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Dive into the research topics where Robert Sévenier is active.

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Featured researches published by Robert Sévenier.


The Plant Cell | 2004

Gain and Loss of Fruit Flavor Compounds Produced by Wild and Cultivated Strawberry Species

Asaph Aharoni; Ashok P. Giri; Francel Verstappen; Cinzia M. Bertea; Robert Sévenier; Zhongkui Sun; Maarten A. Jongsma; Wilfried Schwab; Harro J. Bouwmeester

The blends of flavor compounds produced by fruits serve as biological perfumes used to attract living creatures, including humans. They include hundreds of metabolites and vary in their characteristic fruit flavor composition. The molecular mechanisms by which fruit flavor and aroma compounds are gained and lost during evolution and domestication are largely unknown. Here, we report on processes that may have been responsible for the evolution of diversity in strawberry (Fragaria spp) fruit flavor components. Whereas the terpenoid profile of cultivated strawberry species is dominated by the monoterpene linalool and the sesquiterpene nerolidol, fruit of wild strawberry species emit mainly olefinic monoterpenes and myrtenyl acetate, which are not found in the cultivated species. We used cDNA microarray analysis to identify the F. ananassa Nerolidol Synthase1 (FaNES1) gene in cultivated strawberry and showed that the recombinant FaNES1 enzyme produced in Escherichia coli cells is capable of generating both linalool and nerolidol when supplied with geranyl diphosphate (GPP) or farnesyl diphosphate (FPP), respectively. Characterization of additional genes that are very similar to FaNES1 from both the wild and cultivated strawberry species (FaNES2 and F. vesca NES1) showed that only FaNES1 is exclusively present and highly expressed in the fruit of cultivated (octaploid) varieties. It encodes a protein truncated at its N terminus. Green fluorescent protein localization experiments suggest that a change in subcellular localization led to the FaNES1 enzyme encountering both GPP and FPP, allowing it to produce linalool and nerolidol. Conversely, an insertional mutation affected the expression of a terpene synthase gene that differs from that in the cultivated species (termed F. ananassa Pinene Synthase). It encodes an enzyme capable of catalyzing the biosynthesis of the typical wild species monoterpenes, such as α-pinene and β-myrcene, and caused the loss of these compounds in the cultivated strawberries. The loss of α-pinene also further influenced the fruit flavor profile because it was no longer available as a substrate for the production of the downstream compounds myrtenol and myrtenyl acetate. This phenomenon was demonstrated by cloning and characterizing a cytochrome P450 gene (Pinene Hydroxylase) that encodes the enzyme catalyzing the C10 hydroxylation of α-pinene to myrtenol. The findings shed light on the molecular evolutionary mechanisms resulting in different flavor profiles that are eventually selected for in domesticated species.


Journal of The American College of Nutrition | 2002

Increased production of nutriments by genetically engineered crops.

Robert Sévenier; Ingrid M. van der Meer; Raoul Bino; A.J. Koops

Plants are the basis of human nutrition and have been selected and improved to assure this purpose. Nowadays, new technologies such as genetic engineering and genomics approaches allow further improvement of plants. We describe here three examples for which these techniques have been employed. We introduced the first enzyme involved in fructan synthesis, the sucrose sucrose fructosyltransferase (isolated from Jerusalem artichoke), into sugar beet. The transgenic sugar beet showed a dramatic change in the nature of the accumulated sugar, 90% of the sucrose being converted into fructan. The use of transgenic sugar beet for the production and isolation of fructans will result in a more efficient plant production system of fructans and should promote their use in human food. The second example shows how the over-expression of the key enzyme of flavonoid biosynthesis could increase anti-oxidant levels in tomato. Introduction of a highly expressed chalcone isomerase led to a seventyfold increase of the amount of quercetin glucoside, which is a strong anti-oxidant in tomato. We were also able to modify the essential amino acid content of potato in order to increase its nutritional value. The introduction of a feedback insensitive bacterial gene involved in biosynthesis of aspartate family amino acids led to a sixfold increase of the lysine content. Because the use of a bacterial gene could appear to be controversial, we also introduced a mutated form of the plant key enzyme of lysine biosynthesis (dihydrodipicolinate synthase) in potato. This modification led to a 15 times increase of the lysine content of potato. This increase of the essential amino acid lysine influences the nutritional value of potato, which normally has low levels of several essential amino acids. These three examples show how the metabolism of primary constituents of the plant cell such as sugar or amino acids, but also of secondary metabolites such as flavonoids, can be modified by genetic engineering. Producing fructan, a soluble fiber, increasing the level of flavonoids, an antioxidant, in tomato or increasing the level of essential amino acids in potato are all clear examples of plant genetic modifications with possible positive effects on human nutrition.


Journal of Plant Physiology | 2012

Sink filling, inulin metabolizing enzymes and carbohydrate status in field grown chicory (Cichorium intybus L.)

Jeroen van Arkel; Rudy Vergauwen; Robert Sévenier; Johanna C. Hakkert; André Van Laere; Harro J. Bouwmeester; A.J. Koops; Ingrid M. van der Meer

Inulin is a fructose-based polymer that is isolated from chicory (Cichorium intybus L.) taproots. The degree of polymerization (DP) determines its application and hence the value of the crop. The DP is highly dependent on the field conditions and harvest time. Therefore, the present study was carried out with the objective to understand the regulation of inulin metabolism and the process that determines the chain length and inulin yield throughout the whole growing season. Metabolic aspects of inulin production and degradation in chicory were monitored in the field and under controlled conditions. The following characteristics were determined in taproots: concentrations of glucose, fructose and sucrose, the inulin mean polymer length (mDP), yield, gene expression and activity of enzymes involved in inulin metabolism. Inulin synthesis, catalyzed by sucrose:sucrose 1-fructosyltransferase (EC 2.4.1.99) (1-SST) and fructan:fructan 1-fructosyltransferase (EC 2.4.1.100) (1-FFT), started at the onset of taproot development. Inulin yield as a function of time followed a sigmoid curve reaching a maximum in November. Inulin reached a maximum mDP of about 15 in September, than gradually decreased. Based on the changes observed in the pattern of inulin accumulation, we defined three different phases in the growing season and analyzed product formation, enzyme activity and gene expression in these defined periods. The results were validated by performing experiments under controlled conditions in climate rooms. Our results show that the decrease in 1-SST that starts in June is not regulated by day length and temperature. From mid-September onwards, the mean degree of polymerization (mDP) decreased gradually although inulin yield still increased. The decrease in mDP combined with increased yield results from fructan exohydrolase activity, induced by low temperature, and the back transfer activity of 1-FFT. Overall, this study provides background information on how to improve inulin yield and quality in chicory.


Carbohydrate Polymers | 2013

Tailor-made fructan synthesis in plants: a review.

Jeroen van Arkel; Robert Sévenier; Johanna C. Hakkert; Harro J. Bouwmeester; A.J. Koops; Ingrid M. van der Meer

Fructan, a fructose polymer, is produced by many bacteria and plants. Fructan is used as carbohydrate reserve, and in bacteria also as protective outside layer. Chicory is a commercial fructan producing crop. The disadvantage of this crop is its fructan breakdown before harvest. Studies using genetically modification showed that fructan biosynthesis is difficult to steer in chicory. Alternatives for production of tailor-made fructan, fructan with a desired polymer length and linkage type, are originally non-fructan-accumulating plants expressing introduced fructosyltransferase genes. The usage of bacterial fructosyltransferases hindered plant performance, whereas plant-derived fructan genes can successfully be used for this purpose. The polymer length distribution and the yield are dependent on the origin of the fructan genes and the availability of sucrose in the host. Limitations seen in chicory for the production of tailor-made fructan are lacking in putative new platform crops like sugar beet and sugarcane and rice.


Nature Biotechnology | 1998

High level fructan accumulation in a transgenic sugar beet

Robert Sévenier; Robert D. Hall; I.M. van der Meer; Johanna C. Hakkert; A.J. van Tunen; A.J. Koops


Archive | 1999

Transgenic plants presenting a modified inulin producing profile

A.J. Koops; Robert Sévenier; Arjen Johannes Van Tunen; Lena De Leenheer


Plant Genetic Engineering, volume 7, Metabolic engineering and molecular farming-I | 2006

Fructan: nutritional significance, application, biosynthesis, molecular biology and genetic engineering

Robert Sévenier; J. van Arkel; Johanna C. Hakkert; A.J. Koops


Archive | 2002

Genetic Engineering of Beet and the Concept of the Plant as a Factory

Robert Sévenier; Robert Hall; A.J. Koops


Polysaccharides : Natural Fibers in Food and Nutrition | 2014

Fructan Biosynthesis Regulation and the Production of Tailor-Made Fructan in Plants

J. van Arkel; Robert Sévenier; Johanna C. Hakkert; Harro J. Bouwmeester; A.J. Koops; I.M. (Ingrid) van der Meer


Carbohydrate Polymers | 2012

Tailor-made fructan synthesis in plants: A review (Online First)

Arkel van J; Robert Sévenier; Johanna C. Hakkert; Harro J. Bouwmeester; A.J. Koops; Meer van der I. M

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A.J. Koops

Wageningen University and Research Centre

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Johanna C. Hakkert

Wageningen University and Research Centre

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Harro J. Bouwmeester

Wageningen University and Research Centre

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Ingrid M. van der Meer

Wageningen University and Research Centre

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Jeroen van Arkel

Wageningen University and Research Centre

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Francel Verstappen

Wageningen University and Research Centre

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Maarten A. Jongsma

Wageningen University and Research Centre

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Robert D. Hall

Wageningen University and Research Centre

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