SYNTHPHOTO

Powering cells with light: the synthetic biology of photosynthesis

Coordinatore	THE UNIVERSITY OF SHEFFIELD    more Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	2˙484˙955 €
EC contributo	2˙484˙955 €
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-2013-ADG
Funding Scheme	ERC-AG
Anno di inizio	2014
Periodo (anno-mese-giorno)	2014-02-01   -   2019-01-31

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	THE UNIVERSITY OF SHEFFIELD  Organization address address: FIRTH COURT WESTERN BANK city: SHEFFIELD postcode: S10 2TN contact info Titolo: Ms. Nome: Joanne Cognome: Watson Email: send email Telefono: +44 114 222 4754 Fax: +44 114 222 1452	UK (SHEFFIELD)	hostInstitution	2˙484˙955.00
2	THE UNIVERSITY OF SHEFFIELD  Organization address address: FIRTH COURT WESTERN BANK city: SHEFFIELD postcode: S10 2TN contact info Titolo: Prof. Nome: Christopher Cognome: Hunter Email: send email Telefono: +44 114 2224191 Fax: 441142000000	UK (SHEFFIELD)	hostInstitution	2˙484˙955.00

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 Obiettivo del progetto (Objective)

'Billions of tonnes of chlorophylls are synthesised every year, then incorporated into the photosynthetic complexes that harvest and trap the solar energy that powers the biosphere. An understanding of the mechanisms that deliver chlorophylls to the growing photosynthetic apparatus is important for fundamental reasons, and also for future exploitation of photosynthesis as an energy source.

The SYNTHPHOTO project comprises two interlinked sections: the first (SP1) will provide a step change in our knowledge of photosystem assembly by showing how newly-synthesised pigments emerging from the (bacterio)chlorophyll synthases encounter the membrane-embedded assembly machinery and form the growing photosynthetic unit. Innovations in atomic force microscopy will provide the first nanoscale mapping information on the membrane location of the assembly machinery, and state-of-the-art mass spectrometry will quantify every component in the assembly pathway.

SP2 will harness this knowledge for the design and construction of new biological and bioinspired light-gathering and energy-trapping systems. The synthetic biology approach of SP2 will splice genes for pigment and assembly pathways from a variety of bacteria, reconfiguring the photosynthetic apparatus for enhanced spectral coverage. SP2 will explore the potential for ‘bottom-up’ redesign and in vivo production of tailored arrays of photosynthetic complexes and enzymes. Building hybrid photosystems in SP2 augments the aims of SP1 by testing the adaptability of the native biosynthetic machinery, providing a new level of understanding of pigment biosynthesis and photosystem assembly pathways.

The overall aim of SYNTHPHOTO is to discover the mechanisms of assembly of the bacterial photosynthetic apparatus, and to harness this understanding for the design, development and implementation of new biological and bioinspired light-gathering and energy trapping systems.'