Characterization of a low-density polyethylene-oxidizing enzyme in Pseudomonas aeruginosa via transcriptomic and proteomic analysis

• The transcriptome and proteome of P. aeruginosa degrading polyethylene were analyzed. • Lipid metabolism and hydrophobic amino acid metabolism pathways were activated. • The expression of oxidoreductases targeting CH CH groups was increased. • Phenylalanine monooxygenase oxidizes polyethylene by introducing hydroxyl groups. • Phenylalanine monooxygenase was not contributed to depolymerization. Plastics have become indispensable in modern industries; however, their resistance to natural degradation poses environmental challenges. Biological degradation technologies employing microorganisms offer promising solutions. Here, we analyzed the transcriptome and proteome of Pseudomonas aeruginosa , a plastic-degrading microorganism found in the gut of superworms, to identify the genes and enzymes upregulated during low-density polyethylene (LDPE) degradation. Functional analyses of these upregulated genes and enzymes using the Kyoto Encyclopedia of Genes and Genomes and Gene Ontology databases revealed an increase in lipid and hydrophobic amino acid metabolism, suggesting their involvement in LDPE degradation. Based on these analyses, we identified phenylalanine monooxygenase (PAH), which is capable of oxidizing plastics. To investigate the involvement of the enzyme in LDPE degradation, phhA was transformed into Escherichia coli , and the enzymes were produced and purified. The purified enzymes were then reacted with LDPE and analyzed. The results revealed the formation of hydroxyl (-OH) and C O groups on the LDPE surface after treatment with PAH, confirming its ability to oxidize LDPE. LDPE is highly hydrophobic and exhibits extremely low reactivity, making it resistant to degradation. The PAH introduces oxygen-containing functional groups into LDPE, increasing its reactivity and thereby facilitating its biodegradation. In this study, we discovered an enzyme capable of catalyzing the oxidation step (the initial stage of LDPE biodegradation) and experimentally validated its activity.

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Publication Details

Journal
Journal of Hazardous Materials Advances
Published
2025-04-19
DOI
https://doi.org/10.1016/j.hazadv.2025.100726
Citations
3
Primary Topic
Microplastics and Plastic Pollution
Type
article
Field-Weighted Citation Impact
1.51
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article

Characterization of a low-density polyethylene-oxidizing enzyme in Pseudomonas aeruginosa via transcriptomic and proteomic analysis

E Lee, Dong Geun Choi, Sukkyoo Lee, Hong Rae Kim et al.
3 citations
Journal of Hazardous Materials Advances
Microplastics and Plastic Pollution
1.51
article

Characterization of a low-density polyethylene-oxidizing enzyme in Pseudomonas aeruginosa via transcriptomic and proteomic analysis

E Lee, Dong Geun Choi, Sukkyoo Lee, Hong Rae Kim, Ye Eun Lee, Dong-Eun Suh
article en
3 citations

Abstract

• The transcriptome and proteome of P. aeruginosa degrading polyethylene were analyzed. • Lipid metabolism and hydrophobic amino acid metabolism pathways were activated. • The expression of oxidoreductases targeting CH CH groups was increased. • Phenylalanine monooxygenase oxidizes polyethylene by introducing hydroxyl groups. • Phenylalanine monooxygenase was not contributed to depolymerization. Plastics have become indispensable in modern industries; however, their resistance to natural degradation poses environmental challenges. Biological degradation technologies employing microorganisms offer promising solutions. Here, we analyzed the transcriptome and proteome of Pseudomonas aeruginosa , a plastic-degrading microorganism found in the gut of superworms, to identify the genes and enzymes upregulated during low-density polyethylene (LDPE) degradation. Functional analyses of these upregulated genes and enzymes using the Kyoto Encyclopedia of Genes and Genomes and Gene Ontology databases revealed an increase in lipid and hydrophobic amino acid metabolism, suggesting their involvement in LDPE degradation. Based on these analyses, we identified phenylalanine monooxygenase (PAH), which is capable of oxidizing plastics. To investigate the involvement of the enzyme in LDPE degradation, phhA was transformed into Escherichia coli , and the enzymes were produced and purified. The purified enzymes were then reacted with LDPE and analyzed. The results revealed the formation of hydroxyl (-OH) and C O groups on the LDPE surface after treatment with PAH, confirming its ability to oxidize LDPE. LDPE is highly hydrophobic and exhibits extremely low reactivity, making it resistant to degradation. The PAH introduces oxygen-containing functional groups into LDPE, increasing its reactivity and thereby facilitating its biodegradation. In this study, we discovered an enzyme capable of catalyzing the oxidation step (the initial stage of LDPE biodegradation) and experimentally validated its activity.

Journal of Hazardous Materials AdvancesVol. 18
Daegu Gyeongbuk Institute of Science and Technology (KR)
Openalex Percentile: Top 20%
Microplastics and Plastic Pollution
1.51
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