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Upcycling of Waste Poly(ethylene terephthalate) into 2,4-Pyridine Dicarboxylic Acid by a Tandem Chemo-Microbial Process
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This research presents a chemical process for converting waste polyethylene terephthalate (PET) plastic into 2,4-pyridinedicarboxylic acid, a compound with applications in pharmaceuticals and materials science. The upcycling approach transforms low-value plastic waste into a higher-value chemical product, reducing environmental burden while generating economic benefit. The study demonstrates the feasibility of chemical upcycling as an alternative to conventional plastic recycling.
This study presents a chemo-microbial cascade process for the upcycling of waste poly(ethylene terephthalate) (PET) into valuable compound 2,4-pyridine dicarboxylic acid (2,4-PDCA). Initially, waste PET undergoes efficient hydrolysis to terephthalic acid (TPA) with a high yield of 92.36%, catalyzed by p-toluenesulfonic acid (PTSA). The acid catalyst exhibits excellent reusability, maintaining activity over five cycles. Subsequently, a one-pot, two-step whole-cell conversion system utilizing genetically modified Escherichia coli strains (E. coli PCA and E. coli 2,4-PDCA) converts the generated TPA into 2,4-PDCA. By integrating the PET hydrolysis module with the 2,4-PDCA biosynthesis module, the study achieves an impressive overall efficiency of 94.01% in converting challenging PET waste into valuable 2,4-PDCA. Our research presents a rational design strategy for PET upcycling and 2,4-PDCA synthesis methods. This research provides a systematic approach to PET upcycling, demonstrating its feasibility and potential for industrial application.
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Researchers engineered the bacterium Pseudomonas putida to simultaneously break down PET plastic monomers and express a PET hydrolase enzyme, enabling one-step PET degradation and growth. The engineered strain successfully metabolized both TPA and EG monomers released during PET hydrolysis. This work advances the development of microbial biocatalysts for plastic recycling and upcycling.
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