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Aug 2026

Efficient transformation of lignin-derived syringaldehyde to syringyl acetate via tandem catalysis with alcohol dehydrogenase and lipase.

Efficient valorization of lignin-derived aromatics remains a key challenge in sustainable chemistry. Biobased aromatic alcohols and esters are important value-added compounds widely used in fragrances, pharmaceutical intermediates, fine chemicals, and functional materials. In this study, a whole-cell biocatalytic system co-expressing alcohol dehydrogenase (ADH6) from Saccharomyces cerevisiae and glucose dehydrogenase (GDH) was developed for the efficient conversion of syringaldehyde to syringyl alcohol. The GDH-based cofactor regeneration module enabled in situ reduced nicotinamide adenine dinucleotide phosphate (NADPH) supply, thereby improving catalytic efficiency while reducing the dependence on external cofactors. Under optimized conditions, the system achieved a high analytical yield of 98.3% at 40 mM syringaldehyde in an aqueous system, representing, to the best of our knowledge, the highest substrate concentration reported so far for this biocatalytic conversion. The substrate spectrum was further evaluated using representative lignin-derived aromatic aldehydes, including cinnamaldehyde, p-anisaldehyde, vanillin, and 3,4-dimethoxybenzaldehyde. These substrates were converted into cinnamyl alcohol, 4-methoxybenzyl alcohol, vanillyl alcohol, and 3,4-dimethoxybenzyl alcohol, respectively. Cinnamaldehyde, p-anisaldehyde, and 3,4-dimethoxybenzaldehyde afforded the corresponding alcohols with analytical yields of 99%, whereas vanillin gave vanillyl alcohol with an analytical yield of 86% after 4 h. Molecular docking indicated that these substrates could bind within the ADH6 active pocket through similar orientations, supported by hydrogen-bonding and hydrophobic interactions, providing structural explanation for the observed substrate adaptability. In addition, coupling with immobilized lipase Novozym 435 enabled the conversion of syringyl alcohol into syringyl acetate via transesterification. This work established an efficient tandem biocatalysis with reductase and lipase for upgrading of lignin-derived aromatic compounds.

Haoyu Chai, Xin Li, Yu-Cai He et al. · 0 citations
Open access Aug 2026

Niacin Synthesis from 3-Cyanopyridine by Recombinant Escherichia coli: Optimization and Immobilization

Niacin (vitamin B3) is a high-value chemical widely used in the pharmaceutical and food industries. In this study, a recombinant Escherichia coli strain expressing nitrilase from Pseudomonas putida CGMCC3830 was evaluated for the whole-cell biotransformation of high-concentration 3-cyanopyridine to niacin. Molecular docking predicted important substrate-interacting residues, including T135, K131, F202, and W166. Under optimized conditions (160 g/L wet cells, pH 8.5), free whole cells completely hydrolyzed 3.0 M 3-cyanopyridine within 8 h. To enhance operational stability, the cells were immobilized in sodium alginate beads containing green zeolite. The resulting catalyst achieved complete conversion of 1.4 M 3-cyanopyridine within 4 h and maintained 96.5% conversion after six cycles. These findings demonstrate the potential of this system for future industrial applications.

Zaiheng Wu, Jingyi Zhou, Bo Fan et al. · 0 citations

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