Academic literature on the topic '3-galactose'

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Journal articles on the topic "3-galactose"

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Robinson, J. A., та H. C. Robinson. "Initiation of chondroitin sulphate synthesis by β-d-galactosides. Substrates for galactosyltransferase II". Biochemical Journal 227, № 3 (1985): 805–14. http://dx.doi.org/10.1042/bj2270805.

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beta-Galactosides were found to initiate chondroitin sulphate chain synthesis in chick-embryo cartilage in vitro and thereby relieve inhibition by cycloheximide of [3H]-acetate incorporation into chondroitin sulphate. beta-Galactosides with an apolar aglycan group such as phenyl O-beta-galactoside were active, whereas those with a charged or polar aglycan group such as pyridine 3-O-beta-galactoside or those with sulphur instead of oxygen in the glycosidic linkage (phenyl beta-thiogalactoside) were not. beta-Galactosides also serve as substrates for microsomal galactosyltransferase activity fro
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Gabrielli, Armando, Pietro Leoni, Giovanni Danieli, Konrad Herrmann, Thomas Krieg та Jorgen Wieslander. "Antibodies against galactosyl (α1→3) galactose in connective tissue diseases". Arthritis & Rheumatism 34, № 3 (1991): 375–76. http://dx.doi.org/10.1002/art.1780340321.

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Tai, G. H., T. N. Huckerby, and I. A. Nieduszynski. "N.m.r. spectroscopic studies of fucose-containing oligosaccharides derived from keratanase digestion of articular cartilage keratan sulphates. Influence of fucose residues on keratanase cleavage." Biochemical Journal 291, no. 3 (1993): 889–94. http://dx.doi.org/10.1042/bj2910889.

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Keratan sulphate chains from bovine articular cartilage were fully digested with keratanase from Pseudomonas sp. and the products were reduced with alkaline borohydride. The resultant fragments were fractionated on a Nucleosil 5SB column and the earliest eluting fucose-containing oligosaccharides were isolated. Structural analysis using 1H n.m.r. spectroscopy (600 MHz) showed the two least-charged species to have the following structure: GlcNAc(6S) beta 1-3Gal beta 1-4(Fuc alpha 1-3)GlcNAc(6S) beta 1- 3Gal beta 1-4GlcNAc(6S) beta 1-3Gal-ol and GlcNAc(6S) beta 1-3Gal beta 1- 4(Fuc alpha 1-3)Glc
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Christiane, Y., M. Aghayan, H. Emonard, A. Lallemand, Ph Mahieu, and J. M. Foidart. "Galactose alpha 1-3 galactose and anti-alpha galactose antibody in normal and pathological pregnancies." Placenta 13, no. 5 (1992): 475–87. http://dx.doi.org/10.1016/0143-4004(92)90053-v.

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Sheares, B. T., and A. M. Mercurio. "Modulation of two distinct galactosyltransferase activities in populations of mouse peritoneal macrophages." Journal of Immunology 139, no. 11 (1987): 3748–52. http://dx.doi.org/10.4049/jimmunol.139.11.3748.

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Abstract We have examined two galactosyltransferase activities in membrane preparations obtained from resident macrophages, from resident macrophages maintained in culture for 24 hr, and from thioglycollate (TG)-elicited macrophages. Transfer of galactose from uridine diphosphate (UDP)-galactose to N-acetylglucosamine is 2.6 times higher in membranes prepared from TG macrophages (107 +/- 5.5 nmol/hr/mg) than in membranes prepared from resident macrophages (41 +/- 2.0 nmol/hr/mg). Membranes obtained from resident macrophages cultured for 24 hr exhibit a 2.5 times higher activity (102 +/- 4.4 nm
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Galili, U., B. A. Macher, J. Buehler, and S. B. Shohet. "Human natural anti-alpha-galactosyl IgG. II. The specific recognition of alpha (1----3)-linked galactose residues." Journal of Experimental Medicine 162, no. 2 (1985): 573–82. http://dx.doi.org/10.1084/jem.162.2.573.

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A natural IgG antibody (anti-Gal) with alpha-galactosyl binding specificity has been found in large amounts (0.5 - 1.0% of serum IgG) in all individuals tested. It has been purified by affinity chromatography on a column of melibiose-Sepharose. In addition to its affinity for normal and pathological senescent human red cells, the antibody readily interacts with rabbit red blood cell (RRBC) glycolipids with alpha-galactosyl terminal residues. Two types (glycosidic linkages of 1----3 vs. 1----4) of rabbit red cells glycolipids with terminal alpha-galactosyl residues were tested for antibody bind
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Abdullah, M., and A. L. Kierszenbaum. "Identification of rat testis galactosyl receptor using antibodies to liver asialoglycoprotein receptor: purification and localization on surfaces of spermatogenic cells and sperm." Journal of Cell Biology 108, no. 2 (1989): 367–75. http://dx.doi.org/10.1083/jcb.108.2.367.

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We have found that the rat testis contains a cell surface galactosyl receptor that is antigenically related to the minor species of rat liver asialoglycoprotein receptor (ASGP-r) and has binding affinity for galactose coupled to agarose. In immunoblotting experiments, rat testis galactosyl receptor (RTG-r) is recognized by antiserum raised against the minor ASGP-r species of rat liver (designated rat hepatic lectin-2/3, RHL-2/3). Antiserum raised against the major species RHL-1 does not recognize an antigenic protein equivalent to RTG-r. Triton X-100-extracted rat liver and testes preparations
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Garcia-Jimenez, Pilar, Diana del Rosario-Santana, and Rafael R. Robaina. "Jasmonates and Ethylene Shape Floridoside Synthesis during Carposporogenesis in the Red Seaweed Grateloupia imbricata." Marine Drugs 22, no. 3 (2024): 115. http://dx.doi.org/10.3390/md22030115.

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Floridoside is a galactosyl–glycerol compound that acts to supply UDP-galactose and functions as an organic osmolyte in response to salinity in Rhodophyta. Significantly, the UDP-galactose pool is shared for sulfated cell wall galactan synthesis, and, in turn, affected by thallus development alongside carposporogenesis induced by volatile growth regulators, such as ethylene and methyl jasmonate, in the red seaweed Grateloupia imbricata. In this study, we monitored changes in the floridoside reservoir through gene expression controlling both the galactose pool and glyceride pool under different
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Zafarani-Moattar, Mohammad Taghi, Hemayat Shekaari, and Elnaz Mazaher Haji Agha. "Measurement and Modeling of Solubility of Galactose in Aqueous Ionic Liquids, 1-Butyl-3-Methyl Imidazolium Bromide, 1-Hexyl-3-Methyl Imidazolium Bromide and 1-Butyl-3-Methylimidazolium Chloride at T = (298.15 And 308.15) K." Pharmaceutical Sciences 25, no. 4 (2019): 319–30. http://dx.doi.org/10.15171/ps.2019.32.

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Background: Saccharides are considered as abundant, cheap and renewable starting materials for chemicals and fuels. Recently, ionic liquids have been used as green solvents for saccharides. The solubility values of galactose in aqueous ionic liquid solutions are not available. Thus, the main objective of this research was to determine the solubility of galactose in aqueous solutions containing ionic liquids, 1-butyl-3-methyl imidazolium bromide, [BMIm]Br, 1-butyl-3-methylimidazolium chloride [BMIm]Cl and 1-hexyl-3-methyl imidazolium bromide, [HMIm]Br at different mole fractions of ionic liquid
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Quinn, Gary, James C. Wood, David J. J. Ryan та ін. "Porcine Endogenous Retrovirus Transmission Characteristics of Galactose α1-3 Galactose-Deficient Pig Cells". Journal of Virology 78, № 11 (2004): 5805–11. http://dx.doi.org/10.1128/jvi.78.11.5805-5811.2004.

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ABSTRACT Galactose α1-3 galactose (Gal) trisaccharides are present on the surface of wild-type pig cells, as well as on viruses particles produced from such cells. The recognition of Gal sugars by natural anti-Gal antibodies (NAb) in human and Old World primate serum can cause the lysis of the particles via complement-dependent mechanisms and has therefore been proposed as an important antiviral mechanism. Recently, pigs have been generated that possess disrupted galactosyl-transferase (GGTA1) genes. The cells of these pigs do not express Gal sugars on their surface, i.e., are Gal null. Concer
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Dissertations / Theses on the topic "3-galactose"

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Rousse, Juliette. "Influence des anticorps anti-Neu5Gc et anti-alpha-1-3-Galactose dans la réponse immunitaire." Electronic Thesis or Diss., Nantes, Ecole nationale vétérinaire, 2019. http://www.theses.fr/2019ONIR134F.

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L’espèce humaine a perdu lors de l’évolution la capacité de synthétiser certains hydrates de carbone et voit sa glycosylation des protéines et des lipides modifiée par rapport aux autres mammifères. Certains motifs glycosylés acquis lors de l’ingestion de denrées d’origine animale ou produits par le microbiote intestinal peuvent être incorporés dans nos tissus et représentent de potentiels xénoantigènes stimulant la production d’anticorps. Nous sommes exposés aussi à ces xénoantigènes lors de l’administration de protéines thérapeutiques ou lors de greffe de cellules ou de tissus d’origine anim
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Lau, Tak Bun Stephen. "Mechanistic investigation of 3, 5-epimerases / reductases involved in the biosynthesis of GDP-L-Fucose and GDP-L-Galactose." Thesis, University of British Columbia, 2009. http://hdl.handle.net/2429/14851.

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GDP-fucose synthase (GFS), also known as GDP-4-keto-6-deoxy-mannose 3, 5- epimerase / 4-reductase (GMER), is the key enzyme in the GDP-L-fucose biosynthetic pathway. The pathway begins with a dehydratase that converts GDP-D-mannose into 6-deoxy-4-keto- GDP-D-mannose. Then GFS performs two consecutive epirnerizations, and a final NADPH dependent reduction to generate GDP-L-fucose. The detailed mechanism of GFS has remained a mystery due to limited mechanistic studies as well as the lack of an x-ray crystal structure with any bound GDP-sugar. This thesis investigates the mechanism of the reactio
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REMY, SANDRINE. "Essais de synthese de nouveaux inhibiteurs de la 3-hydroxy-3-methyl glutanyl coenzyme a reductase. Synthese de decalines chirales polysubstituees a partir du d-galactose via la reaction de diels-alder intramoleculaire." Paris 11, 1992. http://www.theses.fr/1992PA112201.

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Cette these expose deux sujets differents, en rapport avec la chimie des hydrates de carbone. La premiere partie concerne la synthese de deux nouveaux inhibiteurs de la 3-hydroxy-3-methylglutaryl coenzyme a reductase, contenant un atome d'azote (fonction amine ou amide) dans le pont entre la lactone et l'aglycone. Le troisieme chapitre decrit les essais de monofluoration et gem-difluoration sur la partie lactonique en remplacement de l'hydroxyle en c-3. Les trois analogues realises ont ete testes pour connaitre leur activite biologique. La deuxieme partie de cette these est une etude de la rea
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Escalante, Chong Renan Antonio. "Genetic and Molecular Dissection of the Integration of Galactose and Glucose Signaling in Saccharomyces Cerevisiae Strains." Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17465312.

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Cells need to sense the environment in order to survive, in particular they need to detect nutrients which will provide different building blocks and energy for the cell. This task is complicated by the fact that there can be multiple sources for the same type of nutrient available for the cell. A classical example of how cells sense multiple signals is given by carbon catabolite repression in the budding yeast S. cerevisiae. In this model the preferred carbon source glucose represses the genes used to metabolize an alternative source such as galactose. This means that the preferred carbohydra
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Gencer, Burcak. "Analysis Of Self-processing Mechanism Of Galactose Oxidase By Site-directed Mutagenesis And Heterologous Expression In Escherichia Coli." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12607081/index.pdf.

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In this study, self-catalytic maturation of heterologously expressed pro-galactose oxidase was analysed in E.coli by altering some amino acids which were supposed to play a crucial role in pro-peptide removal. Galactose oxidase (GOase<br>EC 1.1.3.9) from Fusarium graminearum<br>having a molecular mass of 68kDa, is a monomeric, copper containing enzyme with an unusual thioether bond. The enzyme is produced as a precursor with an additional 8 amino acid pre- and a 17- amino acid pro-sequence at the N terminus. Previous work has shown that the pre-peptide is removed possibly by a protease during
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Karumudi, B. "Synthetic studies toward eupomatilone-6, 4-O-β-D-galactosyl maltose and amphidinol-3". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2008. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2661.

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Mach, Tobias Maximilian von [Verfasser], and Ralf [Akademischer Betreuer] Jacob. "pH-abhängige strukturelle und funktionelle Variationen des ß-Galactosid-bindenden Proteins Galectin-3 / Tobias Maximilian von Mach. Betreuer: Ralf Jacob." Marburg : Philipps-Universität Marburg, 2013. http://d-nb.info/104331668X/34.

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French, Anne Thérèse. "The co-regulation of the mucus associated molecules intelectin, resistin like molecule beta and beta galactoside alpha 2-3 sialyltransferase in a T helper cell type 2 response." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/28071.

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The mucus associated molecules intelectin (ITLN), resistin like molecule beta (RELMβ) and beta galactoside alpha 2-3 sialyltransferase (SIAT4C) are upregulated in nematode infections known to induce a typical T helper cell type 2 (Th2) response in mice. It was hypothesised that these three mucus-associated molecules were co-regulated by Th2 cytokines and that their upregulation was part of a typical anti-parasite response in other species. Sheep were chosen as a model because of the economic importance of both respiratory and gastrointestinal tract parasitic infections. Culture of a human colo
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Vandamme, Valérie. "Régulation des sialyltransférases : comparaison des activités [alpha]-1, 3-galactosylet sialyltransférasiques des cellules NIH3T3 transformées par l'oncogène ras, augmentation de l'activité de la [beta]-galactoside [alpha]-2, 6-sialyltransférase. Régulation par la dexaméthasone de la transcription de la [beta]-galactoside [alpha]-2, 6-sialyltransférase des fibroblastes de rat. Activités sialyltransférasiques des cellules FR3T3 transformées par l'oncogène ras, diminution de l'activité de la CMP-NeuAc : GalBl, 3GalNAc : [alpha]-2, 3-sialyltransférase." Lille 1, 1993. http://www.theses.fr/1993LIL10096.

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L'étude des activités sialyltransférasiques des cellules nih3t3 et fr3t3, nous a permis de montrer que l'activité de la cmp-neuac : gal(betal-4)glcnac alpha-2,6-sialyltransférase (alpha2, 6st(n)), enzyme impliquée dans la sialylation des n-glycosylprotéines, est spécifiquement activée lorsque ces cellules sont transformées par transfection de l'oncogène humain c-ha-ras ou encore cultivées en présence de dexaméthasone. Dans les deux cas, nous avons pu montrer que l'activation de cette enzyme résultait d'une augmentation du taux de transcription d'un arnm de 4. 7 kb correspondant à l'une des tro
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Barreto, Francisco António Freitas. "d-Galactose high-dose administration and oral epigallocatechin-3-gallatte effects on the dendritic trees of developing neurons of young male rats." Master's thesis, 2018. https://hdl.handle.net/10216/112028.

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Books on the topic "3-galactose"

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Bhat, Paike Jayadeva. Galactose Regulon of Yeast. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-74015-5.

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Book chapters on the topic "3-galactose"

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Honke, Koichi. "Galactose-3-O-Sulfotransferase 1-4 (GAL3ST1-4)." In Handbook of Glycosyltransferases and Related Genes. Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_56.

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Schomburg, Dietmar, and Dörte Stephan. "Galactose oxidase." In Enzyme Handbook 10. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-57756-7_105.

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Schomburg, Dietmar, and Dörte Stephan. "Galactoside 3-fucosyltransferase." In Enzyme Handbook 12. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_152.

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Schomburg, Dietmar, and Dörte Stephan. "Galactose 1-dehydrogenase." In Enzyme Handbook 9. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-85200-8_48.

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Timson, David J., Richard J. Reece, James B. Thoden, et al. "Glucose-Galactose Intolerance." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_6288.

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Schomburg, Dietmar, and Dörte Stephan. "Galactose-6-sulfurylase." In Enzyme Handbook 13. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59176-1_5.

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Gitzelmann, R. "Disorders of Galactose Metabolism." In Inborn Metabolic Diseases. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-02613-7_9.

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Berry, Gerard T., John Walter, and Judith L. Fridovich-Keil. "Disorders of Galactose Metabolism." In Inborn Metabolic Diseases. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49771-5_6.

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Schomburg, Dietmar, and Dörte Stephan. "Galactose 1-dehydrogenase (NADP+)." In Enzyme Handbook 9. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-85200-8_115.

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Gitzelmann, R. "Disorders of Galactose Metabolism." In Inborn Metabolic Diseases. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04285-4_7.

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Conference papers on the topic "3-galactose"

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Gohari, Minoo. "Abstract 3166: Inspecting the presence of sialic acid α-2-3- galactose/GalNAC terminal sugar in human stomach adenocarcinoma by lectin histochemistry". У Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-3166.

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Lima, Camila Cristina Sant Ana de, Claudia Regina Faria, Lidia Freire Abdalla Nery, Cyra Mesquita de Araujo, Bruno Oliveira Barreto, and Isabela de Oliveira Moura. "Perfil de alterações em teste de triagem neonatal realizados em um laboratório privado de São José dos Campos." In Resumos do 56º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2024. https://doi.org/10.5327/1516-3180.142s1.10809.

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Objetivo: O diagnóstico precoce, o tratamento adequado e o acompanhamento médico de algumas doenças podem evitar a morte e proporcionar melhor qualidade de vida aos recém-nascidos de uma população. A Triagem Neonatal identifica algumas dessas condições e é responsável por identificar precocemente indivíduos com doenças metabólicas, genéticas, enzimáticas e endocrinológicas, para que estes possam ser tratados em tempo oportuno. Este trabalho teve o objetivo de identificar o perfil dos testes de triagem neonatal alterados e reforçar a importância da prática de confirmação do resultado em segunda
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Wu, Peng, Dachao Li, Jingxin Zhang, Bing Song, and Kexin Xu. "Research on Influencing Factors of Surface Plasmon Resonance Glucose Detection Based on D-Galactose/D-Glucose Protein Immobilizied by Amine Coupling Method." In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-40281.

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Prediction of blood glucose based on measuring the glucose concentration in interstitial fluid is an effectively way to control diabetes. A surface plasmon resonance (SPR) system based on a miniature integrated SPR sensor is set up in this paper to measure the glucose concentration in interstitial fluid, and the D-galactose/D-glucose Binding Protein (GGBP) which can specifically absorb glucose is immobilized onto the SPR sensor surface by amine coupling method for higher sensitivity. The experiment result is affected by various factors, such as the grime on sensor surface, baseline, flow veloc
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Mimuro, Jun, Raymond R. Schleef, and David J. Loskutoff. "THE EXTRACELLULAR MATRIX (ECM) OF CULTURED BOVINE AORTIC ENDOTHELIAL CELLS (BAEs) CONTAINS FUNCTIONALLY ACTIVE TYPE I PLASMINOGEN ACTIVATOR INHIBITOR (PAI-1)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644438.

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The ECM of cultured BAEs was analyzed by immunoblotting and reverse fibrin autography and shown to contain PAI-1. PAI-1 containing ECM was incubated with tissue plasminogen activator (tPA) to determine whether the bound PAI-1 was functionally active or latent. The majority of the detectable PAI-1 in the ECM formed complexes with tPA indicating that it was active. The resulting tPA/PAI-1 complexes were released from ECM and recovered in the reaction solution indicating that the PAI-1 in such complexes had lost its ECM binding site. The PAI-1 could not be removed from ECM by incubating it in hig
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Kiselova-Kaneva, Yoana, Irina Potoroko, and Diana Ivanova. "In Silico 3D/4D QSAR Prediction of 5-O-Caffeoylquinic Acid, Cyanidin-3-O-Galactoside Chloride and L-Epicatechin Anti-Inflammatory Activity, Cytotoxicity and Metabolism." In European Nutrition Conference. MDPI, 2024. http://dx.doi.org/10.3390/proceedings2023091246.

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Gunda, Naga Siva Kumar, Selvaraj Naicker, Maryam S. Ghoraishi, Subir Bhattacharjee, Thomas G. Thundat, and Sushanta K. Mitra. "Microspot With Integrated Wells (MSIW) for the Detection of E.coli." In ASME 2013 11th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icnmm2013-73037.

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There is an increasing problem in getting quality water for developing countries. Water system is contaminated and without proper treatment, it has been consumed as drinking water. It is a big problem for health. Escherichia coli (E.coli) is the main cause for the contamination of water and illness in people. Early detection of E.coli presence in the drinking water followed by subsequent treatment for elimination of E.coli can solve this problem. The present work developed a new method for detecting E.coli in contaminated water using microspot with integrated wells (MSIW). The method involves
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Reports on the topic "3-galactose"

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Sukenik, Assaf, Paul Roessler, and John Ohlrogge. Biochemical and Physiological Regulation of Lipid Synthesis in Unicellular Algae with Special Emphasis on W-3 Very Long Chain Lipids. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7604932.bard.

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Various unicellular algae produce omega-3 (w3) very-long-chain polyunsaturated fatty acids (VLC-PUFA), which are rarely found in higher plants. In this research and other studies from our laboratories, it has been demonstrated that the marine unicellular alga Nannochloropsis (Eustigmatophyceae) can be used as a reliable and high quality source for the w3 VLC-PUFA eicosapentaenoic acid (EPA). This alga is widely used in mariculture systems as the primary component of the artificial food chain in fish larvae production, mainly due to its high EPA content. Furthermore, w3 fatty acids are essentia
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