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Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532
Desulfurococcus amylolyticus DSM 16532 is an anaerobic and hyperthermophilic crenarchaeon known to grow on a variety of different carbon sources, including monosaccharides and polysaccharides. Furthermore, D. amylolyticus is one of the few archaea that are known to be able to grow on cellulose. Here...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182646/ https://www.ncbi.nlm.nih.gov/pubmed/29797222 http://dx.doi.org/10.1007/s12223-018-0612-5 |
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author | Reischl, Barbara Ergal, İpek Rittmann, Simon K.-M. R. |
author_facet | Reischl, Barbara Ergal, İpek Rittmann, Simon K.-M. R. |
author_sort | Reischl, Barbara |
collection | PubMed |
description | Desulfurococcus amylolyticus DSM 16532 is an anaerobic and hyperthermophilic crenarchaeon known to grow on a variety of different carbon sources, including monosaccharides and polysaccharides. Furthermore, D. amylolyticus is one of the few archaea that are known to be able to grow on cellulose. Here, we present the metabolic reconstruction of D. amylolyticus’ central carbon metabolism. Based on the published genome, the metabolic reconstruction was completed by integrating complementary information available from the KEGG, BRENDA, UniProt, NCBI, and PFAM databases, as well as from available literature. The genomic analysis of D. amylolyticus revealed genes for both the classical and the archaeal version of the Embden-Meyerhof pathway. The metabolic reconstruction highlighted gaps in carbon dioxide-fixation pathways. No complete carbon dioxide-fixation pathway such as the reductive citrate cycle or the dicarboxylate-4-hydroxybutyrate cycle could be identified. However, the metabolic reconstruction indicated that D. amylolyticus harbors all genes necessary for glucose metabolization. Closed batch experimental verification of glucose utilization by D. amylolyticus was performed in chemically defined medium. The findings from in silico analyses and from growth experiments are discussed with respect to physiological features of hyperthermophilic organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12223-018-0612-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-61826462018-10-24 Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 Reischl, Barbara Ergal, İpek Rittmann, Simon K.-M. R. Folia Microbiol (Praha) Original Article Desulfurococcus amylolyticus DSM 16532 is an anaerobic and hyperthermophilic crenarchaeon known to grow on a variety of different carbon sources, including monosaccharides and polysaccharides. Furthermore, D. amylolyticus is one of the few archaea that are known to be able to grow on cellulose. Here, we present the metabolic reconstruction of D. amylolyticus’ central carbon metabolism. Based on the published genome, the metabolic reconstruction was completed by integrating complementary information available from the KEGG, BRENDA, UniProt, NCBI, and PFAM databases, as well as from available literature. The genomic analysis of D. amylolyticus revealed genes for both the classical and the archaeal version of the Embden-Meyerhof pathway. The metabolic reconstruction highlighted gaps in carbon dioxide-fixation pathways. No complete carbon dioxide-fixation pathway such as the reductive citrate cycle or the dicarboxylate-4-hydroxybutyrate cycle could be identified. However, the metabolic reconstruction indicated that D. amylolyticus harbors all genes necessary for glucose metabolization. Closed batch experimental verification of glucose utilization by D. amylolyticus was performed in chemically defined medium. The findings from in silico analyses and from growth experiments are discussed with respect to physiological features of hyperthermophilic organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12223-018-0612-5) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-05-24 2018 /pmc/articles/PMC6182646/ /pubmed/29797222 http://dx.doi.org/10.1007/s12223-018-0612-5 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Reischl, Barbara Ergal, İpek Rittmann, Simon K.-M. R. Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title | Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title_full | Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title_fullStr | Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title_full_unstemmed | Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title_short | Metabolic reconstruction and experimental verification of glucose utilization in Desulfurococcus amylolyticus DSM 16532 |
title_sort | metabolic reconstruction and experimental verification of glucose utilization in desulfurococcus amylolyticus dsm 16532 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182646/ https://www.ncbi.nlm.nih.gov/pubmed/29797222 http://dx.doi.org/10.1007/s12223-018-0612-5 |
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