The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen

Abstract Advances in tissue printing and wound healing necessitate a continuous global supply of collagen. Microbial systems are highly desirable to meet these demands as recombinant collagenous proteins can be guaranteed as free from animal viruses. The filamentous cell factory Aspergillus niger ha...

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Main Authors: Tom Morris, Friederike Gerstl, Sascha Jung, Timothy C. Cairns, Vera Meyer
Format: Article
Language:English
Published: BMC 2025-08-01
Series:Biotechnology for Biofuels and Bioproducts
Subjects:
Online Access:https://doi.org/10.1186/s13068-025-02681-y
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author Tom Morris
Friederike Gerstl
Sascha Jung
Timothy C. Cairns
Vera Meyer
author_facet Tom Morris
Friederike Gerstl
Sascha Jung
Timothy C. Cairns
Vera Meyer
author_sort Tom Morris
collection DOAJ
description Abstract Advances in tissue printing and wound healing necessitate a continuous global supply of collagen. Microbial systems are highly desirable to meet these demands as recombinant collagenous proteins can be guaranteed as free from animal viruses. The filamentous cell factory Aspergillus niger has been instrumental for decades in the production of organic acids, enzymes and proteins, yet this fungus has not been explored for recombinant collagen production. In this study, we conducted extensive genetic engineering and fermentation optimization to provide proof of principle that A. niger can produce hydroxylated collagen. We used a modular cloning system to generate a suite of cassettes encoding numerous N-terminal secretion signals, native collagen genes and, additionally, various prolyl-4-hydroxylases (P4H) for protein hydroxylation. Collagen transcription was supported by both luciferase reporter and eGFP tagged approaches. Peptide sequencing from culture supernatant confirmed A. niger produced partially hydroxylated collagen. We then conducted a range of media optimizations and RNA sequencing to, respectively, increase collagen production and identify proteases which we hypothesized were detrimental to recombinant protein titers. Thus, we deleted an endopeptidase encoding gene, protA, which was likely responsible for degrading secreting collagen. Ultimately, we were able to generate an isolate capable of producing hydroxylated collagen at titers of 5 mgL−1 in shake flask models of fermentation. This study thus proves A. niger is a promising heterologous system to address the demand for virus-free collagen.
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series Biotechnology for Biofuels and Bioproducts
spelling doaj-art-291fe63c1fe64f1cb33d8b4a7ded0dca2025-08-20T04:01:53ZengBMCBiotechnology for Biofuels and Bioproducts2731-36542025-08-0118111510.1186/s13068-025-02681-yThe multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagenTom Morris0Friederike Gerstl1Sascha Jung2Timothy C. Cairns3Vera Meyer4Chair of Applied and Molecular Microbiology, Institute of Biotechnology, Technische Universität BerlinChair of Applied and Molecular Microbiology, Institute of Biotechnology, Technische Universität BerlinChair of Applied and Molecular Microbiology, Institute of Biotechnology, Technische Universität BerlinChair of Applied and Molecular Microbiology, Institute of Biotechnology, Technische Universität BerlinChair of Applied and Molecular Microbiology, Institute of Biotechnology, Technische Universität BerlinAbstract Advances in tissue printing and wound healing necessitate a continuous global supply of collagen. Microbial systems are highly desirable to meet these demands as recombinant collagenous proteins can be guaranteed as free from animal viruses. The filamentous cell factory Aspergillus niger has been instrumental for decades in the production of organic acids, enzymes and proteins, yet this fungus has not been explored for recombinant collagen production. In this study, we conducted extensive genetic engineering and fermentation optimization to provide proof of principle that A. niger can produce hydroxylated collagen. We used a modular cloning system to generate a suite of cassettes encoding numerous N-terminal secretion signals, native collagen genes and, additionally, various prolyl-4-hydroxylases (P4H) for protein hydroxylation. Collagen transcription was supported by both luciferase reporter and eGFP tagged approaches. Peptide sequencing from culture supernatant confirmed A. niger produced partially hydroxylated collagen. We then conducted a range of media optimizations and RNA sequencing to, respectively, increase collagen production and identify proteases which we hypothesized were detrimental to recombinant protein titers. Thus, we deleted an endopeptidase encoding gene, protA, which was likely responsible for degrading secreting collagen. Ultimately, we were able to generate an isolate capable of producing hydroxylated collagen at titers of 5 mgL−1 in shake flask models of fermentation. This study thus proves A. niger is a promising heterologous system to address the demand for virus-free collagen.https://doi.org/10.1186/s13068-025-02681-yAspergillus nigerCollagenHeterologous expression systemTranscriptomics
spellingShingle Tom Morris
Friederike Gerstl
Sascha Jung
Timothy C. Cairns
Vera Meyer
The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
Biotechnology for Biofuels and Bioproducts
Aspergillus niger
Collagen
Heterologous expression system
Transcriptomics
title The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
title_full The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
title_fullStr The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
title_full_unstemmed The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
title_short The multipurpose cell factory Aspergillus niger can be engineered to produce hydroxylated collagen
title_sort multipurpose cell factory aspergillus niger can be engineered to produce hydroxylated collagen
topic Aspergillus niger
Collagen
Heterologous expression system
Transcriptomics
url https://doi.org/10.1186/s13068-025-02681-y
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