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Dynamic Docking-Assisted Engineering of Hydrolases for Efficient PET Depolymerization

delete2024-02-21
delete10
PRE
AI
Y
Yi Zheng
Q
Qingbin Li
P
Pan Liu
Y
Yingbo Yuan
典龙阳 封面图
典龙阳 (Longyang Dian)
王
王倩 (Qian Wang)
梁泉峰 封面图
梁泉峰 (Quanfeng Liang)
苏田源 封面图
苏田源 (Tianyuan Su)
祁庆生 封面图
祁庆生 (Qingsheng Qi) *
DOI:10.1021/acscatal.4c00400delete
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摘要

摘要

En 中文
Poly(ethylene terephthalate) (PET) is the most abundant polyester plastic and is causing serious environmental pollution. Rapid biological depolymerization of PET waste at a large scale requires powerful engineered enzymes with excellent performance. Here, we designed a computational strategy to analyze the ligand affinity energy of enzymes to PET chains by molecular docking with the dynamic protein conformations, named affinity analysis based on dynamic docking (ADD). After three rounds of protein engineering assisted by ADD, we drastically enhanced the PET-depolymerizing activity of leaf-branch-compost cutinase (LCC). The best variant LCC-A2 depolymerized >90% of the pretreated, postconsumer PET waste into corresponding monomers within 3.3 h at 78 C-degrees, and over 99% of the products was terminal depolymerization products (terephthalic acid and ethylene glycol), representing the fastest PET depolymerization rate reported to date in the bioreactor under optimal condition. Structural analysis revealed interesting features that improved the ligand affinity and catalytic performance. In conclusion, the proposed strategy and engineered variants represent a substantial advancement of the biological circular economy for PET.
Keyword:
molecular dynamicssimulation
molecular docking
poly(ethylene terephthalate)(PET)
biodepolymerization
specific ligand interaction
affinity energy

期刊

ACS Catalysis 封面图
ACS Catalysis
IF:
13.1
论文数:
1.6W
被引数:
15.0W

机构

S
shandong university
学者数:
9.5W
论文数: 6.4W
被引数: 94
引用论文

引用论文

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