Award details

Integron and omics based acceleratation of industrial strain development

Reference	BB/K011499/2
Principal Investigator / Supervisor	Professor Susan Rosser
Co-Investigators / Co-Supervisors	Professor Mike Barrett, Dr Karl Burgess
Institution	University of Edinburgh
Department	Sch of Biological Sciences
Funding type	Research
Value (£)	144,643
Status	Completed
Type	Research Grant
Start date	01/11/2013
End date	31/10/2015
Duration	24 months

Abstract

This project aims to provide a new set of enabling technologies which will create a step change in the speed and efficiency with which engineered microbes can be constructed for industrial application. This improvement will be achieved by combining novel methods to recombine genes within the genome of industrial organisms with advanced metabolomics techniques and direct screening methods to identify strains with improved process efficiency. The project output will provide methods to overcome the normally time-consuming and laborious empirical process of iterative strain improvement. The initial application is to rapidly improve yeast strains used for bioethanol production but the suite of enabling tools being employed would be capable of accelerating the development of microbes for virtually any industrial application

Summary

Impact Summary

The UK manufactures over 1 billion gallons of bioethanol and the US >12B gallons currently but mandated to increase to over 30 billion gallons by 2022. Despite controversy over the use of food crops for fuel, economic and political factors will dictate bioethanol policy for decades. It is now critical for science to improve ethanol production efficiency from current carbon sources, and adapt production microbes to new carbon sources. This project will greatly impact both issues by accelerating the genetic adaptation of commercial yeast strains to unused carbon in corn or other raw materials used to manufacture bioethanol and to greatly reduce or eliminate the need for added enzymes. This project will utilise a novel, efficient and versatile means to recombine fragments of DNA, along with metabolomics analyses to accelerate the genetic construction and improvement of yeast of extremely high commercial importance in biofuel manufacture. However, the method is potentially applicable to microbial strains for many industrial purposes. This project will provide new scientific advances and state of the art techniques in: 1) Tools for rapid strain improvement and pathway engineering 2) Engineered strains for bioethanol production 3) New assays and screens for bioethanol producing strains 4) Novel insights into the metabolome of industrialy important strains. Following appropriate protection of IP, the success of the project will be publicised widely by the academic groups in high impact scientific journals and through presentations at international symposia focussed on the applications of omics and genetic technologies. This project has a direct route to market via the industrial partner Ingenza. Ingenza has established relationships with three current US bioethanol manufacturers who are prepared to evaluate and potentially implement the output of the project, thereby offering an attractive route to market without a significant change in the business model of the end users.One manufacturer has signed an agreement to test Ingenza's improved strains in its facilities to demonstrate feasibility. These manufacturers are part of a consortium with access to 25 bioethanol plants, representing approximately 5% of total US bioethanol production. The broader economic impact of the project will improve the economic sustainability, adaptability and robustness of the biofuel and subsequently other industries which use renewable feedstocks, reducing fossil fuel, land and fertiliser usage. Successful implementation of the project results and greater predictability in bioprocess improvement will encourage uptake of bioscience technology in the UK, by manufacturing sectors such as medicine, agriculture and personal care which apply these approaches to a degree but consider bioscience to be unpredictable in cost and timeline. This will positively impact the economic sustainability, adaptability and robustness of UK manufacturing with no negative social or environmental impact. The project results will accelerate microbial strain improvement strategies aimed at the more efficient production of biofuels from diverse sources of biomass but will also provide methods to optimise the expression of any endogenous or heterologous proteins in microbial systems. Such improvements would have applications across many industrial sectors that include the production of proteins as biocatalysts or biologics, and the engineering of more complex biochemical pathways to produce secondary metabolites, nutritional supplements or natural products currently sourced from regions endangered by climate change, political or other factors. The technology may also have future application to the production of chemicals, which are out of scope for this competition and so will not be addressed directly in the proposed project.

Committee	Research Committee A (Animal disease, health and welfare)
Research Topics	X – not assigned to a current Research Topic
Research Priority	X – Research Priority information not available
Research Initiative	Innovate UK (TSB) [2011-2015]
Funding Scheme	X – not Funded via a specific Funding Scheme

Associated awards:

BB/K011499/1 Integron and omics based acceleratation of industrial strain development

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