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The growing demand for sustainable biomanufacturing has driven significant interest in 2,5-furandicarboxylic acid (FDCA), a bio-based platform chemical for producing renewable polymers. The eco-friendly oxidoreductase laccase exhibits promising FDCA biosynthesis capacity yet is hampered by pH-dependent activity decay and susceptibility to proteolytic degradation. Herein, we developed a bio-enabled synthesis approach to fabricate three-dimensional laccase-integrated copper hybrid nanoflowers (Lac-NFs) through enzyme-metal coordination-driven self-assembly. The engineered Lac-NFs displayed high enzyme encapsulation efficiency (89.28%) and enhanced environmental robustness compared to free laccase. Furthermore, the Lac-NFs maintained prolonged storage stability with well-preserved activity relative to the native enzyme. Elevated catalytic efficiency and refined enzymatic kinetics were achieved copper-mediated electron transfer networks within the hybrid matrix. Remarkably, Lac-NFs demonstrate exceptional catalytic efficiency and selectivity in the conversion of HMF to FDCA, achieving complete substrate conversion under precisely controlled operational parameters. This nano-biohybrid design establishes a robust and efficient biocatalytic platform for biomass valorization into high-value-added chemicals, exhibiting promising scalability prospects for industrial implementation.
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http://dx.doi.org/10.1039/d5ra04187b | DOI Listing |
RSC Adv
September 2025
Department of Chemical Engineering and Green Technology, Institute of Chemical Technology (ICT) Mumbai Maharashtra 400019 India
The sustainable synthesis of bio-based monomers from renewable biomass intermediates is a central goal in green chemistry and biorefinery innovation. This study introduces a synergistic catalytic-enzymatic strategy for the efficient and eco-friendly oxidation of 5-hydroxymethylfurfural (5-HMF) into 2,5-furandicarboxylic acid (FDCA), a key monomer for next-generation biodegradable plastics. The catalytic phase employed non-noble metal catalysts, MnO and Co-Mn supported on activated carbon (Co-Mn/AC), under mild batch reaction conditions at 90 °C.
View Article and Find Full Text PDFBioresour Technol
September 2025
Department of Polymer Materials and Engineering, College of Materials and Metallurgy, Guizhou University, Guiyang 550025, China; Technology Innovation Center for High-Efficiency Utilization of Bamboo-Based Biomass in Guizhou Province, Guiyang 550025, China. Electronic address:
Worldwide, marine shell waste generated from the seafood industry has emerged as a significant environmental challenge. Indeed, this shell waste represents an abundant source of various valuable products, particularly chitin. However, the extraction and subsequent processing of chitin are hindered by the inherently resistant structure of these chitin-rich feedstocks, coupled with strong hydrogen bonding between chitin chains.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
International Joint Research Center for Photoresponsive Molecules and Materials, School of Chemical and Material Engineering, Jiangnan University, Lihu Street 1800, Wuxi, 214122, P.R. China.
Electrocatalytic coupling of nitrate reduction (NORR) to ammonia with 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA) enables simultaneous wastewater remediation and biomass valorization. However, developing efficient bifunctional electrocatalysts for these multiproton-coupled electron transfer reactions remains challenging as conventional single-active-site catalysts inherently suffer from linear scaling relationships between intermediates and adsorption energies, particularly sluggish proton transfer. To address this, we engineered a triphasic N-doped CuO@CoO@Ni(OH) heterostructure with a gradient built-in electric field (BIEF), which synergistically enhances interfacial charge polarization and accelerates proton transport through dynamic coupling effects in both reactions: sufficient *H supply for NORR and fast Ni(OH)/NiOOH redox cycling during HMF oxidation (HMFOR), thus achieving unprecedented bifunctional performance: at - 0.
View Article and Find Full Text PDFSmall
September 2025
The Liaoning Province Key Laboratory of Paper and Pulp Engineering, The Key Laboratory of High Value Utilization of Botanical Resources of China, Light Industry College of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian, 116034, China.
2,5-Furandicarboxylic acid (FDCA), synthesized via selective oxidation of 5-hydroxymethylfurfural (HMF), is a structural analog to petroleum-derived terephthalic acid (PTA) and a key precursor for renewable polyesters like polyethylene furanoate (PEF). Recent advances in electrocatalytic HMF oxidation (HMFOR) enable efficient synthesis under mild conditions, aligning with renewable energy integration. In this work, catalysts with oxygen-rich vacancies by growing Ce, V bimetallic-dopsynthesizeded Ni(OH) nanosheets in situ on nickel foam for electrocatalytic HMF oxidation to FDCA are prepared.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P.R. China.
Accelerating proton deintercalation and transfer on the catalyst surface is crucial for the electrochemical oxidation of 5-hydroxymethylfurfural (HMF) into the high-value 2,5-furanodicarboxylic acid (FDCA). Herein, we have constructed a Ni(OH)─PO /Ni(PO) heterojunction catalyst that demonstrates exceptional selectivity (97.16%), yield (94.
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