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A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan
Marine algae catalyze half of all global photosynthetic production of carbohydrates. Owing to their fast growth rates, Ulva spp. rapidly produce substantial amounts of carbohydrate-rich biomass and represent an emerging renewable energy and carbon resource. Their major cell wall polysaccharide is th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511951/ https://www.ncbi.nlm.nih.gov/pubmed/34547290 http://dx.doi.org/10.1016/j.jbc.2021.101210 |
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author | Bäumgen, Marcus Dutschei, Theresa Bartosik, Daniel Suster, Christoph Reisky, Lukas Gerlach, Nadine Stanetty, Christian Mihovilovic, Marko D. Schweder, Thomas Hehemann, Jan-Hendrik Bornscheuer, Uwe T. |
author_facet | Bäumgen, Marcus Dutschei, Theresa Bartosik, Daniel Suster, Christoph Reisky, Lukas Gerlach, Nadine Stanetty, Christian Mihovilovic, Marko D. Schweder, Thomas Hehemann, Jan-Hendrik Bornscheuer, Uwe T. |
author_sort | Bäumgen, Marcus |
collection | PubMed |
description | Marine algae catalyze half of all global photosynthetic production of carbohydrates. Owing to their fast growth rates, Ulva spp. rapidly produce substantial amounts of carbohydrate-rich biomass and represent an emerging renewable energy and carbon resource. Their major cell wall polysaccharide is the anionic carbohydrate ulvan. Here, we describe a new enzymatic degradation pathway of the marine bacterium Formosa agariphila for ulvan oligosaccharides involving unsaturated uronic acid at the nonreducing end linked to rhamnose-3-sulfate and glucuronic or iduronic acid (Δ-Rha3S-GlcA/IdoA-Rha3S). Notably, we discovered a new dehydratase (P29_PDnc) acting on the nonreducing end of ulvan oligosaccharides, i.e., GlcA/IdoA-Rha3S, forming the aforementioned unsaturated uronic acid residue. This residue represents the substrate for GH105 glycoside hydrolases, which complements the enzymatic degradation pathway including one ulvan lyase, one multimodular sulfatase, three glycoside hydrolases, and the dehydratase P29_PDnc, the latter being described for the first time. Our research thus shows that the oligosaccharide dehydratase is involved in the degradation of carboxylated polysaccharides into monosaccharides. |
format | Online Article Text |
id | pubmed-8511951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85119512021-10-21 A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan Bäumgen, Marcus Dutschei, Theresa Bartosik, Daniel Suster, Christoph Reisky, Lukas Gerlach, Nadine Stanetty, Christian Mihovilovic, Marko D. Schweder, Thomas Hehemann, Jan-Hendrik Bornscheuer, Uwe T. J Biol Chem Research Article Marine algae catalyze half of all global photosynthetic production of carbohydrates. Owing to their fast growth rates, Ulva spp. rapidly produce substantial amounts of carbohydrate-rich biomass and represent an emerging renewable energy and carbon resource. Their major cell wall polysaccharide is the anionic carbohydrate ulvan. Here, we describe a new enzymatic degradation pathway of the marine bacterium Formosa agariphila for ulvan oligosaccharides involving unsaturated uronic acid at the nonreducing end linked to rhamnose-3-sulfate and glucuronic or iduronic acid (Δ-Rha3S-GlcA/IdoA-Rha3S). Notably, we discovered a new dehydratase (P29_PDnc) acting on the nonreducing end of ulvan oligosaccharides, i.e., GlcA/IdoA-Rha3S, forming the aforementioned unsaturated uronic acid residue. This residue represents the substrate for GH105 glycoside hydrolases, which complements the enzymatic degradation pathway including one ulvan lyase, one multimodular sulfatase, three glycoside hydrolases, and the dehydratase P29_PDnc, the latter being described for the first time. Our research thus shows that the oligosaccharide dehydratase is involved in the degradation of carboxylated polysaccharides into monosaccharides. American Society for Biochemistry and Molecular Biology 2021-09-20 /pmc/articles/PMC8511951/ /pubmed/34547290 http://dx.doi.org/10.1016/j.jbc.2021.101210 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Bäumgen, Marcus Dutschei, Theresa Bartosik, Daniel Suster, Christoph Reisky, Lukas Gerlach, Nadine Stanetty, Christian Mihovilovic, Marko D. Schweder, Thomas Hehemann, Jan-Hendrik Bornscheuer, Uwe T. A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title | A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title_full | A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title_fullStr | A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title_full_unstemmed | A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title_short | A new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
title_sort | new carbohydrate-active oligosaccharide dehydratase is involved in the degradation of ulvan |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511951/ https://www.ncbi.nlm.nih.gov/pubmed/34547290 http://dx.doi.org/10.1016/j.jbc.2021.101210 |
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