# Extracellular Metabolite Profiling in CO2-Fixing Bacterium Rhodobacter sphaeroides Under Autotrophic Conditions

**Authors:** Yu Rim Lee, Suhyeon Hong, Young-Hwan Chu, Soo Youn Lee, Sangmin Lee

PMC · DOI: 10.3390/metabo16030156 · 2026-02-26

## TL;DR

This study identifies extracellular metabolites in Rhodobacter sphaeroides under autotrophic conditions, revealing shifts in metabolic pathways that could improve CO2-based biomanufacturing.

## Contribution

The first comprehensive extracellular metabolite profiling of R. sphaeroides under autotrophic conditions, linking metabolite accumulation to gene expression changes.

## Key findings

- 62 putative extracellular metabolites were detected, with 23 above quantification limits.
- Glycolysis and gluconeogenesis metabolites dominated, with lactic acid showing the highest accumulation.
- Transcriptional analysis revealed downregulation of glycolytic genes and upregulation of cfxA under autotrophic conditions.

## Abstract

Background/Objectives: Rhodobacter sphaeriids is considered a promising biomanufacturing platform due to its capacity to convert CO2 into value-added products. To enhance the yield of CO2-derived products, understanding extracellular metabolite dynamics during autotrophic growth is essential. However, the extracellular metabolite profiles of R. sphaeroides under autotrophic conditions have not been reported. Methods: In this study, we performed a comprehensive analysis of extracellular metabolites produced under autotrophic conditions using capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS) and liquid chromatography time-of-flight mass spectrometry (LC-TOFMS). Results: A total of 62 putative metabolites were detected, of which 23 were measured above the quantification limit. Metabolites involved in glycolysis and gluconeogenesis constituted the largest proportion of extracellular metabolites, with lactic acid exhibiting the highest accumulation levels. To investigate the transcriptional changes associated with metabolite accumulation, we analyzed gene expression and observed the downregulation of glycolytic genes, including pgi, gapB, and lctB, whereas cfxA, encoding fructose-1,6-bisphosphate aldolase, was upregulated under autotrophic conditions compared to heterotrophic conditions. Conclusions: These results suggest that the carbon assimilation metabolic flux in R. sphaeroides shifts toward the CBB cycle and lactic acid overflow metabolism under autotrophic conditions. Collectively, these findings provide new insights into metabolic regulation during autotrophic growth and offer a basis for reducing extracellular byproduct formation and improving CO2-based biological production in R. sphaeroides.

## Linked entities

- **Genes:** BGN (biglycan) [NCBI Gene 633], GAPB (glyceraldehyde-3-phosphate dehydrogenase B subunit) [NCBI Gene 840895], lctB (lactate dehydrogenase subunit LctB) [NCBI Gene 68363108]
- **Chemicals:** lactic acid (PubChem CID 612), fructose-1,6-bisphosphate (PubChem CID 10267)

## Full-text entities

- **Diseases:** injury to (MESH:D014947)
- **Chemicals:** methionine sulfone (MESH:C018332), fat (MESH:D005223), lipid (MESH:D008055), DHAP (MESH:D004099), spermidine (MESH:D013095), biotin (MESH:D001710), glycerol (MESH:D005990), TCA (MESH:D014238), IPP (MESH:C004809), EDTA (MESH:D004492), 1,3-BPG (-), isoprene (MESH:C005059), 2-phosphoglycerate (MESH:C008885), poly-beta-hydroxybutyrate (MESH:C003182), Creatine (MESH:D003401), Methyl sulfate (MESH:C033522), serine (MESH:D012694), G3P (MESH:D005986), H2 (MESH:D006859), PHB (MESH:C000720856), alanine (MESH:D000409), glutamine (MESH:D005973), C1 (MESH:C400149), thiol (MESH:D013438), polyamine (MESH:D011073), fructose-6-phosphate (MESH:C027618), L-lactic acid (MESH:D019344), methionine (MESH:D008715), C (MESH:D002244), fatty acids (MESH:D005227), oxygen (MESH:D010100), isoprenoids (MESH:D013729), threonine (MESH:D013912), ethanol (MESH:D000431), N-Ethylmaleimide (MESH:D005033), ATP (MESH:D000255), ascorbic acid (MESH:D001205), histidine (MESH:D006639), carbohydrate (MESH:D002241), CO2 (MESH:D002245), 3-phosphoglycerate (MESH:C005156), KOH (MESH:C029943), aspartic acid (MESH:D001224), RuBP (MESH:C001933), nicotinic acid (MESH:D009525), sesquiterpene (MESH:D012717), pyruvate (MESH:D019289), choline (MESH:D002794), glucose-6-phosphate (MESH:D019298), cellulose (MESH:D002482), NaCl (MESH:D012965), HMT (MESH:D008709), urea (MESH:D014508), N (MESH:D009584), beta-farnesene (MESH:C062671), Ar (MESH:D001128), proline (MESH:D011392), FPP (MESH:C004808), fructose-1,6-bisphosphate (MESH:C029063), ammonium formate (MESH:C030544)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cupriavidus necator (species) [taxon 106590], Escherichia coli (E. coli, species) [taxon 562], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Cereibacter sphaeroides (species) [taxon 1063], Rhodospirillum rubrum (species) [taxon 1085], Komagataeibacter xylinus (species) [taxon 28448], Citrus junos (kuzu, species) [taxon 135197]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027526/full.md

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Source: https://tomesphere.com/paper/PMC13027526