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使用双酶系统对混合塑料进行一锅法解聚

One-Pot Depolymerization of Mixed Plastics Using a Dual Enzyme System.

作者信息

Branson Yannick, Liu Jiawei, Schmidt Louis, Griebel Jan, Prager Andrea, Stieler Lena, Breite Daniel, Bayer Thomas, Besenmatter Werner, Dong Weiliang, Garscha Ulrike, Bornscheuer Uwe T, Wei Ren

机构信息

Department of Biotechnology & Enzyme Catalysis, Institute of Biochemistry, University of Greifswald, Felix-Hausdorff-Str. 4, 17489, Greifswald, Germany.

Key Laboratory for Waste Plastic Biocatalytic Degradation and Recycling, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, 211800, PR China.

出版信息

ChemSusChem. 2025 May 5;18(9):e202402416. doi: 10.1002/cssc.202402416. Epub 2025 Jan 16.

DOI:10.1002/cssc.202402416
PMID:39714869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12051254/
Abstract

As global plastic consumption and littering escalate, innovative approaches to sustainable waste management are crucial. Enzymatic depolymerization has emerged as a promising recycling method for polyesters via monomer recovery under mild conditions. However, current research mainly focuses on using a single plastic feedstock, which can only be derived from complex and costly plastic waste sorting. This study investigated the enzymatic depolymerization of mixed plastics using a dual-enzyme system in a one-pot approach. Employing the polyester hydrolase PES-H1 FY and the (poly)urethanase UMG-SP-2, mixed or blended polymers consisting of polyethylene terephthalate (PET), polybutylene adipate-co-terephthalate (PBAT), and thermoplastic polyester-polyurethane (TPU) were depolymerized into their monomers. Chromatographic quantification revealed a total yield of monomeric products of up to 39.8±4.4 % after 96 h reactions, which was consistent with the weight loss measurements of 40.9±2.5 %. In addition, a modified dissolution-precipitation method was shown to easily blend the three different polymers while improving their degradability. Our findings suggest that using mixed enzymes is a viable method for recycling mixed or blended waste plastics without polymer sorting. Individual monomers can be separated and purified to produce virgin polymers, while their mixture in the hydrolysate can easily serve as feedstock for microbial upcycling into value-added products.

摘要

随着全球塑料消费量和垃圾量的不断增加,创新的可持续废物管理方法至关重要。酶促解聚已成为一种有前景的聚酯回收方法,可在温和条件下通过单体回收实现。然而,目前的研究主要集中在使用单一塑料原料,而这种原料只能从复杂且成本高昂的塑料垃圾分类中获得。本研究采用双酶体系一锅法研究了混合塑料的酶促解聚。使用聚酯水解酶PES-H1 FY和(聚)聚氨酯酶UMG-SP-2,将由聚对苯二甲酸乙二酯(PET)、聚己二酸丁二醇酯-对苯二甲酸丁二醇酯(PBAT)和热塑性聚酯-聚氨酯(TPU)组成的混合或共混聚合物解聚为单体。色谱定量分析显示,反应96小时后,单体产物的总产率高达39.8±4.4%,这与失重测量结果40.9±2.5%一致。此外,一种改进的溶解沉淀法被证明可以轻松地将三种不同的聚合物共混,同时提高它们的可降解性。我们的研究结果表明,使用混合酶是一种可行的方法,可在不进行聚合物分类的情况下回收混合或共混的废塑料。可以分离和纯化单个单体以生产原始聚合物,而它们在水解产物中的混合物可以很容易地用作微生物升级循环为增值产品的原料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/a4df0f82e6ce/CSSC-18-e202402416-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/d53ece288a20/CSSC-18-e202402416-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/33b2f6c0de3b/CSSC-18-e202402416-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/1e559cfdd0a8/CSSC-18-e202402416-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/49f1b69c1dfa/CSSC-18-e202402416-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/34d6fb5f9687/CSSC-18-e202402416-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/a4df0f82e6ce/CSSC-18-e202402416-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/d53ece288a20/CSSC-18-e202402416-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/33b2f6c0de3b/CSSC-18-e202402416-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/1e559cfdd0a8/CSSC-18-e202402416-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/49f1b69c1dfa/CSSC-18-e202402416-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/34d6fb5f9687/CSSC-18-e202402416-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b29/12051254/a4df0f82e6ce/CSSC-18-e202402416-g001.jpg

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Natural diversity screening, assay development, and characterization of nylon-6 enzymatic depolymerization.
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