# Catechol Siderophores from a Mangrove-Derived Bacteria Serratia marcescens F2-2 and Their Cytotoxic Activity

**Authors:** Gang Zhang, Xunming Wang, Xingwang Zhang, Lin Ye, Longyang Ke, Shimin Fan, Xuan Hong, Guoqiang Li, Bingye Yang, Lianzhong Luo

PMC · DOI: 10.3390/md23060241 · Marine Drugs · 2025-05-30

## TL;DR

This study isolates new iron-chelating compounds from a mangrove bacteria that show potential in fighting liver cancer by inducing cell death.

## Contribution

The discovery of two new catechol siderophores, serratiochelins E and F, and their potential anti-liver cancer activity.

## Key findings

- Serratiochelins E and F are new catechol siderophores isolated from S. marcescens F2-2.
- Serratiochelin B shows selective cytotoxicity against HepG2 liver cancer cells with an IC50 of 50.6 μmol/L.
- The compound induces apoptosis via Bcl-2/Bax/caspase-3 and Fas/FasL/caspase-8 pathways.

## Abstract

Serratia marcescens is a common Gram-negative and facultative anaerobic bacillus that produces serratiochelins with several bioactivities. In this study, four catechol siderphores (1–4), including two new ones named serratiochelins E (1) and F (2), were obtained from the fermentation of a mangrove-derived bacterium, S. marcescens F2-2. The structures were elucidated with various spectroscopic methods such as NMR and HR-ESI-MS. Absolute and geometric configurations of the new compounds were established by employing quantum NMR calculations in conjunction with DP4+ probability analysis, ECD calculations, and the advanced Marfey’s method. The bioactivity test showed that serratiochelin B (3) displayed weak but selective cytotoxicity against HepG2 cancer cells with an IC50 of 50.6 μmol/L and could trigger apoptosis through both Bcl-2/Bax/caspase-3 and Fas/FasL/caspase-8 signaling pathways. These findings deepen the understanding of siderophores of S. marcescens and provide a lead for research on anti-liver cancer drugs.

## Linked entities

- **Proteins:** BCL2 (BCL2 apoptosis regulator), BAX (BCL2 associated X, apoptosis regulator), Casp3 (caspase 3), FAS (Fas cell surface death receptor), FASLG (Fas ligand), casp8 (caspase 8, apoptosis-related cysteine peptidase)
- **Chemicals:** serratiochelin B (PubChem CID 139587640)
- **Diseases:** liver cancer (MONDO:0002691)
- **Species:** Serratia marcescens (taxon 615)

## Full-text entities

- **Diseases:** cytotoxicity (MESH:D064420), liver cancer (MESH:D006528), cancer (MESH:D009369)
- **Chemicals:** Catechol Siderophores (-)
- **Species:** marcescens [taxon 211759], Serratia marcescens (species) [taxon 615]
- **Cell lines:** HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12193787/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12193787/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12193787/full.md

---
Source: https://tomesphere.com/paper/PMC12193787