2026/01/22 by Holly R. Rucker, Kunmanee Bubphamanee, Derek F. Harris +4 · 1 voice
Earth and Planetary Sciences · Energy · Chemical Engineering · #Paleontology and Stratigraphy of Fossils #Metalloenzymes and iron-sulfur proteins #Ammonia Synthesis and Nitrogen Reduction
paper · pdf · doi:10.1038/s41467-025-67423-y
openalex publication_date 2026/01/22 · openalex created_date 2026/01/23 · openalex updated_date 2026/07/29
Nitrogen isotope fractionation (ε15N) in sedimentary rocks has provided evidence for biological nitrogen fixation, and thus primary productivity, on the early Earth. However, the extent to which molecular evolution has influenced the isotopic signatures of nitrogenase, the enzyme that catalyzes the conversion of atmospheric nitrogen (N₂) to bioavailable ammonia, remains unresolved. Here, we reconstruct and experimentally characterize a library of synthetic ancestral nitrogenase genes, spanning over 2 billion years of evolutionary history. We assess the resulting ε¹⁵N values under controlled laboratory conditions. All engineered strains exhibit ε15N values within a narrow range comparable to that of modern microbes, suggesting that molybdenum (Mo)-dependent nitrogenase has been largely invariant throughout evolutionary time since the origins of this pathway. The results of this study support the early origin of molybdenum nitrogenase and the resilience of nitrogen-isotope biosignatures in ancient rocks, while also demonstrating their potential as powerful tools in the search for life beyond Earth. The study shows that nitrogenase enzymes have maintained stable isotope signatures over billions of years, revealing how ancient microbes shaped Earth’s nitrogen cycle and offering a new experimental framework for probing early life.