水解酶
聚对苯二甲酸乙二醇酯
基质(水族馆)
酶
乙二醇
水解
活动站点
化学
丝氨酸水解酶
材料科学
生物化学
有机化学
生物
生态学
丝氨酸
复合材料
作者
Gottfried J. Palm,Lukas Reisky,Dominique Böttcher,Henrik Müller,Emil A. P. Michels,Miriam C. Walczak,Leona Berndt,M.S. Weiss,Uwe T. Bornscheuer,Gert Weber
标识
DOI:10.1038/s41467-019-09326-3
摘要
The extreme durability of polyethylene terephthalate (PET) debris has rendered it a long-term environmental burden. At the same time, current recycling efforts still lack sustainability. Two recently discovered bacterial enzymes that specifically degrade PET represent a promising solution. First, Ideonella sakaiensis PETase, a structurally well-characterized consensus α/β-hydrolase fold enzyme, converts PET to mono-(2-hydroxyethyl) terephthalate (MHET). MHETase, the second key enzyme, hydrolyzes MHET to the PET educts terephthalate and ethylene glycol. Here, we report the crystal structures of active ligand-free MHETase and MHETase bound to a nonhydrolyzable MHET analog. MHETase, which is reminiscent of feruloyl esterases, possesses a classic α/β-hydrolase domain and a lid domain conferring substrate specificity. In the light of structure-based mapping of the active site, activity assays, mutagenesis studies and a first structure-guided alteration of substrate specificity towards bis-(2-hydroxyethyl) terephthalate (BHET) reported here, we anticipate MHETase to be a valuable resource to further advance enzymatic plastic degradation.
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