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A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria
Heptoses are important structural components of Gram-negative bacterium cell wall and participate in bacterial colonization, infection, and immune recognition. Current knowledge of NDP-heptose originating from d-sedoheptulose 7-phosphate in Grampositive bacterium remains limited. Here, in silico ana...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Science China Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502628/ https://www.ncbi.nlm.nih.gov/pubmed/34632535 http://dx.doi.org/10.1007/s11427-021-2000-2 |
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author | Tang, Yue Tang, Wei Wang, Min Zhang, Zhilong Chen, Yihua |
author_facet | Tang, Yue Tang, Wei Wang, Min Zhang, Zhilong Chen, Yihua |
author_sort | Tang, Yue |
collection | PubMed |
description | Heptoses are important structural components of Gram-negative bacterium cell wall and participate in bacterial colonization, infection, and immune recognition. Current knowledge of NDP-heptose originating from d-sedoheptulose 7-phosphate in Grampositive bacterium remains limited. Here, in silico analysis suggested that the special tridomain NDP-heptose synthetases with isomerase, kinase, and nucleotidyltransferase activities are conservatively distributed in Actinobacteria class of Gram-positive bacterium. Enzymatical characterization of the tridomain proteins from different strains showed that they are involved in ADP-d-glycero-β-d-manno-heptose biosynthesis despite the unexpected discovery of kinase activities deficient in some proteins. The presence of three types of NDP-heptose synthetases in Gram-positive bacterium suggests that it is also a rich source of heptoses and the heptose moieties may play important roles in vivo. Our work updates the understanding of NDP-heptose biosynthesis in Gram-positive bacterium and lays a solid foundation for further physiological function explorations. SUPPORTING INFORMATION: The supporting information is available online at 10.1007/s11427-021-2000-2. The supporting materials are published as submitted, without typesetting or editing. The responsibility for scientific accuracy and content remains entirely with the authors. |
format | Online Article Text |
id | pubmed-8502628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Science China Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85026282021-10-12 A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria Tang, Yue Tang, Wei Wang, Min Zhang, Zhilong Chen, Yihua Sci China Life Sci Research Paper Heptoses are important structural components of Gram-negative bacterium cell wall and participate in bacterial colonization, infection, and immune recognition. Current knowledge of NDP-heptose originating from d-sedoheptulose 7-phosphate in Grampositive bacterium remains limited. Here, in silico analysis suggested that the special tridomain NDP-heptose synthetases with isomerase, kinase, and nucleotidyltransferase activities are conservatively distributed in Actinobacteria class of Gram-positive bacterium. Enzymatical characterization of the tridomain proteins from different strains showed that they are involved in ADP-d-glycero-β-d-manno-heptose biosynthesis despite the unexpected discovery of kinase activities deficient in some proteins. The presence of three types of NDP-heptose synthetases in Gram-positive bacterium suggests that it is also a rich source of heptoses and the heptose moieties may play important roles in vivo. Our work updates the understanding of NDP-heptose biosynthesis in Gram-positive bacterium and lays a solid foundation for further physiological function explorations. SUPPORTING INFORMATION: The supporting information is available online at 10.1007/s11427-021-2000-2. The supporting materials are published as submitted, without typesetting or editing. The responsibility for scientific accuracy and content remains entirely with the authors. Science China Press 2021-10-08 2022 /pmc/articles/PMC8502628/ /pubmed/34632535 http://dx.doi.org/10.1007/s11427-021-2000-2 Text en © Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Research Paper Tang, Yue Tang, Wei Wang, Min Zhang, Zhilong Chen, Yihua A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title | A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title_full | A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title_fullStr | A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title_full_unstemmed | A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title_short | A conservative distribution of tridomain NDP-heptose synthetases in actinobacteria |
title_sort | conservative distribution of tridomain ndp-heptose synthetases in actinobacteria |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502628/ https://www.ncbi.nlm.nih.gov/pubmed/34632535 http://dx.doi.org/10.1007/s11427-021-2000-2 |
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