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Enhancing the yield of industrial Actinomycete fermentations
Reference
BB/N023544/1
Principal Investigator / Supervisor
Professor Paul Hoskisson
Co-Investigators /
Co-Supervisors
Dr Iain Hunter
Institution
University of Strathclyde
Department
Inst of Pharmacy and Biomedical Sci
Funding type
Research
Value (£)
696,737
Status
Completed
Type
Research Grant
Start date
01/08/2016
End date
31/07/2019
Duration
36 months
Abstract
A new and radical approach to strain construction is needed for the UK to remain competitive in manufacturing off-patent antibiotics. Antibiotic fermentation processes balance nutrients and cell growth rate with the chemical and physical environments. Cellular output is traditionally improved by selecting higher-producing mutants and optimising fermentation media. However, many antibiotics are unstable in the extracellular environment, with well characterised relationships between pH and degradation rate. The pH range for operation of the biological system often conflicts with the optimum for chemical stability of the product. For an established commercial process we propose to utilise recent advances in synthetic biology and genomics to develop a bacterial strain and industrial fermentation process capable of operating at a lower pH, facilitating stability of the desired product.
Summary
A new and radical approach to strain construction is needed for the UK to remain competitive in manufacturing off-patent antibiotics. Antibiotic fermentation processes balance nutrients and cell growth rate with the chemical and physical environments. Cellular output is traditionally improved by selecting higher-producing mutants and optimising fermentation media. However, many antibiotics are unstable in the extracellular environment, with well characterised relationships between pH and degradation rate. The pH range for operation of the biological system often conflicts with the optimum for chemical stability of the product. For an established commercial process we propose to utilise recent advances in synthetic biology and genomics to develop a bacterial strain and industrial fermentation process capable of operating at a lower pH, facilitating stability of the desired product.
Impact Summary
As described in proposal submitted to IUK
Committee
Research Committee A (Animal disease, health and welfare)
Research Topics
Industrial Biotechnology, Microbiology, Pharmaceuticals, Synthetic Biology
Research Priority
X – Research Priority information not available
Research Initiative
Industrial Biotechnology Catalyst (IBCAT) [2014-2015]
Funding Scheme
X – not Funded via a specific Funding Scheme
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