Ancestral sequence reconstruction of the prokaryotic three-domain laccases for efficiently degrading polyethylene

漆酶 序列(生物学) 领域(数学分析) 聚乙烯 化学 生物降解 微生物学 生物 计算生物学 生物化学 有机化学 数学 数学分析
作者
Bo Zeng,Yishan Fu,Jiacai Ye,Penghui Yang,Cui Shixiu,Wenxuan Qiu,Yangyang Li,Ting-Long Wu,Haiyun Zhang,Yachan Wang,Guocheng Du,Song Liu
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:476: 135012-135012 被引量:12
标识
DOI:10.1016/j.jhazmat.2024.135012
摘要

Biodegradation of polyethylene (PE) plastics is environmentally friendly. To obtain the laccases that can efficiently degrade PE plastics, we generated 9 ancestral laccases from 23 bacterial three-domain laccases through ancestral sequence reconstruction. The optimal temperatures of the ancestral laccases were between 60 °C-80 °C, while their optimal pHs were at 3.0 or 4.0. Without substrate pretreatment and mediator addition, all the ancestral laccases can degrade low-density polyethylene (LDPE) films at pH 7.0 and 60 °C. Among them, Anc52, which shared low sequence identity (18 %-41.7 %) with the reported PE-degrading laccases, was the most effective for LDPE degradation. After the catalytic reactions at 90 °C for 14 h, Anc52 (0.2 mg/mL) induced clear wrinkles and deep pits on the PE film surface detected by scanning electron microscope, and its carbonyl and hydroxyl indices reached 2.08 and 2.42, respectively. Then, we identified the residues 203 and 288 critical for PE degradation through site-directed mutation on Anc52. Moreover, Anc52 be activated by heat treatment (60 °C and 90 °C) at pH 7.0, which gave it a high catalytic efficiency (k
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