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Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices

Certain bacterial species target the polysaccharide glycosaminoglycans (GAGs) of animal extracellular matrices for colonization and/or infection. GAGs such as hyaluronan and chondroitin sulfate consist of repeating disaccharide units of uronate and amino sugar residues, and are depolymerized to unsa...

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Autores principales: Oiki, Sayoko, Nakamichi, Yusuke, Maruyama, Yukie, Mikami, Bunzo, Murata, Kousaku, Hashimoto, Wataru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837340/
https://www.ncbi.nlm.nih.gov/pubmed/31697725
http://dx.doi.org/10.1371/journal.pone.0224753
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author Oiki, Sayoko
Nakamichi, Yusuke
Maruyama, Yukie
Mikami, Bunzo
Murata, Kousaku
Hashimoto, Wataru
author_facet Oiki, Sayoko
Nakamichi, Yusuke
Maruyama, Yukie
Mikami, Bunzo
Murata, Kousaku
Hashimoto, Wataru
author_sort Oiki, Sayoko
collection PubMed
description Certain bacterial species target the polysaccharide glycosaminoglycans (GAGs) of animal extracellular matrices for colonization and/or infection. GAGs such as hyaluronan and chondroitin sulfate consist of repeating disaccharide units of uronate and amino sugar residues, and are depolymerized to unsaturated disaccharides by bacterial extracellular or cell-surface polysaccharide lyase. The disaccharides are degraded and metabolized by cytoplasmic enzymes such as unsaturated glucuronyl hydrolase, isomerase, and reductase. The genes encoding these enzymes are assembled to form a GAG genetic cluster. Here, we demonstrate the Streptococcus agalactiae phosphotransferase system (PTS) for import of unsaturated hyaluronan disaccharide. S. agalactiae NEM316 was found to depolymerize and assimilate hyaluronan, whereas its mutant with a disruption in the PTS genes included in the GAG cluster was unable to grow on hyaluronan, while retaining the ability to depolymerize hyaluronan. Using toluene-treated wild-type cells, the PTS activity for import of unsaturated hyaluronan disaccharide was significantly higher than that observed in the absence of the substrate. In contrast, the PTS mutant was unable to import unsaturated hyaluronan disaccharide, indicating that the corresponding PTS is the only importer of fragmented hyaluronan, which is suitable for PTS to phosphorylate the substrate at the C-6 position. This is distinct from Streptobacillus moniliformis ATP-binding cassette transporter for import of sulfated and non-sulfated fragmented GAGs without substrate modification. The three-dimensional structure of streptococcal EIIA, one of the PTS components, was found to contain a Rossman-fold motif by X-ray crystallization. Docking of EIIA with another component EIIB by modeling provided structural insights into the phosphate transfer mechanism. This study is the first to identify the substrate (unsaturated hyaluronan disaccharide) recognized and imported by the streptococcal PTS. The PTS and ABC transporter for import of GAGs shed light on bacterial clever colonization/infection system targeting various animal polysaccharides.
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spelling pubmed-68373402019-11-14 Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices Oiki, Sayoko Nakamichi, Yusuke Maruyama, Yukie Mikami, Bunzo Murata, Kousaku Hashimoto, Wataru PLoS One Research Article Certain bacterial species target the polysaccharide glycosaminoglycans (GAGs) of animal extracellular matrices for colonization and/or infection. GAGs such as hyaluronan and chondroitin sulfate consist of repeating disaccharide units of uronate and amino sugar residues, and are depolymerized to unsaturated disaccharides by bacterial extracellular or cell-surface polysaccharide lyase. The disaccharides are degraded and metabolized by cytoplasmic enzymes such as unsaturated glucuronyl hydrolase, isomerase, and reductase. The genes encoding these enzymes are assembled to form a GAG genetic cluster. Here, we demonstrate the Streptococcus agalactiae phosphotransferase system (PTS) for import of unsaturated hyaluronan disaccharide. S. agalactiae NEM316 was found to depolymerize and assimilate hyaluronan, whereas its mutant with a disruption in the PTS genes included in the GAG cluster was unable to grow on hyaluronan, while retaining the ability to depolymerize hyaluronan. Using toluene-treated wild-type cells, the PTS activity for import of unsaturated hyaluronan disaccharide was significantly higher than that observed in the absence of the substrate. In contrast, the PTS mutant was unable to import unsaturated hyaluronan disaccharide, indicating that the corresponding PTS is the only importer of fragmented hyaluronan, which is suitable for PTS to phosphorylate the substrate at the C-6 position. This is distinct from Streptobacillus moniliformis ATP-binding cassette transporter for import of sulfated and non-sulfated fragmented GAGs without substrate modification. The three-dimensional structure of streptococcal EIIA, one of the PTS components, was found to contain a Rossman-fold motif by X-ray crystallization. Docking of EIIA with another component EIIB by modeling provided structural insights into the phosphate transfer mechanism. This study is the first to identify the substrate (unsaturated hyaluronan disaccharide) recognized and imported by the streptococcal PTS. The PTS and ABC transporter for import of GAGs shed light on bacterial clever colonization/infection system targeting various animal polysaccharides. Public Library of Science 2019-11-07 /pmc/articles/PMC6837340/ /pubmed/31697725 http://dx.doi.org/10.1371/journal.pone.0224753 Text en © 2019 Oiki et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Oiki, Sayoko
Nakamichi, Yusuke
Maruyama, Yukie
Mikami, Bunzo
Murata, Kousaku
Hashimoto, Wataru
Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title_full Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title_fullStr Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title_full_unstemmed Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title_short Streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
title_sort streptococcal phosphotransferase system imports unsaturated hyaluronan disaccharide derived from host extracellular matrices
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837340/
https://www.ncbi.nlm.nih.gov/pubmed/31697725
http://dx.doi.org/10.1371/journal.pone.0224753
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