Literature DB >> 16667943

Glucosylation of Steviol and Steviol-Glucosides in Extracts from Stevia rebaudiana Bertoni.

H Shibata1, S Sonoke, H Ochiai, H Nishihashi, M Yamada.   

Abstract

To evaluate and characterize stevioside biosynthetic pathway in Stevia rebaudiana Bertoni cv Houten, two enzyme fractions that catalyze glucosylation of steviol (ent-13-hydroxy kaur-16-en-19-oic acid) and steviol-glucosides (steviol-13-O-glucopyranoside, steviolbioside and stevioside), utilizing UDP-glucose as the glucose donor, were prepared from the soluble extracts of S. rebaudiana leaves. Enzyme fraction I, passed through DEAE-Toyopearl equilibrated with 50 millimolar K-phosphate pH 7.5, catalyzed the glucosylation to steviol and 19-O-methylsteviol, but not to iso-steviol and 13-O-methylsteviol, indicating that 13-hydroxyl group of the steviol skeleton is glucosylated first from UDP-glucose to produce steviol-13-O-glucopyranoside. Enzyme fraction II, eluted from the DEAE-Toyopearl column with 0.15 molar KCI, catalyzed the glucose transfer from UDP-glucose to steviol-13-O-glucopyranoside, steviolbioside and stevioside, but not to rubusoside (13, 19-di-O-glucopyranoside) and rebaudioside A. The reaction products glucosylated from steviol-13-O-glucopyranoside, steviolbioside and stevioside were identified to be steviolbioside, stevioside and rebaudioside A, respectively. These results indicate that in the steviol-glucoside biosynthetic pathway, steviol-13-O-glucopyranoside produced from the steviol glucosylation is successively glucosylated to steviolbioside, then to stevioside producing rebaudioside A.

Entities:  

Year:  1991        PMID: 16667943      PMCID: PMC1077498          DOI: 10.1104/pp.95.1.152

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  5 in total

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Authors:  M Ruddat; E Heftmann; A Lang
Journal:  Arch Biochem Biophys       Date:  1965-06       Impact factor: 4.013

2.  Diterpenoid sweeteners. Synthesis and sensory evaluation of stevioside analogues with improved organoleptic properties.

Authors:  G E DuBois; R A Stephenson
Journal:  J Med Chem       Date:  1985-01       Impact factor: 7.446

3.  Gas chromatography of glucuronides.

Authors:  T Imanari; Z Tamura
Journal:  Chem Pharm Bull (Tokyo)       Date:  1967-11       Impact factor: 1.645

4.  Gas chromatography of O-glucuronides.

Authors:  Z Tamura; T Imanari
Journal:  Chem Pharm Bull (Tokyo)       Date:  1964-11       Impact factor: 1.645

5.  Enzymic synthesis of indole-3-acetyl-1-O-beta-d-glucose. II. Metabolic characteristics of the enzyme.

Authors:  A J Leznicki; R S Bandurski
Journal:  Plant Physiol       Date:  1988       Impact factor: 8.340

  5 in total
  3 in total

1.  Leaf Ests from Stevia rebaudiana: a resource for gene discovery in diterpene synthesis.

Authors:  J E Brandle; A Richman; A K Swanson; B P Chapman
Journal:  Plant Mol Biol       Date:  2002-11       Impact factor: 4.076

2.  Enhanced specialized metabolite, trichome density, and biosynthetic gene expression in Stevia rebaudiana (Bertoni) Bertoni plants inoculated with endophytic bacteria Enterobacter hormaechei.

Authors:  Dumas G Oviedo-Pereira; Melina López-Meyer; Silvia Evangelista-Lozano; Luis G Sarmiento-López; Gabriela Sepúlveda-Jiménez; Mario Rodríguez-Monroy
Journal:  PeerJ       Date:  2022-06-28       Impact factor: 3.061

3.  2C-Methyl- D- erythritol 2,4-cyclodiphosphate synthase from Stevia rebaudiana Bertoni is a functional gene.

Authors:  Hitesh Kumar; Kashmir Singh; Sanjay Kumar
Journal:  Mol Biol Rep       Date:  2012-10-12       Impact factor: 2.316

  3 in total

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