References of "Goffin, Dorothée"
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See detailL'analyse de sucres par HPEAC-PAD
Goffin, Dorothée ULg; Gillet, Sébastien ULg

Learning material (2011)

Présentation de l'analyse des sucres par Chromatographie Haute Performance Échangeuse d'Anions, couplée à un Détecteur par Ampérométrie Pulsée (HPAEC-PAD).

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See detailLes Aliments Fonctionnels
Goffin, Dorothée ULg

Scientific conference (2011, November 03)

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See detailPrésentation du projet de Spin-off IMONIC à des investisseurs potentiels
Goffin, Dorothée ULg

Conference (2011, September 02)

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See detailRapport 1 FIRST Spin Off IMONIC
Goffin, Dorothée ULg

Report (2011)

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See detailPrésentation du projet de Spin-off IMONIC
Goffin, Dorothée ULg

Conference (2011, April 28)

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See detailDossier de candidature INNOVACT Campus Award
Goffin, Dorothée ULg

Report (2011)

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See detailEnzymatic production of pectic oligosaccharides from polygalacturonic acid with commercial pectinase preparations
Combo, Agnan Marie Michel ULg; Aguedo, Mario ULg; Goffin, Dorothée ULg et al

in Food and Bioproducts Processing: Transactions of the Institution of Chemical Engineers, Part C (2011), 90(3), 588-596

The present study investigates the individual efficiency of six commercial pectinase preparations (Endopolygalacturonase M2, Pectinase, Viscozyme L, Pectinex Ultra SP-L, Pectinase 62L and Macer8 FJ) in ... [more ▼]

The present study investigates the individual efficiency of six commercial pectinase preparations (Endopolygalacturonase M2, Pectinase, Viscozyme L, Pectinex Ultra SP-L, Pectinase 62L and Macer8 FJ) in catalyzing the liberation of pectic oligosaccharides (POS) from polygalacturonic acid. On the basis of high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD) analysis of the enzymatic hydrolysates, products release kinetics revealed a random cleavage pattern and an exo mode of cleavage for all the enzymes except for Endopolygalacturonase M2. All six enzymes generated oligoGalA with different degree of polymerization (DP); the quantitative composition of oligoGalA depended on the enzyme specificity and the time of enzymatic reaction. Endopolygalacturonase M2 was the best enzyme preparation for production of oligoGalA, with 18% (wt) of digalacturonic acid and 58% (wt) of trigalacturonic acid after 2h of reaction. Concerning galacturonic acid production, Pectinase 62L was superior to the other enzyme preparations with 47% (wt) after 1h of reaction. [less ▲]

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See detailWill isomalto-oligosaccharides, a well-established functional food in Asia, break through the European and American market? The status of knowledge on these prebiotics
Goffin, Dorothée ULg; Delzenne, Nathalie; Blecker, Christophe ULg et al

in Critical Reviews in Food Science & Nutrition (2011)

This critical review article present the current state of knowledge on isomaltooligosaccharides, some well known functional oligosaccharides in Asia, to evaluate their potential as emergent prebiotics in ... [more ▼]

This critical review article present the current state of knowledge on isomaltooligosaccharides, some well known functional oligosaccharides in Asia, to evaluate their potential as emergent prebiotics in the American and European functional food market. It includes first a unique inventory of the different families of compounds which have been considered as IMO and their specific structure. A description of the different production methods including the involved enzymes and their specific activities, the substrates and the types of IMO produced. Considering the structural complexity of IMO products, specific characterization methods are described as well as purification methods which enable the riddance of digestible oligosaccharides. Finally an extensive review of their techno-functional and nutritional properties enables to place IMO inside the growing prebiotic market. This review is of a particular interest considering that IMO commercialization in America and Europe is a topical subject due to the recent submission, by Bioneutra INC. (Canada), of a novel food file to the UK Food Standards Agency as well as several patents for IMO production. [less ▲]

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See detailMise à l'honneur des Docteurs avec Thèse
Bay, Daniel ULg; Goffin, Dorothée ULg

Diverse speeche and writing (2010)

Présentation de la thèse de doctorat de Dorothée Goffin

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See detailA method for the production of prebiotic preparations containing isomaltooligosaccharides and gluconic acid.
Goffin, Dorothée ULg; Blecker, Christophe ULg; Paquot, Michel ULg

Poster (2010, October 14)

Isomaltooligosaccharides (IMOs) are non-digestible oligosaccharides, considered as prebiotics and therefore aim to selectively feed probiotics indigenous to the human colon. IMOs consists of glucose ... [more ▼]

Isomaltooligosaccharides (IMOs) are non-digestible oligosaccharides, considered as prebiotics and therefore aim to selectively feed probiotics indigenous to the human colon. IMOs consists of glucose monomers linked by at least one α-1-6, or in a lower proportion α -1-3 (nigerose family) or α -1-2 (kojibiose family) glucosidic linkages. In our case they are produced from either corn, tapioca, or rice hydrolyzed starch. The enzymatic reaction is achieved using an Aspergillus niger transglucosidase (EC 2.4.1.24). It results in a very complex mixture with molecules characterized at the same time by their DP value (from 2 to ~15), linkages types (α-1-2, 3 or 6) and the proportion and position of each type of linkage (only α -1-6 or combined types). However, the reaction only permits to reach yields between 50-75 % in IMOs. Impurities are composed of residual maltooligosaccharides (glucose with exclusively α -1-4 linkages) from the starting vegetal material and glucose released during the transglucosylation step. These digestible saccharides are deleterious for the prebiotic preparation. Therefore, these compounds must be eliminated from the medium or converted in prebiotic species. Residual maltooligosaccharides are thus specifically hydrolyzed by a thermostable α-glucosidase (EC. 3.2.1.20) in order to produce glucose as the only unwanted specie. This glucose can then be converted to gluconic acid and/or its salts using a glucose-oxidase (EC. 1.1.3.4) in combination with a catalase. Gluconic acid (C6H12O7) is a saccharide derivative which has been recognized as a prebiotic compound. It is also known for its purgative action and proved to be effective for lipid peroxidation prevention. A first option can then be chosen, leaving gluconic acid in the product in order to obtain an original prebiotic product enjoying new prebiotic potential properties due to the combination of both types of prebiotic compounds (IMO and gluconic acid). The second option is to eliminate the gluconic acid from the prebiotic mixture. This separation doesn’t present the same difficulties than for glucose as gluconic acid is charged and can therefore be separated on anion-exchange resins (Dowex AcO-). This overall process, fulfilling the principles of green chemistry and being applicable to produce organic prebiotic, is an elegant solution, from an economical, an environmental, a nutri-functional and a techno-functional point of view. Indeed, it can lead to original prebiotic preparations, with yields close to 100%, by avoiding product loss, as the digestible saccharides portion is converted to gluconic acid. Furthermore, the presence of gluconic acid can provide many functional properties to the prebiotic preparations for their incorporation in food products. [less ▲]

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