New Microbial Glycosidases

Sunrvranv Glycosidases from fungi are useful in the preparation of various glycosides mainly by transglycosylation or reversed glycosylation. The lack ofany requirement for protection- deprotection sequences, mild conditions and easier synthesis of thermodynamically not preferred glycosidic bonds ar...

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Main Author: Charvátová, Andrea
Other Authors: Křen, Vladimír
Format: Doctoral Thesis
Language:English
Published: 2007
Online Access:http://www.nusl.cz/ntk/nusl-373560
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spelling ndltd-nusl.cz-oai-invenio.nusl.cz-3735602018-03-17T04:02:15Z New Microbial Glycosidases New Microbial Glycosidases Charvátová, Andrea Křen, Vladimír Králová, Blanka Walterová, Daniela Sunrvranv Glycosidases from fungi are useful in the preparation of various glycosides mainly by transglycosylation or reversed glycosylation. The lack ofany requirement for protection- deprotection sequences, mild conditions and easier synthesis of thermodynamically not preferred glycosidic bonds are the main advantages of glycosidase-catalysed synthesis of glycosides. In ttris thesis we concentratedon exoglycosidases,mainly B.N.aceýlhexosaminidases, cr-galactosidases and cr-L-rhamnosidases. For the enzyme preparation taxonomically characterised fungal strains from public collections were used. A library comprising more than 200 various glycosidases was developed by modification ofcultivation conditions and by the use ofspecific inducers. The enrymes were used for screening ofsubstrate specificity and stability in organic solvents and subsequently for synthesis and modification of various substrates. Both B-N-acetylgalactosaminidase and B-N-acetylglucosaminidase activities in the series of B-N-acetylhexosaminidases were determined. Saccharides with strong immunomodulation activity $-o-GalpNAc-(i-+4)-o-GlcpNAc and B-o-GalpNAc-(1-+6)-o-GlcpNAc were synthesisedby transglycosylation using B-N-acetylhexosaminidase from Penicillium oxalicum CCF 2430' enryme having the highest B.N-acetylgalactosaminidase activiý.... 2007 info:eu-repo/semantics/doctoralThesis http://www.nusl.cz/ntk/nusl-373560 eng info:eu-repo/semantics/restrictedAccess
collection NDLTD
language English
format Doctoral Thesis
sources NDLTD
description Sunrvranv Glycosidases from fungi are useful in the preparation of various glycosides mainly by transglycosylation or reversed glycosylation. The lack ofany requirement for protection- deprotection sequences, mild conditions and easier synthesis of thermodynamically not preferred glycosidic bonds are the main advantages of glycosidase-catalysed synthesis of glycosides. In ttris thesis we concentratedon exoglycosidases,mainly B.N.aceýlhexosaminidases, cr-galactosidases and cr-L-rhamnosidases. For the enzyme preparation taxonomically characterised fungal strains from public collections were used. A library comprising more than 200 various glycosidases was developed by modification ofcultivation conditions and by the use ofspecific inducers. The enrymes were used for screening ofsubstrate specificity and stability in organic solvents and subsequently for synthesis and modification of various substrates. Both B-N-acetylgalactosaminidase and B-N-acetylglucosaminidase activities in the series of B-N-acetylhexosaminidases were determined. Saccharides with strong immunomodulation activity $-o-GalpNAc-(i-+4)-o-GlcpNAc and B-o-GalpNAc-(1-+6)-o-GlcpNAc were synthesisedby transglycosylation using B-N-acetylhexosaminidase from Penicillium oxalicum CCF 2430' enryme having the highest B.N-acetylgalactosaminidase activiý....
author2 Křen, Vladimír
author_facet Křen, Vladimír
Charvátová, Andrea
author Charvátová, Andrea
spellingShingle Charvátová, Andrea
New Microbial Glycosidases
author_sort Charvátová, Andrea
title New Microbial Glycosidases
title_short New Microbial Glycosidases
title_full New Microbial Glycosidases
title_fullStr New Microbial Glycosidases
title_full_unstemmed New Microbial Glycosidases
title_sort new microbial glycosidases
publishDate 2007
url http://www.nusl.cz/ntk/nusl-373560
work_keys_str_mv AT charvatovaandrea newmicrobialglycosidases
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