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ROAL OY

Country: Finland
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5 Projects, page 1 of 1
  • Funder: European Commission Project Code: 239341
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  • Funder: European Commission Project Code: 222699
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  • Funder: European Commission Project Code: 720729
    Overall Budget: 3,569,720 EURFunder Contribution: 1,934,230 EUR

    The main objective of NeoCel project is to develop innovative and techno-economically feasible alkaline processes enabling the sustainable production of higher quality eco-innovative textile fibres from reactive high-cellulose pulps and integration of these processes with pulp mills. Targets for the development of NeoCel processes are: - wet strength of fibres higher than the wet strength of standard viscose, competing with cotton properties. - lower environmental impact than any other type of existing textile fibre - Reduction of production cost by at least 15% compared to that of best available technology (BAT) viscose The targets will be met through development of adapted pulps with high reactivity/solubility in alkaline water-based solutions, advanced dissolution process to maximize cellulose concentration, novel cellulose regeneration chemistry enabling both recovery of process chemicals and increased strength properties of the spun fibre, design for integration of textile fibre production with the pulp mill for minimized environmental impact, increased energy efficiency and reduced chemical consumption through system analysis using software models of theoretical mills. In NeoCel, a consortium with raw material processing companies, chemical suppliers, equipment producers, SMEs and world-leading research institutes has formed to develop the processes for large scale manufacturing of eco-innovative textile fibres. The consortium expects that a successful NeoCel project will enable creation of 75 000 new jobs and a turn-over increase of 9.5 billion € for European forest products, textile and clothing industries within 15 years. However, already within 3 years, the consortium partners expect their joint turnover to increase by 170 MEuro

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  • Funder: UK Research and Innovation Project Code: BB/F017693/1
    Funder Contribution: 72,540 GBP

    The project aims to provide new information on the transcriptional regulation of expression of cellulase in the filamentous fungus Trichoderma reesei. T. reesei is a fungus exploited extensively commercially for production of native (mainly cellulases) enzymes and, increasingly, heterologous proteins. The genome sequence of T. reesei is available (http://genome.jgi-psf.org/Trire2/Trire2.home.html). Although the T. reesei genome encodes for the expression of several cellulases, the cbh1 gene has been the most extensively studied in relation to its expression and the cbh1 promoter is used to drive expression of heterologous proteins. This project will build upon our unpublished data which show, for the first time, the importance of chromatin in its regulation, including changes in nucleosomal positioning during induction and repression. Moreover, we have preliminary data showing protein binding to the ORF during induction, indicating that the ORF is involved in regulation in addition to the promoter region. That is unprecedented in filamentous fungi. The overall Aim of the project is to define new regulatory principles in the transcriptional control of a target gene in a filamentous fungus. The specific experimental Aims of the project are to confirm the nucleosomal rearrangements of the chb1 promoter and ORF during induction and repression and to specify the roles, if any, of known regulators (e.g. Cre1, Ace1) in the nucleosomal rearrangements. A secondary Aim is to define a model for the regulation of cbh1. The project will also explore the role of protein binding to the ORF during transcriptional regulation. The methodologies available for exploration of nucleosomal positioning (involving the isolation of chromatin, nuclease sensitivity assays, and hybridisation studies), culture conditions for induction and repression (and neutral conditions), and some mutant strains for exploration of the roles of some transcription factors are all in place in Nottingham or the research facility of Roal. This project provides an exciting possibility for defining new mechanisms of transcriptional regulation in fungi. The student will receive training in microbiology, genomics and molecular biology and will have the opportunity to interface with mathematicians in Nottingham in order to define a model for the regulation of the cbh1 gene That model can be tested and its relevance to gene regulation in the fungus as a whole examined using gene array methodology, which is only recently available for T. reesei. This new information will be important for Roal, a company that exploits filamentous fungi, including T. reesei, in its business.

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  • Funder: European Commission Project Code: 213139
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