Osaka University

Department of Macromolecular Science at Graduate School of Science,
Osaka University

Research Theme

Repolymerization and degradation using enzymatic reactions

Resource-recyclable polymer materials using biocatalysts

We have achieved material toughness (stability and longevity) eight times greater than conventional materials by applying specific molecular and material design to biodegradable polymers. In the resulting biodegradable polymer, we also achieved enzyme-catalyzed degradation using lipase, a biocatalyst, a 20-fold increase in degradation rate, and reconstruction of the polymer material, successfully circulating this material. Not only is it possible to recycle by repolymerization in which low molecular weight bodies bond with each other after degradation, but also upcycling by copolymerization incorporating another type of polyester or inorganic polymer at the molecular level has been realized

Resource recycling of polymer materials using lipase, a biocatalyst

Liu, J.; Ikura, R.; Yamaoka, K.; Sugawara, A.; Takahashi, Yuya.; Kure, B.; Takenaka, N.; Park, Junsu.; Uyama, H.; Takashima, Y., Chem 2025, 11, 102327.

Controlling enzymatic reaction degradation by adding cyclic molecules

Controlling the degradability of environmentally low-impact biodegradable polymers is important in the resource recycling of polymers. The degradation rate was reduced by creating a pseudo-rotaxane structure (Figure c) in which PCL-PU penetrated the vacancies of c[n]PS (Figure d). The ƒÎ-ƒÎ interaction between the added c[n]PS inhibited the degradation of PCL ester bonds by the enzyme (Figure e). The degradation rate of biodegradable polymers was successfully controlled by the amount of cyclic molecules added and the formation of supramolecular structures

Chemical structures of (a) PCL-PU and (b) c[n]PS.
(c) Schematic diagram of the pseudo-rotaxane structure and (d) enzyme reaction degradation experiments.
(e) Effect of c[n]PS on the degradability of PCL-PU.

Ding, Y.; Ikura, R.; Yamaoka, K.; Nishida, K.; Sugawara, A.; Uyama, H.; Nara, S.; Takashima, Y., ACS Macro Letters 2024, 13, 1265-1271.

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