Collaborative research: RUI: interrogating catalytic efficiency through kinetic, structural and small-molecule guided investigation of l-dopa 2,3-dioxygenases
Active Project Grant Awarded Last action
- Award ID
- 2449642
- Recipient
-
Rhodes College (") UEI F51NKQLSLHT4
- Awarding agency
-
Division of Chemistry
National Science Foundation
- Obligated
- $180,000
Award facts
- Assistance listing
- 47.049 Mathematical and Physical Sciences
- Completion date 41% complete
- Place of performance
- Memphis, TN 38112, USA
Award details come from USAspending.gov.
About this award
The National Science Foundation (NSF) Division of Chemistry, under the Mathematical and Physical Sciences program (CFDA 47.049), awarded $180,000 to a collaborative research team led by Rhodes College (with co-investigators at Muhlenberg College and State University of New York at Cortland) for the period August 1, 2025, through July 31, 2028. This Research in Undergraduate Institutions (RUI) project delivers fundamental research and educational products centered on understanding and engineering extradiol dioxygenase enzymes, specifically L-DOPA 2,3-dioxygenase, to enhance catalytic efficiency in converting catecholic compounds derived from lignin into useful natural products and materials.
The primary deliverables include: (1) systematic kinetic and structural characterization studies examining how enzyme mutations and variations in substrate size and electronic properties affect catalytic performance; (2) development of a novel toolkit of catecholic compounds for enzymatic testing; (3) expansion of predictive models for substrate oxidizability to guide enzyme engineering; and (4) integrated educational experiences for undergraduate research students across three institutions, with cross-institutional training and course integration to broaden research participation and develop STEM workforce competencies. These outputs advance both catalytic science and undergraduate research training in chemistry and biochemistry.
Description
- Abstract
- With this award, the chemistry of life processes program in the chemistry division is funding DRS. Keri colabroy at muhlenberg college and larryn peterson of rhodes college, in collaboration with DR. Katherine hicks from the state university of new york at cortland to study how extradiol dioxygenase enzymes use oxygen to chemically rearrange catecholic carbon (a primary component of lignin in woody plants) into useful materials, such as natural products. Under the direction of the faculty mentors, undergraduate research students will systematically change the size and electronic properties of these plant-based carbon sources, mutate the enzymes? Structures and study the effect of these changes on the effectiveness of the molecular conversions. These students will experience the interdisciplinary nature of the project through cross-over training at each of the participating laboratories. In addition, parts of the project will be integrated into coursework at each of the home institutions to broaden the reach of original research and help develop the skills that all undergraduate students need to succeed in stem courses, graduate training and stem careers. Expanding the ability to not only predict catalytic efficiency for enzyme-substrate pairs, but also purposefully engineer extradiol dioxygenase enzymes like l-dopa 2,3-dioxygenase to be more effective on non-native substrates is necessary to utilize the powerful chemical capacity of extradiol dioxygenase enzymes to refashion naturally abundant catecholic carbon into useful materials. L-dopa 2,3-dioxygenase exhibits enormous catalytic potential, but the prevailing understanding of ?substrate oxidizability? As a guiding principle behind extradiol dioxygenase reactivity has proven inadequate. Over the course of this project, a ?toolkit? Of novel catechols are synthesized to vary substrate size alongside redox potential over a sufficiently large suite of substrates to be able to visualize the impacts of each variable independently and interdependently. The toolkit is then used in structural study of active site volume and in pre-steady state and equilibrium measurements of rate to measure and ultimately tune catalytic efficiency across evolutionarily diverse l-dopa 2,3-dioxygenase homologs and their mutants. The project is conducted entirely through the efforts of undergraduate students under the direct mentorship of the copis and collaborator. Participating undergraduate students also crossover between the home institutions to experience the project from different perspectives, and part of the project is integrated into undergraduate coursework at each of the home institutions to reach more undergraduates with the high impact learning that comes with original research. These experiences are powerfully effective at developing the skills undergraduate students need to succeed in stem courses, graduate training and in stem careers. This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the foundation's intellectual merit and broader impacts review criteria.- subawards are not planned for this award.
Quick answers
Who received award 2449642?
2449642 was awarded to Rhodes College (") by Division of Chemistry (National Science Foundation) on August 1, 2025.
How much is award 2449642 worth?
$180,000 has been obligated on 2449642.
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