深海でも分解速度が劇的に加速する酵素内包生分解性プラスチックの開発に成功 ~生分解開始スイッチ機能も搭載~

2026-10-22 東京大学

研究グループは、生分解性プラスチックに自然由来の分解酵素をあらかじめ混ぜ込むことで、微生物が少ない深海環境でも分解を大幅に促進する技術を開発した。4種類の生分解性ポリエステルにクチナーゼやリパーゼを内包させたところ、岸壁では1か月以内、水深約757mの深海では5か月以内に、素材によってはほぼ完全に分解した。酵素を含まない素材に比べ、分解速度は岸壁で5~50倍、深海で12~80倍に向上した。また、乾燥した使用中は分解が進まず、環境に流出した後、摩耗や衝撃による破損を通じて酵素が水に触れると分解が始まる「生分解開始スイッチ機能」も備える。海洋プラスチック汚染やマイクロプラスチックの抑制に向けた新たな材料技術として期待される。

深海でも分解速度が劇的に加速する酵素内包生分解性プラスチックの開発に成功 ~生分解開始スイッチ機能も搭載~
酵素内包生分解性プラスチックの作製と深海における分解途中のフィルム

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深海での生分解を促進するための酵素埋め込みポリエステル Enzyme-embedded polyesters for accelerated biodegradation in the deep sea

QiuYuan Huang, Noriko Iida, Noriyuki Isobe, Taizo Kabe, Taku Omura, Manikandan Ilangovan, Satoshi Kimura, Jin Ho Seok, Hidetaka Nomaki, Ken-ichi Kasuya & Tadahisa Iwata
Nature  Published:21 October 2026
DOI:https://doi.org/10.1038/s41586-026-11192-1

Abstract

The accumulation of persistent plastics in the ocean is causing wide-ranging environmental problems1,2,3. Some commercially available compostable plastics4,5,6,7, developed to address these issues, degrade efficiently under industrial composting conditions; however, their degradation in marine environments, particularly in the deep sea, remains limited8,9,10. Here we demonstrate that thermally embedding enzymes into compostable polyesters (poly(butylene succinate) (PBS), poly(butylene succinate-co-adipate) (PBSA), poly(ε-caprolactone) (PCL) and poly(butylene adipate-co-terephthalate) (PBAT)) significantly accelerates their degradation in both coastal and deep-sea environments from water depths of 2–6 m to 5,503 m. Enzyme-embedded polyesters achieved near-complete degradation at a deep-sea depth of 757 m within 5 months. Furthermore, moderate biodegradation of enzyme-embedded polyesters was observed under extreme conditions on deep-sea floors of 5,503 m. In coastal seawater, films embedded with trace amounts (0.1 wt%) of enzyme underwent rapid degradation. The mechanical properties of enzyme-embedded polyesters were similar to those of enzyme-free polyesters. Chemical analysis confirmed the formation of low-molecular-mass degradation products and biochemical oxygen demand measurements supported the mineralization of the enzyme-embedded polyesters. The enzyme-embedding strategy enables enhanced marine degradation of compostable polyesters and represents a potential solution to marine plastic pollution.

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