Characterising Fish Collagen for Expression in Bacterial Systems

Isinglass, a collagen-based fining agent commonly used in the brewing industry for centuries, is traditionally produced from the swim bladder of tropical and sub-tropical fishes. However, the production of isinglass raises sustainability concerns, such as overfishing and environmental impact. Ariu...

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Main Author: Shi, Xiaoqin
Format: Thesis (University of Nottingham only)
Language:English
Published: 2025
Subjects:
Online Access:https://eprints.nottingham.ac.uk/80151/
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author Shi, Xiaoqin
author_facet Shi, Xiaoqin
author_sort Shi, Xiaoqin
building Nottingham Research Data Repository
collection Online Access
description Isinglass, a collagen-based fining agent commonly used in the brewing industry for centuries, is traditionally produced from the swim bladder of tropical and sub-tropical fishes. However, the production of isinglass raises sustainability concerns, such as overfishing and environmental impact. Arius maculatus, the species widely used in commercial isinglass production, there is limited data available on the specific protein characteristics of the collagen derived from this source. This study aimed to optimise the extraction and preliminary characterisation of collagen from isinglass from Arius maculatus swim bladders in a laboratory setting, addressing the gap in existing knowledge. The collagen extraction process was refined using acid extraction techniques. The resultants were analysed through SDS-PAGE, revealing the presence of two α-chains and a β-chain with molecular weights slightly over 115kDa and 190kDa, respectively. The study provided essential preliminary data on the molecular structure of this collagen for the future work on the full confirmation of the protein structure. The functionality of these crude extracts as a fining agent was compared against commercial products. The findings reveal that laboratory-extracted protein crude shared structural characteristics with collagen type I and potential in maintaining functionality in finings. The study also pursued the goal of expressing this collagen in a bacterial host; however, achieving suitable DNA templates for PCR was challenging. Repeated failures with commercial DNA extraction kits led to the development of an optimized protocol using conventional methods, yielding high-molecular-weight genomic DNA (>10 kb) for potential future applications. While time constraints prevented the completion of gene expression efforts, this research successfully refined both collagen and DNA extraction techniques, providing a critical foundation for future work on sustainable isinglass production and related collagen-based applications.
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spelling nottingham-801512025-07-31T04:40:07Z https://eprints.nottingham.ac.uk/80151/ Characterising Fish Collagen for Expression in Bacterial Systems Shi, Xiaoqin Isinglass, a collagen-based fining agent commonly used in the brewing industry for centuries, is traditionally produced from the swim bladder of tropical and sub-tropical fishes. However, the production of isinglass raises sustainability concerns, such as overfishing and environmental impact. Arius maculatus, the species widely used in commercial isinglass production, there is limited data available on the specific protein characteristics of the collagen derived from this source. This study aimed to optimise the extraction and preliminary characterisation of collagen from isinglass from Arius maculatus swim bladders in a laboratory setting, addressing the gap in existing knowledge. The collagen extraction process was refined using acid extraction techniques. The resultants were analysed through SDS-PAGE, revealing the presence of two α-chains and a β-chain with molecular weights slightly over 115kDa and 190kDa, respectively. The study provided essential preliminary data on the molecular structure of this collagen for the future work on the full confirmation of the protein structure. The functionality of these crude extracts as a fining agent was compared against commercial products. The findings reveal that laboratory-extracted protein crude shared structural characteristics with collagen type I and potential in maintaining functionality in finings. The study also pursued the goal of expressing this collagen in a bacterial host; however, achieving suitable DNA templates for PCR was challenging. Repeated failures with commercial DNA extraction kits led to the development of an optimized protocol using conventional methods, yielding high-molecular-weight genomic DNA (>10 kb) for potential future applications. While time constraints prevented the completion of gene expression efforts, this research successfully refined both collagen and DNA extraction techniques, providing a critical foundation for future work on sustainable isinglass production and related collagen-based applications. 2025-07-31 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en cc_by https://eprints.nottingham.ac.uk/80151/1/Shi%2C%20Xiaoqin%2C%2020398717%2C%20Re-submission%20.pdf Shi, Xiaoqin (2025) Characterising Fish Collagen for Expression in Bacterial Systems. MRes thesis, University of Nottingham. Isinglass; Fish collagen; Heterologous expression; Collagen extraction; DNA extraction
spellingShingle Isinglass; Fish collagen; Heterologous expression; Collagen extraction; DNA extraction
Shi, Xiaoqin
Characterising Fish Collagen for Expression in Bacterial Systems
title Characterising Fish Collagen for Expression in Bacterial Systems
title_full Characterising Fish Collagen for Expression in Bacterial Systems
title_fullStr Characterising Fish Collagen for Expression in Bacterial Systems
title_full_unstemmed Characterising Fish Collagen for Expression in Bacterial Systems
title_short Characterising Fish Collagen for Expression in Bacterial Systems
title_sort characterising fish collagen for expression in bacterial systems
topic Isinglass; Fish collagen; Heterologous expression; Collagen extraction; DNA extraction
url https://eprints.nottingham.ac.uk/80151/