**Job Description**
This 3-year Ph.D. position, part of an Alliance Ph.D. funded by DTU and Villum Fonden, is available in the Enzymatic Synthesis Technology group at the Department of Biotechnology and Biomedicine, DTU. Supervised by Associate Professor Birgitte Zeuner and co-supervised by Associate Professor Gaston Courtade (NTNU), the project focuses on ligand-observed NMR analysis of carbohydrate-active enzymes to investigate the molecular basis of enzyme-substrate interactions in regioselective carbohydrate synthesis catalyzed by glycoside hydrolases, contributing to new sustainable bioprocessing applications. The successful candidate will join a project team and collaborate with other Ph.D. students and postdocs, with work primarily at DTU and including extended stays at NTNU.
**Skills & Abilities**
• Strong background in analytical chemistry, biochemistry, enzyme technology or similar
• Documented knowledge and experience with carbohydrate-active enzymes (prioritized)
• Well organized, structured, self-driven
• Enjoy interacting and collaborating with colleagues
• Documented practical experience with NMR analysis, preferably with ligand-observed methods for studying protein-ligand interactions
• Knowledge of carbohydrate chemistry (carbohydrate structures and terminology)
• Experience in working with carbohydrate-active enzymes (advantage, while interest in learning it is a requirement)
• Experience in chemical carbohydrate synthesis and/or recombinant protein expression (advantageous)
• Excellent communication skills in English (written and spoken)
**Qualifications**
Required Degree(s) in:
• Analytical Chemistry
• Biochemistry
• Enzyme Technology
• Related fields
**Experience**
Other:
• Documented knowledge and experience with carbohydrate-active enzymes is prioritized.
• Documented practical experience with NMR analysis, preferably with ligand-observed methods for studying protein-ligand interactions.
• Experience in working with carbohydrate-active enzymes is an advantage.
• Experience in chemical carbohydrate synthesis and/or recombinant protein expression are considered advantageous.
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