AOX1 PROMOTER

Purification and Characterization of Regulatory Proteins of the Alcohol Oxidase 1 (AOX1) Promoter of Pichia pastoris

 Coordinatore AKDENIZ UNIVERSITY 

 Organization address address: DUMLUPINAR BULVARI Kampus
city: Antalya
postcode: 7058

contact info
Titolo: Prof.
Nome: Muharrem
Cognome: Certel
Email: send email
Telefono: -3102119
Fax: -2275536

 Nazionalità Coordinatore Turkey [TR]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 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-2009-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-09-01   -   2014-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    AKDENIZ UNIVERSITY

 Organization address address: DUMLUPINAR BULVARI Kampus
city: Antalya
postcode: 7058

contact info
Titolo: Prof.
Nome: Muharrem
Cognome: Certel
Email: send email
Telefono: -3102119
Fax: -2275536

TR (Antalya) coordinator 100˙000.00

Mappa


 Word cloud

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

acting    determine       promoter    protein    utilize    strains    host    proteins    aox    regulatory    pastoris    expression    cis   

 Obiettivo del progetto (Objective)

'The methylotrophic yeast Pichia pastoris is used as a host system to produce recombinant proteins for a variety of applications, from food products to pharmaceuticals. However, despite the success of the P. pastoris expression system, relatively little is known about the molecular biology of the promoter utilized in this system, namely alcohol oxidase I (AOX1) promoter. In order to better utilize the AOX1 promoter, I propose to study regulation of the promoter using three approaches, 1) purify and characterize the regulatory proteins that bind to the AOX1 promoter and 2) overexpress his-tagged Methanol Expression Regulator 1 (Mrx1) protein to determine binding sites on the AOX1 promoter 3) determine the cis-acting regulatory sequences and design synthetic promoters. In addition, I will generate new host strains in which activator protein(s) will be over-expressed and expression of the repressor protein(s) will be suppressed. These studies will identify cis- and trans-acting factors that dictate the AOX1 promoter strength, in turn effect heterologous protein production. The elucidation of the AOX1 promoter control mechanism will benefit industrial and academic scientists who utilize P. pastoris expressions system in their studies.'

Introduzione (Teaser)

Researchers investigated how yeasts regulate protein production in order to create new strains with maximised protein yield.

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