Добірка наукової літератури з теми "Oligo- polysaccharides"
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Статті в журналах з теми "Oligo- polysaccharides"
Kadokawa, Jun-ichi. "α-Glucan Phosphorylase-Catalyzed Enzymatic Reactions Using Analog Substrates to Synthesize Non-Natural Oligo- and Polysaccharides". Catalysts 8, № 10 (19 жовтня 2018): 473. http://dx.doi.org/10.3390/catal8100473.
Повний текст джерелаIravani, Siavash, and Rajender S. Varma. "Important Roles of Oligo- and Polysaccharides against SARS-CoV-2: Recent Advances." Applied Sciences 11, no. 8 (April 14, 2021): 3512. http://dx.doi.org/10.3390/app11083512.
Повний текст джерелаVessella, Giulia, Serena Traboni, Antonio Laezza, Alfonso Iadonisi, and Emiliano Bedini. "(Semi)-Synthetic Fucosylated Chondroitin Sulfate Oligo- and Polysaccharides." Marine Drugs 18, no. 6 (June 1, 2020): 293. http://dx.doi.org/10.3390/md18060293.
Повний текст джерелаCuthbertson, Leslie, Veronica Kos, and Chris Whitfield. "ABC Transporters Involved in Export of Cell Surface Glycoconjugates." Microbiology and Molecular Biology Reviews 74, no. 3 (September 2010): 341–62. http://dx.doi.org/10.1128/mmbr.00009-10.
Повний текст джерелаTurdumambetov, K., D. A. Rakhimov, and M. Kh Malikova. "Oligo- and polysaccharides from Cousinia umbrosa." Chemistry of Natural Compounds 43, no. 3 (May 2007): 308–9. http://dx.doi.org/10.1007/s10600-007-0112-3.
Повний текст джерелаTANAKA, Toshio. "Enzymic Synthesis of Oligo- and Polysaccharides." Journal of the Japanese Society of Starch Science 40, no. 2 (1993): 203–8. http://dx.doi.org/10.5458/jag1972.40.203.
Повний текст джерелаPálvölgyi, Adrienn, Veronika Deák, Véréna Poinsot, Tibor Nagy, Enik Nagy, Ildikó Kerepesi, and Péter Putnoky. "Genetic Analysis of the rkp-3 Gene Region in Sinorhizobium meliloti 41: rkpY Directs Capsular Polysaccharide Synthesis to KR5 Antigen Production." Molecular Plant-Microbe Interactions® 22, no. 11 (November 2009): 1422–30. http://dx.doi.org/10.1094/mpmi-22-11-1422.
Повний текст джерелаWang, Yvonne, Michael G. Gänzle, and Clarissa Schwab. "Exopolysaccharide Synthesized by Lactobacillus reuteri Decreases the Ability of Enterotoxigenic Escherichia coli To Bind to Porcine Erythrocytes." Applied and Environmental Microbiology 76, no. 14 (May 14, 2010): 4863–66. http://dx.doi.org/10.1128/aem.03137-09.
Повний текст джерелаLi, Xiaowei, and Yan Zhao. "Synthetic glycosidases for the precise hydrolysis of oligosaccharides and polysaccharides." Chemical Science 12, no. 1 (2021): 374–83. http://dx.doi.org/10.1039/d0sc05338d.
Повний текст джерелаUhr�n, Du?an, Jean-Robert Brisson, and DavidR Bundle. "Pseudo-3D NMR spectroscopy: Application to oligo- and polysaccharides." Journal of Biomolecular NMR 3, no. 3 (May 1993): 367–73. http://dx.doi.org/10.1007/bf00212523.
Повний текст джерелаДисертації з теми "Oligo- polysaccharides"
Ruff, Yves. "Biopolymères dynamiques : Oligo- et polysaccharides." Université Louis Pasteur (Strasbourg) (1971-2008), 2008. https://publication-theses.unistra.fr/public/theses_doctorat/2008/RUFF_Yves_2008.pdf.
Повний текст джерелаReversible polymers, or dynamic polymers, result from the reversible association of monomers using covalent (dynamic covalent polymers) or non covalent (supramolecular polymers) chemical bonds. As the polymerisation is reversible, the structure, the molecular weight distribution, and the composition of the polymer are susceptible to evolve even after polymerisation. According to their dynamic character this polymers are adaptative and can respond to an external stimuli (temperature, pH, presence of a molecular target) by a constitutional change, and so they can be considered as smart materials. Our goal was to prepare dynamic covalent polymers, based on reversible imine bonds formation (hydrazones or oximes), that are analogs of natural polysaccharides. This dynamic glycopolymers could be interesting as materials, and have biorecognition properties combined with the possibility to adapt their sequence and composition in presence of a biological target
Ruff, Yves Lehn Jean-Marie. "Biopolymères dynamiques Oligo- et polysaccharides /." Strasbourg : Université Louis Pasteur, 2008. http://eprints-scd-ulp.u-strasbg.fr:8080/955/01/RUFF_Yves_2008.pdf.
Повний текст джерелаLarsson, Andreas. "Synthesis, structure and conformation of oligo- and polysaccharides." Doctoral thesis, Stockholm University, Department of Organic Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-172.
Повний текст джерелаCarbohydrates are a complex group of biomolecules with a high structural diversity. Their almost omnipresent occurrence has generated a broad field of research in both biology and chemistry. This thesis focuses on three different aspects of carbohydrate chemistry, synthesis, structure elucidation and the conformational analysis of carbohydrates.
The first paper describes the synthesis of a penta- and a tetrasaccharide related to the highly branched capsular polysaccharide from Streptococcus pneumoniae type 37. In the second paper, the structure of the O-antigenic repeating unit from the lipopolysaccharide of E. coli 396/C1 was determined along with indications of the structure of the biological repeating unit. In addition, its structural and immunological relationship with E. coli O126 is discussed. In the third paper, partially protected galactopyranosides were examined to clarify the origin of an intriguing 4JHO,H coupling, where a W-mediated coupling pathway was found to operate. In the fourth paper, the conformation of methyl a-cellobioside is studied with a combination of molecular dynamics simulations and NMR spectroscopy. In addition to the expected syn-conformation, detection and quantification of anti-ø and anti-ψ conformers was also possible.
Larsson, E. Andreas. "Synthesis, structure and conformation of oligo- and polysaccharides /." Stockholm : Institutionen för organisk kemi, Univ, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-172.
Повний текст джерелаZaccheus, Mona. "Structural and Conformational Studies of Oligo- and Polysaccharides." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-75050.
Повний текст джерелаAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 4: Submitted. Paper 6: Submitted.
Gullfot, Fredrika. "Synthesis of xyloglucan oligo- and polysaccharides with glycosynthase technology." Licentiate thesis, KTH, School of Biotechnology (BIO), 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-10178.
Повний текст джерелаXyloglucans are polysaccharides found as storage polymers in seeds and tubers, and as cross-linking glycans in the cell wall of plants. Their structure is complex with intricate branching patterns, which contribute to the physical properties of the polysaccharide including its binding to and interaction with other glycans such as cellulose.
Xyloglucan is widely used in bulk quantities in the food, textile and paper making industries. With an increasing interest in technically more advanced applications of xyloglucan, such as novel biocomposites, there is a need to understand and control the properties and interactions of xyloglucan with other compounds, to decipher the relationship between xyloglucan structure and function, and in particular the effect of different branching patterns. However, due to the structural heterogeneity of the polysaccharide as obtained from natural sources, relevant studies have not been possible to perform in practise. This fact has stimulated an interest in synthetic methods to obtain xyloglucan mimics and analogs with well-defined structure and decoration patterns.
Glycosynthases are hydrolytically inactive mutant glycosidases that catalyse the formation of glycosidic linkages between glycosyl fluoride donors and glycoside acceptors. Since its first conception in 1998, the technology is emerging as a useful tool in the synthesis of large, complex polysaccharides. This thesis presents the generation and characterisation of glycosynthases based on xyloglucanase scaffolds for the synthesis of well-defined homogenous xyloglucan oligo- and polysaccharides with regular substitution patterns.
Dal, Bó Alexandre Gonçalves. "Préparation et caractérisation de nouveaux amphiphiles fonctionnalisés par des oligo-et polysaccharides." Thesis, Grenoble, 2011. http://www.theses.fr/2011GRENV012/document.
Повний текст джерелаThis thesis reports the preparation and characterization of new rod-coil amphiphiles functionalized with oligo- and polysaccharides through Huisgen 1,3-dipolar cycloaddition reactions between species functionalized by an azide group on one side and an terminal alkyne on the other catalyzed by copper. The amphiphiles were synthesized and characterized based on different hydrophobic parts conjugated with the polymer poly(ethylene oxide) PEO with a hydrophilic spacer arm and the oligo- and polyssaccharides 2-propargyl-2-acetamido-2-deoxy-β-D-glucopyranose (GlcNAc) and propargyl β-D-galactopyranosyl-(14)-β-D-glucopyranose (Lac). The amphiphiles synthesized were characterized in terms of their chemical structure and composition through nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR) spectroscopy, mass spectroscopy (MALDI-TOF-MS and ESI-MS) and high resolution mass spectroscopy (HRMS). After the dissolution in water, the amphiphiles self-associate in highly regular micelles with an average diameter of 2RH ~ 10 nm. Dynamic light scattering (DLS), transmission electron microscopy (TEM) and small angle x-ray scattering (SAXS) were used in order to investigate the structure and dynamics of these saccharide amphiphiles. The presence of carbohydrate epitopes on the surface of the micelles and their bioavailability for the segmentation of lectin were also demonstrated by DLS. Specific interactions of GlcNAc and Lac residues with lectins from wheat germ agglutinin (WGA) and peanut agglutinin (PNA), respectively, reveal the potential applications of such amphiphilic derivatives of carbohydrates as vectorizing systems, both simple and specific to a drug delivery site
Goncalves, Dal Bo Alexandre. "Préparation et caractérisation de nouveaux amphiphiles fonctionnalisés par des oligo-et polysaccharides." Phd thesis, Université de Grenoble, 2011. http://tel.archives-ouvertes.fr/tel-00604432.
Повний текст джерелаJonsson, Hanna. "Exploring the structure of oligo- and polysaccharides synthesis and NMR spectroscopy studies /." Doctoral thesis, Stockholm : Department of Organic Chemistry, Stockholm University, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-37680.
Повний текст джерелаAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 4: Manuscript. Paper 5: Manuscript.
Broberg, Susanna. "Studies of oligo- and polysaccharides by MALDI-TOF and ESI-ITMSn mass spectrometry /." Uppsala : Dept. of Chemistry, Swedish Univ. of Agricultural Sciences, 2004. http://epsilon.slu.se/a452.pdf.
Повний текст джерелаЧастини книг з теми "Oligo- polysaccharides"
Garozzo, D. "MALDI MS of Oligo and Polysaccharides." In Selected Topics in Mass Spectrometry in the Biomolecular Sciences, 477–99. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5165-8_25.
Повний текст джерелаWilson, Iain B. H. "Biosynthesis and Degradation of Mono-, Oligo-, and Polysaccharides: Introduction." In Glycoscience, 2243–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-30429-6_58.
Повний текст джерелаWilson, Iain B. H., Christelle Breton, Anne Imberty, and Igor Tvaroška. "Molecular Basis for the Biosynthesis of Oligo- and Polysaccharides." In Glycoscience, 2265–323. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-30429-6_59.
Повний текст джерелаMischnick, Petra. "Mass Spectrometric Characterization of Oligo- and Polysaccharides and Their Derivatives." In Mass Spectrometry of Polymers – New Techniques, 105–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/12_2011_134.
Повний текст джерелаGorton, L., G. Marko-Varga, E. Domínguez, and J. Emnéus. "Analysis of Mono-, oligo- and polysaccharides by enzyme reaction detection." In Analytical Applications of Immobilized Enzyme Reactors, 51–130. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1310-6_3.
Повний текст джерелаLifely, M. R., U. T. Nowicka, E. Krambovitis, and J. Esdaile. "Antigenicity of meningococcal group B oligo- and polysaccharides of defined chain length." In Gonococci and Meningococci, 147–52. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1383-7_25.
Повний текст джерелаKadokawa, Jun-ichi. "Enzymatic Synthesis of Non-Natural Oligo- and Polysaccharides by Phosphorylase-Catalyzed Glycosylations Using Analogue Substrates." In ACS Symposium Series, 87–99. Washington, DC: American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1192.ch006.
Повний текст джерелаFromm, Herbert J., and Mark S. Hargrove. "Carbohydrate Metabolism B: Di-, Oligo-, and Polysaccharide Synthesis and Degradation." In Essentials of Biochemistry, 239–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19624-9_11.
Повний текст джерела"72 Carbohydrates: Oligo- and Polysaccharides." In Efficiently Studying Organic Chemistry, edited by Eberhard Breitmaier. Stuttgart: Georg Thieme Verlag, 2016. http://dx.doi.org/10.1055/b-0036-135270.
Повний текст джерела"Fungal Degradation of Plant Oligo- and Polysaccharides." In Handbook of Carbohydrate-Modifying Biocatalysts, 837–924. Jenny Stanford Publishing, 2016. http://dx.doi.org/10.1201/9781315185392-25.
Повний текст джерелаТези доповідей конференцій з теми "Oligo- polysaccharides"
Stenutz, Roland, Per-Erik Jansson, and Goran Widmalm. "SEQUENCE DETERMINATION OF OLIGO- AND POLYSACCHARIDES FROM NMR USING A WWW-INTERFACE TO THE COMPUTER PROGRAM CASPER." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.705.
Повний текст джерела