Proceedings of the National Academy of SciencesBiochemistryPeer-reviewed journal article
In vivo directed evolution of an ultra-fast RuBisCO from a semi-anaerobic environment imparts oxygen resistance
Julie Lynn McDonaldiD, Nathan P. Shapiro, Amanuella A. Mengiste, Sarah KainesiD, Spencer Michael WhitneyiD, Robert H. WilsoniD, Matthew D. ShouldersiD
Abstract
Carbon dioxide (CO2) assimilation by the enzyme Ribulose-1,5-bisphosphate Carboxylase/Oxygenase (Rubisco) underpins biomass accumulation in photosynthetic bacteria and eukaryotes. Despite its pivotal role, Rubisco has a slow carboxylation rate [Formula] and is competitively inhibited by oxygen (O2). These traits impose limitations on photosynthetic efficiency, making Rubisco a compelling target for improvement. Interest in Form II Rubisco from Gallionellaceae bacteria, which comprise a dimer or hexamer of large subunits, arises from their nearly 5-fold higher [Formula] than the average Rubisco enzyme. As well as having a fast [Formula] (25.8 s-1 at 25 {degrees}C), we show that Gallionellaceae Rubisco (GWS1B) is extremely sensitive to O2 inhibition, consistent with its evolution under semi-anaerobic environments. We therefore used a novel in vivo mutagenesis-mediated screening pipeline to evolve GWS1B over six rounds under oxygenic selection, identifying three catalytic point mutants with improved ambient carboxylation efficiency; Thr-29-Ala (T29A), Glu-40-Lys (E40K) and Arg-337-Cys (R337C). Full kinetic characterization showed that each substitution enhanced the CO2 affinity of GWS1B under oxygenic conditions by subduing oxygen affinity, leading to 25% (E40K), 11% (T29A) and 8% (R337C) enhancements in carboxylation efficiency under ambient O2 at 25 {degrees}C. By contrast, under the near anaerobic natural environment of Gallionellaceae, the carboxylation efficiency of each mutant was impaired [~]16%. These findings demonstrate the efficacy of artificial directed evolution to access novel regions of catalytic space in Rubisco. SignificanceGiven Rubiscos crucial role in carbon dioxide assimilation, addressing its slow carboxylation rate and oxygen inhibition is a significant challenge. Utilizing one of the fastest known, yet also highly oxygen-sensitive, Rubisco - from the bacteria Gallionellaceae - we applied a novel in vivo directed evolution pipeline in Escherichia coli to discover mutations that specifically enhance carboxylation efficiency under ambient oxygen, a condition distinct from Gallionellaceaes natural semi-anaerobic environment. Our findings underscore the potential of directed evolution to unlock new catalytic capabilities for Rubisco, with implications for both fundamental research and practical agricultural applications.
- Citations
- 21
- FWCI
- 6.28
- Field percentile
- top 2%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Rubisco is evolving for improved catalytic efficiency and CO2 assimilation in plants
J. Bouvier, D. Emms, S. Kelly·bioRxiv·Jul 6, 2022
- A microbial growth-coupled platform for in vivo interrogation of Rubisco oxygenase activity
Enrico Orsi, Kai Kabuth, … Pablo I. Nikel·bioRxiv·Jul 10, 2026
- The fitness landscape of a Form II Rubisco in a photosynthetic bacterium guides engineering of oxygen tolerance
Ute A. Hoffmann, Axel Knave, … Elton Paul Hudson·Science AdvancesPeer-reviewed·Sep 4, 2026
- Systematic exploration of bacterial form I rubisco maximal carboxylation rates
Benoit de Pins, Lior Greenspoon, … Ron Milo·The EMBO JournalPeer-reviewed·May 28, 2024
- A Genetically Encoded System to Quantify and Evolve RuBisCO-Catalyzed Carbon Fixation
David L. Lanster, Zhiyi Li, Ahmed H. Badran·bioRxiv·May 15, 2024
- A cyanobacterial screening platform for Rubisco mutant variants
Ute A. Hoffmann, Anna Zoey Schuppe, … Elton Paul Hudson·ACS Synthetic BiologyPeer-reviewed·Jul 7, 2025