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The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger

Aspergillus niger is widely used as a cell factory for the industrial production of enzymes. Previously, it was shown that deletion of α-1–3 glucan synthase genes results in smaller micro-colonies in liquid cultures of Aspergillus nidulans. Also, it has been shown that small wild-type Aspergillus ni...

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Autores principales: Lyu, Jun, Torchia, Costanza, Post, Harm, Moran Torres, Juan P., Altelaar, A. F. Maarten, de Cock, Hans, Wösten, Han A. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371888/
https://www.ncbi.nlm.nih.gov/pubmed/37316742
http://dx.doi.org/10.1007/s10482-023-01853-w
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author Lyu, Jun
Torchia, Costanza
Post, Harm
Moran Torres, Juan P.
Altelaar, A. F. Maarten
de Cock, Hans
Wösten, Han A. B.
author_facet Lyu, Jun
Torchia, Costanza
Post, Harm
Moran Torres, Juan P.
Altelaar, A. F. Maarten
de Cock, Hans
Wösten, Han A. B.
author_sort Lyu, Jun
collection PubMed
description Aspergillus niger is widely used as a cell factory for the industrial production of enzymes. Previously, it was shown that deletion of α-1–3 glucan synthase genes results in smaller micro-colonies in liquid cultures of Aspergillus nidulans. Also, it has been shown that small wild-type Aspergillus niger micro-colonies secrete more protein than large mirco-colonies. We here assessed whether deletion of the agsC or agsE α-1–3 glucan synthase genes results in smaller A. niger micro-colonies and whether this is accompanied by a change in protein secretion. Biomass formation was not affected in the deletion strains but pH of the culture medium had changed from 5.2 in the case of the wild-type to 4.6 and 6.4 for ΔagsC and ΔagsE, respectively. The diameter of the ΔagsC micro-colonies was not affected in liquid cultures. In contrast, diameter of the ΔagsE micro-colonies was reduced from 3304 ± 338 µm to 1229 ± 113 µm. Moreover, the ΔagsE secretome was affected with 54 and 36 unique proteins with a predicted signal peptide in the culture medium of MA234.1 and the ΔagsE, respectively. Results show that these strains have complementary cellulase activity and thus may have complementary activity on plant biomass degradation. Together, α-1–3 glucan synthesis (in)directly impacts protein secretion in A. niger. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10482-023-01853-w.
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spelling pubmed-103718882023-07-28 The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger Lyu, Jun Torchia, Costanza Post, Harm Moran Torres, Juan P. Altelaar, A. F. Maarten de Cock, Hans Wösten, Han A. B. Antonie Van Leeuwenhoek Original Paper Aspergillus niger is widely used as a cell factory for the industrial production of enzymes. Previously, it was shown that deletion of α-1–3 glucan synthase genes results in smaller micro-colonies in liquid cultures of Aspergillus nidulans. Also, it has been shown that small wild-type Aspergillus niger micro-colonies secrete more protein than large mirco-colonies. We here assessed whether deletion of the agsC or agsE α-1–3 glucan synthase genes results in smaller A. niger micro-colonies and whether this is accompanied by a change in protein secretion. Biomass formation was not affected in the deletion strains but pH of the culture medium had changed from 5.2 in the case of the wild-type to 4.6 and 6.4 for ΔagsC and ΔagsE, respectively. The diameter of the ΔagsC micro-colonies was not affected in liquid cultures. In contrast, diameter of the ΔagsE micro-colonies was reduced from 3304 ± 338 µm to 1229 ± 113 µm. Moreover, the ΔagsE secretome was affected with 54 and 36 unique proteins with a predicted signal peptide in the culture medium of MA234.1 and the ΔagsE, respectively. Results show that these strains have complementary cellulase activity and thus may have complementary activity on plant biomass degradation. Together, α-1–3 glucan synthesis (in)directly impacts protein secretion in A. niger. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10482-023-01853-w. Springer International Publishing 2023-06-14 2023 /pmc/articles/PMC10371888/ /pubmed/37316742 http://dx.doi.org/10.1007/s10482-023-01853-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Lyu, Jun
Torchia, Costanza
Post, Harm
Moran Torres, Juan P.
Altelaar, A. F. Maarten
de Cock, Hans
Wösten, Han A. B.
The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title_full The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title_fullStr The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title_full_unstemmed The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title_short The α-(1,3)-glucan synthase gene agsE impacts the secretome of Aspergillus niger
title_sort α-(1,3)-glucan synthase gene agse impacts the secretome of aspergillus niger
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371888/
https://www.ncbi.nlm.nih.gov/pubmed/37316742
http://dx.doi.org/10.1007/s10482-023-01853-w
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