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Targeted Genome Mining Facilitates the Discovery of a Promiscuous, Hyperthermostable Amidase from Thermovenabulum Gondwanense with Notable Nylon‐Degrading Capacity
Summary
Researchers used targeted genome mining to discover a heat-stable amidase enzyme from the thermophilic bacterium Thermovenabulum gondwanense that can degrade nylon. The enzyme showed broad substrate versatility and maintained its activity at high temperatures, making it a promising candidate for industrial plastic recycling applications. The study demonstrates that mining genomes of heat-loving microorganisms can yield new biotechnologies for breaking down synthetic polymers that contribute to microplastic pollution.
Abstract Plastics are ubiquitous in our ecosystems, and microplastic accumulation in the environment is an emerging global health concern. Since available recycling technologies are not economically competitive with primary plastic production, global use is expected to reach 1231 megatons by 2060, with 493 megatons leeching into the environment each year. To identify new nylon‐recycling biotechnologies, targeted genome mining was used to identify thermostable enzymes capable of degrading polyamides. Here, we describe the characterization of a novel protein sourced from Thermovenabulum gondwanense : TvgC. TvgC is extremely stable, exhibiting a melting temperature of 93 °C and no detectable losses in hydrolytic activity after one week at 60 °C. While nylonases primarily process nylon‐6, TvgC catalysed the degradation of both nylon‐6 and nylon‐6,6 films, which are considerably more difficult to degrade. Finally, conversion experiments demonstrate that TvgC achieves a 1.2 wt % conversion of nylon‐6 film, comparable to that of the most highly engineered nylonases. This novel hyperthermostable protein represents an excellent starting point for future engineering of increasingly efficient nylonases.