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Metabolic engineering of Pseudomonas putida KT2440 for valorization of terephthalic acid to produce catechol and muconic acid
- Title
- Metabolic engineering of Pseudomonas putida KT2440 for valorization of terephthalic acid to produce catechol and muconic acid
- Authors
- Lee E.S.; Son J.; Song H.M.; Lim H.J.; Jeon B.W.; Cha H.G.; Kim Y.; Jeong K.J.; Joo J.C.; Park S.J.
- Ewha Authors
- 박시재
- SCOPUS Author ID
- 박시재

- Issue Date
- 2026
- Journal Title
- New Biotechnology
- ISSN
- 1871-6784
- Citation
- New Biotechnology vol. 93, pp. 226 - 233
- Keywords
- Catechol; cis,cis-Muconic acid; PET upcycling; Pseudomonas putida; Terephthalic acid
- Publisher
- Elsevier B.V.
- Indexed
- SCIE; SCOPUS

- Document Type
- Article
- Abstract
- Polyethylene terephthalate (PET) is one of the most widely used synthetic plastics, yet its environmental persistence necessitates sustainable end-of-life management strategies. Microbial upcycling of PET-derived monomers, particularly terephthalic acid (TPA), into high-value chemicals represents a promising alternative to conventional recycling. In this study, Pseudomonas putida KT2440 was engineered as a modular bioconversion platform for efficient TPA valorization into aromatic products, including catechol and muconic acid (MA). Introduction of the Comamonas sp. E6 tphBAabc operon combined with deletion of pcaHG in the chromosome of P. putida enabled conversion of TPA into protocatechuate (PCA). However, limited native TPA uptake was found. To overcome this bottleneck, nine TPA transporters were screened, identifying Acinetobacter baylyi ADP1 MucKmut and Rhodococcus opacus TpaK as superior transporters that enhanced TPA assimilation. Using these transporters, catechol biosynthesis was enabled by plasmid-based expression of Enterobacter cloacae aroY and chromosomal deletion of catA1 and catA2. Notably, the tpaK-expressing strain achieved catechol production of 8.51 mM with an 86.0% molar yield. Extension of the pathway toward MA through plasmid-based expression of aroY, catA1 and catA2, and chromosomal deletion of catB and catC enabled efficient MA production, reaching 8.45 mM MA with a 93.1% molar yield. In addition, TPA derived from chemically depolymerized post-consumer PET was effectively utilized for catechol production. Furthermore, fed-batch fermentation validated process scalability, achieving 15.04 mM catechol from 16.76 mM TPA. Collectively, this work demonstrates that recombinant P. putida KT2440 can be constructed as a robust chassis for sustainable PET upcycling through implementation of an efficient TPA transporter. © 2026
- DOI
- 10.1016/j.nbt.2026.03.009
- Appears in Collections:
- 공과대학 > 화공신소재공학과 > Journal papers
- Files in This Item:
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1-s2.0-S1871678426000427-main.pdf(2.55 MB)
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