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从解淀粉欧文氏菌中分离得到的 PET 降解酶 PETase 和 MHETase 的结构分析。

Structural analysis of PET-degrading enzymes PETase and MHETase from Ideonella sakaiensis.

机构信息

Macromolecular Crystallography, Institute of Biochemistry, University of Greifswald, Greifswald, Germany.

Biotechnology, University of Applied Sciences Bremerhaven, Bremerhaven, Germany.

出版信息

Methods Enzymol. 2021;648:337-356. doi: 10.1016/bs.mie.2020.12.015. Epub 2021 Jan 16.

Abstract

The concept of biocatalytic PET degradation for industrial recycling processes had made a big step when the bacterium Ideonella sakaiensis was discovered to break PET down to its building blocks at ambient temperature. This process involves two enzymes: cleavage of ester bonds in PET by PETase and in MHET, the resulting intermediate, by MHETase. To understand and further improve this unique capability, structural analysis of the involved enzymes was aimed at from early on. We describe a repertoire of methods to this end, including protein expression and purification, crystallization of apo and substrate-bound enzymes, and modeling of PETase complexed with a ligand.

摘要

当发现细菌 Ideonella sakaiensis 能够在环境温度下将 PET 分解为其组成单元时,用于工业回收过程的生物催化 PET 降解概念迈出了一大步。该过程涉及两种酶:PETase 分解 PET 中的酯键,以及 MHETase 分解所得中间体 MHET。为了理解并进一步提高这种独特的能力,从早期开始就针对相关酶进行了结构分析。我们描述了一系列达到此目的的方法,包括蛋白质表达和纯化、apo 和底物结合酶的结晶以及与配体结合的 PETase 的建模。

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