# Genome mining and screening for plastic-degrading potential in marine bacteria

**Authors:** Rafaela Perdigão, Diogo A. M. Alexandrino, Maria F. Carvalho, Catarina Magalhães, C. Marisa R. Almeida, Ana P. Mucha

PMC · DOI: 10.1007/s00253-026-13767-4 · Applied Microbiology and Biotechnology · 2026-03-03

## TL;DR

This study identifies marine bacteria from plastic fishing nets that can degrade plastics and explores their genetic potential for biodegradation.

## Contribution

A new workflow for screening and genome mining of plastic-degrading marine bacteria from submerged plastic nets is introduced.

## Key findings

- Eleven bacterial strains showed enhanced growth on plastic polymers and eight exhibited esterase/lipase activity.
- Genes linked to plastic degradation were predominantly found in Actinomycetes strains.
- Genome mining revealed enzymes potentially capable of degrading polyethylene terephthalate, low-density PE, and nylon.

## Abstract

Marine plastic litter, including microplastics, has a profound impact on the ocean and its wildlife, and strategies to remove/eliminate it are needed. Microbial biodegradation, particularly by bacteria, offers a potential solution, where a link between hydrocarbon and plastic-degradation has been hypothesized. This study screened the plastic-degrading potential of 18 bacterial strains isolated from 1-month-old biofilms developed in three submerged plastic fishing nets (braided polyethylene (PE), braided nylon, thin nylon). In addition, three highly efficient hydrocarbon-degrading strains were also tested. Strains were cultivated on solid minimal media with fishing net small pieces (new/unused nets) added as a carbon source for 1 month, followed by tributyrin-agar assays to assess esterase/lipase activity. Eleven bacteria exhibited enhanced growth with net polymers, mainly from the genera Sulfitobacter, Rhodococcus, Bacillus, and Pseudomonas, and eight of which bacteria also demonstrated esterase/lipase activity. Then, genes encoding hydrocarbon or plastic-degrading enzymes (alkB and almA homologs, PETase-like enzymes) were screened by PCR in the 21 mentioned bacteria and in ca.100 other strains found in submerged nets biofilm. Amplification of the investigated genes was predominantly observed in Actinomycetes strains. Genome mining of six promising strains revealed hits with enzymes linked to degradation of synthetic polymers like polyethylene terephthalate, low-density PE and nylon. The workflow developed here enabled the selection of marine bacteria with plastic-degrading potential, sourced from biofilms of submerged plastic fishing nets and hydrocarbon-enriched environments.

• A comprehensive lab workflow was developed to assess plastic-degrading potential.

• Genome mining in Rhodococcus and Pseudomonas strains revealed plastic-degrading enzymes.

• Hydrocarbon-degrading bacteria could hold plastic-degrading capabilities.

The online version contains supplementary material available at 10.1007/s00253-026-13767-4.

## Linked entities

- **Genes:** ALKBH1 (alkB homolog 1, histone H2A dioxygenase) [NCBI Gene 8846]
- **Chemicals:** nylon (PubChem CID 12332)
- **Species:** Sulfitobacter (taxon 60136), Rhodococcus (taxon 1827), Bacillus (taxon 1386), Pseudomonas (taxon 286), Actinomycetes (taxon 1760)

## Full-text entities

- **Genes:** ALKBH1 (alkB homolog 1, histone H2A dioxygenase) [NCBI Gene 8846] {aka ABH, ABH1, ALKBH, alkB, hABH}
- **Chemicals:** CaCl2 (MESH:D002122), alkane (MESH:D000473), A (MESH:D001151), PET (MESH:D011093), PU (MESH:D011140), LDPE (MESH:D020959), PAHs (MESH:D011084), H2SO4 (MESH:C033158), NaOH (MESH:D012972), water (MESH:D014867), PS (MESH:D011137), styrene (MESH:D020058), PE polymer (MESH:C443715), agarose (MESH:D012685), Poly(butylene adipate-co-terephthalate (MESH:C488797), PP (MESH:D011126), (NH4)2SO4 (MESH:D000645), EG (MESH:D019855), PVA (MESH:D011142), Na2SO4 (MESH:C012036), polyester (MESH:D011091), MgSO4 (MESH:D008278), EDTA (MESH:D004492), Agar (MESH:D000362), Tributyrin (MESH:C005830), Hydrocarbon (MESH:D006838), polymer (MESH:D011108), TPA (MESH:C011363), carbon (MESH:D002244), TCA (MESH:D014233), Nylon (MESH:D009757), Ca2+ (-), saline (MESH:D012965), salt (MESH:D012492), nylon 6 (MESH:C009916), plastic (MESH:D010969)
- **Species:** Exiguobacterium (genus) [taxon 33986], Bacillus sp. (in: firmicutes) (species) [taxon 1409], Rhodococcoides fascians (species) [taxon 1828], Thermobifida fusca (species) [taxon 2021], Bacillus (genus) [taxon 55087], Streptomyces sp. SM14 (species) [taxon 1736045], Erythrobacteraceae (family) [taxon 335929], Sulfitobacter (genus) [taxon 60136], Pseudophaeobacter (genus) [taxon 1541822], Acinetobacter lwoffii (species) [taxon 28090], Rhodococcus qingshengii (species) [taxon 334542], Thermobifida cellulosilytica (species) [taxon 144786], Sphingomonas (genus) [taxon 13687], Stutzerimonas stutzeri (species) [taxon 316], Dietzia sp. (species) [taxon 1871616], Sulfitobacter geojensis (species) [taxon 1342299], Pseudomonas (RNA similarity group I, genus) [taxon 286], Marinobacter (genus) [taxon 2742], Staphylococcus aureus (species) [taxon 1280], Rhodococcus (genus) [taxon 1661425], Bacillus pumilus (species) [taxon 1408], Thermobifida alba (species) [taxon 53522], Amycolatopsis mediterranei (species) [taxon 33910], Alcanivorax sp. (species) [taxon 1872427], Priestia sp. (species) [taxon 2800375], Homo sapiens (human, species) [taxon 9606], Streptomyces sp. (species) [taxon 1931], Pseudomonas sp. (species) [taxon 306], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Neochloris sp. LCR (species) [taxon 408120], Exiguobacterium oxidotolerans (species) [taxon 223958], Rhodococcus erythropolis (species) [taxon 1833], Oerskovia (genus) [taxon 162491], Rhodococcus sp. (in: high G+C Gram-positive bacteria) (species) [taxon 1831], Bacillus subtilis (species) [taxon 1423], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** NLCR_57 — Mus musculus (Mouse), Hybridoma (CVCL_A9KB), PS13 — Homo sapiens (Human), Finite cell line (CVCL_A8DL), NLBR_41 — Mus musculus (Mouse), Mouse kidney carcinoma, Cancer cell line (CVCL_0151), 1.7L — Mus musculus (Mouse), Hybridoma (CVCL_XK51), NLCR_54 — Homo sapiens (Human), Ataxia telangiectasia syndrome, Transformed cell line (CVCL_ZT26), NLAR_29 — Homo sapiens (Human), Amyotrophic lateral sclerosis 1, Induced pluripotent stem cell (CVCL_8999), NLAR_30 — Mus musculus (Mouse), Hybridoma (CVCL_J925), NLBR_39 — Mus musculus (Mouse), Hybridoma (CVCL_XX77), ATCC 29213 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), NLBR_22 — Mus musculus (Mouse), Hybridoma (CVCL_B4FN)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12960351/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960351/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960351/full.md

---
Source: https://tomesphere.com/paper/PMC12960351