# Genomic and functional characterization of Pseudosulfitobacter pseudonitzschiae BPC-C4-2: a growth-promoting symbiont in Antarctic Ulva communities

**Authors:** Tia Wünschmann, Fatemeh Ghaderiardakani, Timo Homeier-Bachmann, Maria Liliana Quartino, Thomas Wichard, Anne Busch

PMC · DOI: 10.1186/s12864-026-12626-w · BMC Genomics · 2026-02-07

## TL;DR

This paper characterizes a cold-adapted marine bacterium and its role in promoting growth of Antarctic algae through genomic and functional analysis.

## Contribution

The study provides a detailed genomic and phylogenetic analysis of Pseudosulfitobacter pseudonitzschiae and its functional role in algal morphogenesis.

## Key findings

- The genome of P. pseudonitzschiae BPC-C4-2 contains 5,380 coding sequences and multiple RNA genes, suggesting metabolic flexibility.
- A sox gene cluster involved in sarcosine oxidation and DMSP degradation was identified, indicating functional adaptations to cold environments.
- Affinity propagation clustering improved phylogenetic placement of P. pseudonitzschiae within a taxonomically complex group.

## Abstract

Pseudosulfitobacter pseudonitzschiae is a species within the genus Pseudosulfitobacter, which belongs to the Roseobacteraceae. This family is closely associated with algae and is essential to marine ecosystems, particularly through interactions with phytoplankton. Notably, this bacterium can produce bioactive compounds that influence microbial dynamics and algal growth in marine environments. In addition to essential nutritional factors, the marine green macroalgal genus Ulva (Chlorophyta) relies on a combination of regulatory morphogenetic compounds produced by its associated epiphytic bacteria to achieve proper morphogenesis. Since P. pseudonitzschiae is rarely described and phylogenetic clustering within this genus is challenging, we conducted phylogenetic and genomic analyses to better resolve its taxonomic position and to explore its functional potential in the Antarctic environment.

P. pseudonitzschiae BPC-C4-2 was isolated and integrated into a tripartite model system alongside Maribacter sp. BPC-D8 (CP128187.1) and Ulva sp. UPC-109 (PP091299.1). This biosystem was designed to study the mechanisms of cold-water adaptation involved in the morphogenetic development of the genus Ulva.

The hybrid genome assembly of P. pseudonitzschiae BPC-C4-2 consisted of seven contigs totaling 5,450,390 bp, with a GC content of 59.0%. Genome annotation identified 5,380 coding sequences (CDSs), 6 rRNA genes, 85 tRNA genes, and 1 tmRNA. The relatively large number of coding sequences and RNA genes observed may reflect an expanded genetic toolkit that enables metabolic flexibility and stress tolerance, potentially supporting adaptation to the extreme conditions of Antarctic and cold-water environments.

Given the taxonomic complexity within the bacterial family, both 16S rRNA gene sequencing and average nucleotide identity (ANI) analyses were conducted. Using affinity propagation clustering, these analyses enabled a more robust phylogenetic placement of P. pseudonitzschiae within this challenging group, providing deeper ecological and evolutionary insights.

In this study, we searched for gene clusters associated with metabolic adaptations. Functionally, the genome harbors a modularly organized sox gene cluster involved in the sarcosine oxidation pathway and dimethylsulfoniopropionate (DMSP) degradation. Additional pathways involved in osmolyte metabolism and methylation were also identified and found to be phylogenetically distinct from closely related species.

Our findings provide the basis for a cold-water bioassay system to study the morphogenesis of Ulva collected from polar regions, in association with Maribacter sp. BPC-D8 and P. pseudonitzschiae BPC-C4-2. Genomic analyses of P. pseudonitzschiae BPC-C4-2 provide insights into its revised phylogeny based on affinity propagation clustering, along with a detailed analysis of genes involved in key metabolic pathways.

The online version contains supplementary material available at 10.1186/s12864-026-12626-w.

## Linked entities

- **Genes:** SOX (sulfite oxidase) [NCBI Gene 820118], rRNA (12S ribosomal RNA) [NCBI Gene 44804684], TRNA (tRNA-Ala) [NCBI Gene 4553], tmRNA (miscRNA) [NCBI Gene 884092]
- **Chemicals:** dimethylsulfoniopropionate (PubChem CID 23736), sarcosine (PubChem CID 1088)
- **Species:** Pseudosulfitobacter pseudonitzschiae (taxon 1402135), Maribacter sp. BPC-D8 (taxon 3053613), Chlorophyta (taxon 3041)

## Full-text entities

- **Chemicals:** FAD (MESH:D005182), thallusin (MESH:C498021), Betaine (MESH:D001622), thiosulfate (MESH:D013885), glycerin (MESH:D005990), Sulfur (MESH:D013455), DMSOP (-), H2O2 (MESH:D006861), auxin (MESH:D007210), DMSO (MESH:D004121), CH3SH (MESH:C005231), formaldehyde (MESH:D005557), quinone (MESH:C004532), Sulfite (MESH:D013447), IAA (MESH:C030737), saxitoxin (MESH:D012530), Ectoine (MESH:C045628), dimethylglycine (MESH:C025138), cytokinin (MESH:D003583), carbon (MESH:D002244), Sulfide (MESH:D013440), sulfate (MESH:D013431), acrylate (MESH:C036658), glycine (MESH:D005998), DMS (MESH:C004784), Sarcosine (MESH:D012521), DMSP (MESH:C068078), sulfur compound (MESH:D013457)
- **Species:** Maribacter sp. (species) [taxon 1897614], Ulva mutabilis (species) [taxon 498180], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Paracoccus pantotrophus (species) [taxon 82367], Roseobacter (genus) [taxon 2433], Pseudosulfitobacter pseudonitzschiae (species) [taxon 1402135], Hyphomonas polymorpha (species) [taxon 74319], PX clade (clade) [taxon 569578], Ulva compressa (species) [taxon 63659], Ulva linza (species) [taxon 63409], Ulva (sea lettuces, genus) [taxon 3118], Halomonas (genus) [taxon 2745], Roseovarius sp. (species) [taxon 1486281], Usnea mutabilis (species) [taxon 143885], Ulva sp. (species) [taxon 2812607], Marinobacter (genus) [taxon 2742], Thiobacillus (genus) [taxon 919], Ulva intestinalis (hollow green seaweed, species) [taxon 3116]
- **Cell lines:** UPC-109 — Homo sapiens (Human), Supernumerary circular chromosome, Finite cell line (CVCL_4D75), FLO-MIN106 — Homo sapiens (Human), Barrett adenocarcinoma, Cancer cell line (CVCL_2045), CP128187.1 — Mus musculus (Mouse), Carcinoma of the mouse prostate gland, Cancer cell line (CVCL_VQ84)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930554/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930554/full.md

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Source: https://tomesphere.com/paper/PMC12930554