Machine learning–assisted directed evolution of plant Rubisco

Ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) is foundational to life on Earth, catalyzing carbon dioxide (CO 2 ) fixation to generate biomass. However, Rubisco is a slow and inefficient enzyme that has proven challenging to engineer. We applied the structure-informed machine learning (ML) model ESM-IF1 to identify plausible amino acid sites in the large subunit of Nicotiana tabacum Rubisco to target for directed evolution. ML-assisted library design followed by selection in Rubisco-dependent Escherichia coli identified multiple enriched variants displaying improved catalytic efficiency. Several improved variants carried amino acid changes not found in the evolutionary lineage of plants, despite being assembly competent in plant chloroplasts, demonstrating that ML-assisted protein design can explore functional sequence space beyond what is observed from natural sequence diversity. Most prominently, the T391I substitution improved carboxylation rate by 29% and aerobic carboxylation efficiency by 43%. Our findings illustrate the utility of ML-assisted evolution for engineering Rubisco with improved carboxylation efficiency and potential for enhancing crop productivity.

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Publication Details

Journal
Science Advances
Published
2026-10-07
DOI
https://doi.org/10.1126/sciadv.aeh3246
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
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article

Machine learning–assisted directed evolution of plant Rubisco

Brian Hie, Robert H. Wilson, Mary A. Gehring, Jiacheng Lin et al.
Science Advances
Photosynthetic Processes and Mechanisms
article

Machine learning–assisted directed evolution of plant Rubisco

Brian Hie, Robert H. Wilson, Mary A. Gehring, Jiacheng Lin, Bryan D. Bryson, Julie L. McDonald, Rosemary J. Birch, Matthew D. Shoulders, Spencer Michael Whitney, Yunlong Zhao
article en

Abstract

Ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) is foundational to life on Earth, catalyzing carbon dioxide (CO 2 ) fixation to generate biomass. However, Rubisco is a slow and inefficient enzyme that has proven challenging to engineer. We applied the structure-informed machine learning (ML) model ESM-IF1 to identify plausible amino acid sites in the large subunit of Nicotiana tabacum Rubisco to target for directed evolution. ML-assisted library design followed by selection in Rubisco-dependent Escherichia coli identified multiple enriched variants displaying improved catalytic efficiency. Several improved variants carried amino acid changes not found in the evolutionary lineage of plants, despite being assembly competent in plant chloroplasts, demonstrating that ML-assisted protein design can explore functional sequence space beyond what is observed from natural sequence diversity. Most prominently, the T391I substitution improved carboxylation rate by 29% and aerobic carboxylation efficiency by 43%. Our findings illustrate the utility of ML-assisted evolution for engineering Rubisco with improved carboxylation efficiency and potential for enhancing crop productivity.

Science AdvancesVol. 12(41)
Broad Institute (US), Australian National University (AU), Howard Hughes Medical Institute (US), Ragon Institute of MGH, MIT and Harvard (US), Stanford Medicine (US), Whitehead Institute for Biomedical Research (US), Massachusetts Institute of Technology (US), Stanford University (US)
Openalex Percentile: Top 22%
Photosynthetic Processes and Mechanisms
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