Thermal melting degrades recycled plastics into brittle, low-value textiles; bacterial cutinases disassemble rigid synthetic polymers back into pure, virgin-grade chemical building blocks. Initially overlooked as a slow academic oddity in 2005, this enzymatic breakdown process now powers commercial bio-recycling plants that digest plastic waste in hours.

Every year, hundreds of millions of tons of plastic water bottles and polyester fabrics end up in landfills because traditional mechanical recycling degrades plastic quality with every melt cycle. Clear plastic bottles could only be downcycled once or twice before turning into useless, brittle waste.
In 2005, microbiologists discovered that soil bacteria from compost heaps possessed a natural protein capable of cutting plastic. The bacterial enzyme behaves like a pair of molecular scissors, selectively snipping synthetic polyester bonds and disassembling complex plastics into pristine liquid chemical ingredients.
This dormant biological discovery enables infinitely circular recycling. By digesting mixed colored fabrics without manual sorting, by producing virgin-grade plastic bottles from landfill waste, and by operating in room-temperature water baths, enzyme bio-recycling eliminates plastic pollution.
Enzymatic Degradation of Poly(ethylene terephthalate): Rapid Hydrolyse using a Hydrolase from T. fusca
Abstract Summary: It is demonstrated that PET, which is usually regarded as ‘non‐biodegradable’, can effectively be depolymerized by a hydrolase from the actinomycete Thermobifida fusca . Erosion rates of 8 to 17 µm per week were obtained upon incubation at 55 °C. Lipases from Pseudomonas sp. and Candida antarctica did not degrade PET under comparable conditions. The influences of crystallinity, melting point, and glass transition temperature on the enzymatic attack on PET, PBT, and PHB are discussed. Outline of the degradation of PET. image Outline of the degradation of PET.
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