CAZypedia needs your help!
We have many unassigned pages in need of Authors and Responsible Curators. See a page that's out-of-date and just needs a touch-up? - You are also welcome to become a CAZypedian. Here's how.
Scientists at all career stages, including students, are welcome to contribute.
Learn more about CAZypedia's misson here and in this article.
Totally new to the CAZy classification? Read this first.
Difference between revisions of "User:Emil Stender"
Emil Stender (talk | contribs) |
Harry Brumer (talk | contribs) m |
||
| Line 1: | Line 1: | ||
[[Image:Emil_Stender.png|200px|right]] | [[Image:Emil_Stender.png|200px|right]] | ||
| − | Emil G. P. Stender obtained his M.Sc. in biochemistry from University of Copenhagen - Denmark in 2014 and completed his PhD in 2018 at Technical University of Denmark (DTU) under supervision of Birte Svensson and co-supervised by Maher Abou Hachem. The project involved characterization of whey protein-alginate interactions and identification of alginate binding sites on the surface of β-lactoglobulin <cite>Stender2019 Stender2017</cite>. He has since been employed as a postdoc at DTU – Bioengineering in a project identifying and characterizing enzymes enabling human gut microbiota to utilize alginate. His main research interests are protein biophysics, polysaccharide lyases and alginate modifying enzymes. | + | Emil G. P. Stender obtained his M.Sc. in biochemistry from University of Copenhagen - Denmark in 2014 and completed his PhD in 2018 at Technical University of Denmark (DTU) under supervision of ^^^Birte Svensson^^^ and co-supervised by Maher Abou Hachem. The project involved characterization of whey protein-alginate interactions and identification of alginate binding sites on the surface of β-lactoglobulin <cite>Stender2019 Stender2017</cite>. He has since been employed as a postdoc at DTU – Bioengineering in a project identifying and characterizing enzymes enabling human gut microbiota to utilize alginate. His main research interests are protein biophysics, polysaccharide lyases and alginate modifying enzymes. |
Revision as of 07:02, 6 June 2019
Emil G. P. Stender obtained his M.Sc. in biochemistry from University of Copenhagen - Denmark in 2014 and completed his PhD in 2018 at Technical University of Denmark (DTU) under supervision of ^^^Birte Svensson^^^ and co-supervised by Maher Abou Hachem. The project involved characterization of whey protein-alginate interactions and identification of alginate binding sites on the surface of β-lactoglobulin [1, 2]. He has since been employed as a postdoc at DTU – Bioengineering in a project identifying and characterizing enzymes enabling human gut microbiota to utilize alginate. His main research interests are protein biophysics, polysaccharide lyases and alginate modifying enzymes.
-
Stender, E. G. P., Birch, J., Kjeldsen, C., Nielsen, L. D., Duus, J. O., Kragelund, B. B., and Svensson, B. (2019) Alginate trisaccharide binding sites on the surface of β-Lactoglobulin identified by NMR spectroscopy: implications for molecular network formation. ACS Omega. 4, 6165–6174
-
Stender, E. G. P., Khan, S., Ipsen, R., Madsen, F., Hägglund, P., Abou Hachem, M., Almdal, K., Westh, P., and Svensson, B. (2017) Effect of alginate size, mannuronic/guluronic acid content and pH on particle size, thermodynamics and composition of complexes with β-lactoglobulin. Food Hydrocoll. 75, 157–163
- Stender EGP , Koutina G , Almdal K , Hassenkam T , Mackie A , Ipsen R , and Svensson B . (2018). Isoenergic modification of whey protein structure by denaturation and crosslinking using transglutaminase. Food Funct. 2018;9(2):797-805. DOI:10.1039/c7fo01451a |
- Stender EG, O'Shea C, and Skriver K. (2015). Subgroup-specific intrinsic disorder profiles of Arabidopsis NAC transcription factors: Identification of functional hotspots. Plant Signal Behav. 2015;10(6):e1010967. DOI:10.1080/15592324.2015.1010967 |
- O'Shea C, Kryger M, Stender EG, Kragelund BB, Willemoës M, and Skriver K. (2015). Protein intrinsic disorder in Arabidopsis NAC transcription factors: transcriptional activation by ANAC013 and ANAC046 and their interactions with RCD1. Biochem J. 2015;465(2):281-94. DOI:10.1042/BJ20141045 |