No description available.

Steroidal glycoalkaloids (SGAs) are secondary metabolites produced by approximately 350 species in the Solanaceae family. SGAs are reported to be important for pest resistance and flavor enhancement at low concentrations but are toxic to humans and other mammals at high concentrations. Studies on sterol / SGA biosynthesis have implicated squalene synthase as a key regulatory enzyme because it catalyzes an irreversible step from the mevalonic acid pathway. However, the regulatory mechanisms of squalene synthase are not yet known. A study was conducted to elucidate the distribution pattern of SGAs and to clone the squalene synthase gene in order to determine a relationship between SGAs and gene expression levels. Solanum chacoense, a wild potato species was used as a model plant from which tissues were harvested at specified developmental stages and analyzed for SGA content. The results from the SGA analysis suggest a qualitative and quantitative tissue- and age-dependent accumulation of SGAs. Regenerative tissues such as, axiliary shoots, flowers and floral buds had the highest levels of 88, 49 and 63 µmole/g DW, respectively. The roots, stems and tubers showed the lowest amounts of SGAs of 1 to 8, 5 to 15 and 7 to 15 µmole/g DW, respectively. Stolons and tubers accumulated higher amounts of α-chaconine (59 to 67%) than α-solanine (61 to 64%) at all developmental stages analyzed. On the other hand, in young expanding, fully expanded, and old senescing leaves where leptine and leptinines tend to dominate, α-solanine and α-chaconine together accounted for only 8 to 15%, 7 to 15%, and 8 to 45%, respectively. Plant organs that showed the highest biosynthetic activity for SGA production also had high levels of transcripts coding for genes of isoprenoid biosynthesis. The results from the cloning and characterization of squalene synthase suggest that the cloned cDNA fragment is a putative S. chacoense squalene synthase gene with an open reading frame / predicted protein precursor of 411 amino acids. The cloned cDNA has high similarity (68-100%) to known plant squalene synthase genes and contains six deduced peptide domains observed in other species. The 3â untranslated regions of floral buds, young leaves (early vegetative stage), and fully expanded leaves (anthesis) were different in length with, 249, 335, and 202 nucleotides, respectively. The Southern blot analysis suggests a single copy gene although the existence of a gene family cannot be ruled out. / Ph. D.

The distribution, absorption, metabolism and tissue binding of radioactivity were studied in hamsters after oral and intraperitoneal administration of alpha-chaconine- (3H). The material was well absorbed from the gastrointestinal tract and nearly 22 percent of the label was excreted via urine and feces in 7 days. The excretion was higher in urine (21 percent) than in feces ( < 1 percent). Tissue concentrations of radioactivity peaked at 12 hours following oral administration, with the highest concentrations found in lungs, liver, spleen, skeletal muscle, kidney and pancreas, with heart and brain containing moderate amounts. Concentrations of radioactivity in tissues following intraperitoneal administration were significantly higher than those observed after oral treatment. Excretion of chloroform-soluble products in the feces was 10 times higher than that of the chloroform-insoluble metabolites after both oral and intraperitoneal administration. In the urine, the activity was predominantly in the chloroform-insoluble form and the chloroform-soluble metabolites were relatively minor in amounts (0.27, 0.85, and 2.45 percent versus 0.005, 0.14 and 0.19 percent of dose for 12, 24 and 72 hours, respectively). After 7 days, the chloroform-soluble metabolites in urine increased to 20 percent of the excreted radioactivity, while the amount of chloroform-insoluble metabolites was less than 1 percent. Subcellular distribution of the labeled compound indicated the highest concentration of radioactivity in the nuclear and microsomal fractions of brain, liver and heart tissues. A small amount of radioactivity, shown by a minor peak, was also observed in the fractions between the mitochondrial and microsomal fractions on a sucrose gradient. Binding of radioactivity was observed in brain, testes, kidney, lung, liver and heart . All of the label in the brain appeared to be in the bound form . The results indicated that alpha-chaconine is slowly absorbed from the gastrointestinal tract after oral administration, and persists in various tissues, much of it in bound (non-extractable) form (in nuclear and microsomal fractions). Excretion of alpha-chaconine- (3H) and its metabolites was investigated after oral and intraperitoneal administration in hamsters. The separation of the glycoalkaloid and its metabolites in feces and urine was accomplished by thin-layer chromatography. An increase in the concentration of excreted alpha-chaconine metabolites in feces and urine was observed. In urine over 50 percent of the eliminated radioactivity during the initial 24 hours was due to the aglycone, solanidine. The fraction of the total dose administered which was excreted represented only 27 percent (26 percent in feces and less than 1 percent in urine) during the 7 day test period. Contrary to the general belief that potato glycoalkaloid absorption is poor following oral administration, only 5 percent or less was excreted in feces during the initial 72 hours, a fact explained by the binding of radioactivity to tissues. Inhibition of acetylcholinesterases by alpha-chaconine was studied. The inhibition of purified erythrocyte acetylcholinesterase and horse serum cholinesterase by alpha-chaconine was found to be a mixed-type with kinetic constants. An inhibition constant (Ki) for both the specific and pseudocholinesterases was 8.3 x 10-6 M and 4.0 x 10-4 M, respectively. Kinetic constants obtained for both enzymes were as follows: Vmax of 7.14 x 10-5 and 3.76 x 10-4 max moles/liter/min, respectively, and Km of 6.2 x 10-5 and 1.33 x 10-4, respectively. The distribution of acetylcholinesterase among the subcellular fractions of rat brain homogenate separated by sucrose density gradient centrifugation was determined, as well as the inhibition pattern of these fractions following in vitro incubation with 0.016 M alpha-chaconine. Enzyme activity was found to be distributed equally between the mitochondrial and microsomal fractions, with the nuclear fraction having the least activity. Percentage inhibition of the various fractions obtained was: whole homogenate 43, nuclear fraction 55, mitochondria 35, and microsomes 33. Brain acetyl cholinesterase activity of animals given intraperitoneal doses (10, 30, 60 mg / Kg) of alpha-chaconine was 79, 55 and 18 percent of the control group. Acetylcholinesterase activity of heart and plasma of animals administered alpha-chaconine did not show the dose-related response observed in the brain. Inhibition of heart acetylcholinesterase was 61 percent, while plasma gave 51 percent for the rats given a dose of 10 mg/Kg and no inhibition for rats given 30 mg/ Kg. Acrylamide gel electrophoretic separation of cholinesterases in aqueous homogenates from whole brain and heart of adult male rats administered alpha-chaconine was investigated. Brain acetylcholinesterase isoenzymes were found to be inhibited by 30 and 60 mg/ Kg dosage levels of alpha-chaconine administered intraperitoneally. Electrophoretic separation of plasma from the treated animals resulted in five anodally migrating zones having properties of cholinesterases. These sites hydrolyze acetylthiocholine and alpha-naphthylacetate, and all were inhibited by alpha-chaconine except the slowest migrating band (band 5). Inhibition of isoenzyme activity of bands 1 and 2 is observed for the groups administered 10 and 30 mg/Kg alpha-chaconine with the percentage inhibition of both bands (l and 2) being 40 and 77 percent for animals given 10 mg/Kg and 100 and 75 percent for the latter group. Isoenzyme bands 3 and 4 were completely absent in the alkaloid treated animals. Inhibition of non-specific cholinesterase isoenzymes (butyrylthiocholine hydrolyzable bands) by alpha-chaconine was clearly demonstrated. In vitro inhibition of plasma, erythrocyte and brain esterase isoenzymes was estimated by incubating gels with 10-4 M alpha-chaconine after the electrophoretic separations. With this concentration of alpha-chaconine, the various isoenzymes in rat plasma, erythrocyte and brain showed some response to the inhibitory potency of alpha-chaconine. The slower-moving isoenzyme bands were inhibited to 100 percent with the different concentrations of inhibitor. The fast migrating isoenzyme bands in plasma and erythrocytes were least affected by alpha-chaconine (10-4 M), with no inhibition. Plasma protein isoenzymes from adult male rats were not affected by alphachaconine.

La pomme de terre produit des glycoalcaloïdes comme la plupart des Solanacées. Deux composés, en particulier, l’α-solanine et l’α-chaconine, sont produits en plus grande quantité lorsque le tubercule est exposé à la lumière et subit des dégradations. Ces molécules sont toxiques et peuvent représenter un danger pour le consommateur et des nuisances pour l’environnement. Dans le cadre de cette thèse, les teneurs en α-solanine et α-chaconine dans la chaire de pomme de terre verdie, en germination ou en décomposition retrouvées sur les marchés d’Abidjan (Côte d'Ivoire) ont été analysées. Les résultats ont montré que la chaire de ces pommes de terre contient des quantités élevées de ces deux composés, dépassant 2 à 5 fois la limite recommandée. Pour des raisons de sécurité sanitaire, ces pommes de terre doivent être proscrites de l’alimentation humaine. En revanche, la teneur élevée en glycoalcaloïdes dans ces pommes de terre représente une source de solanidine, un précurseur pour la synthèse d'hormones et de composés pharmacologiquement actifs, qui mérite d’être exploitée. Dans cet objectif, nous avons développé une méthode chimio-enzymatique simple, comprenant un traitement acide partiel suivi d’une hydrolyse enzymatique par la β-glycosidase de la blatte Periplaneta americana dont le gène a été isolé à partir d’une librairie génomique de cDNA afin de détoxifier ces composés et produire la solanidine. / Potato produce glycoalkaloids as most plants of Solanaceae family. The principal glycoalkaloids, α-chaconine and α-solanine are produced in greater quantities when potato tubers are exposed to light and are subject to deteriorations. These compounds are toxic and can represent a real danger for the consumer and the environment where they are discharged during their degradation. In this work, the estimation of glycoalkaloids in the flesh of different types of decayed potatoes usually found in different market places of Abidjan (Ivory Coast) was evaluated. The results showed that turned green and also sprouting or rotting potato flesh contain high amounts of toxic solanine and chaconine, exceeding by 2 to 5-fold the recommended limit. For safety consideration, these decayed potatoes should be systematically set aside. The accumulation of α-chaconine and solanine in potatoes can be seen as an attractive source of solanidine that is an important precursor for hormone synthesis and some pharmacologically active compounds. To this end, we proposed herein a simple chemo-enzymatic protocol comprising a partial acidic hydrolysis followed by an enzymatic treatment with the β-glycosidase from Periplaneta americana whose gene was isolated from a cDNA genomic library in order to detoxify these compounds and produce solanidine.