CFILP

Characterization of factors involved in proliferation of Bacillus subtilis L-forms

 Coordinatore UNIVERSITY OF NEWCASTLE UPON TYNE 

 Organization address address: Kensington Terrace 6
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU

contact info
Titolo: Ms.
Nome: Aleona
Cognome: Blinova
Email: send email
Telefono: +44 0191 282 4528
Fax: +44 0191 222 7424

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 172˙240 €
 EC contributo 172˙240 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-01-01   -   2012-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF NEWCASTLE UPON TYNE

 Organization address address: Kensington Terrace 6
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU

contact info
Titolo: Ms.
Nome: Aleona
Cognome: Blinova
Email: send email
Telefono: +44 0191 282 4528
Fax: +44 0191 222 7424

UK (NEWCASTLE UPON TYNE) coordinator 172˙240.80

Mappa


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   forms    remarkable    form    bacteria    cell    genes    membrane    proliferation    biology    subtilis   

 Obiettivo del progetto (Objective)

'The main objective of the project will be to characterize the molecular cell biology of proliferation in cell-wall deficient (L-form) derivatives of Bacillus. subtilis. L-forms can apparently arise from a wide range of bacteria and are often found in clinical situations. Recent work in the Errington lab has provided a highly tractable model system for studying the L-form state. B. subtilis L-forms proliferate via a remarkable membrane extrusion and resolution mechanism. The aim of the project is to improve our understanding of L-form biology by identifying and characterizing genes required specifically for growth in the L-form state. Two complementary approaches will be used. First, a candidate gene approach, looking at whether genes involved in chromosome segregation or various forms of membrane dynamics are involved. Second, an unbiased genetic screen for such factors. The project will shed light on the basic cell biology of this important and neglected bacterial way of life and provide insights into their remarkable and unexpected mode of proliferation. It may also provide new antibacterial targets for the development of antimicrobial agents acting on persistent bacteria.'

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