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An Aspergillus nidulans β-mannanase with high transglycosylation capacity revealed through comparative studies within glycosidase family 5 [PDF]
β-Mannanases are involved in the conversion and modification of mannan-based saccharides. Using a retaining mechanism, they can, in addition to hydrolysis, also potentially perform transglycosylation reactions, synthesizing new glyco-conjugates ...
Anna Rosengren +2 more
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Enzymatic transglycosylation of xylose using a glycosynthase
Carbohydrate Research, 2005The application of the hyperactive glycosynthase derived from Agrobacterium sp. beta-glucosidase (AbgE358G-2F6) to the synthesis of xylo-oligosaccharides by using alpha-D-xylopyranosyl fluoride as donor represents the first successful use of glycosynthase technology for xylosyl transfer.
Young-Wan, Kim +2 more
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Transglycosylation Reactions of 6-Thioguanine Acyclonucleosides
Nucleosides, Nucleotides and Nucleic Acids, 20009-(2-Acetoxyethoxy)methyl-N2-acetyl-6-thoguanine (2) undergoes two different transglycosylation reactions: i) the 79 isomerization, which gives the respective 7-regioisomer (3) as the major product, ii) the 9S6 glycosyl migration, which leads to a 9,S6-disubstituted product (4). S6-Methylation completely stopped the reversibility of transglycosylation.
A, Manikowski, J, Boryski
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Transglycosylation of L-ascorbic acid
Applied Biochemistry and Microbiology, 2007Cyclodextrin glucanotransferases (CGTs, EC 2.4.1.19) from mesophilic, thermophilic, and halophilic bacteria and maltase (EC 3.2.1.20) from the yeast Saccharomyces cerevisiae were used for transglycosylation of ascorbic acid with starch, maltodextrin, γ-cyclodextrin, and maltose. These compounds served as donors of glucosyl residues.
A. A. Markosyan +4 more
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Benzimidazoles in the Reaction of Enzymatic Transglycosylation
Nucleosides, Nucleotides and Nucleic Acids, 1995Abstract Substrate activity of a broad spectrum of derivatives of benzimidazole in the reaction of enzymatic ribo- and 2-deoxyribosylation catalyzed by purine nucleoside phosphorylase of whole cells of E. coli BMT-1D/1A has been studied. Guanosine or 2′-deoxyguanosine were used as glycosyl donors.
Igor Mikhailopulo +5 more
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2009
The most important functions of carbohydrates are structural roles and energy storage, but carbohydrate parts of glycoproteins and glycolipids are involved in biological functions mainly related to cell recognition events. Carbohydrates are also important molecules in the technological domain.
A Tramice +3 more
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The most important functions of carbohydrates are structural roles and energy storage, but carbohydrate parts of glycoproteins and glycolipids are involved in biological functions mainly related to cell recognition events. Carbohydrates are also important molecules in the technological domain.
A Tramice +3 more
openaire +1 more source
Oligosaccharide synthesis by enzymatic transglycosylation
Glycoconjugate Journal, 1990Agricultural Research Service, United States Department of Agriculture, Northern Regional Research Center, 1815 N. University St., Peoria, IL 61604, U.S.A. 2 Biochemical and Food Process Engineering, Agricultural Engineering Department, Purdue University, West Lafayette, IN 47907, U.S.A.
Gregory L Cote, Bernard Y Tao
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[Transglycosylation of benzo[h]quinazolines].
Prikladnaia biokhimiia i mikrobiologiia, 2009This was the first study to apply cyclodextrin glucanotransferases (CGTase, EC 2.4.1.19) produced by mesophilic, thermophilic, alkaliphilic, and halophilic bacilli as well as pullulanase, beta-amylase, beta-galactosidase, and beta-fructofuranosidase for transglycosylation of benzo[h]quinazolines.
A A, Markosian +3 more
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Transglycosylation Reaction of 6-Thioguanosine
Nucleosides and Nucleotides, 1999Abstract Peracetylated 6-thioguanosine (2) undergoes the so far unknown N→S transglycosylation reaction to form a stable 9,S6 -bis(ribosyl) derivative (3) and N2-acetyl-6-thioguanine (4). The reaction takes place at elevated temperatures with no catalyst, or in solution in the presence of acidic catalysts.
Andrzej Manikowski, Jerzy Boryski
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Transglycosylation in the Modification and Isotope Labeling of Pyrimidine Nucleosides
Organic Letters, 2020Transglycosylation of pyrimidine nucleosides is demonstrated in a one-pot synthesis of uridine derivatives under microwave irradiation. Inductive activation of 2',3',5'-tri-O-acetyl uridine with a 5-nitro group produces a more-reactive glycosyl donor. Under optimized Vorbrüggen conditions, the 5-nitrouridine facilitates a reversible nucleobase exchange
Yong Gong +3 more
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