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Global niche partitioning of purine and pyrimidine cross-feeding among ocean microbes

Rogier Braakman, Brandon M. Satinsky, Tyler J. O’Keefe, Krista Longnecker, Shane Hogle, Jamie W. Becker, R.C.M. Li, Keven Dooley, Aldo A. Arellano, Melissa C. Kido Soule, Elizabeth B. Kujawinski, Sallie W. Chisholm

2025Science Advances14 citationsDOIOpen Access PDF

Abstract

Cross-feeding involves microbes consuming exudates of other surrounding microbes, mediating elemental cycling. Characterizing the diversity of cross-feeding pathways in ocean microbes illuminates evolutionary forces driving self-organization of ocean ecosystems. Here, we uncover a purine and pyrimidine cross-feeding network in globally abundant groups. The cyanobacterium Prochlorococcus exudes both compound classes, which metabolic reconstructions suggest follows synchronous daily genome replication. Co-occurring heterotrophs differentiate into purine- and pyrimidine-using generalists or specialists that use compounds for different purposes. The most abundant heterotroph, SAR11, is a specialist that uses purines as sources of energy, carbon, and/or nitrogen, with subgroups differentiating along ocean-scale gradients in the supply of energy and nitrogen, in turn producing putative cryptic nitrogen cycles that link many microbes. Last, in an SAR11 subgroup that dominates where Prochlorococcus is abundant, adenine additions to cultures inhibit DNA synthesis, poising cells for replication. We argue that this subgroup uses inferred daily adenine pulses from Prochlorococcus to synchronize to the daily photosynthate supply from surrounding phytoplankton.

Topics & Concepts

ProchlorococcusBiologyPurineCyanobacteriaPyrimidineNitrogen cycleGeomicrobiologyNichePhytoplanktonEcologyEcosystemMicrobial ecologyEnvironmental biotechnologyBiochemistryNitrogenNutrientChemistryBacteriaGeneticsSynechococcusOrganic chemistryEnzymeMicrobial Community Ecology and PhysiologyAmino Acid Enzymes and MetabolismProtist diversity and phylogeny