脱羧
对苯二甲酸
辅因子
化学
生物催化
酶
立体化学
黄素单核苷酸
生物化学
基质(水族馆)
生物转化
定向进化
蛋白质工程
黄素组
底物特异性
分子进化
联苯
酶催化
收敛演化
生物
有机化学
热稳定性
作者
Yuqing Wang,Mingdong Wang,Xianglong Li,Xinyu Che,Xuanyu Cao,Jiangang Ren,Yanbin Feng,Song Xue
标识
DOI:10.1021/acs.jafc.5c14497
摘要
Enzymatic conversion of poly(ethylene terephthalate) into terephthalic acid (TPA) represents a major frontier in environmental biotechnology, yet downstream TPA biotransformation remains constrained by dioxygenases, and no natural TPA decarboxylase has been reported. Here, we combine ancestral sequence reconstruction with structure-guided evolution to engineer HmfF, a 2,5-furandicarboxylic acid decarboxylase, yielding TPA decarboxylase activity. Guided by phylogenetic and structural analyses, 17 ancestral variants were reconstructed, among which HmfF_N1 exhibits exceptional thermostability with Tm over 86 °C and enhances prenylated flavin mononucleotide (prFMN) cofactor binding. Substrate profiling across furandicarboxylic acids, terephthalic acid, and hydroxybenzoic acids shows that HmfF_N1 catalyzes decarboxylation with superior efficiency toward TPA. Relative to the reported enzyme PtHmfF from Pelotomaculum thermopropionicum, HmfF_N1 harbors 42 distal substitutions, and molecular dynamics simulations reveal that HmfF_N1 stabilizes both the prFMN cofactor and the TPA substrate. This study demonstrates that integrating structural insights into ancestral evolution enables the generation of robust enzymes, providing a promising biocatalyst for sustainable plastic utilization.
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