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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
박시재scopus
Issue Date
2026
Journal Title
New Biotechnology
ISSN
1871-6784JCR Link
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 WOS 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
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