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Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation
A central step in nucleoside and nucleobase salvage pathways is the hydrolysis of nucleosides to their respective nucleobases. In plants this is solely accomplished by nucleosidases (EC 3.2.2.x). To elucidate the importance of nucleosidases for nucleoside degradation, general metabolism, and plant g...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3147060/ https://www.ncbi.nlm.nih.gov/pubmed/21599668 http://dx.doi.org/10.1111/j.1469-8137.2011.03711.x |
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author | Riegler, Heike Geserick, Claudia Zrenner, Rita |
author_facet | Riegler, Heike Geserick, Claudia Zrenner, Rita |
author_sort | Riegler, Heike |
collection | PubMed |
description | A central step in nucleoside and nucleobase salvage pathways is the hydrolysis of nucleosides to their respective nucleobases. In plants this is solely accomplished by nucleosidases (EC 3.2.2.x). To elucidate the importance of nucleosidases for nucleoside degradation, general metabolism, and plant growth, thorough phenotypic and biochemical analyses were performed using Arabidopsis thaliana T-DNA insertion mutants lacking expression of the previously identified genes annotated as uridine ribohydrolases (URH1 and URH2). Comprehensive functional analyses of single and double mutants demonstrated that both isoforms are unimportant for seedling establishment and plant growth, while one participates in uridine degradation. Rather unexpectedly, nucleoside and nucleotide profiling and nucleosidase activity screening of soluble crude extracts revealed a deficiency of xanthosine and inosine hydrolysis in the single mutants, with substantial accumulation of xanthosine in one of them. Mixing of the two mutant extracts, and by in vitro activity reconstitution using a mixture of recombinant URH1 and URH2 proteins, both restored activity, thus providing biochemical evidence that at least these two isoforms are needed for inosine and xanthosine hydrolysis. This mutant study demonstrates the utility of in vivo systems for the examination of metabolic activities, with the discovery of the new substrate xanthosine and elucidation of a mechanism for expanding the nucleosidase substrate spectrum. |
format | Online Article Text |
id | pubmed-3147060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-31470602011-08-03 Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation Riegler, Heike Geserick, Claudia Zrenner, Rita New Phytol Research A central step in nucleoside and nucleobase salvage pathways is the hydrolysis of nucleosides to their respective nucleobases. In plants this is solely accomplished by nucleosidases (EC 3.2.2.x). To elucidate the importance of nucleosidases for nucleoside degradation, general metabolism, and plant growth, thorough phenotypic and biochemical analyses were performed using Arabidopsis thaliana T-DNA insertion mutants lacking expression of the previously identified genes annotated as uridine ribohydrolases (URH1 and URH2). Comprehensive functional analyses of single and double mutants demonstrated that both isoforms are unimportant for seedling establishment and plant growth, while one participates in uridine degradation. Rather unexpectedly, nucleoside and nucleotide profiling and nucleosidase activity screening of soluble crude extracts revealed a deficiency of xanthosine and inosine hydrolysis in the single mutants, with substantial accumulation of xanthosine in one of them. Mixing of the two mutant extracts, and by in vitro activity reconstitution using a mixture of recombinant URH1 and URH2 proteins, both restored activity, thus providing biochemical evidence that at least these two isoforms are needed for inosine and xanthosine hydrolysis. This mutant study demonstrates the utility of in vivo systems for the examination of metabolic activities, with the discovery of the new substrate xanthosine and elucidation of a mechanism for expanding the nucleosidase substrate spectrum. Blackwell Publishing Ltd 2011-07 /pmc/articles/PMC3147060/ /pubmed/21599668 http://dx.doi.org/10.1111/j.1469-8137.2011.03711.x Text en Copyright © 2011 New Phytologist Trust http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Riegler, Heike Geserick, Claudia Zrenner, Rita Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title | Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title_full | Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title_fullStr | Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title_full_unstemmed | Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title_short | Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
title_sort | arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3147060/ https://www.ncbi.nlm.nih.gov/pubmed/21599668 http://dx.doi.org/10.1111/j.1469-8137.2011.03711.x |
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