DEGRADEPLANT

Directed evolution and semi-rational engineering of plant cell wall-degrading enzymes

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Dr.
Nome: Florian
Cognome: Hollfelder
Email: send email
Telefono: 441224000000
Fax: 441224000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 200˙049 €
 EC contributo 200˙049 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-06-01   -   2013-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Dr.
Nome: Florian
Cognome: Hollfelder
Email: send email
Telefono: 441224000000
Fax: 441224000000

UK (CAMBRIDGE) coordinator 200˙049.60

Mappa


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related    evolution    libraries    enzymes    strategies    directed    screening   

 Obiettivo del progetto (Objective)

'This proposal focuses on the development of new techniques and strategies for the directed evolution of enzymes useful for industrial (white) biotechnology, including the development of new genetic methodologies to improve the potential of variant libraries, as well as new screening tools to broaden the range of targets for directed evolution. Specifically, the proposed project will apply these new methodologies to plant cell-wall degrading enzymes, namely cellulases and hemicellulases, which are crucial biocatalysts for the production of second-generation lignocellulose-derived biofuels. The enzymes targeted in this proposal are phylogenetically-related, share the same fold, catalyze the same chemical transformation on a large number of structurally related substrates and thus provide good starting points to switch substrate specificities by directed evolution. In order to achieve these challenging objectives, the proposed project will combine new technical advances: on the one hand methodologies to construct gene libraries and stability compensation strategies, and on the other hand new screening approaches of unprecedented throughput based on compartmentalized screening in microdroplets that are processed in microfluidic devices.'

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