Abundant and metabolically flexible lineages within the SAR324 and gammaproteobacteria dominate the potential for rubisco-mediated carbon fixation in the dark ocean

BackgroundRubisco is among the most abundant enzymes on Earth and is a critical conduit for inorganic carbon into the biosphere. Despite this, the full extent of rubisco diversity and the biology of organisms that employ it for carbon fixation are still emerging, particularly in unlit ecosystems like the deep sea. ResultsHere, we generate fifteen deeply-sequenced metagenomes along a spatially-resolved transect off the California coast, and combine them with globally-distributed public data to examine the diversity, distribution, and metabolic features of rubisco-encoding organisms from the dark water column. Organisms with rubisco were detected in the vast majority of all samples, spanning over 1,000 species groups and together comprising up to [~]20% of the total microbial community. At 150 meters and below, potential for carbon fixation via rubisco was dominated by just two orders of gammaproteobacteria and SAR324, encoding either the form I or II rubisco. Many of these organisms also possessed genes for the oxidation of reduced sulfur compounds, which may energetically support carbon fixation. Transcriptomic profiling in the epi- and mesopelagic suggested that all major forms of rubisco can be highly expressed in the deep water column, but are not done so constitutively, consistent with metabolic flexibility. ConclusionOur results demonstrate that the genetic potential to fix carbon via rubisco is significant and spatially widespread in the dark ocean. We identify several rubisco-encoding species groups that are particularly abundant and cosmopolitan, highlighting the key role they may play in deep-sea chemoautotrophy and the global marine carbon cycle.