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Qiang Yong

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Review Open access Sep 2026

Targeted Preparation of Low-Degree Polymerization Xylooligosaccharides From Lignocellulosic Biomass: Advances, Structure-Activity Relationships, and Applications.

Xylooligosaccharides (XOS) are highly promising functional prebiotics with excellent stability and intestinal regulatory activity, whose physiological efficacy is strictly dependent on their degree of polymerization (DP), with low-DP XOS (DP 2-3, mainly xylobiose and xylotriose) being the core active components. Recent advances in lignocellulosic biorefinery and enzymatic engineering have greatly expanded XOS feedstock sources and improved production efficiency, while the controllable preparation and efficient application of high-purity low-DP XOS remain the core bottleneck restricting the high-quality development of the XOS industry. This review systematically summarizes the latest research progress of lignocellulose-derived XOS, covering feedstock screening and evaluation, preparation technology comparison, DP-dependent functional mechanisms, and multi-scenario application advances. It highlights the unique advantages of mild organic acid pretreatment combined with specific enzymatic hydrolysis in low-DP XOS production, and the broad application prospects of low-DP XOS in precision nutrition and biomedicine, providing a comprehensive theoretical reference for subsequent research. Emerging promising approaches include continuous-flow reactors with real-time DP monitoring and high-specificity GH11 xylanase engineering, while future research will focus on targeted synthesis of specific DP XOS, in-depth dissection of molecular action mechanisms, and development of customized functional products.

Xuan Ge, Chen-Huan Lai, Caoxing Huang et al. · 0 citations
Jul 2026

Temperature Regulating Evaporation‐Induced Self‐Assembly of Chiral Nematic Cellulose Nanocrystals for Rational Design of Iridescent Films

Cellulose nanocrystals (CNCs) are one of the promising bio‐based nanomaterials with a distinctive chiral nematic structure for fabricating optically iridescent films, yet their long evaporation time for self‐assembly and poor flexibility greatly inhibit practical applications. Herein, pure CNCs and modified CNCs films by various molecules (PEG, glucose, and glycerol) were prepared via evaporation‐induced self‐assembly (EISA) under the regulation of environmental temperature, in order to investigate the synergistic effects of modifiers and temperature gradients on CNCs' self‐assembly and film properties. A series of characterizations revealed that cooperation of PEG may improve CNCs dispersion, while glucose induced excessive hydrogen‐bonded agglomeration. The CNCs/PEG/glucose composite (CGP) films prepared via evaporation at 55°C exhibited optimal applicable performance, with enhanced thermal stability, tensile strength and toughness as compared with pure CNCs and single‐modified films. These results suggest that the dual‐modification system by the ternary molecules achieved a synergistic balance of interparticle interactions, effectively suppressing high‐temperature agglomeration, accelerating self‐assembly and maintaining chiral nematic order. This temperature‐modification synergy strategy provides a feasible approach for the efficient preparation of high‐performance CNCs iridescent films, promoting their applications in flexible, optical, and smart functional materials.

Zhe Ling, Huilin Chen, Yu-Zhen Zhou et al. · 0 citations

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