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See detailAspergillus fumigatus detection by PCR in broncho-alveolar fluid
Hayette, Marie-Pierre ULg; Boland, Pascal; Evrard, Béatrice et al

Poster (1999, September 29)

Background: The usefullness of a nested PCR for detection of Aspergillus fumigatus DNA was evaluated in bronchoalveolar lavage (BAL) fluid during a period of two years (1996- 1998). The aim of the study ... [more ▼]

Background: The usefullness of a nested PCR for detection of Aspergillus fumigatus DNA was evaluated in bronchoalveolar lavage (BAL) fluid during a period of two years (1996- 1998). The aim of the study was to assess the role of PCR in diagnosing invasive pulmonary aspergillosis (IPA). Methods: A nested PCR-based amplification of fragments of genes-encoding alkaline proteases from A. fumigatus was used to test 167 BAL samples. All samples were checked for the absence of amplification inhibitors. Medical, radiological, microbiological records and autopsy findings were reviewed for assessing invasive aspergillosis. All successive patients investigated by BAL were included in the study. They were distributed in three groups: A, proven or probable aspergillosis (n=11); B, colonization (n=2); C, no evidence of IPA (n=154). PCR results were compared to culture détection as gold standard and to clinical data. Results: BAL fluids from 10 patients of group A were PCR positive. One case was falsely negative. Among group B, one case was PCR positive, and the second one PCR negative but had negative BAL cultures (only culture positive sputum). No false positive was detected among group C. Comparing to culture, sensitivity was 91%, specificity, 100%, positive predictive value, 100% and négative predictive value, 99%. Conclusion: 1. Aspergillus fumigatus PCR in BAL fluid was an accurate test to diagnose culture negative patients with IPA and to confirm culture positive samples; however it doesn't make difference between infection and colonization. 2. It is an appropriate test to exclude Aspergillus infection in patients at risk of invasive illness. [less ▲]

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See detailSynthesis and evaluation of non-carboxylic pyridinic derivatives as cyclooxygenase inhibitors
Dogne, J. M.; De Leval, X.; Delarge, J. et al

Poster (1999, September 17)

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See detailComparative effects of nimesulide, nimesulide L-lysine and nimesulide L-lysine L-arginine on human articular chondrocytes in vitro
De Leval, X.; Dogne, J. M.; Delarge, J. et al

Poster (1999, September 17)

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See detailLearning new names for new stimuli : Making the connection
Thi, Jean-Pierre; Comblain, Annick ULg

Poster (1999, September)

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See detailUse of LIPA Mycobacteria (Innogenetics) to identify mycobacteria in a routine laboratory
Fauville-Dufaux, Maryse; Hayette, Marie-Pierre ULg; Vanfleteren, B. et al

Poster (1999, September)

The test consists in the PCR amplification of the DNA region coding for the 16S~23S rRNA space! of Mycobacterium species followed by the hybridization and the stringent wash of the amplified product with ... [more ▼]

The test consists in the PCR amplification of the DNA region coding for the 16S~23S rRNA space! of Mycobacterium species followed by the hybridization and the stringent wash of the amplified product with species specific probes immobilized on a strip. Thirteen different probes are placed on the strip enabling the specific identification of the most frequent mycobacterial strains isolated in clinical samples. One hundred twenty strains isolated from clinical specimens on Lowenstein-Jensen medium were included in the evaluation study. Lipa. identification of all the 120 strains was in agreement with identification obtained by other methods like classical bacteriological tests) Gen Probe hybridization tests, species specific PCRs. PeR-restriction fragment length polymorphism analysis ofthe fup65 gene (PRA) and, in some cases, DNA sequencing of an amplified fragment ofthe 168 rRNA gene. On the other hand, 35 early growing Bactec cultures from clinical specimens, taken at a GI as low as 9, were analysed by Lips Mycobacteria. 69 % ofthem could be identified on the aliquot taken when the GI was between 9 to 50. The remaining cultures could be identified on an aliquot ofBaetec mediwn taken one or 2 days later. In comparison to the other identification methods. Lipa Mycobacteria gives results by far faster than bacteriological tests and is easier to perfonn than PRA and DNA sequencing. It takes longer to perform than the Gen Probe hybridization test (lh30 PeR plus 3h30 hybridizationwashing procedure versus 2h for the Gen Probe test), but it allows, in the same procedure, identification of 9 different mycobacterial species though Gen Probe hyridiution only identifies 1 or maximum 2 species. Lipa Mycobacteria is also usable on early growing Bactec cultures. [less ▲]

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See detailSurveillance of antimicrobial resistance in Streptococcus agalactiae isolated from patients in Belgium (1989-1991 versus 1996-1999)
MELIN, Pierrette ULg; Rodriguez Cuns, Grisel; Vincento Fernandez, Walter et al

Poster (1999, September)

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See detailProduction and freeze-drying of Lactococcus starters isolated from Tunisian Lben.
Hamdi, M.; Cornelius, C.; Achour, M. et al

Poster (1999, September)

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See detailPurification and characterization of Yarrowia lipolytica exracellular lipase.
Destain, Jacqueline ULg; Swiatkowski, T.; van Beumen, J. et al

Poster (1999, September)

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See detailPhytoplankton control: the role of in situ nutrient recycling?
Darchambeau, François ULg; Thys, Isabelle; Leporcq, Bruno et al

Poster (1999, August 25)

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See detailRearrangement of 1-alkynyltrialkylaluminates
Debuigne, Antoine ULg; Gérard, Julien; Hevesi, Làszlò

Poster (1999, July 19)

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See detailImportance of the apoprotein in the catalysis of hydroperoxide lyase
Delcarte, J.; Jacques, P.; Fauconnier, Marie-Laure ULg et al

Poster (1999, July 15)

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See detailConversion of green note aldehydes into alcohols by yeast alcohol dehydrogenase
Fauconnier, Marie-Laure ULg; Mpambara, A.; Delcarte, J. et al

Poster (1999, July 11)

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See detailStress-induced metabolites in potato in response to ampicillin elicitation.
Ongena, Marc ULg; Antoine, P.; Thonart, Philippe ULg et al

Poster (1999, July)

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See detailDesiccation-tolerance : an advantage for the biotechnological applications of bacteria
Weekers, F.; Jacques, Ph.; Springael, D. et al

Poster (1999, July)

See detailThe monitoring of the enzymatic depolymerisation of pectins by spectroscopic techniques.
Sinnaeve, G.; Ciza, A.; Deconinck, T. et al

Poster (1999, July)

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See detailIn vivo et in vitro effect of new glibenclamide isosteres
Lebrun, P.; Ouedraogo, R.; Nguyen, Q. A. et al

Poster (1999, July)

See detailSurfactin and iturin A effects on Bacillus subtilis surface hydrophobicity
Ahimou, F.; Deleu, Magali ULg; Jacques, Ph. et al

Poster (1999, July)

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See detailMicrobiological and chemical study of « Tiéré », senegalese millet fermented food.
Leite, N.; Diop, M.; Tine, E. et al

Poster (1999, July)

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See detailComparative study of bile salts hydrolase activity from Lactobacilli ssp.
El Mejdoub, Thami ULg; Roblain, D.; Destain, Jacqueline ULg et al

Poster (1999, July)

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See detailIn vivo et in vitro effect of new glibenclamide isosteres
Lebrun, P.; Ouedraogo, R.; Nguyen, Q. A. et al

Poster (1999, July)

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See detailScreening of new microorganisms for pectinases production
Ciza, A.; Sinnaeve, G.; Deconinck, T. et al

Poster (1999, July)

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See detailScreening of pectolytic microorganisms by near infrared reflectance spectroscopy.
Sinnaeve, G.; Ciza, A.; Deconinck, T. et al

Poster (1999, June)

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See detailThe development of visual memory span : The role of expertise
Thibaut, Jean-Pierre; Comblain, Annick ULg

Poster (1999, May 20)

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See detailThe Nitroxides in Polymerization
Olive, Gilles ULg; Göttgens, Christianne; Smulders, Wilfred et al

Poster (1999, May 20)

The Nitroxides in Polymerization arepresented here with explanation.

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See detailAntifungal lipopeptides from B. subtilis induce defense-related phenolics in potato
Ongena, Marc ULg; Akpa, E.; Thonart, Philippe ULg et al

Poster (1999, May 04)

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See detailSynthèse du 6-fluoro-a-méthyl-L-tryptophane et d'un de ses métabolites
Lambin, D.; Tadino, V.; Olynyk, Ch et al

Poster (1999, May 03)

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See detailComparative evaluation of Fungitest, Neosensitabs and broth microdilution method for yeasts susceptibility testing
Hayette, Marie-Pierre ULg; Bolland, Pascal; Seidel, Laurence ULg et al

Poster (1999, May)

The need of a simple and reliable method for routine yeasts susceptibility testing led us to evaluate two commercially available methods. We investigated the in vitro susceptibility of 67 clinical ... [more ▼]

The need of a simple and reliable method for routine yeasts susceptibility testing led us to evaluate two commercially available methods. We investigated the in vitro susceptibility of 67 clinical isolates (26 C. albicans, 32 C. glabrata, 4 C. krusei, 2 C. tropicalis, 2 C. kefyr and 1 S. cerevisiae) to 6 drugs flucytosine (FC), amphotericin B (A), fluconazole (FZ), itraconazole (IT), kétoconazole (K), miconazole (M), comparing two methods Fungitest (Sanofi Pasteur) and Neosensitabs (Rosco). A broth microdilution adaptation from the NCCLS-M27A procedure was used as reference method. Fungitests consist of individually packed 16 wells microplates containing 6 drugs at two critical concentrations in buffered medium. Reading was performed after 24 and 48h incubation. Neosensitabs is an agar diffusion method on Shadomy agar using antifungals tablets. Reading was performed after 24h. For all strains Neosensitabs was in concordance with NCCLS M27-A for FC (94%), A (98%), FZ (55%) I (53%) with p<0.05. Fungitest correlated with NCCLS method for all antifungals after 24 and 48h incubation time (p<0.05) with respectively 95/95% for FC, 100/100% for A, 80/76% for FZ, 81/55% for I and 93/75% for K, and 88/81 for M. Candida glabrata gave the poorest result with Neosensitabs with 28% concordance for FZand 39% for I; therefore the method can't be recommended for this species. Fungitest concordance observed was 55% for I after 48h. Our results suggest that Fungitest is appropriate for routine yeast susceptibility testing. However itraconazole testing has to be improved with this method. [less ▲]

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See detailSynthèse et évaluation pharmacologique de 3-alkylamino-7-chloro-4H-pyrido[2,3-e]-1,2,4-thiadiazine 1,1-dioxydes
Ouedraogo, R.; Fontaine, J.; Antoine, M. H. et al

Poster (1999, May)

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See detailMécanisme d’inactivation de l’α-chymotrypsine par les dérivés coumariniques: étude de l’ouverture de la lactone
Pochet, L.; Dive, G.; Alin, V. et al

Poster (1999, May)

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See detailImpact d’antagonistes du thromboxane A2 dérivés du torasémide sur la fonction plaquettaire
Dogne, J. M.; Neven, Ph.; Rolin, S. et al

Poster (1999, May)

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See detailEvaluation de la sélectivité COX-1 vs COX-2 de drogues à potentialités anti-inflammatoires
De Leval, X.; Dogne, J. M.; Neven, Ph. et al

Poster (1999, May)

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See detailSynthesis of polynorbornene grafted with poly(ε-caprolactone) by sequential controlled ring opening polymerization
Lecomte, Philippe ULg; Mecerreyes, David; Dubois, Philippe et al

Poster (1999, April 12)

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See detailSynthesis of new copolymers of polypyrrole-poly-ε-caprolactone
Jérôme, Christine ULg; Martinot, Lucien; Louette, P. et al

Poster (1999, April 12)

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See detailAdaptation of the European crop growth monitoring system to the Belgian conditions.
Buffet, D.; Dehem, Didier; Wouters, K. et al

Poster (1999, April)

The aim of the Belgian Crop Growth Monitoring System (B-CGMS) is the elaboration of an integrated information system predicting reliable, timely and objective estimates of crop yields and monitoring ... [more ▼]

The aim of the Belgian Crop Growth Monitoring System (B-CGMS) is the elaboration of an integrated information system predicting reliable, timely and objective estimates of crop yields and monitoring calamity sites at regional scales. Seven major crops are concerned by the project : winter wheat, winter barley, fodder maize, winter rape seed, potatoes, sugar beet and permanent meadow. The main tasks in the adaptation of the European model come down to the completion and the improvement of the databases to specify the local conditions and particularities of Belgium, to modify the scale of the forecasting system, to incorporate satellite information and to develop a web-based mapping interface. [less ▲]

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See detailL'HACCP et la maîtrise de l'hygiène chez les artisans producteurs
Tollet, Myriam; Frere, Pol ULg; Sindic, Marianne ULg

Poster (1999, January 27)

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See detailAmélioration de la qualité chez les artisans.
Duculot, Jacqueline; Vanwijnsberghe, Caroline; Sindic, Marianne ULg

Poster (1999, January)

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See detailPeriotontitis as a risk factor for coronary heart disease
Geerts, Sabine ULg; Nys, Monique; Legrand, Victor et al

Poster (1999)

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See detailOne-photon mazer resonances for arbitrary field modes
Bastin, Thierry ULg; Solano, E.

Poster (1999)

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See detailGentle mastication induces endotoxemia in periodontitis-affected patients
Geerts, Sabine ULg; Nys, Monique; Legrand, Victor et al

Poster (1999)

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See detailCCD Detection of beam-foil light
Quevrin, A.; Bastin, Thierry ULg; Dumont, Paul-Dominique ULg et al

Poster (1999)

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See detailPhenotypic analysis on media containing drugs
Vandenbol, Micheline ULg; Hilger, François; Portetelle, Daniel ULg

Poster (1999)

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See detailQualitative phenotypic analysis of yeast genes with unknown function.
Bianchi, M.; Vandenbol, Micheline ULg; Ngo, S. et al

Poster (1999)

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See detailElectron-microscopic tomography of silver-stained interphase and metaphase nucleolar organizer regions
Cheutin, T; O'Donohue, M-F; Kaplan, H et al

Poster (1999)

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See detailLysosomal phospholipases inhibition by emetine, strychnopentamine and usambarensine
Quetin-Leclercq, Joelle; Schomer, G; Van Bambeke, F et al

Poster (1999)

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See detailDeactivation mechanisms and regeneration of a bimetallic hydrodechlorination catalyst
Heinrichs, Benoît ULg; Noville, Francis ULg; Schoebrechts, Jean-Paul et al

Poster (1999)

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See detailExtended Analysis of the Highly Ionized Neon Spectra
Kramida, A. E.; Bastin, Thierry ULg; Biémont, Emile ULg et al

Poster (1999)

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See detailCapture for coorbital moons
Champenois, Sylvain; Henrard, Jacques; Jancart, Sylvie ULg

Poster (1999)

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See detailOPTIMAL LEVEL OF RAPESEED MEAL IN DIETS OF LAMBS.
Mandiki, S.; Bister, J.-L.; Deryke, G. et al

Poster (1999)

Two experiments were carried out in order to improve the strategy of rapeseed meal (RPM) incorporation in the diets of lambs. In a first experiment, the effects of RPM obtained from either a high ... [more ▼]

Two experiments were carried out in order to improve the strategy of rapeseed meal (RPM) incorporation in the diets of lambs. In a first experiment, the effects of RPM obtained from either a high-glucosinolate (HG) cultivar (Honk RPM) or a double-low strain (Samourai RPM) were studied. Two types of concentrates containing 25% of RPM were compared to a Control concentrate. In a second experiment, the effects of various proportions (0 – 40%) of an industrial low glucosinolate (LG)-RPM were studied in order to determine the disorder-threshold in diets for young ruminants. One hundred forty six Texel, Suffolk or crossbred lambs ranged in age from 1 to 2 months were used. Neither the Samourai nor the Honk RPM did affect negatively animal performance whatever the parameter considered (growth, food intake and conversion, slaughter performances). Low (P < 0.05) proportions of C10:0, C12:0 and C14:0 and high contents of C18:1trans, C22:2 were determined in the perirenal fat of lambs receiving the Honk RPM. The industrial LG-RPM had no negative effects on animalperformance, best results were obtained with 25 and 30% of RPM. The Samourai RPM had no effect on the thyroid weight, whereas, the Honk RPM modified (P < 0.05) the histology of this organ; the percentages of large thyroid follicles being higher (P < 0.05) in the Honk group than in the Control and Samourai groups. High levels of Canola industrial LG-RPM(from 20%) induced also an hyperthyroidism. The Samourai and Honk RPM decreased (P < 0.05) the secretions of thyroid hormones while the industrial LG-RPM did not affect these hormones in any way. RPM had no significative effects on other hormones. It was concluded that disturbance in thyroid histology and activity induced by the ingestion of RPM did not affect the physiology and performance of lambs and that the levels between 25 to 30% of a LG-RPM were optimal for growing and fattening lambs. [less ▲]

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See detailOPTIMIZATION OF RAPESEED MEAL USE FOR FATTENING BULLS
Paquay, R.; Mandiki, S.; Bister, J.-L. et al

Poster (1999)

Two experiments were conducted in order to optimize the incorporation of rapeseed meal (RPM) in diets for growing and fattening of bulls. In a first experiment, the effects of 20% of a low glucosinolate ... [more ▼]

Two experiments were conducted in order to optimize the incorporation of rapeseed meal (RPM) in diets for growing and fattening of bulls. In a first experiment, the effects of 20% of a low glucosinolate (LG) RPM (3.14 mmoles/g DM of concentrate) were studied. In a second experiment, various proportions (0, 10, 20, 34%) of an LG- industrial RPM were tested in order to determine the optimal level in diet of young bulls. Thirty six young Belgian White Blue bulls were used. In the two experiments, large amount of industrial RPM (20 - 34%) did not reduce animal performance whatever the parameter considered (liveweight, daily weight gains, food intake, feed conversion, carcass weight, dressing percentages). Values did not also vary with the level of LG-RPM in the diet. Any effects were observed on the thyroid weight and the size of thyroid follicles. The secretion of thyroid hormones was not affected by RPM except for a decrease (P < 0.05) in the production of thyroxin by thyroid tissue decreased (P < 0.05) with 34% in the diet in Experiment 2. Results concerning plasma testosterone and cortisol contrasted between the two experiments with negative effects or no influence of LG-RPM. It was concluded that levels 20 ≤ A < 34% of double 00 – RPM in diet may be used for fattening bulls but investigations are still needed to outline the long-term effects on steroids and reproductive performance [less ▲]

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See detailENZYMATIC TRANSFORMATION OF DESULFO-GLUCOSINOLATES IN PURE NITRILES USING A RECOMBINANT beta-O-GLUCOSIDASE
Iori, R.; Wathelet, Jean-Paul ULg; Leoni, O. et al

Poster (1999)

The recombinant b-O-glucosidase (EC 3.2.1.21) from the thermophilic bacterium Tp8 does not catalyse glucosinolate degradation but transforms desulfo-glucosinolates viz. desulfo-sinigrin, desulfo ... [more ▼]

The recombinant b-O-glucosidase (EC 3.2.1.21) from the thermophilic bacterium Tp8 does not catalyse glucosinolate degradation but transforms desulfo-glucosinolates viz. desulfo-sinigrin, desulfo-gluconapin, desulfo-progoitrin, desulfo-epiprogoitrin, desulfo-glucotropaeolin, desulfogluconasturtiin, desulfo-sinalbin, desulfo-limnantin, desulfo-glucoerucin and desulfo-glucoiberin in the corresponding pure nitriles (GC purity: +/- 99%). Prop-3-enyl, but-3-enyl, (2R)-2-hydroxybut-3-enyl, (2S)-2-hydroxybut-3-enyl, benzyl, phenethyl, 4-hydroxybenzyl, 3-methoxybenzyl, 4-methylthiobutyl and 3-methylsulphinylpropyl cyanides have been respectively identified by GC-MS. This thermostable enzyme is very different from myrosinase, a b-S-glucosidase (EC 3.2.3.1) present in Brassicaceae, which easily hydrolyses glucosinolates producing mainly a mixture of isothiocyanates, nitriles and eventually thiones. This endogenous b-S-glucosidase is totally inactive towards desulfo-glucosinolates, while the b-O-glucosidase tested is not active with synthetic S-glucose substrates such as the p-nitrophenyl-S-glucose. It is the first time that a b-O-glucosidase has been found to hydrolyse natural S-glucose substrates such as desulfoglucosinolates. The possibility to produce pure nitriles by this way, especially chiral compounds ((2R)-2-hydroxybut-3-enyl, (2S)-2-hydroxybut-3-enyl...), appears to be interesting for application in fine chemistry. The effect of pH (2 to 9) and temperature (40 to 85°C) on the recombinant b-O-glucosidase activity has been determined with desulfo-sinigrin as substrate. Optimal activity of this thermostable enzyme is reached at pH 6. [less ▲]

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See detailMEASUREMENT OF AROMATIC CHOLINE ESTERS IN RAPESEED BY HPLC
Mabon, N.; Wathelet, Jean-Paul ULg; Marlier, M.

Poster (1999)

Aromatic choline esters are natural compounds occurring in Brassicaceae especially in rapeseed among whom the most important is called sinapine (choline ester of the 3,5-dimethoxy-4 hydroxycinnamic acid ... [more ▼]

Aromatic choline esters are natural compounds occurring in Brassicaceae especially in rapeseed among whom the most important is called sinapine (choline ester of the 3,5-dimethoxy-4 hydroxycinnamic acid). Choline esters are easily hydrolysed by entero bacteria in digestive tractus giving the correspondent acid and a choline molecule. Choline could then be broken down, by a deaminase, into trimethylamine, compound inducing a negative flavour ("fishy odour") in the milk, the meat or in yolk. So, the method improved in our laboratory is a power tool for breeders and other scientists who would like to evaluate individual aromatic choline esters in seeds or meals. Seeds (10 g) are first ground in a coffee mill (20 sec). 200 mg of ground seeds are weighed in a test tube and then placed in a water bath (75°C). Then 10 ml of boiling methanol/acetic acid (0.05M) mixture (70/30) are added plus 0.5 ml of internal standard solution (3,5-dimethoxybenzoic choline ester, 10 µmol/ml).The heterogeneous content is stirred with a magnetic stirrer for 10 min. Only one extraction step is necessary to obtain good results. Then, 1 ml of crude extract is purified with a cation exchange column (CM Sephadex C25-120). Aromatic choline esters are eluted with acetic acid 1N. Separation and quantification of individual choline esters are further realised by high performance liquid chromatography with an Inertsil 5 ODS-2 (3 x 250 mm, 5 µm) using a ternary solvent gradient (water-acetonitrile-phosphate buffer: NaH2PO4, 20 mM at pH 2 with o-phosphoric acid). In these optimised chromatographic conditions, the choline esters are separated and quantified. The retention times and the response factors have been determinated for the 36 different choline esters (benzoic or cinnamic structures with hydroxy or methoxy groups in ortho, para or meta position) synthesised in our laboratory. [less ▲]

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See detailSYNTHESIS AND PURIFICATION OF 36 AROMATIC CHOLINE ESTERS AS STANDARDS
Wathelet, Jean-Paul ULg; Mabon, N.; Marlier, M.

Poster (1999)

Natural aromatic choline esters occurring in seeds of Brassicaceae are determined, after extraction with a mixture of methanol and acetic acid 0.01N (70/30), by high performance liquid chromatography. So ... [more ▼]

Natural aromatic choline esters occurring in seeds of Brassicaceae are determined, after extraction with a mixture of methanol and acetic acid 0.01N (70/30), by high performance liquid chromatography. So, from a qualitative and a quantitative point of view, it is very useful to have in the laboratory pure standards for confirm retention times, response factors and for the constitution of u.v., infra-red or mass spectra libraries. As choline esters are not available by a commercial way, we decided to synthesise different aromatic choline esters (36). The structure of the acidic part of all the choline esters prepared are derived from benzoic or cinnamic acids with hydroxy or methoxy substituants in ortho, para or meta position. Pure aromatic choline esters were synthesised according to a fast method using bromocholine bromide. An aromatic acid (in excess) in methanol is first neutralised by NaOH (0.1 N). Then bromocholine bromide in methanol is added in the evaporation flask. Solvent is evaporated to dryness using a rotative evaporator Büchi (40°C). The flask containing the dried mixture is placed in an oven (107°C) during 5 hours, avoiding carbonisation. The choline ester is taken up with 2 x 3 ml of distilled water and purified on a SP Sephadex C25-120 resin. After washing with distilled water, the ester is eluted HCl (1N). The elution is followed by measuring u.v. absorbance at 280 nm. The eluate is evaporated to dryness with a rotative evaporator (Büchi) and the crystals obtained are washed with acetone. The purity obtained for all the choline esters produced was close to 98% and total amount between 5 to 100 mg. An u.v. spectra library of each aromatic choline esters has been constituted for rapid identification when a diode array detector is coupled with the HPLC. [less ▲]

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See detailDETERMINATION OF GLUCOSINOLATES IN RAPESEED
Wathelet, Jean-Paul ULg; Mabon, N.; Marlier, M.

Poster (1999)

The official ISO protocol (similar to U.E. recommendations established in 1987 by six european laboratories) for determination of individual glucosinolate content in rapeseed using HPLC was published for ... [more ▼]

The official ISO protocol (similar to U.E. recommendations established in 1987 by six european laboratories) for determination of individual glucosinolate content in rapeseed using HPLC was published for the first time in 1992 (ISO 9167-1). Numerous laboratories, all over the world, use now this method, especially in order to control the 00 varieties. The goals of our research were to considerably reduce the analysis time without loosing precision. A single extraction is now suggested (200 mg of ground seeds stirred in 10 ml of 75°C methanol/water 70/30 with an internal standard for 10 min). Then 1-6 ml of the crude extract is directly put on DEAE A-25 resin prepared according to the ISO method. Glucosinolates are desulfated by addition of 100 µl of concentrated Helix pomatia sulfatase (H1, EC 3.1.6.1) quickly prepared by ethanol precipitation. The desulfatation process can be reduced to 1 hour without any problems with all kind of glucosinolate (alcenyl, benzyl, indolyl, methylthio, methylsulfinyl, methylsulfonyl...). Elution of the desulfo-glucosinolates is realised with 4 x 0.5 ml of distilled water. Desulfo-glucosinolates are separated by HPLC using an Inertsil 3 ODS-3 column (100 x 3 mm, 3 µm) with a water/acetonitrile gradient (from 2 to 25% in 35 min). Resolution is very nice and the limited flow (0.4 ml/min) reduce the solvent costs and the elimination of wastes. The suggested fast method has been compared with the official ISO method analysing the three certified reference materials prepared by BCR (now IRMM) and recommended by U.E. and ISO (CRMs 366, 190 and 367). The recovery of indolyl desulfo-glucosinolates, specially 4-OH glucobrassicin, is higher with the quicker method. Results obtained with the two methods are very close for other desulfo-glucosinolates. [less ▲]

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See detailNumerical modelling of the photorefractive effect in II-VI semiconductors
Nguyen, Ngoc Duy ULg; Schmeits, Marcel

Poster (1999)

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See detailPeriodontitis as potential risk factor for coronary heart disease
Geerts, Sabine ULg; Nys, Monique; Legrand, Victor et al

Poster (1999)

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See detailMastication-induced release of endotoxins in the bloodstream of periodontitis patients
Geerts, Sabine ULg; Nys, Monique; Legrand, Victor et al

Poster (1999)

Detailed reference viewed: 4 (0 ULg)
See detailDynamics of rRNA transcripts within the nucleolus as revealed with confocal and electron microscopy
Thiry, Marc ULg; O'Donohue, Marie-Christine; Kaplan, Hervé et al

Poster (1999)

Detailed reference viewed: 2 (0 ULg)
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See detailLa qualité : un outil de repositionnement de la viande bovine dans le marché des produits alimentaires
Burny, Philippe ULg

Poster (1999)

La qualité, dans tous les sens du terme, constitue un élément indispensable à l'avenir de la viande bovine. Pour réussir, la coopération de tous les acteurs est impérative, sous l'égide des pouvoirs ... [more ▼]

La qualité, dans tous les sens du terme, constitue un élément indispensable à l'avenir de la viande bovine. Pour réussir, la coopération de tous les acteurs est impérative, sous l'égide des pouvoirs publics. Par rapport aux autres viandes, la viande bovine possède une connotation plus "naturelle". Les consommateurs semblent prêts à assumer le coût des contrôles nécessaires. [less ▲]

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See detailPanorama des démarches qualité: à chaque stratégie son outil.
Sindic, Marianne ULg; Fumière, Olivier; Romnée, Jean-Marie et al

Poster (1999)

Detailed reference viewed: 12 (1 ULg)
See detailIpsilateral responses after a stroke : an electrophysiological study by focal TMS
Alagona, Giovanna; Rapisarda, giuseppe; DELVAUX, Valérie ULg

Poster (1999)

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See detailEnantiomeric separation of clenbuterol by transient ITP-CE-MS
Toussaint, B.; Bergmann, J.; Hubert, Philippe ULg et al

Poster (1999)

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See detailIn-line concentration and enantioseparation of clenbuterol by transient ITP-CE-UV
Toussaint, B.; Bergmann, J.; Hubert, Philippe ULg et al

Poster (1999)

Detailed reference viewed: 3 (0 ULg)
See detailPeriotontitis as a risk factor for coronary heart disease
Geerts, Sabine ULg; Nys, Monique; Legrand, Victor et al

Poster (1999)

Detailed reference viewed: 3 (0 ULg)