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A Quantum Mechanism Study of the C-C Bond Cleavage to Predict the Bio-Catalytic Polyethylene Degradation

机译:C-C键断裂预测生物催化聚乙烯降解的量子机理研究

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摘要

The growing amount of plastic solid waste (PSW) is a global concern. Despite increasing efforts to reduce the residual amounts of PSW to be disposed off through segregated collection and recycling, a considerable amount of PSW is still landfilled and the extent of PSW ocean pollution has become a worldwide issue. Particularly, polyethylene (PE) and polystyrene (PS) are considered as notably recalcitrant to biodegradation due to the carbon-carbon backbone that is highly resistant to enzymatic degradation via oxidative reactions. The present research investigated the catalytic mechanism of P450 monooxygenases by quantum mechanics to determine the bio-catalytic degradation of PE or PS. The findings indicated that the oxygenase-induced free radical transition caused the carbon-carbon backbone cleavage of aliphatic compounds. This work provides a fundamental knowledge of the biodegradation process of PE or PS at the atomic level and facilitates predicting the pathway of plastics’ biodegradation by microbial enzymes.
机译:越来越多的塑料固体废物(PSW)是全球关注的问题。尽管加大了减少通过分离收集和再循环处理而残留的PSW残留量的努力,但仍有大量PSW被填埋,并且PSW海洋污染的程度已成为全球性问题。特别地,由于碳-碳主链高度抵抗经由氧化反应的酶促降解,因此聚乙烯(PE)和聚苯乙烯(PS)被认为对生物降解具有顽固性。本研究通过量子力学研究了P450单加氧酶的催化机理,以确定PE或PS的生物催化降解。该发现表明加氧酶诱导的自由基转变引起脂族化合物的碳-碳主链裂解。这项工作为PE或PS在原子级的生物降解过程提供了基础知识,并有助于预测微生物酶对塑料进行生物降解的途径。

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