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Degradation of PET microplastic particles to monomers in human serum by PETase
Summary
This study tested whether PETase — an enzyme originally discovered in plastic-eating bacteria — can break down PET microplastic particles found in human blood serum, finding that it can degrade the particles into monomers even in complex biological fluids. The results open a potential avenue for enzyme-based therapies to clear plastic particles from the human body, though further toxicity and efficacy studies are needed.
<title>Abstract</title> More than 8 bton of plastic waste has been generated posing severe environmental consequences and health risks. Due to prolonged exposure, microplastic particles are found in human blood and other bodily fluids. Despite a lack of toxicity studies regarding microplastics, harmful effects for humans seem plausible and cannot be excluded. As small plastic particles readily translocate from the gut to body fluids, enzyme-based treatment of serum could constitute a promising futureavenue to clear synthetic polymers and their responding oligomers by their degradation into monomers of lower toxicity than the material they originate from. Still, whereas it is known that enzymatic depolymerization rate of synthetic polymers varies orders of magnitude depending on buffer and media composition, the activity of plastic degrading enzymes in serum was unknown. Here we report how an engineered PETase can expediently depolymerize crystalline microplastic-like particles of the commodity polymer polyethylene terephthalate (PET) into its non-toxic monomer terephthalic acid (TPA) alongside mono(2-hydroxyethyl) terephthalate (MHET) in human serum at 37°C. By developing an efficient method to depolymerize microplastics <italic>in vitro,</italic> our work takes a step closer to find a solution to the problem that microplastics in the bloodstream may pose in the future.
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