Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.04.04.716520

Protein without farms: What comparative genomics reveals about ''Power-to-Food'' microbes

Abstract

Conventional agriculture is increasingly incompatible with planetary boundaries, such as land and water demand, greenhouse-gas emissions, and disruption of the nitrogen cycle. Hydrogen-oxidizing bacteria (HOB) enable a scalable "power-to-food" approach in which aerobic gas fermentation turns CO2 and renewable H2, along with N2 in some strains, into protein-rich biomass, largely decoupling protein production from arable land and climate variability. The same chemistry is attractive for closed-loop space life support, where crew CO2 and electrolysis-derived H2 can be recycled into edible biomass. Here, we compare two leading HOB chassis strains, Cupriavidus necator H16 and Xanthobacter sp. SoF1, using standardized re-annotation, orthology-based comparison, pathway reconstruction, and safety-oriented genome screening. Importantly, SoF1 is the production strain for Solar Foods Solein(R), a dried microbial biomass ingredient, which is approved as a novel food in Singapore and has a self-affirmed GRAS status in the United States. H16 has a larger, multipartite genome of 7.41 Mb split across two chromosomes and the pHG1 megaplasmid, whereas SoF1 is more compact at 4.91 Mb and encoded on a single replicon. Both encode Calvin-Benson-Bassham CO2 fixation and multiple [NiFe]-hydrogenase systems supporting growth on CO2/H2, but nitrogen economy differentiates the hosts. SoF1 encodes a complete nitrogen-fixation module (nifHDK) and nitrate-assimilation genes, whereas H16 lacks nif and instead encodes nitrate/nitrite respiration for oxygen-limited flexibility. Safety screening revealed no evidence of canonical virulence determinants, integron or plasmid-linked antimicrobial resistant (AMR) cassettes, or high-confidence foodborne exotoxins under strict thresholds. These results convert genome-level features into actionable design constraints for selecting and engineering food-grade HOB, strengthening robust air-to-protein bioprocesses on Earth and informing a blueprint for closed-loop, space-compatible protein production. HighlightsO_LIHydrogen-oxidizing bacteria enable power-to-protein from CO2, H2 with minimal land use. C_LIO_LIHead-to-head genomics defines design rules for food-grade "air-to-protein" bioprocesses. C_LIO_LIContrasting nitrogen routes guide media design, nutrient inputs, and closed-loop operation. C_LIO_LICO2 fixation and hydrogenase gene sets reveal complementary robustness and control features. C_LIO_LIGenome architecture and COG shifts inform safety, stability, and regulatory-ready strain choice. C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kumar, K., Pitkänen, J.-P., Alter, T. B., Blank, L. M.. 2026-04-07. Protein without farms: What comparative genomics reveals about ''Power-to-Food'' microbes. https://doi.org/10.64898/2026.04.04.716520

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

RNA isoform-resolved multiplexed sequencing with bioorthogonal barcoding

RNA isoform dysregulation drives disease pathogenesis and is the target of FDA-approved splice-switching therapeutics. However, multiplexed sequencing methods discard splice junction information because only 3' termini are barcoded and counted. Here, we repurpose acylation and click chemistries to conjugate bioorthogonal barcodes (bobcodes) directly onto multiple internal positions along cellular RNAs. Bobcoded RNAs from multiple samples are pooled for multiplexed cDNA synthesis, during which reverse transcriptase switches from each RNA template onto its tethered bobcode with greater than 99% accuracy in species mixing experiments. Bobcode attachment intervals set cDNA insert sizes without a library fragmentation step, and priming with poly(dT) or random hexamers selects between 3'-end counting and full-length isoform capture. A bioorthogonal barcode-sequencing (BOB-seq v0.1) drug screen identifies transcriptome-wide on- and off-target RNA splicing effects and outperforms existing multiplexing RNA sequencing methods in workflow simplicity, sample-to-sample variability, and barcoding accuracy. Bobcodes add isoform resolution to scalable multiplexed RNA sequencing.

genomics↗

Integrative Nanopore and Illumina sequencing reveals age-associated tRNA modification and CCA-tail dynamics in yeast

Aging is characterized by a progressive loss of proteostasis. Transfer RNAs (tRNAs) are essential regulators of translation, yet their dynamics during aging remain poorly understood due to challenges in sequencing highly modified RNAs. Here we present a benchmarked Nanopore direct RNA sequencing (RNA004 chemistry) resource that profiles the Saccharomyces cerevisiae tRNAome during replicative aging at single-molecule resolution. Using in vitro transcribed tRNA controls, we establish modification detection thresholds and validate key findings with orthogonal Illumina sequencing. While overall tRNA abundance remains largely stable, our resource reveals age-associated terminal A cleavage at the 3' CCA tail of mature tRNAs, targeted T-loop and anticodon modification changes, and single-molecule evidence of modification co-occurrence. This dataset provides a resource for exploring tRNA regulation, translation fidelity, and longevity.

genomics↗

A hydrogen-producing mitochondrion in an anaerobic eukaryotrophic rhizarian

Diverse eukaryotes thrive under low oxygen conditions, in part through highly modified mitochondrion-related organelles (MROs) that use alternate metabolic pathways to support ATP production and cofactor recycling. Anaerobic lifestyles have evolved repeatedly across the eukaryotic tree of life, each providing an independent opportunity to understand how eukaryotes adapt to life in low oxygen conditions. Here, we use single-cell transcriptomics to reconstruct the MRO metabolism of PCE SSF, a benthic eukaryotrophic flagellate and the first cultivated representative of Novel Clade 12 (NC12; Rhizaria), an independently anaerobic rhizarian lineage. PCE SSF possesses an anaerobic hydrogen-producing mitochondrion capable of hydrogenosome-type substrate-level phosphorylation. It also retains a nearly complete but likely branched tricarboxylic acid pathway that lacks citrate synthase and malate dehydrogenase. The function of citrate synthase may instead be fulfilled by the typically cytosolic ATP citrate lyase, previously reported in this context only in the anaerobic cercozoan, Brevimastigomonas motovehiculus. Unlike B. motovehiculus, however, PCE SSF retains only Complex II and the NuoE/NuoF subunits of the electron transport chain and lacks a mitochondrial genome. Together, these features indicate an atypical and reduced mitochondrial metabolism, highlighting the diversity of evolutionary solutions to anaerobic energy metabolism in eukaryotes.

genomics↗