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Difference between revisions of "User:Florence Vincent"

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(Created page with ' Normal.dotm 0 0 1 65 372 CNRS 3 1 456 12.0 0 false 21 18 pt 18 pt 0 0 false false false From 1998 to 2001,…')
 
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I return to Marseille in 2004 to start new research in the glycobiology field in the group of Yves Bourne. Since then I’ve been working on a GH73 and two putative carbohydrate binding domain appended to two global regulators involved in the regulation of biofilm formation in pseudomonas aeruginosa
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From 1998 to 2001, I did my PhD in the group of Christian Cambillau in Marseille working on the structure-function relationships of several mammalian odorant binding proteins (OBPs). In January 2002 I joined the group of [[Gideon Davies]] in the YSBL laboratory (York Structural Biology laboratory) as a postdoctoral fellow to study various aarbohydrate esterases and their role in bacterial cell wall formation and breakdown. We worked on family [[CE4]], [[CE9]], and also [[GH5]] as well as other carbohydrate active enzyme like NagA from ''Bacillus subtilis'' a glucosamine-6-phophate deacetylase and NagB a frustose-6-phosphate isomerase.
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I return to Marseille in 2004 to join the group of structural glycobiology directed by Yves Bourne. Since then I’ve been interested in a GH73, an isoprenoid binding module appended to a [[CBM2]] and possibly involved in oxydoreduction events during plant cell wall breakdown; two putative carbohydrate binding domain appended two global regulators as well as several[[ GT2]] and [[GT4]], all involved in biofilm formation in ''Pseudomonas aeruginosa''

Revision as of 05:55, 19 July 2010

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From 1998 to 2001, I did my PhD in the group of Christian Cambillau in Marseille working on the structure-function relationships of several mammalian odorant binding proteins (OBPs). In January 2002 I joined the group of Gideon Davies in the YSBL laboratory (York Structural Biology laboratory) as a postdoctoral fellow to study various aarbohydrate esterases and their role in bacterial cell wall formation and breakdown. We worked on family CE4, CE9, and also GH5 as well as other carbohydrate active enzyme like NagA from Bacillus subtilis a glucosamine-6-phophate deacetylase and NagB a frustose-6-phosphate isomerase.

I return to Marseille in 2004 to join the group of structural glycobiology directed by Yves Bourne. Since then I’ve been interested in a GH73, an isoprenoid binding module appended to a CBM2 and possibly involved in oxydoreduction events during plant cell wall breakdown; two putative carbohydrate binding domain appended two global regulators as well as severalGT2 and GT4, all involved in biofilm formation in Pseudomonas aeruginosa