SYNPLANTMET

Synthetic Metabolism in Plants: Elucidating Vinblastine Biosynthesis and Implementing Strategies to Overproduce Complex Plant Metabolites

 Coordinatore JOHN INNES CENTRE 

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 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 1˙497˙920 €
 EC contributo 1˙497˙920 €
 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-2012-StG_20111109
 Funding Scheme ERC-SG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-02-01   -   2018-01-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF EAST ANGLIA

 Organization address address: EARLHAM ROAD
city: NORWICH
postcode: NR4 7TJ

contact info
Titolo: Dr.
Nome: Chris
Cognome: Killen
Email: send email
Telefono: +44 1603 593713
Fax: +44 1603 591550

UK (NORWICH) beneficiary 278˙519.94
2    JOHN INNES CENTRE

 Organization address address: "Norwich Research Park, Colney"
city: NORWICH
postcode: NR4 7UH

contact info
Titolo: Dr.
Nome: Mary
Cognome: Anderson
Email: send email
Telefono: +44 1603 450244
Fax: +44 1603 450045

UK (NORWICH) hostInstitution 1˙219˙400.10
3    JOHN INNES CENTRE

 Organization address address: "Norwich Research Park, Colney"
city: NORWICH
postcode: NR4 7UH

contact info
Titolo: Dr.
Nome: Sarah Ellen
Cognome: O'connor
Email: send email
Telefono: +44 1603 450334
Fax: +44 1603 450045

UK (NORWICH) hostInstitution 1˙219˙400.10

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

metabolic    recently    molecules    plant    moreover    roseus    time    planta    candidates    metabolism    gene    group    synthetic    biosynthetic    produces    vinblastine    biology    function    pathways    specialised    data   

 Obiettivo del progetto (Objective)

'Nature produces a spectacularly diverse array of complex molecules that are exploited for many applications. Elucidating the biosynthetic pathways that are used to construct these complex molecules allows implementation of metabolic engineering or synthetic biology strategies that can dramatically improve production levels of these compounds. Moreover, identifying the biosynthetic genes facilitates study of the unprecedented biochemistry harboured within these specialised metabolic pathways. Unfortunately, research progress in plant specialised metabolism has lagged, in large part due to the complexities of plant systems. This has hampered the application of state-of-the-art synthetic biology approaches that can exploit this rich metabolism. The availability of inexpensive sequence data makes this an outstanding time to revisit difficult questions in plant metabolism. My group has recently obtained RNA-seq data for 24 tissues for Catharanthus roseus, which produces vinblastine, an anti-cancer drug that is arguably one of the most complex natural products found in plants. Moreover, my group has recently pioneered the implementation of gene silencing technology in C. roseus, which provides, for the first time, the means to rapidly assess C. roseus gene function in planta. This ensures that we will have a reasonably high-throughput platform by which we can assess gene candidates identified by hierarchical clustering analysis. In Objective 1, we outline a plan to identify vinblastine biosynthetic gene candidates using our transcriptome data and then screen these candidates for function in planta. We also propose a series of in vitro assays by which to characterise promising gene candidates biochemically. In Objective 2, we propose to reconstitute portions of the vinblastine pathway in Saccharomyces cerevisiae (yeast) and the model plant Nicotiana benthamiana (tobacco) to create high-yielding platforms for production of valuable plant metabolites.'

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