Cargando…

Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components

Fungi produce a wide range of enzymes that allow them to grow on diverse plant biomass. Wheat bran is a low‐cost substrate with high potential for biotechnological applications. It mainly contains cellulose and (arabino)xylan, as well as starch, proteins, lipids and lignin to a lesser extent. In thi...

Descripción completa

Detalles Bibliográficos
Autores principales: Kun, Roland S., Garrigues, Sandra, Di Falco, Marcos, Tsang, Adrian, de Vries, Ronald P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313289/
https://www.ncbi.nlm.nih.gov/pubmed/34114741
http://dx.doi.org/10.1111/1751-7915.13835
_version_ 1783729314099888128
author Kun, Roland S.
Garrigues, Sandra
Di Falco, Marcos
Tsang, Adrian
de Vries, Ronald P.
author_facet Kun, Roland S.
Garrigues, Sandra
Di Falco, Marcos
Tsang, Adrian
de Vries, Ronald P.
author_sort Kun, Roland S.
collection PubMed
description Fungi produce a wide range of enzymes that allow them to grow on diverse plant biomass. Wheat bran is a low‐cost substrate with high potential for biotechnological applications. It mainly contains cellulose and (arabino)xylan, as well as starch, proteins, lipids and lignin to a lesser extent. In this study, we dissected the regulatory network governing wheat bran degradation in Aspergillus niger to assess the relative contribution of the regulators to the utilization of this plant biomass substrate. Deletion of genes encoding transcription factors involved in (hemi‐)cellulose utilization (XlnR, AraR, ClrA and ClrB) individually and in combination significantly reduced production of polysaccharide‐degrading enzymes, but retained substantial growth on wheat bran. Proteomic analysis suggested the ability of A. niger to grow on other carbon components, such as starch, which was confirmed by the additional deletion of the amylolytic regulator AmyR. Growth was further reduced but not impaired, indicating that other minor components provide sufficient energy for residual growth, displaying the flexibility of A. niger, and likely other fungi, in carbon utilization. Better understanding of the complexity and flexibility of fungal regulatory networks will facilitate the generation of more efficient fungal cell factories that use plant biomass as a substrate.
format Online
Article
Text
id pubmed-8313289
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-83132892021-07-30 Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components Kun, Roland S. Garrigues, Sandra Di Falco, Marcos Tsang, Adrian de Vries, Ronald P. Microb Biotechnol Research Articles Fungi produce a wide range of enzymes that allow them to grow on diverse plant biomass. Wheat bran is a low‐cost substrate with high potential for biotechnological applications. It mainly contains cellulose and (arabino)xylan, as well as starch, proteins, lipids and lignin to a lesser extent. In this study, we dissected the regulatory network governing wheat bran degradation in Aspergillus niger to assess the relative contribution of the regulators to the utilization of this plant biomass substrate. Deletion of genes encoding transcription factors involved in (hemi‐)cellulose utilization (XlnR, AraR, ClrA and ClrB) individually and in combination significantly reduced production of polysaccharide‐degrading enzymes, but retained substantial growth on wheat bran. Proteomic analysis suggested the ability of A. niger to grow on other carbon components, such as starch, which was confirmed by the additional deletion of the amylolytic regulator AmyR. Growth was further reduced but not impaired, indicating that other minor components provide sufficient energy for residual growth, displaying the flexibility of A. niger, and likely other fungi, in carbon utilization. Better understanding of the complexity and flexibility of fungal regulatory networks will facilitate the generation of more efficient fungal cell factories that use plant biomass as a substrate. John Wiley and Sons Inc. 2021-06-11 /pmc/articles/PMC8313289/ /pubmed/34114741 http://dx.doi.org/10.1111/1751-7915.13835 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kun, Roland S.
Garrigues, Sandra
Di Falco, Marcos
Tsang, Adrian
de Vries, Ronald P.
Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title_full Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title_fullStr Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title_full_unstemmed Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title_short Blocking utilization of major plant biomass polysaccharides leads Aspergillus niger towards utilization of minor components
title_sort blocking utilization of major plant biomass polysaccharides leads aspergillus niger towards utilization of minor components
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313289/
https://www.ncbi.nlm.nih.gov/pubmed/34114741
http://dx.doi.org/10.1111/1751-7915.13835
work_keys_str_mv AT kunrolands blockingutilizationofmajorplantbiomasspolysaccharidesleadsaspergillusnigertowardsutilizationofminorcomponents
AT garriguessandra blockingutilizationofmajorplantbiomasspolysaccharidesleadsaspergillusnigertowardsutilizationofminorcomponents
AT difalcomarcos blockingutilizationofmajorplantbiomasspolysaccharidesleadsaspergillusnigertowardsutilizationofminorcomponents
AT tsangadrian blockingutilizationofmajorplantbiomasspolysaccharidesleadsaspergillusnigertowardsutilizationofminorcomponents
AT devriesronaldp blockingutilizationofmajorplantbiomasspolysaccharidesleadsaspergillusnigertowardsutilizationofminorcomponents