http://www.cnr.it/ontology/cnr/individuo/prodotto/ID14719
Enzymatic synthesis of 2-deoxyglycosides using the b-glycosidase of the archaeon Sulfolobus solfataricus (Articolo in rivista)
- Type
- Label
- Enzymatic synthesis of 2-deoxyglycosides using the b-glycosidase of the archaeon Sulfolobus solfataricus (Articolo in rivista) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
- Alternative label
Trincone, A., Pagnotta, E., Giordano, A., Perugino, G., Rossi, M., Moracci M. (2003)
Enzymatic synthesis of 2-deoxyglycosides using the b-glycosidase of the archaeon Sulfolobus solfataricus
in Biocatalysis and biotransformation (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Trincone, A., Pagnotta, E., Giordano, A., Perugino, G., Rossi, M., Moracci M. (literal)
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- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Titolo
- Enzymatic synthesis of 2-deoxyglycosides using the b-glycosidase of the archaeon Sulfolobus solfataricus (literal)
- Abstract
- The synthesis of 2-deoxyglycosides and, for the first time, of 2-deoxygalactosides is reported using a thermophilic and thermostable b-glycosyl hydrolase from the archeon Sulfolobus solfataricus and glucal or galactal as donors. The yields observed with alkyl acceptors confirmed that
the robustness of the biocatalyst is of great help in designing practical syntheses of pure b-anomers of 2-deoxy derivatives of 4-penten-1-ol (obtained in 80% yield at 20 fold molar excess) and 3,4-dimethoxybenzyl alcohol (obtained in 19% yield at 3.3 fold molar excess. The attachment of 2-deoxyglyco units was performed on various pyranosidic acceptors (p-nitrophenyl a-D-glucopyranoside, o-nitrophenyl 2-deoxy-N-acetyl-a-D-glucosamine and p-nitrophenyl 2-deoxy-N-acetyl-b-Dglucosamine). At low molecular excesses of the acceptors, satisfactory yields (20/40%) of chromophoric 2-deoxy di- and trisaccharides were obtained. The different regioselectivity of our enzyme with respect
to mesophilic counterparts reflects the importance of
biodiversity in this field for the construction of a library
of different glycosidases with different specificity. (literal)
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- Autore CNR
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