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酶催化酯键的合成与水解:塑料可持续利用的关键步骤。

Enzyme catalyzes ester bond synthesis and hydrolysis: The key step for sustainable usage of plastics.

作者信息

Lai Jinghui, Huang Huiqin, Lin Mengwei, Xu Youqiang, Li Xiuting, Sun Baoguo

机构信息

Key Laboratory of Brewing Microbiology and Enzymatic Molecular Engineering of China General Chamber of Commence, Beijing Technology and Business University, Beijing, China.

Key Laboratory of Brewing Molecular Engineering of China Light Industry, Beijing Technology and Business University, Beijing, China.

出版信息

Front Microbiol. 2023 Jan 12;13:1113705. doi: 10.3389/fmicb.2022.1113705. eCollection 2022.

Abstract

Petro-plastic wastes cause serious environmental contamination that require effective solutions. Developing alternatives to petro-plastics and exploring feasible degrading methods are two solving routes. Bio-plastics like polyhydroxyalkanoates (PHAs), polylactic acid (PLA), polycaprolactone (PCL), poly (butylene succinate) (PBS), poly (ethylene furanoate) s (PEFs) and poly (ethylene succinate) (PES) have emerged as promising alternatives. Meanwhile, biodegradation plays important roles in recycling plastics (e.g., bio-plastics PHAs, PLA, PCL, PBS, PEFs and PES) and petro-plastics poly (ethylene terephthalate) (PET) and plasticizers in plastics (e.g., phthalate esters, PAEs). All these bio- and petro-materials show structure similarity by connecting monomers through ester bond. Thus, this review focused on bio-plastics and summarized the sequences and structures of the microbial enzymes catalyzing ester-bond synthesis. Most of these synthetic enzymes belonged to α/β-hydrolases with conserved serine catalytic active site and catalyzed the polymerization of monomers by forming ester bond. For enzymatic plastic degradation, enzymes about PHAs, PBS, PCL, PEFs, PES and PET were discussed, and most of the enzymes also belonged to the α/β hydrolases with a catalytic active residue serine, and nucleophilically attacked the ester bond of substrate to generate the cleavage of plastic backbone. Enzymes hydrolysis of the representative plasticizer PAEs were divided into three types (I, II, and III). Type I enzymes hydrolyzed only one ester-bond of PAEs, type II enzymes catalyzed the ester-bond of mono-ester phthalates, and type III enzymes hydrolyzed di-ester bonds of PAEs. Divergences of catalytic mechanisms among these enzymes were still unclear. This review provided references for producing bio-plastics, and degrading or recycling of bio- and petro-plastics from an enzymatic point of view.

摘要

石化塑料废弃物会造成严重的环境污染,这需要有效的解决办法。开发石化塑料的替代品并探索可行的降解方法是两条解决途径。聚羟基脂肪酸酯(PHA)、聚乳酸(PLA)、聚己内酯(PCL)、聚丁二酸丁二醇酯(PBS)、聚呋喃二甲酸乙二酯(PEF)和聚丁二酸乙二酯(PES)等生物塑料已成为有前景的替代品。同时,生物降解在塑料(如生物塑料PHA、PLA、PCL、PBS、PEF和PES)、石化塑料聚对苯二甲酸乙二酯(PET)以及塑料中的增塑剂(如邻苯二甲酸酯,PAE)的回收利用中发挥着重要作用。所有这些生物和石化材料通过酯键连接单体,显示出结构相似性。因此,本综述聚焦于生物塑料,总结了催化酯键合成的微生物酶的序列和结构。这些合成酶大多属于具有保守丝氨酸催化活性位点的α/β水解酶,通过形成酯键催化单体聚合。对于酶促塑料降解,讨论了关于PHA、PBS、PCL、PEF、PES和PET的酶,并且大多数酶也属于具有催化活性残基丝氨酸的α/β水解酶,亲核攻击底物的酯键以产生塑料主链的裂解。代表性增塑剂PAE的酶促水解分为三种类型(I、II和III)。I型酶仅水解PAE的一个酯键,II型酶催化单酯邻苯二甲酸酯的酯键,III型酶水解PAE的二酯键。这些酶之间催化机制的差异仍不清楚。本综述从酶学角度为生物塑料的生产以及生物和石化塑料的降解或回收提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e6a/9878459/022515c1d534/fmicb-13-1113705-g001.jpg

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