, Singapore, Singapore.

Junshi Zheng (J)

Temasek Life Sciences Laboratory, National University of Singapore, Singapore, Singapore.
Department of Biological Sciences, National University of Singapore, Singapore, Singapore.

Ming Hui Liao (MH)

Temasek Life Sciences Laboratory, National University of Singapore, Singapore, Singapore.

In-Cheol Jang (IC)

Temasek Life Sciences Laboratory, National University of Singapore, Singapore, Singapore.
Department of Biological Sciences, National University of Singapore, Singapore, Singapore.

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Classifications MeSH