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Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase

[Image: see text] The current drive for applications of biomass-derived compounds, for energy and advanced materials, has led to a resurgence of interest in the manipulation of plant polymers. The xyloglucans, a family of structurally complex plant polysaccharides, have attracted significant interes...

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Autores principales: Spadiut, Oliver, Ibatullin, Farid M., Peart, Jonelle, Gullfot, Fredrika, Martinez-Fleites, Carlos, Ruda, Marcus, Xu, Chunlin, Sundqvist, Gustav, Davies, Gideon J., Brumer, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2011
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135005/
https://www.ncbi.nlm.nih.gov/pubmed/21618981
http://dx.doi.org/10.1021/ja202788q
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author Spadiut, Oliver
Ibatullin, Farid M.
Peart, Jonelle
Gullfot, Fredrika
Martinez-Fleites, Carlos
Ruda, Marcus
Xu, Chunlin
Sundqvist, Gustav
Davies, Gideon J.
Brumer, Harry
author_facet Spadiut, Oliver
Ibatullin, Farid M.
Peart, Jonelle
Gullfot, Fredrika
Martinez-Fleites, Carlos
Ruda, Marcus
Xu, Chunlin
Sundqvist, Gustav
Davies, Gideon J.
Brumer, Harry
author_sort Spadiut, Oliver
collection PubMed
description [Image: see text] The current drive for applications of biomass-derived compounds, for energy and advanced materials, has led to a resurgence of interest in the manipulation of plant polymers. The xyloglucans, a family of structurally complex plant polysaccharides, have attracted significant interest due to their intrinsic high affinity for cellulose, both in muro and in technical applications. Moreover, current cell wall models are limited by the lack of detailed structure–property relationships of xyloglucans, due to a lack of molecules with well-defined branching patterns. Here, we have developed a new, broad-specificity “xyloglucan glycosynthase”, selected from active-site mutants of a bacterial endoxyloglucanase, which catalyzed the synthesis of high molar mass polysaccharides, with complex side-chain structures, from suitable glycosyl fluoride donor substrates. The product range was further extended by combination with an Arabidopsis thaliana α(1→2)-fucosyltransferase to achieve the in vitro synthesis of fucosylated xyloglucans typical of dicot primary cell walls. These enzymes thus comprise a toolkit for the controlled enzymatic synthesis of xyloglucans that are otherwise impossible to obtain from native sources. Moreover, this study demonstrates the validity of a chemo-enzymatic approach to polysaccharide synthesis, in which the simplicity and economy of glycosynthase technology is harnessed together with the exquisite specificity of glycosyltransferases to control molecular complexity.
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spelling pubmed-31350052011-07-13 Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase Spadiut, Oliver Ibatullin, Farid M. Peart, Jonelle Gullfot, Fredrika Martinez-Fleites, Carlos Ruda, Marcus Xu, Chunlin Sundqvist, Gustav Davies, Gideon J. Brumer, Harry J Am Chem Soc [Image: see text] The current drive for applications of biomass-derived compounds, for energy and advanced materials, has led to a resurgence of interest in the manipulation of plant polymers. The xyloglucans, a family of structurally complex plant polysaccharides, have attracted significant interest due to their intrinsic high affinity for cellulose, both in muro and in technical applications. Moreover, current cell wall models are limited by the lack of detailed structure–property relationships of xyloglucans, due to a lack of molecules with well-defined branching patterns. Here, we have developed a new, broad-specificity “xyloglucan glycosynthase”, selected from active-site mutants of a bacterial endoxyloglucanase, which catalyzed the synthesis of high molar mass polysaccharides, with complex side-chain structures, from suitable glycosyl fluoride donor substrates. The product range was further extended by combination with an Arabidopsis thaliana α(1→2)-fucosyltransferase to achieve the in vitro synthesis of fucosylated xyloglucans typical of dicot primary cell walls. These enzymes thus comprise a toolkit for the controlled enzymatic synthesis of xyloglucans that are otherwise impossible to obtain from native sources. Moreover, this study demonstrates the validity of a chemo-enzymatic approach to polysaccharide synthesis, in which the simplicity and economy of glycosynthase technology is harnessed together with the exquisite specificity of glycosyltransferases to control molecular complexity. American Chemical Society 2011-05-27 2011-07-20 /pmc/articles/PMC3135005/ /pubmed/21618981 http://dx.doi.org/10.1021/ja202788q Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Spadiut, Oliver
Ibatullin, Farid M.
Peart, Jonelle
Gullfot, Fredrika
Martinez-Fleites, Carlos
Ruda, Marcus
Xu, Chunlin
Sundqvist, Gustav
Davies, Gideon J.
Brumer, Harry
Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title_full Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title_fullStr Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title_full_unstemmed Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title_short Building Custom Polysaccharides in Vitro with an Efficient, Broad-Specificity Xyloglucan Glycosynthase and a Fucosyltransferase
title_sort building custom polysaccharides in vitro with an efficient, broad-specificity xyloglucan glycosynthase and a fucosyltransferase
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135005/
https://www.ncbi.nlm.nih.gov/pubmed/21618981
http://dx.doi.org/10.1021/ja202788q
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