Matthias Wüst

Dr. Matthias Wüst

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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 June 2010 in European Food Research and Technology
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UWUrsula Wölwer-Rieck
Ursula Wölwer-Rieck
CLChrista Lankes
Christa Lankes
AWAndreas Wawrzun
Andreas Wawrzun
MWMatthias Wüst
Matthias Wüst

1 May 2014 in Plant Physiology
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Journal Article
Closed access
FBFriedericke Bönisch
Friedericke Bönisch
JFJohanna Frotscher
Johanna Frotscher
SSSarah Stanitzek
Sarah Stanitzek
ERErnst Rühl
Ernst Rühl
MWMatthias Wüst
Matthias Wüst
WSWilfried Schwab
Wilfried Schwab
Terpenoids represent one of the major classes of natural products and serve different biological functions. In grape (Vitis vinifera), a large fraction of these compounds is present as nonvolatile terpene glycosides. We have extracted putative glycosyltransferase (GT) sequences from the grape genome database that show similarity to Arabidopsis (Arabidopsis thaliana) GTs whose encoded proteins glucosylate a diversity of terpenes. Spatial and temporal expression levels of the potential VvGT genes were determined in five different grapevine varieties. Heterologous expression and biochemical assays of candidate genes led to the identification of a UDP-glucose:monoterpenol β-d-glucosyltransferase (VvGT7). The VvGT7 gene was expressed in various tissues in accordance with monoterpenyl glucoside accumulation in grape cultivars. Twelve allelic VvGT7 genes were isolated from five cultivars, and their encoded proteins were biochemically analyzed. They varied in substrate preference and catalytic activity. Three amino acids, which corresponded to none of the determinants previously identified for other plant GTs, were found to be important for enzymatic catalysis. Site-specific mutagenesis along with the analysis of allelic proteins also revealed amino acids that impact catalytic activity and substrate tolerance. These results demonstrate that VvGT7 may contribute to the production of geranyl and neryl glucoside during grape ripening.


29 July 2014 in Plant Physiology
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Journal Article
Open access
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FBFriedericke Bönisch
Friedericke Bönisch
JFJohanna Frotscher
Johanna Frotscher
SSSarah Stanitzek
Sarah Stanitzek
ERErnst Rühl
Ernst Rühl
MWMatthias Wüst
Matthias Wüst
WSWilfried Schwab
Wilfried Schwab
Monoterpenols serve various biological functions and accumulate in grape (Vitis vinifera), where a major fraction occurs as nonvolatile glycosides. We have screened the grape genome for sequences with similarity to terpene URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASES (UGTs) from Arabidopsis (Arabidopsis thaliana). A ripening-related expression pattern was shown for three candidates by spatial and temporal expression analyses in five grape cultivars. Transcript accumulation correlated with the production of monoterpenyl β-d-glucosides in grape exocarp during ripening and was low in vegetative tissue. Targeted functional screening of the recombinant UGTs for their biological substrates was performed by activity-based metabolite profiling (ABMP) employing a physiologic library of aglycones built from glycosides isolated from grape. This approach led to the identification of two UDP-glucose:monoterpenol β-d-glucosyltransferases. Whereas VvGT14a glucosylated geraniol, R,S-citronellol, and nerol with similar efficiency, the three allelic forms VvGT15a, VvGT15b, and VvGT15c preferred geraniol over nerol. Kinetic resolution of R,S-citronellol and R,S-linalool was shown for VvGT15a and VvGT14a, respectively. ABMP revealed geraniol as the major biological substrate but also disclosed that these UGTs may add to the production of further glycoconjugates in planta. ABMP of aglycone libraries provides a versatile tool to uncover novel biologically relevant substrates of small-molecule glycosyltransferases that often show broad sugar acceptor promiscuity.

1 February 2005 in Phytochemistry
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Journal Article
Closed access
FLF Luan
F Luan
AMA Mosandl
A Mosandl
AMA Munch
A Munch
MWMatthias Wüst
Matthias Wüst