Chemical modification of botryosphaeran: structural characterization and anticoagulant activity of a water-soluble sulfonated (1-->3)(1-->6)-β-D-glucan.

3)(1-->6)-β-D-glucan. -->
Autoři: Brandi J; Departamento de Física, Química e Biologia, Faculdade de Ciências e Technologia, Universidade Estadual Paulista, CEP 19060-900, Presidente Prudente - São Paulo, Brazil., Oliveira ÉC, Monteiro N, Vasconcelos AF, Dekker RF, Barbosa AM, Silveira JL, Mourão PA, Corradi da Silva Mde L
Zdroj: Journal of microbiology and biotechnology [J Microbiol Biotechnol] 2011 Oct; Vol. 21 (10), pp. 1036-42.
Způsob vydávání: Journal Article; Research Support, Non-U.S. Gov't
Jazyk: English
Informace o časopise: Publisher: Korean Society for Microbiology and Biotechnology Country of Publication: Korea (South) NLM ID: 9431852 Publication Model: Print Cited Medium: Internet ISSN: 1738-8872 (Electronic) Linking ISSN: 10177825 NLM ISO Abbreviation: J Microbiol Biotechnol Subsets: MEDLINE
Imprint Name(s): Publication: 2002- : Seoul : Korean Society for Microbiology and Biotechnology
Original Publication: Seoul : Korean Society for Applied Microbiology, 1991-2001.
Výrazy ze slovníku MeSH: Anticoagulants/*chemistry , Glucans/*chemistry, Anticoagulants/metabolism ; Anticoagulants/pharmacology ; Ascomycota/chemistry ; Ascomycota/metabolism ; Blood Coagulation/drug effects ; Glucans/metabolism ; Glucans/pharmacology ; Humans ; Molecular Structure ; Structure-Activity Relationship
Abstrakt: The exopolysaccharide botryosphaeran (EPS(GLC); a (1--> 3)(1-->6)-β-D-glucan from Botryosphaeria rhodina MAMB- 05) was sulfonated to produce a water-soluble fraction (EPS(GLC)-S) using pyridine and chlorosulfonic acid in formamid. This procedure was then repeated twice to produce another fraction (EPSGLC-RS) with a higher degree of substitution (DS, 1.64). The purity of each botryosphaeran sample (unsulfonated and sulfonated) was assessed by gel filtration chromatography (Sepharose CL-4B), where each polysaccharide was eluted as a single symmetrical peak. The structures of the sulfonated and re-sulfonated botryosphaerans were investigated using ultraviolet-visible (UV-Vis), Fourier-transform infrared (FT-IR), and (13)C nuclear magnetic resonance ((13)C NMR) spectroscopies. EPS(GLC) and EPS(GLC)-RS were also assayed for anticoagulation activity, and EPS(GLC)-RS was identified as an anticoagulant.
Substance Nomenclature: 0 (Anticoagulants)
0 (Glucans)
0 (botryosphaeran)
Entry Date(s): Date Created: 20111028 Date Completed: 20120207 Latest Revision: 20190923
Update Code: 20240829
DOI: 10.4014/jmb.1105.05020
PMID: 22031027
Autor: Brandi J; Departamento de Física, Química e Biologia, Faculdade de Ciências e Technologia, Universidade Estadual Paulista, CEP 19060-900, Presidente Prudente - São Paulo, Brazil., Oliveira ÉC, Monteiro N, Vasconcelos AF, Dekker RF, Barbosa AM, Silveira JL, Mourão PA, Corradi da Silva Mde L
Jazyk: angličtina
Zdroj: Journal of microbiology and biotechnology [J Microbiol Biotechnol] 2011 Oct; Vol. 21 (10), pp. 1036-42.
DOI: 10.4014/jmb.1105.05020
Abstrakt: The exopolysaccharide botryosphaeran (EPS(GLC); a (1--> 3)(1-->6)-β-D-glucan from Botryosphaeria rhodina MAMB- 05) was sulfonated to produce a water-soluble fraction (EPS(GLC)-S) using pyridine and chlorosulfonic acid in formamid. This procedure was then repeated twice to produce another fraction (EPSGLC-RS) with a higher degree of substitution (DS, 1.64). The purity of each botryosphaeran sample (unsulfonated and sulfonated) was assessed by gel filtration chromatography (Sepharose CL-4B), where each polysaccharide was eluted as a single symmetrical peak. The structures of the sulfonated and re-sulfonated botryosphaerans were investigated using ultraviolet-visible (UV-Vis), Fourier-transform infrared (FT-IR), and (13)C nuclear magnetic resonance ((13)C NMR) spectroscopies. EPS(GLC) and EPS(GLC)-RS were also assayed for anticoagulation activity, and EPS(GLC)-RS was identified as an anticoagulant.
Databáze: MEDLINE