Complete Depolymerization of PET Wastes by an Evolved PET Hydrolase from Directed Evolution

Author:

Shi Lixia123,Liu Pi23,Tan Zijian24,Zhao Wei23,Gao Junfei23,Gu Qun23,Ma Hongwu23,Liu Haifeng4,Zhu Leilei23ORCID

Affiliation:

1. University of Chinese Academy of Sciences 19A Yuquan Road Beijing 100049 China

2. Tianjin Institute of Industrial Biotechnology Chinese Academy of Sciences 32 West 7th Avenue, Tianjin Airport Economic Area Tianjin 300308 P. R. China

3. National Technology Innovation Center of Synthetic Biology 32 West 7th Avenue, Tianjin Airport Economic Area Tianjin 300308 P. R. China

4. Jiangsu Collaborative Innovation Centre of Chinese Medicinal Resources Industrialization School of Pharmacy Nanjing University of Chinese Medicine Nanjing 210023 China

Abstract

AbstractPETase displays great potential in PET depolymerization. Directed evolution has been limited to engineer PETase due to the lack of high‐throughput screening assay. In this study, a novel fluorescence‐based high‐throughput screening assay employing a newly designed substrate, bis (2‐hydroxyethyl) 2‐hydroxyterephthalate (termed BHET‐OH), was developed for PET hydrolases. The best variant DepoPETase produced 1407‐fold more products towards amorphous PET film at 50 °C and showed a 23.3 °C higher Tm value than the PETase WT. DepoPETase enabled complete depolymerization of seven untreated PET wastes and 19.1 g PET waste (0.4 % Wenzyme/WPET) in liter‐scale reactor, suggesting that it is a potential candidate for industrial PET depolymerization processes. The molecular dynamic simulations revealed that the distal substitutions stabilized the loops around the active sites and transmitted the stabilization effect to the active sites through enhancing inter‐loop interactions network.

Funder

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Medicine

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