Optimization of polyethylene terephthalate biodegradation using a self-assembled multi-enzyme cascade strategy

Although many efforts have been devoted to the modification of polyethylene terephthalate (PET) hydrolases for improving the efficiency of PET degradation, the catalytic performance of these enzymes at near-ambient temperatures remains a challenge. Herein, a multi-enzyme cascade system (PT-EC) was d...

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Veröffentlicht in:Journal of hazardous materials 2024-09, Vol.476, p.134887, Article 134887
Hauptverfasser: Aer, Lizhu, Jiang, Qifa, Zhong, Linling, Si, Qiuyue, Liu, Xianghong, Pan, Yan, Feng, Juan, Zeng, Hongjuan, Tang, Lixia
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container_issue
container_start_page 134887
container_title Journal of hazardous materials
container_volume 476
creator Aer, Lizhu
Jiang, Qifa
Zhong, Linling
Si, Qiuyue
Liu, Xianghong
Pan, Yan
Feng, Juan
Zeng, Hongjuan
Tang, Lixia
description Although many efforts have been devoted to the modification of polyethylene terephthalate (PET) hydrolases for improving the efficiency of PET degradation, the catalytic performance of these enzymes at near-ambient temperatures remains a challenge. Herein, a multi-enzyme cascade system (PT-EC) was developed and validated by assembling three well-developed PETases, PETaseEHA, Fast-PETase, and Z1-PETase, respectively, together with carboxylesterase TfCa, and hydrophobic binding module CBM3a using scaffold proteins. The resulting PT-ECEHA, PT-ECFPE, PT-ECZPE all demonstrated outstanding PET degradation efficacy. Notably, PT-ECEHA exhibited a 16.5-fold increase in product release compared to PETaseEHA, and PT-ECZPE yielded the highest amount of product. Subsequently, PT-ECs were displayed on the surface of Escherichia coli, respectively, and their degradation efficiency toward three PET types was investigated. The displayed PT-ECEHA exhibited a 20-fold increase in degradation efficiency with PET film compared to the surface-displayed PETaseEHA. Remarkably, an almost linear increase in product release was observed for the displayed PT-ECZPE over a one-week degradation period, reaching 11.56 ± 0.64 mM after 7 days. TfCaI69W/L281Y evolved using a docking-based virtual screening strategy showed a further 2.5-fold increase in the product release of PET degradation. Collectively, these advantages of PT-EC demonstrated the potential of a multi-enzyme cascade system for PET bio-cycling. [Display omitted] •Multi-enzyme complexes (PT-ECs) exhibit efficient PET degradation at 40 ℃.•The activity of PT-ECEHA in degrading PET is 16.5-fold more than that of PETaseEHA.•Surface-displayed PT-ECEHA has 20-fold higher activity than displayed PETaseEHA.•Surface-displayed PT-EC enhances enzyme tolerance against organic solvent.•TfCaI69W/L281Y enhances the surface-displayed PT-EC enzyme activity by 2.5-fold.
doi_str_mv 10.1016/j.jhazmat.2024.134887
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Herein, a multi-enzyme cascade system (PT-EC) was developed and validated by assembling three well-developed PETases, PETaseEHA, Fast-PETase, and Z1-PETase, respectively, together with carboxylesterase TfCa, and hydrophobic binding module CBM3a using scaffold proteins. The resulting PT-ECEHA, PT-ECFPE, PT-ECZPE all demonstrated outstanding PET degradation efficacy. Notably, PT-ECEHA exhibited a 16.5-fold increase in product release compared to PETaseEHA, and PT-ECZPE yielded the highest amount of product. Subsequently, PT-ECs were displayed on the surface of Escherichia coli, respectively, and their degradation efficiency toward three PET types was investigated. The displayed PT-ECEHA exhibited a 20-fold increase in degradation efficiency with PET film compared to the surface-displayed PETaseEHA. Remarkably, an almost linear increase in product release was observed for the displayed PT-ECZPE over a one-week degradation period, reaching 11.56 ± 0.64 mM after 7 days. TfCaI69W/L281Y evolved using a docking-based virtual screening strategy showed a further 2.5-fold increase in the product release of PET degradation. Collectively, these advantages of PT-EC demonstrated the potential of a multi-enzyme cascade system for PET bio-cycling. 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[Display omitted] •Multi-enzyme complexes (PT-ECs) exhibit efficient PET degradation at 40 ℃.•The activity of PT-ECEHA in degrading PET is 16.5-fold more than that of PETaseEHA.•Surface-displayed PT-ECEHA has 20-fold higher activity than displayed PETaseEHA.•Surface-displayed PT-EC enhances enzyme tolerance against organic solvent.•TfCaI69W/L281Y enhances the surface-displayed PT-EC enzyme activity by 2.5-fold.</description><subject>Biodegradation, Environmental</subject><subject>Carboxylesterase - chemistry</subject><subject>Carboxylesterase - metabolism</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Enzymes, Immobilized - metabolism</subject><subject>Escherichia coli - metabolism</subject><subject>Hydrolases - chemistry</subject><subject>Hydrolases - metabolism</subject><subject>IsPETase</subject><subject>Multi-enzyme cascade</subject><subject>PET degradation</subject><subject>Polyethylene Terephthalates - chemistry</subject><subject>Polyethylene Terephthalates - metabolism</subject><subject>Surface display</subject><subject>TfCa</subject><issn>0304-3894</issn><issn>1873-3336</issn><issn>1873-3336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2LFDEQhoMo7uzqT1By9NJj5aM_5iSyqCss7EXPoZKunsmQ_jBJCz2_3l569OqpoHjet6iHsXcC9gJE9fG8P5_w0mPeS5B6L5RumvoF24mmVoVSqnrJdqBAF6o56Bt2m9IZAERd6tfsZt2BkKXYseFpyr73F8x-HPjY8WkMC-XTEmggninSdMonDJiJWz-2dIzYbvCc_HDkyBOFrsCUqLeBWt7PIfuChsvSE3eYHLbEU45rw3F5w151GBK9vc479vPrlx_3D8Xj07fv958fCye1yoWtrLRaKluiPtTK2ba2IJpD1ckSlBXaIqLrqANZg62EJq1qAlm6ilCXQt2xD1vvFMdfM6Vsep8chYADjXMyCmpoVCMbvaLlhro4phSpM1P0PcbFCDDPqs3ZXFWbZ9VmU73m3l9PzLan9l_qr9sV-LQBtD7621M0yXkaHLU-ksumHf1_TvwBxvOVHw</recordid><startdate>20240905</startdate><enddate>20240905</enddate><creator>Aer, Lizhu</creator><creator>Jiang, Qifa</creator><creator>Zhong, Linling</creator><creator>Si, Qiuyue</creator><creator>Liu, Xianghong</creator><creator>Pan, Yan</creator><creator>Feng, Juan</creator><creator>Zeng, Hongjuan</creator><creator>Tang, Lixia</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240905</creationdate><title>Optimization of polyethylene terephthalate biodegradation using a self-assembled multi-enzyme cascade strategy</title><author>Aer, Lizhu ; 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subjects Biodegradation, Environmental
Carboxylesterase - chemistry
Carboxylesterase - metabolism
Enzymes, Immobilized - chemistry
Enzymes, Immobilized - metabolism
Escherichia coli - metabolism
Hydrolases - chemistry
Hydrolases - metabolism
IsPETase
Multi-enzyme cascade
PET degradation
Polyethylene Terephthalates - chemistry
Polyethylene Terephthalates - metabolism
Surface display
TfCa
title Optimization of polyethylene terephthalate biodegradation using a self-assembled multi-enzyme cascade strategy
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