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Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger

Acid formation in Aspergillus niger is known to be subjected to tight regulation, and the acid production profiles are fine-tuned to respond to the ambient pH. Based on transcriptome data, putative trans-acting pH responding transcription factors were listed and through knock out studies, mutants ex...

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Autores principales: Poulsen, Lars, Andersen, Mikael Rørdam, Lantz, Anna Eliasson, Thykaer, Jette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520943/
https://www.ncbi.nlm.nih.gov/pubmed/23251373
http://dx.doi.org/10.1371/journal.pone.0050596
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author Poulsen, Lars
Andersen, Mikael Rørdam
Lantz, Anna Eliasson
Thykaer, Jette
author_facet Poulsen, Lars
Andersen, Mikael Rørdam
Lantz, Anna Eliasson
Thykaer, Jette
author_sort Poulsen, Lars
collection PubMed
description Acid formation in Aspergillus niger is known to be subjected to tight regulation, and the acid production profiles are fine-tuned to respond to the ambient pH. Based on transcriptome data, putative trans-acting pH responding transcription factors were listed and through knock out studies, mutants exhibiting an oxalate overproducing phenotype were identified. The yield of oxalate was increased up to 158% compared to the wild type and the corresponding transcription factor was therefore entitled Oxalic Acid repression Factor, OafA. Detailed physiological characterization of one of the ΔoafA mutants, compared to the wild type, showed that both strains produced substantial amounts of gluconic acid, but the mutant strain was more efficient in re-uptake of gluconic acid and converting it to oxalic acid, particularly at high pH (pH 5.0). Transcriptional profiles showed that 241 genes were differentially expressed due to the deletion of oafA and this supported the argument of OafA being a trans-acting transcription factor. Furthermore, expression of two phosphoketolases was down-regulated in the ΔoafA mutant, one of which has not previously been described in fungi. It was argued that the observed oxalate overproducing phenotype was a consequence of the efficient re-uptake of gluconic acid and thereby a higher flux through glycolysis. This results in a lower flux through the pentose phosphate pathway, demonstrated by the down-regulation of the phosphoketolases. Finally, the physiological data, in terms of the specific oxygen consumption, indicated a connection between the oxidative phosphorylation and oxalate production and this was further substantiated through transcription analysis.
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spelling pubmed-35209432012-12-18 Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger Poulsen, Lars Andersen, Mikael Rørdam Lantz, Anna Eliasson Thykaer, Jette PLoS One Research Article Acid formation in Aspergillus niger is known to be subjected to tight regulation, and the acid production profiles are fine-tuned to respond to the ambient pH. Based on transcriptome data, putative trans-acting pH responding transcription factors were listed and through knock out studies, mutants exhibiting an oxalate overproducing phenotype were identified. The yield of oxalate was increased up to 158% compared to the wild type and the corresponding transcription factor was therefore entitled Oxalic Acid repression Factor, OafA. Detailed physiological characterization of one of the ΔoafA mutants, compared to the wild type, showed that both strains produced substantial amounts of gluconic acid, but the mutant strain was more efficient in re-uptake of gluconic acid and converting it to oxalic acid, particularly at high pH (pH 5.0). Transcriptional profiles showed that 241 genes were differentially expressed due to the deletion of oafA and this supported the argument of OafA being a trans-acting transcription factor. Furthermore, expression of two phosphoketolases was down-regulated in the ΔoafA mutant, one of which has not previously been described in fungi. It was argued that the observed oxalate overproducing phenotype was a consequence of the efficient re-uptake of gluconic acid and thereby a higher flux through glycolysis. This results in a lower flux through the pentose phosphate pathway, demonstrated by the down-regulation of the phosphoketolases. Finally, the physiological data, in terms of the specific oxygen consumption, indicated a connection between the oxidative phosphorylation and oxalate production and this was further substantiated through transcription analysis. Public Library of Science 2012-12-12 /pmc/articles/PMC3520943/ /pubmed/23251373 http://dx.doi.org/10.1371/journal.pone.0050596 Text en © 2012 Poulsen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Poulsen, Lars
Andersen, Mikael Rørdam
Lantz, Anna Eliasson
Thykaer, Jette
Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title_full Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title_fullStr Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title_full_unstemmed Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title_short Identification of a Transcription Factor Controlling pH-Dependent Organic Acid Response in Aspergillus niger
title_sort identification of a transcription factor controlling ph-dependent organic acid response in aspergillus niger
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520943/
https://www.ncbi.nlm.nih.gov/pubmed/23251373
http://dx.doi.org/10.1371/journal.pone.0050596
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