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Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253
The genome of Rhodothermus marinus DSM 4253 encodes six glycoside hydrolases (GH) classified under GH family 3 (GH3): RmBgl3A, RmBgl3B, RmBgl3C, RmXyl3A, RmXyl3B and RmNag3. The biochemical function, modelled 3D-structure, gene cluster and evolutionary relationships of each of these enzymes were stu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987092/ https://www.ncbi.nlm.nih.gov/pubmed/31992772 http://dx.doi.org/10.1038/s41598-020-58015-5 |
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author | Ara, Kazi Zubaida Gulshan Månberger, Anna Gabriško, Marek Linares-Pastén, Javier A. Jasilionis, Andrius Friðjónsson, Ólafur H. Hreggviðsson, Guðmundur Ó. Janeček, Štefan Nordberg Karlsson, Eva |
author_facet | Ara, Kazi Zubaida Gulshan Månberger, Anna Gabriško, Marek Linares-Pastén, Javier A. Jasilionis, Andrius Friðjónsson, Ólafur H. Hreggviðsson, Guðmundur Ó. Janeček, Štefan Nordberg Karlsson, Eva |
author_sort | Ara, Kazi Zubaida Gulshan |
collection | PubMed |
description | The genome of Rhodothermus marinus DSM 4253 encodes six glycoside hydrolases (GH) classified under GH family 3 (GH3): RmBgl3A, RmBgl3B, RmBgl3C, RmXyl3A, RmXyl3B and RmNag3. The biochemical function, modelled 3D-structure, gene cluster and evolutionary relationships of each of these enzymes were studied. The six enzymes were clustered into three major evolutionary lineages of GH3: β-N-acetyl-glucosaminidases, β-1,4-glucosidases/β-xylosidases and macrolide β-glucosidases. The RmNag3 with additional β-lactamase domain clustered with the deepest rooted GH3-lineage of β-N-acetyl-glucosaminidases and was active on acetyl-chitooligosaccharides. RmBgl3B displayed β-1,4-glucosidase activity and was the only representative of the lineage clustered with macrolide β-glucosidases from Actinomycetes. The β-xylosidases, RmXyl3A and RmXyl3B, and the β-glucosidases RmBgl3A and RmBgl3C clustered within the major β-glucosidases/β-xylosidases evolutionary lineage. RmXyl3A and RmXyl3B showed β-xylosidase activity with different specificities for para-nitrophenyl (pNP)-linked substrates and xylooligosaccharides. RmBgl3A displayed β-1,4-glucosidase/β-xylosidase activity while RmBgl3C was active on pNP-β-Glc and β-1,3-1,4-linked glucosyl disaccharides. Putative polysaccharide utilization gene clusters were also investigated for both R. marinus DSM 4253 and DSM 4252(T) (homolog strain). The analysis showed that in the homolog strain DSM 4252(T) Rmar_1080 (RmXyl3A) and Rmar_1081 (RmXyl3B) are parts of a putative polysaccharide utilization locus (PUL) for xylan utilization. |
format | Online Article Text |
id | pubmed-6987092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69870922020-01-31 Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 Ara, Kazi Zubaida Gulshan Månberger, Anna Gabriško, Marek Linares-Pastén, Javier A. Jasilionis, Andrius Friðjónsson, Ólafur H. Hreggviðsson, Guðmundur Ó. Janeček, Štefan Nordberg Karlsson, Eva Sci Rep Article The genome of Rhodothermus marinus DSM 4253 encodes six glycoside hydrolases (GH) classified under GH family 3 (GH3): RmBgl3A, RmBgl3B, RmBgl3C, RmXyl3A, RmXyl3B and RmNag3. The biochemical function, modelled 3D-structure, gene cluster and evolutionary relationships of each of these enzymes were studied. The six enzymes were clustered into three major evolutionary lineages of GH3: β-N-acetyl-glucosaminidases, β-1,4-glucosidases/β-xylosidases and macrolide β-glucosidases. The RmNag3 with additional β-lactamase domain clustered with the deepest rooted GH3-lineage of β-N-acetyl-glucosaminidases and was active on acetyl-chitooligosaccharides. RmBgl3B displayed β-1,4-glucosidase activity and was the only representative of the lineage clustered with macrolide β-glucosidases from Actinomycetes. The β-xylosidases, RmXyl3A and RmXyl3B, and the β-glucosidases RmBgl3A and RmBgl3C clustered within the major β-glucosidases/β-xylosidases evolutionary lineage. RmXyl3A and RmXyl3B showed β-xylosidase activity with different specificities for para-nitrophenyl (pNP)-linked substrates and xylooligosaccharides. RmBgl3A displayed β-1,4-glucosidase/β-xylosidase activity while RmBgl3C was active on pNP-β-Glc and β-1,3-1,4-linked glucosyl disaccharides. Putative polysaccharide utilization gene clusters were also investigated for both R. marinus DSM 4253 and DSM 4252(T) (homolog strain). The analysis showed that in the homolog strain DSM 4252(T) Rmar_1080 (RmXyl3A) and Rmar_1081 (RmXyl3B) are parts of a putative polysaccharide utilization locus (PUL) for xylan utilization. Nature Publishing Group UK 2020-01-28 /pmc/articles/PMC6987092/ /pubmed/31992772 http://dx.doi.org/10.1038/s41598-020-58015-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ara, Kazi Zubaida Gulshan Månberger, Anna Gabriško, Marek Linares-Pastén, Javier A. Jasilionis, Andrius Friðjónsson, Ólafur H. Hreggviðsson, Guðmundur Ó. Janeček, Štefan Nordberg Karlsson, Eva Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title | Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title_full | Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title_fullStr | Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title_full_unstemmed | Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title_short | Characterization and diversity of the complete set of GH family 3 enzymes from Rhodothermus marinus DSM 4253 |
title_sort | characterization and diversity of the complete set of gh family 3 enzymes from rhodothermus marinus dsm 4253 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987092/ https://www.ncbi.nlm.nih.gov/pubmed/31992772 http://dx.doi.org/10.1038/s41598-020-58015-5 |
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