Literature DB >> 19875083

beta-Glycosyl azides as substrates for alpha-glycosynthases: preparation of efficient alpha-L-fucosynthases.

Beatrice Cobucci-Ponzano1, Fiorella Conte, Emiliano Bedini, Maria Michela Corsaro, Michelangelo Parrilli, Gerlind Sulzenbacher, Alexandra Lipski, Fabrizio Dal Piaz, Laura Lepore, Mosè Rossi, Marco Moracci.   

Abstract

Fucose-containing oligosaccharides play a central role in physio-pathological events, and fucosylated oligosaccharides have interesting potential applications in biomedicine. No methods for the large-scale production of oligosaccharides are currently available, but the chemo-enzymatic approach is very promising. Glycosynthases, mutated glycosidases that synthesize oligosaccharides in high yields, have been demonstrated to be an interesting alternative. However, examples of glycosynthases available so far are restricted to a limited number of glycosidases families and to only one retaining alpha-glycosynthase. We show here that new mutants of two alpha-L-fucosidases are efficient alpha-L-fucosynthases. The approach shown utilized beta-L-fucopyranosyl azide as donor substrate leading to transglycosylation yields up to 91%. This is the first method exploiting a beta-glycosyl azide donor for alpha-glycosynthases; its applicability to the glycosynthetic methodology in a wider perspective is presented.

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Year:  2009        PMID: 19875083     DOI: 10.1016/j.chembiol.2009.09.013

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  13 in total

1.  1,3-1,4-α-L-fucosynthase that specifically introduces Lewis a/x antigens into type-1/2 chains.

Authors:  Haruko Sakurama; Shinya Fushinobu; Masafumi Hidaka; Erina Yoshida; Yuji Honda; Hisashi Ashida; Motomitsu Kitaoka; Hidehiko Kumagai; Kenji Yamamoto; Takane Katayama
Journal:  J Biol Chem       Date:  2012-03-26       Impact factor: 5.157

Review 2.  α-L-Fucosidases and their applications for the production of fucosylated human milk oligosaccharides.

Authors:  Li Wan; Yingying Zhu; Wenli Zhang; Wanmeng Mu
Journal:  Appl Microbiol Biotechnol       Date:  2020-05-01       Impact factor: 4.813

Review 3.  Translational recoding in archaea.

Authors:  Beatrice Cobucci-Ponzano; Mosè Rossi; Marco Moracci
Journal:  Extremophiles       Date:  2012-09-27       Impact factor: 2.395

Review 4.  Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: an update for 2009-2010.

Authors:  David J Harvey
Journal:  Mass Spectrom Rev       Date:  2014-05-26       Impact factor: 10.946

Review 5.  Harnessing glycoenzyme engineering for synthesis of bioactive oligosaccharides.

Authors:  Mounir Benkoulouche; Régis Fauré; Magali Remaud-Siméon; Claire Moulis; Isabelle André
Journal:  Interface Focus       Date:  2019-02-15       Impact factor: 3.906

Review 6.  Chemoenzymatic Methods for the Synthesis of Glycoproteins.

Authors:  Chao Li; Lai-Xi Wang
Journal:  Chem Rev       Date:  2018-08-24       Impact factor: 60.622

7.  Designer α1,6-Fucosidase Mutants Enable Direct Core Fucosylation of Intact N-Glycopeptides and N-Glycoproteins.

Authors:  Chao Li; Shilei Zhu; Christopher Ma; Lai-Xi Wang
Journal:  J Am Chem Soc       Date:  2017-10-16       Impact factor: 15.419

8.  Building custom polysaccharides in vitro with an efficient, broad-specificity xyloglucan glycosynthase and a fucosyltransferase.

Authors:  Oliver Spadiut; Farid M Ibatullin; Jonelle Peart; Fredrika Gullfot; Carlos Martinez-Fleites; Marcus Ruda; Chunlin Xu; Gustav Sundqvist; Gideon J Davies; Harry Brumer
Journal:  J Am Chem Soc       Date:  2011-06-27       Impact factor: 15.419

9.  Insight into the Mechanism of Intramolecular Inhibition of the Catalytic Activity of Sirtuin 2 (SIRT2).

Authors:  Jinyu Li; Franziska Flick; Patricia Verheugd; Paolo Carloni; Bernhard Lüscher; Giulia Rossetti
Journal:  PLoS One       Date:  2015-09-25       Impact factor: 3.240

Review 10.  Synthesis of Glycosides by Glycosynthases.

Authors:  Marc R Hayes; Jörg Pietruszka
Journal:  Molecules       Date:  2017-08-30       Impact factor: 4.411

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