Computationally guided genome rewiring of Escherichia coli and its application for nanopolyethylene terephthalate (PET) biodegradation and upcycling

Numerous strategies for the biodegradation and upcycling of polyethylene terephthalate (PET) are under investigation. Here, we present a proof-of-concept study for reprogramming the Escherichia coli BL21(DE3) strain to degrade PET nanoparticles (nPET) without introducing foreign DNA and compromising native cellular fitness. In brief, native proteins selected in silico from the genome were repurposed to acquire artificial PETase activity without compromising their function and were subsequently replaced via CRISPR/Cas9 editing. A variant of the transport protein LsrB, selected for its ability to bind PET, was engineered to degrade PET powder (at 37-60°C). Building on LsrB periplasmic localization, we engineered a strain that degrades nPET at 37°C. The strain was further engineered to grow on nPET degradation products and produce valuable compounds. Our method, which is applicable across diverse genomes and microbial chassis, expands the potential of metabolic engineering to address plastic biodegradation and upcycling while reducing reliance on foreign DNA.

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Publication Details

Journal
Trends in biotechnology
Published
2025-08-15
DOI
https://doi.org/10.1016/j.tibtech.2025.07.008
Citations
3
Primary Topic
Microplastics and Plastic Pollution
Type
article
Field-Weighted Citation Impact
1.51
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article

Computationally guided genome rewiring of Escherichia coli and its application for nanopolyethylene terephthalate (PET) biodegradation and upcycling

Mario Luengo, David Almendral, José L. González-Alfonso, Karl‐Erich Jaeger et al.
3 citations
Trends in biotechnology
Microplastics and Plastic Pollution
1.51
article

Computationally guided genome rewiring of Escherichia coli and its application for nanopolyethylene terephthalate (PET) biodegradation and upcycling

Mario Luengo, David Almendral, José L. González-Alfonso, Karl‐Erich Jaeger, Laura Fernández-López, Pablo Pérez-García, Ana Robles‐Martín, Luzie Kruse, Rafael Bargiela, Joan Giménez-Dejoz, Manuel Ferrer, Vı́ctor Guallar, Mireia Martinez, Patrick Shahgaldian, Seyed Amirabbas Nazemi, Sergi Rodà, Martin Floor, Wolfgang R. Streit, Sonia Lidia Romero Vela, Francisco J. Plou, Paula Vidal
article en
3 citations

Abstract

Numerous strategies for the biodegradation and upcycling of polyethylene terephthalate (PET) are under investigation. Here, we present a proof-of-concept study for reprogramming the Escherichia coli BL21(DE3) strain to degrade PET nanoparticles (nPET) without introducing foreign DNA and compromising native cellular fitness. In brief, native proteins selected in silico from the genome were repurposed to acquire artificial PETase activity without compromising their function and were subsequently replaced via CRISPR/Cas9 editing. A variant of the transport protein LsrB, selected for its ability to bind PET, was engineered to degrade PET powder (at 37-60°C). Building on LsrB periplasmic localization, we engineered a strain that degrades nPET at 37°C. The strain was further engineered to grow on nPET degradation products and produce valuable compounds. Our method, which is applicable across diverse genomes and microbial chassis, expands the potential of metabolic engineering to address plastic biodegradation and upcycling while reducing reliance on foreign DNA.

Trends in biotechnologyVol. 43(11)
Institució Catalana de Recerca i Estudis Avançats (ES), Universität Hamburg (DE), Forschungszentrum Jülich (DE), Barcelona Supercomputing Center (ES), FHNW University of Applied Sciences and Arts Northwestern Switzerland (CH), Instituto de Catálisis y Petroleoquímica (ES), Sunny BioDiscovery (United States) (US), Heinrich Heine University Düsseldorf (DE), Universitat Politècnica de Catalunya (ES)
Responsible consumption and production
Openalex Percentile: Top 17%
Microplastics and Plastic Pollution
1.51
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