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Difference between revisions of "User:Marie Couturier"
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| − | Marie Couturier started working on carbohydrate-active enzymes in 2008 at INRA (Fungal Biodiversity and | + | Marie Couturier started working on carbohydrate-active enzymes in 2008 at INRA (Fungal Biodiversity and Biotechnology Lab, Marseilles, France), first as a research assistant and then as a PhD student supervised by ^^^Jean-Guy Berrin^^^. Her PhD studies focused on the characterization of a variety of fungal CAZymes ([[GH5]], [[GH26]], [[GH45]]) <cite>Couturier2011a Couturier2011b Couturier2013</cite>. In 2013 she obtained a Marie Curie fellowship to join Emma Master’s team at the University of Toronto (Bioproducts Lab, Toronto, Canada) where she was involved in metagenomic exploration of microflora originating from moose and beaver intestinal tracts <cite>Wong2017</cite>. She also studied there the enzymatic arsenal of ''Pycnoporus coccineus'' by means of transcriptomic, proteomic and functional analyses <cite>Couturier2015</cite>. This work led to the discovery of the LPMO family [[AA14]] and structure-function characterization of its first member <cite>Couturier2018</cite>. In 2017 she started a postdoctoral contract at CERMAV (Centre for Research on Plant Macromolecules, CNRS, Grenoble, France) with William Helbert where she studied several mannanase families ([[GH26]], [[GH113]]) as well as mannan degrading Polysaccharide Utilization Loci. She recently obtained a research scientist position at CERMAV to pursue her research on enzymes involved in the deconstruction of polysaccharides. |
Revision as of 23:57, 8 May 2019
Marie Couturier started working on carbohydrate-active enzymes in 2008 at INRA (Fungal Biodiversity and Biotechnology Lab, Marseilles, France), first as a research assistant and then as a PhD student supervised by ^^^Jean-Guy Berrin^^^. Her PhD studies focused on the characterization of a variety of fungal CAZymes (GH5, GH26, GH45) [1, 2, 3]. In 2013 she obtained a Marie Curie fellowship to join Emma Master’s team at the University of Toronto (Bioproducts Lab, Toronto, Canada) where she was involved in metagenomic exploration of microflora originating from moose and beaver intestinal tracts [4]. She also studied there the enzymatic arsenal of Pycnoporus coccineus by means of transcriptomic, proteomic and functional analyses [5]. This work led to the discovery of the LPMO family AA14 and structure-function characterization of its first member [6]. In 2017 she started a postdoctoral contract at CERMAV (Centre for Research on Plant Macromolecules, CNRS, Grenoble, France) with William Helbert where she studied several mannanase families (GH26, GH113) as well as mannan degrading Polysaccharide Utilization Loci. She recently obtained a research scientist position at CERMAV to pursue her research on enzymes involved in the deconstruction of polysaccharides.
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- Wong MT, Wang W, Couturier M, Razeq FM, Lombard V, Lapebie P, Edwards EA, Terrapon N, Henrissat B, and Master ER. (2017). Comparative Metagenomics of Cellulose- and Poplar Hydrolysate-Degrading Microcosms from Gut Microflora of the Canadian Beaver (Castor canadensis) and North American Moose (Alces americanus) after Long-Term Enrichment. Front Microbiol. 2017;8:2504. DOI:10.3389/fmicb.2017.02504 |
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