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  • Fungal glucans represent various structurally different d-glucose polymers with a large diversity of molecular mass and configuration. According to glucose anomeric structure, it is possible to distinguish alpha-d-glucans, beta-d-glucans and mixed alpha, beta-d-glucans. Further discrimination could be made on the basis of glycosidic bond position in a pyranoid ring, distribution of specific glycosidic bonds along a chain, branching and molecular mass. Fungal glucans can be chemically modified to obtain various derivatives of potential industrial or medicinal importance. NMR spectroscopy is a powerful tool in structural analysis of fungal glucans. Together with chemolytic methods like methylation analysis and periodate oxidation, NMR is able to determine exact structure of these polysaccharides. Fungal glucans or their derivatives exert various biological activities, which are usually linked to structure, molecular mass and substitution degree.
  • Fungal glucans represent various structurally different d-glucose polymers with a large diversity of molecular mass and configuration. According to glucose anomeric structure, it is possible to distinguish alpha-d-glucans, beta-d-glucans and mixed alpha, beta-d-glucans. Further discrimination could be made on the basis of glycosidic bond position in a pyranoid ring, distribution of specific glycosidic bonds along a chain, branching and molecular mass. Fungal glucans can be chemically modified to obtain various derivatives of potential industrial or medicinal importance. NMR spectroscopy is a powerful tool in structural analysis of fungal glucans. Together with chemolytic methods like methylation analysis and periodate oxidation, NMR is able to determine exact structure of these polysaccharides. Fungal glucans or their derivatives exert various biological activities, which are usually linked to structure, molecular mass and substitution degree. (en)
Title
  • Structural diversity of fungal glucans
  • Structural diversity of fungal glucans (en)
skos:prefLabel
  • Structural diversity of fungal glucans
  • Structural diversity of fungal glucans (en)
skos:notation
  • RIV/60461373:22330/13:43894591!RIV14-GA0-22330___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA525/09/1133), Z(MSM6046137305)
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 108352
http://linked.open...ai/riv/idVysledku
  • RIV/60461373:22330/13:43894591
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • fungal glucans, structural diversity, nuclear magnetic resonance, chemical modification, structure-activity relationship (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [1C813092DB3B]
http://linked.open...i/riv/nazevZdroje
  • Carbohydrate Polymers
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 92
http://linked.open...iv/tvurceVysledku
  • Novák, Miroslav
  • Synytsya, Andriy
http://linked.open...ain/vavai/riv/wos
  • 000313146900112
http://linked.open...n/vavai/riv/zamer
issn
  • 0144-8617
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.carbpol.2012.09.077
http://localhost/t...ganizacniJednotka
  • 22330
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