http://www.cnr.it/ontology/cnr/individuo/prodotto/ID167183
Highly productive autocondensation and transglycosylation reactions using Sulfolobus solfataricus glycosynthase (Articolo in rivista)
- Type
- Label
- Highly productive autocondensation and transglycosylation reactions using Sulfolobus solfataricus glycosynthase (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/cbic.200400430 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- A Trincone; A Giordano; G Perugino; M Rossi; M Moracci (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://onlinelibrary.wiley.com/doi/10.1002/cbic.200400430/abstract (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
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- PubMe (literal)
- ISI Web of Science (WOS) (literal)
- Scopu (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica Biomolecolare--Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, 80072 Pozzuoli, Naples (Italy); Institute of Protein Biochemistry--Consiglio Nazionale delle Ricerche, Via P. Castellino 111, 80131, Naples (Italy); Dipartimento di Chimica Biologica, Università di Napoli \"Federico II\" Via Mezzocannone 16, 80134, Naples (Italy (literal)
- Titolo
- Highly productive autocondensation and transglycosylation reactions using Sulfolobus solfataricus glycosynthase (literal)
- Abstract
- Transglycosylation reactions (autocondensation of the substrate or transfer of the glycon donor moiety to different acceptors) with the hyperthermophilic glycosynthase from Sulfolobus solfataricus acting in dilute sodium formate buffer at pH 4.0 are reported; the use of 4-nitrophenyl beta-glucopyranoside as both donor and acceptor in the self-transfer reaction and a highly productive reaction with 1.1 M 2-nitrophenyl beta-glucopyranoside were possible. Interesting effects, governed by the anomeric configuration and lipophilicity of heteroacceptors, on the regioselectivity and yield of reactions were found for the first time with this enzyme and are discussed. The results demonstrate the unexplored synthetic potential of this glycosynthase; the tuning of the reaction conditions and the choice of different donors/acceptors can lead to products of applicative interest. (literal)
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