Search Results (77)

Residual lignin generated by pulp, paper, and biorefining industries is commonly burned for energy, despite its potential as a renewable source of aromatic compounds. Studies focusing on microbial lignin degradation contribute to lignin valorization and represent a sustainable strategy to enhance biomass circularity. Here, we report the isolation of Klebsiella sp. IL2_9 from a ruminal consortium and demonstrate its ability to degrade and metabolize organosolv lignin. After 24 h of cultivation, the strain removed 22% of the initial lignin content. FTIR analysis revealed alterations in functional groups associated with guaiacyl and syringyl units, indicating structural modification of the polymer. GC–MS analyses further showed the consumption of lignin-derived aromatics, including vanillin, 2-aminobenzoic acid, and 4-hydroxybenzoic acid, along with the formation of vanillyl alcohol and phenyllactic acid derivatives. Overall, these findings highlight the potential of Klebsiella sp. IL2_9 as a promising biotechnological candidate for lignin valorization under anaerobic conditions. Full article

This study presents an integrated chemical and anatomical characterization of leaves from seven Asparagaceae species (Agave convallis Trel., A. salmiana Otto ex Salm.-Dyck, A. striata Zucc., Dasylirion acrotrichum Zucc., Nolina excelsa García-Mend. & E. Solano, Yucca filifera Chabaud, and Y. periculosa Baker). Leaf biomass was subjected to successive Soxhlet extractions to quantify extractives, followed by isolation of lignocellulosic fractions. Lignin and cellulose were analyzed by Fourier-transform infrared (FTIR) spectroscopy to determine the syringyl/guaiacyl (S/G) ratio and total crystallinity index. Leaf anatomy was examined using fluorescence microscopy. Total extractives ranged from 13.4 to 24.0%, with A. salmiana and D. acrotrichum showing the highest values. Lignin content varied markedly among genera, reaching up to 45.1% in Yucca species, whereas cellulose content ranged from 31.3 to 42.2%. Crystalline cellulose accounted for 42.1–56.9% of total cellulose, with the highest crystallinity observed in A. convallis. FTIR analysis revealed a predominance of guaiacyl-type lignin in all species except Y. periculosa (S/G = 1.2). Multivariate analyses discriminated between genera primarily based on lignin, hemicellulose, and cellulose contents. These findings highlight genus-level differences in leaf lignocellulosic composition and support the potential use of Asparagaceae leaves as feedstocks for bioenergy and biomaterial applications. Full article

This study focuses on obtaining lignin-based hydrogels from pruning residues of orange trees in the Safor region (Valencia) using an alkaline extraction method. The structural analysis of the obtained lignin was carried out using Fourier-transform infrared spectroscopy (FTIR), which revealed the characteristic functional groups of lignin, as well as its structural monolignols: syringyl and guaiacyl. The thermal properties were analyzed using differential scanning calorimetry (DSC) and thermogravimetric analysis. The DSC thermogram revealed a relatively low glass transition temperature (T_g) of 67 °C, which may be attributed to partial lignin chain degradation during alkaline extraction. Soda lignin was obtained at 190 °C with an approximate yield of 10.8% relative to the initial biomass and subsequently used to synthesize poly(vinyl alcohol) (PVA)-based hydrogels for ibuprofen encapsulation. Finally, the release experiments of the encapsulated ibuprofen were carried out in an aqueous phosphate buffer medium (pH = 7) at room temperature. A multi-curve response analysis (MCR) algorithm using the Korsmeyer–Peppas (KP) concentration model was used to analyze the release curves, which concluded that the drug and water-soluble lignin fraction (SLF) were released at different rates. For both components, a good correlation was obtained between the measured responses and those provided by the KP model. The release profile indicated that approximately 87% of the initial ibuprofen load was released from the hydrogel within 5 h, highlighting the promising potential of lignin-based hydrogels for drug delivery applications. Full article

This study focused on optimising the saccharification of cardoon mixed residues through acid or base-catalysed steam explosion, using a Response Surface Methodology (RSM) to optimise the main process parameters. Despite the increasing interest in cardoon as a lignocellulosic feedstock, its efficient fractionation remains challenging, with limited cellulose hydrolysis and incomplete hemicellulose recovery under non-optimised steam explosion conditions. Therefore, a systematic evaluation of catalytic severity is required to improve biomass valorisation. H₂SO₄-catalysed steam explosion significantly improved glucan hydrolysis in the following enzymatic saccharification process, achieving 78 mol% glucose yield after a pretreatment carried out at 200 °C, 5 min, and 25 mM catalyst concentration. Xylan recovery required a higher catalyst concentration of 50 mM and temperatures lower than 220 °C to avoid the dehydration reaction of xylose to furfural. The optimal conditions for maximising glucose and xylose yields were 196 °C for 5 min with 50 mM H₂SO₄, resulting in 80.5 mol% glucose yield and 70.3 mol% xylose yield. Alkaline-catalysed steam explosion at 200 °C with 25 mM NaOH increased the enzymatic hydrolysis of glucan and favoured the production of lignin with a higher syringyl/guaiacyl ratio, making it more reactive. Overall, this research provides valuable insights into catalytic steam explosion coupled with the enzymatic saccharification step for the complete valorisation of lignocellulosic cardoon residues. Full article

Lignin is one of the most abundant natural biopolymers and plays a crucial role in the development of safe and sustainable alternatives for healthcare products. In this study, we employed molecular dynamics simulations and free energy calculations to investigate lignin derivatives’ interactions with skin-like membranes. Specifically, we designed a small lignin derivative composed of syringyl and guaiacyl subunits. Our results reveal that molecular size, concentration, and thermal conditions critically influence the insertion, interaction dynamics, and localization behavior of lignin derivatives. Notably, variations in these parameters induce distinct behaviors, including rapid membrane insertion, hydrogen bonding, clustering, and surface adhesion. The findings provide insights into the molecular mechanisms governing lignin derivatives’ interactions with skin-like membranes, with implications for developing bio-based skincare formulations and transdermal delivery systems. Our results highlight the importance of molecular size and concentration in optimizing lignin-derived compounds for dermatological and therapeutic applications. Full article

Almond hulls and shells, the byproducts of the almond industry, were analyzed to assess their potential valorization pathways. Shells showed a higher content in lignin and polysaccharides, but very low levels of extractives and inorganics. Hull’s high polar extractives fraction showed poor phenolic preponderance and antioxidant activity, but high sugar and mineral contents, and its lipophilic extracts were highly enriched in triterpenes (from 73.5% to 91.3%), while shells presented more fatty acids (27.4% to 34.2%) and sterols (17.4% to 29.1%). Shells exhibited much higher S/G ratio (syringyl to guaiacyl units) in their lignin polymer (1.0 to 1.4), compared to hulls (0.5 to 0.6). After mineral analyses, hulls showed high amounts of potassium (3.7–4.9%). Fixed carbon content was similar for both materials, but shells showed a higher energetic content, ~20 MJ/kg. Finally, both hulls and pellets increased the water holding capacity (WHC) of the soil by 50%, when added in weight percentages of 6.25% (hulls) and 25% (pellets). With these results, the range of possibilities for these waste materials is exciting: shells could be used to obtain hemicellulose oligosaccharides, while hulls could be used in sugar extraction for biotransformation or as a soil amendment. Full article

The integration of manure and straw substantially affects soil organic carbon (SOC) dynamics, transformation, and long-term stabilization in agricultural systems. Dissolved organic carbon (DOC), particulate organic carbon (POC), and mineral-associated organic carbon (MOC) are the three main components of the SOC pool, each influencing soil carbon dynamics and nutrient cycling. Current research gaps remain regarding how combined fertilization practices affect the inputs of plant-originated and microbe-derived carbon into SOC pools and stability mechanisms. Our investigation measured SOC fractions (DOC, POC, MOC), SOC mineralization rate (SCMR), microbial necromass carbon, lignin phenols, enzyme activities, and microbial phospholipid fatty acids (PLFAs) over a long-term (17 years) field experiment with four treatments: mineral fertilization alone (CF), manure-mineral combination (CM), straw-mineral application (CS), and integrated manure-straw-mineral treatment (CMS). The CMS treatment exhibited notably elevated levels of POC (7.42 g kg⁻¹), MOC (10.7 g kg⁻¹), and DOC (0.108 g kg⁻¹), as well as a lower SCMR value (1.85%), compared with other fertilization treatments. Additionally, the CMS treatment stimulated the buildup of both bacterial and fungal necromass while enhancing the concentrations of ligneous biomarkers (vanillin, syringyl, and cinnamic derivatives), which correlated strongly with the elevated contents of fungal and bacterial PLFAs and heightened activity of carbon-processing enzymes (α-glucosidase, polyphenol oxidase, cellobiohydrolase, peroxidase, N-acetyl-β-D-glucosidase). Furthermore, fungal and bacterial microbial necromass carbon, together with lignin phenols, significantly contributed to shaping the composition of SOC. Through random forest analysis, we identified that the contents of bacterial and fungal necromass carbon were the key factors influencing DOC and MOC. The concentrations of syringyl phenol and cinnamyl phenols, and the syringyl-to-cinnamyl phenols ratio were the primary determinants for POC, while the fungal-to-bacterial necromass carbon ratio, as well as the concentrations of vanillyl, syringyl, and cinnamyl phenols, played a critical role in SCMR. In conclusion, the manure combined with straw incorporation not only promoted microbial growth and enzyme activity but also enhanced plant- and microbial-derived carbon inputs. Consequently, this led to an increase in the contents and stability of SOC fractions (DOC, POC, and MOC). These results suggest that manure combined with straw is a viable strategy for soil fertility due to its improvement in SOC sequestration and stability. Full article

Soil salinity is a growing threat to agricultural sustainability, particularly in arid and semi-arid regions. Understanding how salinity affects soil organic matter (OM) is critical for improving land management and maintaining soil health. This study addresses these challenges by exploring the molecular-level impact of salinity on OM dynamics. Salinity exerts a depth-dependent influence on lignin and microbial lipid biomarkers, which are used to trace plant inputs and microbial activity, respectively. For lignin biomarkers, in the surface layer (0–20 cm), higher salinity levels are associated with increased Syringyl/Vanillyl (S/V) and Cinnamyl/Vanillyl (C/V) ratios, suggesting enhanced preservation of syringyl (S) and cinnamyl (C) units. In the middle layer (−20 to −60 cm), higher salinity correlates with elevated SVC (total lignin phenols), Acid/aldehyde (Ad/Al) ratios, and other markers of selective lignin degradation. For lipid biomarkers, salinity modulates microbial adaptation and turnover, as seen in variations in i17 (iso-C17), a17 (anteiso-C17), and unsaturation indices such as C16:1/C16, reflecting Gram-positive and Gram-negative bacterial activity. These trends indicate that salinity stress alters microbial lipid profiles, leading to reduced turnover and enhanced preservation in deeper, more anoxic environments. Principal Component Analysis (PCA) revealed depth- and salinity-driven patterns that distinguish between surface microbial transformations and deep-layer molecular preservation. Correlation analysis of Principal Components (PCs) with salinity revealed that higher salinity favored molecular stability in deeper layers, while lower salinity was associated with microbial transformations in surface layers. These findings underscore salinity’s critical role in OM stabilization and turnover, and provide a molecular framework to guide sustainable management of saline soils. Full article

This study examines a boreal peatland (the Sagnes peatland, Fanay, Limousin, France) with a depth of 1 m. This peatland is currently in the late stages of organic deposition, as evidenced by the growth of Carex species, along with Sphagnum mosses, in the uppermost level. To gain molecular insights, we conducted an analysis of the lignin and polyphenolic counterparts using HMDS (hexamethyldisilazane) thermochemolysis, enabling the identification of lignin degradation proxies. The goal was to develop characteristic indicators for the state of lignin degradation based on the relative distribution of lignin phenols, measured by gas chromatography coupled with mass spectrometry (GC-MS) after the HMDS thermochemolysis. For that purpose, the singular contribution of the 11 aromatic moieties yielded, along with SGC (sum of lignin moieties) and the most lignin degradation proxies, were applied. It has been shown that HMDS thermochemolysis exhibited the capacity to reveal oxidized and degraded lignin fractions, following the increasing trend yielded for most moieties and SGC proxy, in the mesotelm and catotelm layers. In addition, the C/G (Cinnamyl/Guaiacyl) and S/G (Syringyl/Guaiacyl) ratios showed their highest input in the upper half of the core. This bias in the aforementioned ratios could indicate that HMDS thermochemolysis is to be applied for geological samples, where low G-compounds exist. For the sake of validating HMDS thermochemolysis’ application, Principal Component Analysis (PCA) was then applied to the molecular fingerprint. For ratios and proxies of aromatic moieties of HMDS thermochemolysis, the PCA approach exhibited a higher contribution (79%). This indicates the efficiency of these ratios in describing the molecular fingerprint of peat depth records. In addition, a higher separation between the contributions of the investigated variables (molecular proxies) along the first two PCs was noticed. In other words, the variables that showed a high contribution towards PC₁ exhibited a low contribution towards PC₂, and vice versa. These findings indicate the high reliance of applying the ratios and proxies of HMDS thermochemolysis. Full article

This study focuses on three different regions of moso bamboo (Phyllostachys edulis): an inner layer (IB), middle layer (MB), and outer layer (OB), to comprehensively characterize the structural features, chemical composition (ash, extractives and lignin contents), and the lignin monomeric composition as determined by analytical pyrolysis. The results show that bamboo presents a gradient structure. From the IB to OB, the vascular bundle density and fiber sheath ratio increase, the porosity decreases (from 45.92% to 18.14%), and the vascular bundle diameter–chord ratio increases (from 0.85 to 1.48). In terms of chemical composition, the ash, extractives, and acid-soluble lignin content gradually decrease from IB to OB. The holocellulose content follows the trend: MB (66.3%) > OB (65.9%) > IB (62.8%), while the acid-insoluble lignin content exhibits the opposite trend: IB (22.6%) > OB (17.8%) > MB (17.7%). Pyrolysis products reveal the diversity of carbohydrates and lignin derivatives, with a lignin monomeric composition rich in syringyl and guaiacyl units and lower amounts of H-units: the IB has an H:G:S relation of 18:26:55, while 15:27:58 is the ratio for the MB and 15:40:45 for the OB; S/G ratio values were, respectively, 1.22, 1.46, and 0.99. A comprehensive analysis highlights significant gradient variations in the structure and chemistry of bamboo, providing robust support for the classification and refinement methods of bamboo residues for potential applications. Full article

Stems are prone to bending or lodging due to inadequate stem strength, which seriously reduces the cut-flower ornamental quality of herbaceous peony (Paeonia lactiflora Pall.). Plant LACCASE (LAC), a copper-containing polyphenol oxidase, has been shown to participate in the polymerization process of monolignols; however, the role of LAC in regulating the stem strength of P. lactiflora remains unclear. Here, the full-length cDNA of PlLAC15, which demonstrated a positive association with stem strength, was isolated. It consisted of 1790 nucleotides, encoding 565 amino acids that had four typical laccase copper ion-binding domains. Moreover, PlLAC15 was highly expressed in the stem, and its expression level gradually significantly increased during stem development. Furthermore, PlLAC15 was found to be localized specifically to the cell wall, and its recombinant protein exhibited laccase activity. Additionally, the role of PlLAC15 in regulating the stem strength of P. lactiflora was confirmed by transgenic studies. When PlLAC15 was overexpressed in tobacco, stem strength increased by more than 50%, S-lignin was significantly deposited, and the lignification degree of stem xylem fiber cells increased. These results suggested that PlLAC15 facilitated S-lignin deposition to enhance stem strength in P. lactiflora, which would provide precious information that benefits future exploration of stem bending or lodging resistance in plants. Full article

Lignin, the earth’s second-most abundant biopolymer after cellulose, has long been relegated to low-value byproducts in the pulp and paper industry. However, recent advancements in valorization are transforming lignin into a sustainable and versatile feedstock for producing high-value biofuels, bioplastics, and specialty chemicals. This review explores the conversion of lignin’s complex structure, composed of syringyl (S), guaiacyl (G), and p-hydroxyphenyl (H) units, into value-added products. We critically assess various biochemical and analytical techniques employed for comprehensive lignin characterization. Additionally, we explore strategies for lignin upgrading and functionalization to enhance its suitability for advanced biomaterials. The review emphasizes key areas of lignin valorization, including catalytic depolymerization methods, along with the associated challenges and advancements. We discuss its potential as a feedstock for diverse products such as biofuels, bioplastics, carbon fibers, adhesives, and phenolic compounds. Furthermore, the review briefly explores lignin’s inherent properties as a UV protectant and antioxidant, alongside its potential for incorporation into polymer blends and composites. By presenting recent advancements and case studies from the literature, this review highlights the significant economic and environmental benefits of lignin valorization, including waste reduction, lower greenhouse gas emissions, and decreased reliance on non-renewable resources. Finally, we address future perspectives and challenges associated with achieving large-scale, techno-economically feasible, and environmentally sustainable lignin valorization. Full article

Lignin is endowed with antioxidant activity due to its diverse chemical structure. It is necessary to explore the relationship between antioxidant activity and the chemical structure of the lignin to develop its high-value utilization. Herein, we employed maleic acid (MA) as a hydrotropic agent to preferably isolate the lignin from distinct herbaceous sources (wheat straw and switchgrass) under atmospheric pressure conditions. The resultant acid hydrotropic lignin (AHL) isolated from wheat straw exhibited high radical scavenging rates, up to 98% toward DPPH and 94% toward ABTS. Further investigations indicated that during the MA hydrotropic fractionation (MAHF) process, lignin was carboxylated by MA at γ-OH of the side-chain, providing additional antioxidant activity from the carboxy group. It was also found that the radical scavenging rate of AHL has a positive correlation with carboxyl, phenolic hydroxyl contents, and the S–G (syringyl–guaiacyl) ratio, which could be realized by increasing the MAHF severity. Overall, this work underlies the enhancement origin of the antioxidant property of lignin, which will facilitate its application in biological fields as an efficient, cheap, and renewable antioxidant additive. Full article

Rising atmospheric CO₂ levels, a significant consequence of anthropogenic activities, profoundly impact global agriculture and food security by altering plant physiological processes. Despite extensive research, a comprehensive understanding of the specific effects of elevated CO₂ on maize (Zea mays L.)’s primary and secondary metabolism remains elusive. This study investigated the responses of maize seedlings cultivated in open-top chambers (OTCs) under three CO₂ concentrations: ambient (380 ppm), elevated (600 ppm), and high (1800 ppm). Key growth parameters, including plant height, leaf area, and aboveground biomass (leaf and stem), were assessed alongside metabolic profiles encompassing nonstructural and structural carbohydrates, syringyl (S) and guaiacyl lignin, the syringyl-to-guaiacyl (S/G)-lignin ratio, photosynthetic pigments, total soluble protein, and malondialdehyde (MDA) levels. The results demonstrated that exposure to 600 ppm CO₂ significantly enhanced plant height, leaf area, and aboveground biomass compared to ambient conditions. Concurrently, there were notable increases in the concentrations of primary metabolites. In contrast, exposure to 1800 ppm CO₂ severely inhibited these growth parameters and induced reductions in secondary metabolites, such as chlorophyll and soluble proteins, throughout the growth stages. The findings underscore the intricate responses of maize metabolism to varying CO₂ levels, highlighting adaptive strategies in primary and secondary metabolism under changing atmospheric conditions. This research contributes to a nuanced understanding of maize’s physiological adaptations to future climate scenarios characterized by elevated CO₂, with implications for sustainable agriculture and food security. Full article

The densification of solid wood is a well-studied technique that aims to increase the strength and hardness of the material by permanently compressing the wood tissue. To optimise the densification process in this study, a pre-treatment with sodium sulphite was used (delignification). With delignification prior to densification, one achieves higher compression ratios and better mechanical properties compared to densification without pre-treatment. The reactivity of syringyl (dominant in hardwoods) and guaiacyl (dominant in softwoods) lignin towards delignification is different. The influences of this difference on the delignification and densification of softwoods and hardwoods need to be investigated. This study aimed to densify wood after delignification and investigate how variations in chemical composition between coniferous and deciduous species affect the densification process. Scots pine and Eurasian aspen specimens with a similar initial density were investigated to study the influence of the different lignin chemistry in softwoods and hardwoods on the densification process. Both timbers were delignified with sodium sulphite and sodium hydroxide and subsequently densified. While the delignification was twice as efficient in aspen than in pine, the compression ratios were almost identical in both species. The Brinell hardness and compressive strength showed a more significant increase in aspen than in Scots pine; however, one exception was the compressive strength in a radial direction, which increased more effectively in Scots pine. Scanning electron microscopy (SEM) revealed the microstructure of densified aspen and Scots pine, showing the crushing and collapse of the cells. Full article