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Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters

BACKGROUND: The development of biological processes that replace the existing petrochemical-based industry is one of the biggest challenges in biotechnology. Aspergillus niger is one of the main industrial producers of lignocellulolytic enzymes, which are used in the conversion of lignocellulosic fe...

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Autores principales: Sloothaak, J., Odoni, D. I., de Graaff, L. H., Martins dos Santos, V. A. P., Schaap, P. J., Tamayo-Ramos, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574540/
https://www.ncbi.nlm.nih.gov/pubmed/26388937
http://dx.doi.org/10.1186/s13068-015-0317-9
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author Sloothaak, J.
Odoni, D. I.
de Graaff, L. H.
Martins dos Santos, V. A. P.
Schaap, P. J.
Tamayo-Ramos, J. A.
author_facet Sloothaak, J.
Odoni, D. I.
de Graaff, L. H.
Martins dos Santos, V. A. P.
Schaap, P. J.
Tamayo-Ramos, J. A.
author_sort Sloothaak, J.
collection PubMed
description BACKGROUND: The development of biological processes that replace the existing petrochemical-based industry is one of the biggest challenges in biotechnology. Aspergillus niger is one of the main industrial producers of lignocellulolytic enzymes, which are used in the conversion of lignocellulosic feedstocks into fermentable sugars. Both the hydrolytic enzymes responsible for lignocellulose depolymerisation and the molecular mechanisms controlling their expression have been well described, but little is known about the transport systems for sugar uptake in A. niger. Understanding the transportome of A. niger is essential to achieve further improvements at strain and process design level. Therefore, this study aims to identify and classify A. niger sugar transporters, using newly developed tools for in silico and in vivo analysis of its membrane-associated proteome. RESULTS: In the present research work, a hidden Markov model (HMM), that shows a good performance in the identification and segmentation of functionally validated glucose transporters, was constructed. The model (HMM(gluT)) was used to analyse the A. niger membrane-associated proteome response to high and low glucose concentrations at a low pH. By combining the abundance patterns of the proteins found in the A. niger plasmalemma proteome with their HMM(gluT) scores, two new putative high-affinity glucose transporters, denoted MstG and MstH, were identified. MstG and MstH were functionally validated and biochemically characterised by heterologous expression in a S. cerevisiae glucose transport null mutant. They were shown to be a high-affinity glucose transporter (K(m) = 0.5 ± 0.04 mM) and a very high-affinity glucose transporter (K(m) = 0.06 ± 0.005 mM), respectively. CONCLUSIONS: This study, focusing for the first time on the membrane-associated proteome of the industrially relevant organism A. niger, shows the global response of the transportome to the availability of different glucose concentrations. Analysis of the A. niger transportome with the newly developed HMM(gluT) showed to be an efficient approach for the identification and classification of new glucose transporters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0317-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-45745402015-09-19 Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters Sloothaak, J. Odoni, D. I. de Graaff, L. H. Martins dos Santos, V. A. P. Schaap, P. J. Tamayo-Ramos, J. A. Biotechnol Biofuels Research Article BACKGROUND: The development of biological processes that replace the existing petrochemical-based industry is one of the biggest challenges in biotechnology. Aspergillus niger is one of the main industrial producers of lignocellulolytic enzymes, which are used in the conversion of lignocellulosic feedstocks into fermentable sugars. Both the hydrolytic enzymes responsible for lignocellulose depolymerisation and the molecular mechanisms controlling their expression have been well described, but little is known about the transport systems for sugar uptake in A. niger. Understanding the transportome of A. niger is essential to achieve further improvements at strain and process design level. Therefore, this study aims to identify and classify A. niger sugar transporters, using newly developed tools for in silico and in vivo analysis of its membrane-associated proteome. RESULTS: In the present research work, a hidden Markov model (HMM), that shows a good performance in the identification and segmentation of functionally validated glucose transporters, was constructed. The model (HMM(gluT)) was used to analyse the A. niger membrane-associated proteome response to high and low glucose concentrations at a low pH. By combining the abundance patterns of the proteins found in the A. niger plasmalemma proteome with their HMM(gluT) scores, two new putative high-affinity glucose transporters, denoted MstG and MstH, were identified. MstG and MstH were functionally validated and biochemically characterised by heterologous expression in a S. cerevisiae glucose transport null mutant. They were shown to be a high-affinity glucose transporter (K(m) = 0.5 ± 0.04 mM) and a very high-affinity glucose transporter (K(m) = 0.06 ± 0.005 mM), respectively. CONCLUSIONS: This study, focusing for the first time on the membrane-associated proteome of the industrially relevant organism A. niger, shows the global response of the transportome to the availability of different glucose concentrations. Analysis of the A. niger transportome with the newly developed HMM(gluT) showed to be an efficient approach for the identification and classification of new glucose transporters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0317-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-17 /pmc/articles/PMC4574540/ /pubmed/26388937 http://dx.doi.org/10.1186/s13068-015-0317-9 Text en © Sloothaak et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sloothaak, J.
Odoni, D. I.
de Graaff, L. H.
Martins dos Santos, V. A. P.
Schaap, P. J.
Tamayo-Ramos, J. A.
Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title_full Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title_fullStr Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title_full_unstemmed Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title_short Aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
title_sort aspergillus niger membrane-associated proteome analysis for the identification of glucose transporters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574540/
https://www.ncbi.nlm.nih.gov/pubmed/26388937
http://dx.doi.org/10.1186/s13068-015-0317-9
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