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Difference between revisions of "User:Julie Grondin"
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'''Julie Grondin''' obtained her PhD in 2009 with Dr. Steven Smith at [http://www.queensu.ca Queen's University] (Kingston, ON, Canada), where she used NMR, XRC, and SAXS toward the structural characterization of large multi-modular GHs from the human gut pathogen ''Clostridium perfringens''. From 2014-2017, she worked in ^^^Wade Abbott^^^'s group at [http://profils-profiles.science.gc.ca/en/research-centre/lethbridge-research-and-development-centre Agriculture and Agri-Food Canada] (Lethbridge, AB, Canada) as a postdoctoral fellow, where she designed nutrient utilization, inducible expression, metabolic selection, and reverse genetics systems into the human gut symbiont ''Bacteroides thetaiotaomicron''. She is currently a post-doctoral fellow in ^^^Harry Brumer^^^'s group at the [http://www.msl.ubc.ca/ Michael Smith Laboratories] at the [http://www.ubc.ca/ University of British Columbia] (Vancouver, BC, Canada). | '''Julie Grondin''' obtained her PhD in 2009 with Dr. Steven Smith at [http://www.queensu.ca Queen's University] (Kingston, ON, Canada), where she used NMR, XRC, and SAXS toward the structural characterization of large multi-modular GHs from the human gut pathogen ''Clostridium perfringens''. From 2014-2017, she worked in ^^^Wade Abbott^^^'s group at [http://profils-profiles.science.gc.ca/en/research-centre/lethbridge-research-and-development-centre Agriculture and Agri-Food Canada] (Lethbridge, AB, Canada) as a postdoctoral fellow, where she designed nutrient utilization, inducible expression, metabolic selection, and reverse genetics systems into the human gut symbiont ''Bacteroides thetaiotaomicron''. She is currently a post-doctoral fellow in ^^^Harry Brumer^^^'s group at the [http://www.msl.ubc.ca/ Michael Smith Laboratories] at the [http://www.ubc.ca/ University of British Columbia] (Vancouver, BC, Canada). | ||
| − | Julie has contributed to the | + | Julie has contributed to the structural and functional characterization of several [[CBM32]] from ''Clostridium perfringens'' [[GH84]] and [[GH31]] <cite>Grondin2012,Grondin2014,Grondin2017</cite>, as well as the characterization of full-length ''Cp''GH84A (unpublished), and the agarose utilization system in ''Bacteroides uniformis'' <cite>Pluvinage2018</cite>. She was also involved in the development of a carbohydrate-inducible heterologous expression system in ''Bacteroides thetaiotaomicron'' <cite>Jones2019</cite>. |
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Revision as of 08:48, 27 April 2020
Julie Grondin obtained her PhD in 2009 with Dr. Steven Smith at Queen's University (Kingston, ON, Canada), where she used NMR, XRC, and SAXS toward the structural characterization of large multi-modular GHs from the human gut pathogen Clostridium perfringens. From 2014-2017, she worked in ^^^Wade Abbott^^^'s group at Agriculture and Agri-Food Canada (Lethbridge, AB, Canada) as a postdoctoral fellow, where she designed nutrient utilization, inducible expression, metabolic selection, and reverse genetics systems into the human gut symbiont Bacteroides thetaiotaomicron. She is currently a post-doctoral fellow in ^^^Harry Brumer^^^'s group at the Michael Smith Laboratories at the University of British Columbia (Vancouver, BC, Canada).
Julie has contributed to the structural and functional characterization of several CBM32 from Clostridium perfringens GH84 and GH31 [1, 2, 3], as well as the characterization of full-length CpGH84A (unpublished), and the agarose utilization system in Bacteroides uniformis [4]. She was also involved in the development of a carbohydrate-inducible heterologous expression system in Bacteroides thetaiotaomicron [5].
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