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Comparative genomic analysis of azasugar biosynthesis
Azasugars are monosaccharide analogs in which the ring oxygen is replaced with a nitrogen atom. These well-known glycosidase inhibitors are of interest as therapeutics, yet several aspects of azasugars remain unknown including their distribution, structural diversity, and chemical ecology. The hallm...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382821/ https://www.ncbi.nlm.nih.gov/pubmed/34424396 http://dx.doi.org/10.1186/s13568-021-01279-5 |
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author | Beal, Hailey E. Horenstein, Nicole A. |
author_facet | Beal, Hailey E. Horenstein, Nicole A. |
author_sort | Beal, Hailey E. |
collection | PubMed |
description | Azasugars are monosaccharide analogs in which the ring oxygen is replaced with a nitrogen atom. These well-known glycosidase inhibitors are of interest as therapeutics, yet several aspects of azasugars remain unknown including their distribution, structural diversity, and chemical ecology. The hallmark signature of bacterial azasugar biosynthesis is a three gene cluster (3GC) coding for aminotransferase, phosphatase, and dehydrogenase enzymes. Using the bioinformatics platform Enzyme Similarity Tool (EST), we identified hundreds of putative three gene clusters coding for azasugar production in microbial species. In the course of this work, we also report a consensus sequence for the aminotransferase involved in azasugar biosynthesis as being: SGNXFRXXXFPNXXXXXXXLXVPXPYCXRC. Most clusters are found in Bacillus and Streptomyces species which typically inhabit soil and the rhizosphere, but some clusters are found with diverse species representation such as Photorhabdus and Xenorhabdus which are symbiotic with entomopathogenic nematodes; the human skin commensal Cutibacterium acnes, and the marine Bacillus rugosus SPB7, a symbiont to the sea sponge Spongia officinalis. This pan-taxonomic survey of the azasugar 3GC signature may lead to the identification of new azasugar producers, facilitate studies of their natural functions, and lead to new potential therapeutics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-021-01279-5. |
format | Online Article Text |
id | pubmed-8382821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-83828212021-09-09 Comparative genomic analysis of azasugar biosynthesis Beal, Hailey E. Horenstein, Nicole A. AMB Express Original Article Azasugars are monosaccharide analogs in which the ring oxygen is replaced with a nitrogen atom. These well-known glycosidase inhibitors are of interest as therapeutics, yet several aspects of azasugars remain unknown including their distribution, structural diversity, and chemical ecology. The hallmark signature of bacterial azasugar biosynthesis is a three gene cluster (3GC) coding for aminotransferase, phosphatase, and dehydrogenase enzymes. Using the bioinformatics platform Enzyme Similarity Tool (EST), we identified hundreds of putative three gene clusters coding for azasugar production in microbial species. In the course of this work, we also report a consensus sequence for the aminotransferase involved in azasugar biosynthesis as being: SGNXFRXXXFPNXXXXXXXLXVPXPYCXRC. Most clusters are found in Bacillus and Streptomyces species which typically inhabit soil and the rhizosphere, but some clusters are found with diverse species representation such as Photorhabdus and Xenorhabdus which are symbiotic with entomopathogenic nematodes; the human skin commensal Cutibacterium acnes, and the marine Bacillus rugosus SPB7, a symbiont to the sea sponge Spongia officinalis. This pan-taxonomic survey of the azasugar 3GC signature may lead to the identification of new azasugar producers, facilitate studies of their natural functions, and lead to new potential therapeutics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-021-01279-5. Springer Berlin Heidelberg 2021-08-23 /pmc/articles/PMC8382821/ /pubmed/34424396 http://dx.doi.org/10.1186/s13568-021-01279-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Beal, Hailey E. Horenstein, Nicole A. Comparative genomic analysis of azasugar biosynthesis |
title | Comparative genomic analysis of azasugar biosynthesis |
title_full | Comparative genomic analysis of azasugar biosynthesis |
title_fullStr | Comparative genomic analysis of azasugar biosynthesis |
title_full_unstemmed | Comparative genomic analysis of azasugar biosynthesis |
title_short | Comparative genomic analysis of azasugar biosynthesis |
title_sort | comparative genomic analysis of azasugar biosynthesis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382821/ https://www.ncbi.nlm.nih.gov/pubmed/34424396 http://dx.doi.org/10.1186/s13568-021-01279-5 |
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