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David Barondeau is an Associate Professor at Texas A&M University in the College of Arts and Sciences. His research focuses on bioinorganic chemistry and chemical biology, leveraging techniques like X-ray crystallography, molecular biology, and biochemistry to unravel the chemistry that underpins biological mechanisms. Barondeau's work is crucial for understanding eukaryotic iron-sulfur cluster biogenesis and the role of metal ions in biochemical reactions, which are essential to prevent toxic byproducts like reactive oxygen species. The Barondeau Research Group studies the mechanisms of escort proteins and their role in functional protein assembly, particularly under conditions that lead to human diseases such as neurodegenerative disorders and cancer. Another significant aspect of his research involves developing novel oxygen-tolerant [FeFe] hydrogenases aimed at producing low-emission fuels through sustainable hydrogen production, addressing the challenge of light energy capture and storage. Furthermore, his group investigates the DNA repair mechanisms in spore-forming pathogens that pose significant threats to human health, such as Bacillus anthracis and Clostridium species. David obtained his B.A. from Southern Utah State College and his Ph.D. from Texas A&M University, followed by a fellowship at La Jolla Interfaces in Sciences.
NIH • USA
Conducted advanced research in bioinorganic chemistry.
Scripps Research Institute • USA
Led projects on chemical biology and DNA repair mechanisms.
Department: Department of Communication and Journalism. Ph.D. program only currently admitting. GRE is test-optional.