Related Experiment Video
Updated: Jan 15, 2026

Anaerobic Protein Purification and Kinetic Analysis via Oxygen Electrode for Studying DesB Dioxygenase Activity and Inhibition
Published on: October 3, 2018
Rieske Oxygenase-Catalyzed Biotransformations in Recombinant Cupriavidus necator Fueled by Formate Oxidation
Marleen Hallamaa1,2, Hannah Pia Franziska Meier1, Matteo Vajente1
1Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV, Groningen, Netherlands.
None:
The use of single carbon (C1) molecules, such as carbon dioxide or formate, is crucial in the transition from a linear, petroleum-based economy to a circular bioeconomy. Formate can serve as both a carbon and energy source, further enhancing its attractiveness as a feedstock. Cupriavidus necator, a lithoautotrophic microbial chassis strain, provides an opportunity to leverage formate for the synthesis of valuable products. However, its ability to grow on formate and the subsequent coupling of that process to recombinantly produced redox enzymes for the efficient production of high-value-added products in a biotransformation has not yet been established. Here, we report the development of a formate-driven C. necator whole-cell chassis that recombinantly produces Rieske oxygenases (ROs) and elaborate on possible stress responses of the cells during formatotrophic cultivation. The whole-cell chassis efficiently catalyzes the oxyfunctionalization of olefins fueled by formate oxidation. For instance, styrene is dihydroxylated to (R)-1-phenylethane-1,2-diol in an excellent 95% yield and with good enantioselectivity (74% ee) under formatotrophic conditions. The product yield and optical purity obtained demonstrate the synthetic usefulness of formate-fueled whole-cell bio-transformations in C. necator.
Related Concept Videos
Carbon-dioxide Fixation
Respiration Pathways
Pyruvate Oxidation
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
Lipid Catabolism
The Calvin Benson Cycle
Fates of Pyruvate
In aerobic organisms, pyruvate is metabolized via the citric acid cycle to produce reduced coenzymes NADH and FADH2. These coenzymes are then oxidized in the electron transport chain to produce ATP and, in the process, regenerate the NAD+ and FAD. As seen in some cell types and organisms, fermentation...

