文献类型：期刊文献

英文题名：Novel iterative genome mining and engineering of a bifunctional KvVDH enable selective production of furan carboxylic acids from high-concentration 5-hydroxymethylfurfural

作者：Cui, Yanan[1,2];Zhang, Jie[1,2];Xing, Xijun[1,2];Zhang, Hanwen[1,2];Chen, Yutong[1,2];Fan, Liqiang[1,2];Li, Xu[1,2];Qiu, Yongjun[1,2];Deng, Chen[1,2];Zhao, Liming[1,2,3]

机构：[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China;[2]Shanghai Collaborat Innovat Ctr Biomfg Technol SCI, Shanghai 200237, Peoples R China;[3]East China Univ Sci & Technol, Shanghai Frontiers Sci Ctr Optogenet Tech Cell Met, Sch Pharm, 130 Mei Long Rd, Shanghai 200237, Peoples R China

年份：2026

卷号：28

期号：12

起止页码：5409

外文期刊名：GREEN CHEMISTRY

收录：;EI(收录号：20261020222760);WOS:【SCI-EXPANDED(收录号:WOS:001707865200001)】；

基金：This work was financially supported by the National Key Research and Development Program of China (2022YFC2104500), the National Natural Science Foundation of China (32301214 and 32327801), the Shanghai Commission of Science and Technology (24HC2820700), and ECUST-Jingbo Joint Research Institute of Applied Technology Exploratory Research Projects (JJHP2020029-12).

语种：英文

外文关键词：Biosynthesis - Carboxylic acids - Catalysis - Catalyst activity - Computational efficiency - Conformations - Enzymes - Genes - Genome - Hydrogen bonds - Iterative methods - Screening

摘要：Enzyme catalysis provides a promising strategy for the selective conversion of the biomass-derived chemical 5-hydroxymethylfurfural (HMF) into value-added furan carboxylic acids. However, the enzymatic synthesis of 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), 5-formyl-2-furancarboxylic acid (FFCA) and 2,5-furandicarboxylic acid (FDCA) faces two critical bottlenecks: scarcity of bifunctional enzymes active toward HMF, HMFCA and FFCA and their low activity, as well as severe high-concentration HMF inhibition. In this study, to address these gaps and expand the enzymatic synthesis pathway of furan carboxylic acids, we developed a data-driven "molecular probe and function-mediated iterative genome mining" strategy (32.1% functional enzyme discovery rate, a threefold improvement over traditional homology screening) to identify 7 novel target enzymes from 13 HMF-tolerant strains and a protein database. Among them, novel bifunctional vanillin dehydrogenase KvVDH exhibited the highest HMF activity (873.1 mU mg-1). Subsequently, we further engineered KvVDH via KnowVolution (computational design and directed evolution), obtaining the optimal variant M3 (A50S/Y370W) with 57.5-fold higher catalytic efficiency (kcat/Km = 5.75 vs. 0.10 s-1 mM-1 for WT KvVDH), 68.8% residual activity at 40 degrees C for 1 h (15.6-fold vs. WT KvVDH), and exceptional high-HMF tolerance: whole-cell catalysts achieved a 97.8% HMFCA yield from 240 mM HMF. Structural and molecular dynamics analysis results indicated that the potential factors enhancing M3 (A50S/Y370W) activity and thermostability include the remodeling of the restructuring of the hydrogen bond network, conformational changes in the substrate channel, regulation of the local conformation at the active site, and reduction in the binding free energy. Furthermore, coupling M3 (A50S/Y370W) with nicotinamide oxidase (NOX) to catalyze 90 mM HMF afforded FFCA with a yield as high as 98.6%. Based on these results, a one-pot two-step enzymatic process was established. Starting from 90 mM HMF, the final FDCA yield was as high as 95.3% through sequential catalysis by M3 (A50S/Y370W), NOX and EcALDH. This study has developed an excellent enzymatic toolkit for the high efficiency and high selectivity conversion of HMF, laying the foundation for the green and economical production of furan carboxylic acids.