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The reactivity of the hydroxyl groups of methyl beta-D-glucopyranoside in the Koenigs-Knorr reactionBills, Alan M. 01 January 1967 (has links)
No description available.
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The synthesis of several azasugars, glycosylated azasugars and disaccharides of biological interest /Meloncelli, Peter J. January 2007 (has links)
Thesis (Ph.D.)--University of Western Australia, 2007.
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Effect of protein-calorie malnutrition on intestinal disaccharidase activities and disaccharide absorption in the ratWilson, Judith Leslie January 1973 (has links)
The purpose of the present investigation was to study the effect of prolonged protein-calorie malnutrition on intestinal disaccharidase activities and on disaccharide absorption, as carbohydrate intolerance is a major problem in children suffering from protein-calorie malnutrition.
Four groups of rats (90 to 120 grams) were fed the following diets for 8 to 9 weeks: control (18% lactalbumin, 66% carbohydrate); low protein low carbohydrate (0.5% lactalbumin, 66% carbohydrate); low protein high carbohydrate (0.5% lactalbumin, 83.5% carbohydrate); and low protein restricted (1% lactalbumin, restricted to 4 grams per day). After 8.5 weeks, part of the group on the 0.5% lactalbumin low carbohydrate diet was fed the control diet (18% lactalbumin, 66% carbohydrate) for 8 weeks.
At the end of the feeding period, the following assays were performed: 1) in vivo absorption of radioactive (¹⁴C) lactose, sucrose, and maltose; 2) activities of intestinal lactase, sucrase, and maltase; 3) plasma albumin concentrations; and 4) mucosal protein concentrations.
In the three protein deficient groups (0.5% lactalbumin low carbohydrate, 0.5% lactalbumin high carbohydrate, and 1% lactalbumin), the activity of both the jejunal and ileal disaccharidases and the absorption of lactose, sucrose and maltose were significantly higher when compared with the controls. The jejunal sucrase and maltase activities were significantly higher in the 0.5% lactalbumin high carbohydrate group than in the 0.5% lactalbumin low carbohydrate group, but the absorption of lactose, sucrose and maltose were alike. When the 1% lactalbumin (restricted to 4 grams per day) and the 0.5% lactalbumin low carbohydrate groups were compared, there were no statistically significant differences in the specific activities of the intestinal disaccharidases or the absorption of the disaccharides.
The absorption of lactose, sucrose, or maltose were similar in the controls and the protein repleted group. The disaccharidase activities were also similar in these two groups except for a significant depression of jejunal maltase and ileal sucrase and maltase activities in the protein repleted group.
Therefore, these results indicate that protein deprivation in rats for 8.5 weeks causes an increase in specific activities of the intestinal disaccharidases in both the jejunum and ileum, and that these changes caused by protein depletion may be reversed by feeding a diet high in protein. Also, an increase in the carbohydrate content of the protein deficient diet results in an induction of jejunal sucrase and maltase activities. The high specific activity of the intestinal disaccharidases following protein-calorie malnutrition may be in part due to a preferential loss of structural proteins rather than to an increase in enzymatic protein in the intestinal mucosa.
The increase in the disaccharidase activities in the protein deficient rats is accompanied by an increase in disaccharide absorption which could be due to the higher levels of disaccharidases or to an increase in the transport of the constituent monosaccharides. The demonstration of statistically significant differences in sucrase and maltase activities between the 0.5% lactalbumin high carbohydrate and the 0.5% lactalbumin low carbohydrate groups without a concomitant increase in sucrose and maltose absorption, supports the view that the higher absorption of sucrose and maltose in the protein deficient rats is a result of increased monosaccharide transport.
The results of this study are not consistent with the suggestion that protein-calorie malnutrition is responsible for disaccharide intolerance in children. / Land and Food Systems, Faculty of / Graduate
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Effect of a 2-O-acetyl substituent on the stereoselectivity of Koenigs-Knorr reactions involving 1,2-cis-glucopyranosyl bromides.Wallace, Jerry E. 01 January 1975 (has links)
No description available.
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Koenigs-Knorr syntheses of beta-1,4-linked disaccharidesRudie, Glenn Frank, January 1973 (has links) (PDF)
Thesis (Ph. D.)--Institute of Paper Chemistry, 1973. / Includes bibliographical references (p. 85-89).
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A study of some reaction rates in the homogeneous system water-sodium hydroxide-cellobioseMacLaurin, Donald James. January 1969 (has links) (PDF)
Thesis (Ph. D.)--Institute of Paper Chemistry, 1969. / Bibliography: leaves 48-52.
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Observations on the absorption of sugars by animal intestineKarrar, O. K. El S. January 1968 (has links)
No description available.
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Syntheses of pseudoaminodisaccharides. / CUHK electronic theses & dissertations collectionJanuary 2004 (has links)
Cheung Wai-chit. / "July 2004." / Thesis (Ph.D.)--Chinese University of Hong Kong, 2004 / Includes bibliographical references (p. 135-140) / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web. / Abstracts in English and Chinese.
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Enantiospecific syntheses of N-linked carbadisaccharides. / CUHK electronic theses & dissertations collectionJanuary 2006 (has links)
*Please refer to dissertation for diagrams. / In this thesis, a review concerning enantiospecific syntheses and structure activity relationship of N-linked carbadisaccharides from 1994 to 2005 is presented. / Valienamine was isolated from microbial degradation products of validoxylamine A with Pseudomonas denitrificans. It showed alpha-glycosidase inhibitory activity and antibiotic activity. Isopropylidene protected allylic chlorides, 2-epi-valienamine and 4-amino-6-deoxy-alpha- D-pseudomannopyranose were synthesized from (-)-quinic acid. The acetonide blocking groups were shown to be the best hydroxyl protecting groups for coupling precursors, compatible with palladium-catalyzed coupling reaction which afforded high yields of the 1,1'- and 1,4'-N-linked carbadisaccharides 83-88 and 89-91, respectively, with a minimum amount of an elimination diene side-product. 2-epi-Valienamines 92 and N-alkyl 2-epi-valienamine 93 and 94 were also prepared. The key palladium-catalyzed coupling reaction was shown to be a regio- and stereospecific reaction. Acid hydrolysis was used to obtain free pseudoaminosugars as glycosidase inhibitors. The inhibitory activities of these pseudoaminosugars were evaluated by the Biochemistry Department of the Chinese University of Hong Kong.* / Kwong Suk Kwan. / "January 2006." / Adviser: Tony K. M. Shing. / Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6409. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references (p. 146-154). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstracts in English and Chinese. / School code: 1307.
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A study of some reaction rates in the homogeneous system water-sodium hydroxide-cellobioseMacLaurin, Donald James 01 January 1969 (has links)
The broad objective of the study was to gain further knowledge of the reaction
rates and mechanisms by which carbohydrates, particularly 3(l-4) glucans, are transformed
and degraded in aqueous alkaline solutions.
While the isomerization, epimerization, and degradation of carbohydrates has
been extensively studied and reviewed, there are practically no kinetic data available
on these important reactions due apparently to a lack of reasonable procedures
for assay of the reaction systems.
Because of the important theoretical, physiological, and industrial implications
of these reactions, it appeared useful to have kinetic data on them and concomitantly
thus to develop a method for obtaining such data. The specific problem selected for study from this broad area was the measurement
of reaction rates prevailing in the homogeneous system: cellobiose-l molar
sodium hydroxide-water at 22°C. and to derive-the related rate constants from the
reaction rate expressions and then to assess current understanding of these reactions
in light of the kinetic data obtained.
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