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Difference between revisions of "User:Didier Ndeh"
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| + | Didier Ndeh is a postdoctoral research associate at the Institute for Cell and Molecular Biosciences (ICAMB), Newcastle University, UK. Didier completed his PhD at Newcastle University in the year 2013. Since then, Didier’s research has focused on the understanding of host-microbial interactions involving the human gut microbiota. Prior to his PhD, Didier obtained a BSc in Biochemistry from the University of Buea in Cameroon in 2007. He was later offered a UK Commonwealth Scholarship to study for his MSc in Biotechnology at Nottingham Trent University, which he completed in 2009. Didier later worked as a research assistant on an Onchocerciasis Drug Research programme at the Biotechnology Unit of the University of Buea before obtaining another UK Commonwealth Scholarship to study for his PhD at Newcastle University. Didier’s work on complex glycan metabolism by the human gut microbiota has led to the discovery of several novel carbohydrate-acting enzyme families including GH137, GH138, GH139, GH140, GH141, GH142, and GH143 <cite>Ndeh2017</cite>. Didier (in collaboration with Arnaud Basle and Harry J Gilbert) determined the first crystal structure of a GH137 enzyme, specifically the pectin degrading BT1002 fucosidase encoded by the human gut bacterium Bacteroides thetaiotaomicron <cite>Ndeh2017</cite>. | ||
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| + | References | ||
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#Gilbert2008 pmid=18430603 | #Gilbert2008 pmid=18430603 | ||
| + | #Ndeh2017 pmid=28329766 | ||
</biblio> | </biblio> | ||
Revision as of 01:04, 18 January 2018
Didier Ndeh is a postdoctoral research associate at the Institute for Cell and Molecular Biosciences (ICAMB), Newcastle University, UK. Didier completed his PhD at Newcastle University in the year 2013. Since then, Didier’s research has focused on the understanding of host-microbial interactions involving the human gut microbiota. Prior to his PhD, Didier obtained a BSc in Biochemistry from the University of Buea in Cameroon in 2007. He was later offered a UK Commonwealth Scholarship to study for his MSc in Biotechnology at Nottingham Trent University, which he completed in 2009. Didier later worked as a research assistant on an Onchocerciasis Drug Research programme at the Biotechnology Unit of the University of Buea before obtaining another UK Commonwealth Scholarship to study for his PhD at Newcastle University. Didier’s work on complex glycan metabolism by the human gut microbiota has led to the discovery of several novel carbohydrate-acting enzyme families including GH137, GH138, GH139, GH140, GH141, GH142, and GH143 [1]. Didier (in collaboration with Arnaud Basle and Harry J Gilbert) determined the first crystal structure of a GH137 enzyme, specifically the pectin degrading BT1002 fucosidase encoded by the human gut bacterium Bacteroides thetaiotaomicron [1].
References
- Ndeh D, Rogowski A, Cartmell A, Luis AS, Baslé A, Gray J, Venditto I, Briggs J, Zhang X, Labourel A, Terrapon N, Buffetto F, Nepogodiev S, Xiao Y, Field RA, Zhu Y, O'Neil MA, Urbanowicz BR, York WS, Davies GJ, Abbott DW, Ralet MC, Martens EC, Henrissat B, and Gilbert HJ. (2017). Complex pectin metabolism by gut bacteria reveals novel catalytic functions. Nature. 2017;544(7648):65-70. DOI:10.1038/nature21725 |
- Gilbert HJ, Stålbrand H, and Brumer H. (2008). How the walls come crumbling down: recent structural biochemistry of plant polysaccharide degradation. Curr Opin Plant Biol. 2008;11(3):338-48. DOI:10.1016/j.pbi.2008.03.004 |