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Development of a Vibrio natriegens-based plate-clearing assay for rapid screening of PET-hydrolyzing enzymes

Susanne Hansen TroøyeniD, Ingrid Moa Bolstad, Nora Drøivoldsmo, Davide LucianoiD, Evamaria I. PeterseniD, Gastón CourtadeiD

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Abstract

Polyethylene terephthalate (PET) is a major contributor to plastic waste. Enzymatic PET degradation offers a sustainable recycling approach, but screening for effective enzymes remains challenging. Herein, we established an experimental plate-clearing assay using Vibrio natriegens, exploiting its protein secretion system to rapidly identify catalytic activity without time-consuming downstream processing. To validate the assay's robustness, we tested variants of Fusarium solani pisi cutinase (FsC) and found that one variant, T45P, exhibited threefold higher PET-film degradation yield than the wild type and favored production of terephthalic acid. As a further test case, we screened an error-prone PCR library of FsC using the assay, obtaining a 25% hit rate after screening 150 colonies. This demonstrates the scalability of the method to large enzyme libraries.

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