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Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger

Filamentous fungi are important producers of plant polysaccharide degrading enzymes that are used in many industrial applications. These enzymes are produced by the fungus to liberate monomeric sugars that are used as carbon source. Two of the main components of plant polysaccharides are l-arabinose...

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Autores principales: Battaglia, Evy, Hansen, Sara Fasmer, Leendertse, Anne, Madrid, Susan, Mulder, Harm, Nikolaev, Igor, de Vries, Ronald P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125510/
https://www.ncbi.nlm.nih.gov/pubmed/21484208
http://dx.doi.org/10.1007/s00253-011-3242-2
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author Battaglia, Evy
Hansen, Sara Fasmer
Leendertse, Anne
Madrid, Susan
Mulder, Harm
Nikolaev, Igor
de Vries, Ronald P.
author_facet Battaglia, Evy
Hansen, Sara Fasmer
Leendertse, Anne
Madrid, Susan
Mulder, Harm
Nikolaev, Igor
de Vries, Ronald P.
author_sort Battaglia, Evy
collection PubMed
description Filamentous fungi are important producers of plant polysaccharide degrading enzymes that are used in many industrial applications. These enzymes are produced by the fungus to liberate monomeric sugars that are used as carbon source. Two of the main components of plant polysaccharides are l-arabinose and d-xylose, which are metabolized through the pentose catabolic pathway (PCP) in these fungi. In Aspergillus niger, the regulation of pentose release from polysaccharides and the PCP involves the transcriptional activators AraR and XlnR, which are also present in other Aspergilli such as Aspergillus nidulans. The comparative analysis revealed that the regulation of the PCP by AraR differs in A. nidulans and A. niger, whereas the regulation of the PCP by XlnR was similar in both species. This was demonstrated by the growth differences on l-arabinose between disruptant strains for araR and xlnR in A. nidulans and A. niger. In addition, the expression profiles of genes encoding l-arabinose reductase (larA), l-arabitol dehydrogenase (ladA) and xylitol dehydrogenase (xdhA) differed in these strains. This data suggests evolutionary changes in these two species that affect pentose utilisation. This study also implies that manipulating regulatory systems to improve the production of polysaccharide degrading enzymes, may give different results in different industrial fungi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-011-3242-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-31255102011-08-09 Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger Battaglia, Evy Hansen, Sara Fasmer Leendertse, Anne Madrid, Susan Mulder, Harm Nikolaev, Igor de Vries, Ronald P. Appl Microbiol Biotechnol Applied Microbial and Cell Physiology Filamentous fungi are important producers of plant polysaccharide degrading enzymes that are used in many industrial applications. These enzymes are produced by the fungus to liberate monomeric sugars that are used as carbon source. Two of the main components of plant polysaccharides are l-arabinose and d-xylose, which are metabolized through the pentose catabolic pathway (PCP) in these fungi. In Aspergillus niger, the regulation of pentose release from polysaccharides and the PCP involves the transcriptional activators AraR and XlnR, which are also present in other Aspergilli such as Aspergillus nidulans. The comparative analysis revealed that the regulation of the PCP by AraR differs in A. nidulans and A. niger, whereas the regulation of the PCP by XlnR was similar in both species. This was demonstrated by the growth differences on l-arabinose between disruptant strains for araR and xlnR in A. nidulans and A. niger. In addition, the expression profiles of genes encoding l-arabinose reductase (larA), l-arabitol dehydrogenase (ladA) and xylitol dehydrogenase (xdhA) differed in these strains. This data suggests evolutionary changes in these two species that affect pentose utilisation. This study also implies that manipulating regulatory systems to improve the production of polysaccharide degrading enzymes, may give different results in different industrial fungi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-011-3242-2) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-04-12 2011 /pmc/articles/PMC3125510/ /pubmed/21484208 http://dx.doi.org/10.1007/s00253-011-3242-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Applied Microbial and Cell Physiology
Battaglia, Evy
Hansen, Sara Fasmer
Leendertse, Anne
Madrid, Susan
Mulder, Harm
Nikolaev, Igor
de Vries, Ronald P.
Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title_full Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title_fullStr Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title_full_unstemmed Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title_short Regulation of pentose utilisation by AraR, but not XlnR, differs in Aspergillus nidulans and Aspergillus niger
title_sort regulation of pentose utilisation by arar, but not xlnr, differs in aspergillus nidulans and aspergillus niger
topic Applied Microbial and Cell Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125510/
https://www.ncbi.nlm.nih.gov/pubmed/21484208
http://dx.doi.org/10.1007/s00253-011-3242-2
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