ENERGYBIOCATALYSIS

Understanding and Exploiting Biological Catalysts for Energy Cycling: Development of Infrared Spectroelectrochemistry for Studying Intermediates in Metalloenzyme Catalysis

Coordinatore	THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD    more Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	1˙373˙322 €
EC contributo	1˙373˙322 €
Programma	FP7-IDEAS-ERC Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
Code Call	ERC-2010-StG_20091028
Funding Scheme	ERC-SG
Anno di inizio	2011
Periodo (anno-mese-giorno)	2011-02-01   -   2016-01-31

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD  Organization address address: University Offices, Wellington Square city: OXFORD postcode: OX1 2JD contact info Titolo: Dr. Nome: Kylie Alison Cognome: Vincent Email: send email Telefono: +44 1865 282611 Fax: +44 1865 272690	UK (OXFORD)	hostInstitution	1˙373˙322.00
2	THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD  Organization address address: University Offices, Wellington Square city: OXFORD postcode: OX1 2JD contact info Titolo: Dr. Nome: Stephen Cognome: Conway Email: send email Telefono: +44 1865 289800 Fax: +44 1865 289801	UK (OXFORD)	hostInstitution	1˙373˙322.00

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 Obiettivo del progetto (Objective)

'Advanced catalysts for energy cycling will be essential to a future sustainable energy economy. Interconversion of water and hydrogen allows solar and other green electricity to be stored in transportable form as H2 - a fuel for electricity generation on demand. Precious metals (Pt) are the best catalysts currently available for H2 oxidation in fuel cells. In contrast, readily available Ni/Fe form the catalytic centres of robust enzymes used by micro-organisms to oxidise or produce H2 selectively, at rates rivalling platinum. Metalloenzymes also efficiently catalyse redox reactions of the nitrogen and carbon cycles. Electrochemistry of enzyme films on a graphite electrode provides a direct route to studying and exploiting biocatalysis, for example a fuel cell that produces electricity from dilute H2 in air using an electrode modified with hydrogenase. Understanding structures and complex chemistry of enzyme active sites is now an important challenge that underpins exploitation of enzymes and design of future catalysts. This project develops sensitive IR methods for metalloenzymes on conducting surfaces or particles. Ligands with strong InfraRed vibrational signatures (CO, CN-) are exploited as probes of active site chemistry for hydrogenases and carbon-cycling enzymes. The proposal unites physical techniques (surface vibrational spectroscopy, electrochemistry), microbiology (mutagenesis, microbial energy cycling), inorganic chemistry (reactions at unusual organometallic centres) and technology development (energy-catalysis) in addressing enzyme chemistry. Understanding the basis for the extreme catalytic selectivity of enzymes will contribute to knowledge of biological energy cycling and provide inspiration for new catalysts.'