A systematic exploration of bacterial form I rubisco maximal carboxylation rates
Benoit de Pins, Lior Greenspoon, Yinon M. Bar‐On, Melina Shamshoum, Roee Ben-Nissan, Eliya Milshtein, Dan Davidi, Itai Sharon, Oliver Mueller‐Cajar, Εlad Noor, Ron Milo
Abstract
Abstract Autotrophy is the basis for complex life on Earth. Central to this process is rubisco—the enzyme that catalyzes almost all carbon fixation on the planet. Yet, with only a small fraction of rubisco diversity kinetically characterized so far, the underlying biological factors driving the evolution of fast rubiscos in nature remain unclear. We conducted a high-throughput kinetic characterization of over 100 bacterial form I rubiscos, the most ubiquitous group of rubisco sequences in nature, to uncover the determinants of rubisco’s carboxylation velocity. We show that the presence of a carboxysome CO 2 concentrating mechanism correlates with faster rubiscos with a median fivefold higher rate. In contrast to prior studies, we find that rubiscos originating from α-cyanobacteria exhibit the highest carboxylation rates among form I enzymes (≈10 s −1 median versus <7 s −1 in other groups). Our study systematically reveals biological and environmental properties associated with kinetic variation across rubiscos from nature.