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The positron annihilation lifetime (PAL) spectroscopy characteristics of ethylene-propylene-diene monomer rubber (EPDM) composites reinforced with treated wheat husk fibers (WHFs) were investigated for the first time. PAL spectroscopy is employed to study the free volume of polymers. The use of lignocellulosic materials as reinforcement in polymeric composites has gained attention due to their low cost, availability, and eco-friendliness. In this study, the impact of the loading concentration on the interfacial adhesion between the EPDM matrix and WHFs is quantified, along with the evaluation of swelling measurement and tensile properties. Additionally, the nanoscopic properties derived from PAL spectroscopy correlate with the composites' macroscopic properties. In addition, the dielectric properties of the investigated samples have been studied, and their conductivity has been calculated. To determine the conduction mechanism within these samples and how it is affected by the addition of WHF, the change in electrical conductivity with the frequency of the external electric field applied to the samples was studied, and from this, the conduction mechanism was determined, and the barrier height value was calculated. The experimental results provide insights into the relationship between the structure and properties of EPDM-WHF biocomposites, offering valuable knowledge for developing sustainable and high-performance materials. [ABSTRACT FROM AUTHOR]

Background: The microbial landscape within termite guts varies across termite families. The gut microbiota of lower termites (LT) is dominated by cellulolytic flagellates that sequester wood particles in their digestive vacuoles, whereas in the flagellate-free higher termites (HT), cellulolytic activity has been attributed to fiber-associated bacteria. However, little is known about the role of individual lineages in fiber digestion, particularly in LT. Results: We investigated the lignocellulolytic potential of 2223 metagenome-assembled genomes (MAGs) recovered from the gut metagenomes of 51 termite species. In the flagellate-dependent LT, cellulolytic enzymes are restricted to MAGs of Bacteroidota (Dysgonomonadaceae, Tannerellaceae, Bacteroidaceae, Azobacteroidaceae) and Spirochaetota (Breznakiellaceae) and reflect a specialization on cellodextrins, whereas their hemicellulolytic arsenal features activities on xylans and diverse heteropolymers. By contrast, the MAGs derived from flagellate-free HT possess a comprehensive arsenal of exo- and endoglucanases that resembles that of termite gut flagellates, underlining that Fibrobacterota and Spirochaetota occupy the cellulolytic niche that became vacant after the loss of the flagellates. Furthermore, we detected directly or indirectly oxygen-dependent enzymes that oxidize cellulose or modify lignin in MAGs of Pseudomonadota (Burkholderiales, Pseudomonadales) and Actinomycetota (Actinomycetales, Mycobacteriales), representing lineages located at the hindgut wall. Conclusions: The results of this study refine our concept of symbiotic digestion of lignocellulose in termite guts, emphasizing the differential roles of specific bacterial lineages in both flagellate-dependent and flagellate-independent breakdown of cellulose and hemicelluloses, as well as a so far unappreciated role of oxygen in the depolymerization of plant fiber and lignin in the microoxic periphery during gut passage in HT. Ak1UNwnHwhcNN-Fj12kHob Video Abstract [ABSTRACT FROM AUTHOR]

The production of bioethanol from lignocellulosic biomass requires the efficient conversion of glucose and xylose to ethanol, a process that depends on the ability of microorganisms to internalize these sugars. Although glucose transporters exist in several species, xylose transporters are less common. Several types of transporters have been identified in diverse microorganisms, including members of the Major Facilitator Superfamily (MFS) and Sugars Will Eventually be Exported Transporter (SWEET) families. Considering that Saccharomyces cerevisiae lacks an effective xylose transport system, engineered yeast strains capable of efficiently consuming this sugar are critical for obtaining high ethanol yields. This article reviews the structure–function relationship of sugar transporters from the MFS and SWEET families. It provides information on several tools and approaches used to identify and characterize them to optimize xylose consumption and, consequently, second-generation ethanol production. [ABSTRACT FROM AUTHOR]

Volvariella volvacea is one of the world-famous edible mushroom varieties cultivated in lignocellulosic agricultural waste as a growth media. The present study aimed to investigate the growth and characteristics of V. volvacea and analyze the difference between the V. volvacea production yield using pineapple leaves medium compared to the oil palm empty fruit bunch (EFB) medium. The biochemical analysis of the substrate was conducted to estimate the substrate's moisture percentage, crude fiber, ash content, and mineral content. The study results revealed that the type of substrate significantly (P < 0.05) affected the mycelial growth, moisture content, and yield of V. volvacea. The fastest growth of mycelium was exhibited on pineapple leaves substrate with mycelium invasion within 3 days. Pineapple leaves also have the highest fruiting body formation diameter (2.57 cm) and moisture content (91.61%). However, there were no significant differences (P > 0.05) observed in other parameters, including cap diameter and stipe length, weight, and biological efficiency (BE) of V. volvacea. In summary, the results demonstrate the possible expenditure of pineapple leaves to cultivate V. volvacea, which would provide a protein-rich food source and help farmers grow V. volvacea with the biological conversion processes of agro-industrial wastes. [ABSTRACT FROM AUTHOR]

Novel lignocellulosic biomass‐based fertilizers are developed to enhance crop yields while minimizing ecological impacts. These fertilizers, enriched with macro and micronutrients, feature slow‐release properties, reducing nutrient loss compared to conventional fertilizers. The study emphasizes their potential in sustainable agriculture, offering a viable alternative for soil fertility and crop yield. [ABSTRACT FROM AUTHOR]

The production of bioethanol from lignocellulosic biomass requires the efficient conversion of glucose and xylose to ethanol, a process that depends on the ability of microorganisms to internalize these sugars. Although glucose transporters exist in several species, xylose transporters are less common. Several types of transporters have been identified in diverse microorganisms, including members of the Major Facilitator Superfamily (MFS) and Sugars Will Eventually be Exported Transporter (SWEET) families. Considering that Saccharomyces cerevisiae lacks an effective xylose transport system, engineered yeast strains capable of efficiently consuming this sugar are critical for obtaining high ethanol yields. This article reviews the structure-function relationship of sugar transporters from the MFS and SWEET families. It provides information on several tools and approaches used to identify and characterize them to optimize xylose consumption and, consequently, second-generation ethanol production. [ABSTRACT FROM AUTHOR]

Effective fractionation of lignocelluosic biomass and subsequent valorization of all three major components under mild conditions were achieved. Pretreatment with acidified monophasic phenoxyethanol (EPH) efficiently removed 92.6 % lignin and 80 % xylan from poplar at 110 °C in 60 min, yielding high‐value EPH‐xyloside, EPH‐modified lignin (EPHL), and a solid residue nearly purely composed of carbohydrates. After removing the grafted acetyl groups using 1 % NaOH at 50 °C, the highest enzymatic digestibility reached 92.3 %. EPHL could be recovered in high yield and purity with an uncondensed structure, while xylose was converted to EPH‐xyloside, a potential precursor in biomedical industries. Additionally, the acidified monophasic EPH solvent could effectively fractionate biomass from species other than hardwood, achieving over 70 % delignification from recalcitrant pinewood under the same mild conditions, demonstrating the high potential of monophasic EPH pretreatment. [ABSTRACT FROM AUTHOR]

Lignocellulosic biomass (LB) represents a sustainable and abundant feedstock with diverse applications, particularly in microbial fermentation processes for the production of biofuels and biochemical. This biomass serves as a promising alternative to conventional fossil fuels. Extensive research on the decomposition of wood has elucidated various microbial enzymatic and non-enzymatic mechanisms that facilitate the utilization of this resource. This review systematically examines the chemical and structural factors contributing to biomass recalcitrance, emphasizing recent advancements in analytical tools for their assessment. Furthermore, we explore innovative predictive models for hydrolysis, which are crucial for optimizing the conversion of LB into biofuels and bio-based chemicals. A comprehensive cost analysis of hydrolysis processes is also presented, offering insights into the economic feasibility of these conversion methods. The findings underscore the potential of lignocellulosic biomass as a key player in sustainable energy and material production. Article Highlights: Lignocellulosic biomass can be efficiently converted into biofuels using specific enzymes to break down plant materials. Factors like microbial strain choice and substrate type greatly impact the success of the hydrolysis process. Economic challenges must be addressed to make biomass conversion a viable alternative to fossil fuels. [ABSTRACT FROM AUTHOR]

Alkaline-catalyzed organosolv pretreatment of lignocellulosic biomass affords excellent delignification, yielding a holocellulose-rich substrate for fermentable sugar production. However, complete lignin removal is impractical, and residual lignin also exacerbates negative effects on subsequent enzymatic hydrolysis. Herein, a novel strategy of developing surfactant-assisted organosolv pretreatment (Triton-X 100, AEO 9 and Tween 80) for in situ lignin modification was proposed to overcome this issue. The results indicated that the pretreated substrates showed considerable enzymatic hydrolyzability with a 15.7%–38.3% higher sugar yield compared to the control group without surfactants. Surfactants could graft on both residual and dissolved lignin through etherification, forming α-etherified lignin, though without significantly changing the component distribution and substrate-related properties. Quantum chemical calculations provided theoretical evidence of strong H-bonding and pronounced interaction energy between lignin and surfactants (maximally at −48.4 kcal mol−1). In particular, this surfactant modification decreased the aliphatic –OH and phenolic –OH contents of residual lignin by 16.0%–22.4% and 13.8%–28.8%, respectively. The reduction of –OH groups mitigated non-productive adsorption between lignin and cellulases via H-bonding interaction, which exhibited a significant correlation with the increased enzymatic hydrolyzability (>−0.9). Overall, this study offers valuable insight into the fundamental understanding of the mechanism involved in lignin modification during surfactant-assisted pretreatment and lignin–enzyme interaction during enzymatic hydrolysis. The new findings underscore the potential application of surfactants in organosolv pretreatment to achieve a feasible approach for developing an efficient enzyme-mediated lignocellulosic sugar platform. [ABSTRACT FROM AUTHOR]

As a crucial component of batteries, the binder connects the granular active material and the conductive additive into a whole electrode and attaches to the surface of the current collector through a variety of interactions to maintain the electron/ion transport and the integrity of the electrode during the charge–discharge cycles. However, conventional binders are mostly synthetic polymers with single structures and properties and are not renewable, thus the development of multifunctional green renewable binders derived from biomass materials is attracting increasing attention. The distribution and function of lignocellulose in plants are similar to those of binders in electrodes. They strengthen the structure of the plants via hydrogen bonding, π–π conjugation, hydrophobicity, etc., and maintain the diffusion and transport of molecules, aligning with the criteria for the next generation of battery binders. In the context of the significant impact of binders on the performance of advanced battery systems, recent progress in research on lignocellulose derivative-based binders in various batteries is summarized. The research potential and challenges of lignocellulose and its derivatives as binder materials are discussed, with the hope of shedding light on the rational construction of robust and stable lignocellulose-based binders for high-energy-density batteries. [ABSTRACT FROM AUTHOR]

To address the problem of non-renewable resources and energy shortages, converting biomass, the only renewable carbon resource on Earth, into various fine chemicals holds significant value. Furfural stands out as one of the most promising platform compounds derived from lignocellulosic biomass. Due to its highly functional molecular structure, furfural can be selectively converted into various fuels and high-value compounds. This review discusses recent developments in furfural production and its conversion into related chemicals, such as furfuryl alcohol, γ-valerolactone, pentanediols, and nitrogen-containing compounds. It provides an in-depth understanding of the catalysts, systems, and mechanisms used in the selective transformation of furfural. The review also explores primary pathways and catalytic mechanisms, with a focus on advances in heterogeneous catalytic systems. Furthermore, it outlines future research directions and offers insights into potential applications in this field. This review presents several research trends, aiming to provide innovative ideas for further exploration of furfural downstream products in a greener, more efficient, and cost-effective manner. [ABSTRACT FROM AUTHOR]

An attempt has been made to optimize areal density and number of layers of needle-punched jute nonwoven fabric for the development of a rigid composite with desirable performance properties using Taguchi L9 experimental design. The hand lay-up followed by compression molding protocol was used to prepare composite sheet with jute nonwoven fabric as reinforcement and unsaturated polyester resin as matrix. We evaluated the tensile strength, flexural strength, and volume of reinforcement of the developed composites, and analyzed the data in Minitab 18.0 software to optimize the processing conditions. Results inferred that the areal density of jute fabric reinforcement positively influenced the mechanical properties of the composite sheet, while the number of layers had a negative impact. Statistical analysis revealed that 400 GSM jute nonwoven fabric in three layers could be an optimum condition to develop a rigid composite sheet with the desirable properties of an automobile product. [ABSTRACT FROM AUTHOR]

d-Xylitol is a naturally occurring sugar alcohol present in diverse plants that is used as an alternative sweetener based on a sweetness similar to sucrose and several health benefits compared to conventional sugar. However, current industrial methods for d-xylitol production are based on chemical hydrogenation of d-xylose, which is energy-intensive and environmentally harmful. However, efficient conversion of l-arabinose as an additional highly abundant pentose in lignocellulosic materials holds great potential to broaden the range of applicable feedstocks. Both pentoses d-xylose and l-arabinose are converted to d-xylitol as a common metabolic intermediate in the native fungal pentose catabolism. To engineer a strain capable of accumulating d-xylitol from arabinan-rich agricultural residues, pentose catabolism was stopped in the ascomycete filamentous fungus Aspergillus niger at the stage of d-xylitol by knocking out three genes encoding enzymes involved in d-xylitol degradation (ΔxdhA, ΔsdhA, ΔxkiA). Additionally, to facilitate its secretion into the medium, an aquaglyceroporin from Saccharomyces cerevisiae was tested. In S. cerevisiae, Fps1 is known to passively transport glycerol and is regulated to convey osmotic stress tolerance but also exhibits the ability to transport other polyols such as d-xylitol. Thus, a constitutively open version of this transporter was introduced into A. niger, controlled by multiple promoters with varying expression strengths. The strain expressing the transporter under control of the PtvdA promoter in the background of the pentose catabolism-deficient triple knock-out yielded the most favorable outcome, producing up to 45% d-xylitol from l-arabinose in culture supernatants, while displaying minimal side effects during osmotic stress. Due to its additional ability to extract d-xylose and l-arabinose from lignocellulosic material via the production of highly active pectinases and hemicellulases, A. niger emerges as an ideal candidate cell factory for d-xylitol production from lignocellulosic biomasses rich in both pentoses. In summary, we are showing for the first time an efficient biosynthesis of d-xylitol from l-arabinose utilizing a filamentous ascomycete fungus. This broadens the potential resources to include also arabinan-rich agricultural waste streams like sugar beet pulp and could thus help to make alternative sweetener production more environmentally friendly and cost-effective. [ABSTRACT FROM AUTHOR]

d-Xylitol is a naturally occurring sugar alcohol present in diverse plants that is used as an alternative sweetener based on a sweetness similar to sucrose and several health benefits compared to conventional sugar. However, current industrial methods for d-xylitol production are based on chemical hydrogenation of d-xylose, which is energy-intensive and environmentally harmful. However, efficient conversion of l-arabinose as an additional highly abundant pentose in lignocellulosic materials holds great potential to broaden the range of applicable feedstocks. Both pentoses d-xylose and l-arabinose are converted to d-xylitol as a common metabolic intermediate in the native fungal pentose catabolism. To engineer a strain capable of accumulating d-xylitol from arabinan-rich agricultural residues, pentose catabolism was stopped in the ascomycete filamentous fungus Aspergillus niger at the stage of d-xylitol by knocking out three genes encoding enzymes involved in d-xylitol degradation (ΔxdhA, ΔsdhA, ΔxkiA). Additionally, to facilitate its secretion into the medium, an aquaglyceroporin from Saccharomyces cerevisiae was tested. In S. cerevisiae, Fps1 is known to passively transport glycerol and is regulated to convey osmotic stress tolerance but also exhibits the ability to transport other polyols such as d-xylitol. Thus, a constitutively open version of this transporter was introduced into A. niger, controlled by multiple promoters with varying expression strengths. The strain expressing the transporter under control of the PtvdA promoter in the background of the pentose catabolism-deficient triple knock-out yielded the most favorable outcome, producing up to 45% d-xylitol from l-arabinose in culture supernatants, while displaying minimal side effects during osmotic stress. Due to its additional ability to extract d-xylose and l-arabinose from lignocellulosic material via the production of highly active pectinases and hemicellulases, A. niger emerges as an ideal candidate cell factory for d-xylitol production from lignocellulosic biomasses rich in both pentoses. In summary, we are showing for the first time an efficient biosynthesis of d-xylitol from l-arabinose utilizing a filamentous ascomycete fungus. This broadens the potential resources to include also arabinan-rich agricultural waste streams like sugar beet pulp and could thus help to make alternative sweetener production more environmentally friendly and cost-effective. [ABSTRACT FROM AUTHOR]

This paper investigates bioethanol production from switchgrass, focusing on enhancement of efficiency through various pretreatment methods and comparing two bioethanol production processes: simultaneous saccharification and fermentation (SSF) and separate hydrolysis and fermentation (SHF). Physical, chemical, and biological pretreatment processes are applied to enhance the breakdown of switchgrass's lignocellulosic structure. Effects of pretreatments, enzymatic hydrolysis, and fermentation on ethanol yield are discussed in detail. The comparative analysis reveals that SSF yields higher ethanol outputs within shorter times by integrating hydrolysis and fermentation into a single process. In contrast, SHF offers more control by separating these stages. The comparative analysis highlights that SSF achieves higher ethanol yields more efficiently, although it might restrict SHF's operational flexibility. This study aims to provide a comprehensive overview of the current pretreatments, hydrolysis methods, and fermentation processes in bioethanol production from switchgrass, offering insights into their scalability, economic viability, and potential environmental benefits. The findings are expected to contribute to the ongoing discussions and developments in renewable bioenergy solutions, supporting advancing more sustainable and efficient bioethanol production techniques. [ABSTRACT FROM AUTHOR]

The aim of this study was to determine the effect of sorption of Basic Red 46 (BR46) dye by lignocellulosic biomass on the susceptibility of the sorbed waste to anaerobic decomposition by anaerobic digestion. The research material used in the experiment consisted of two types of biomass: stalks with leaves and inflorescences after mowing Canadian goldenrod (Solidago canadensis L.) (GB), and rapeseed hulls (RHs) after oil pressing. During the anaerobic decomposition of RHs, 732.30 NmL/gVS and 646.63 NmL/gVS of methane were obtained from the non-sorbed substrate and the plant material after dye sorption, respectively. Similarly, in the variants using Canadian goldenrod, the production was 220.70 NmL/gVS and 183.20 NmL/gVS. The GB sorbent sorbed 34% more BR46 dye than the RH sorbent, which is likely to have resulted in the accumulation of VFA and contributed to the partial inhibition of methane production. In light of the obtained results and the literature data, it is concluded that there is a possibility of effective use of dye sorption waste for methane production. [ABSTRACT FROM AUTHOR]

Brewer's spent grains (BSG) offer valuable opportunities for valorization beyond its conventional use as animal feed. Among its components, lignin—a natural polymer with inherent antioxidant properties—holds significant industrial potential. This work investigates the use of microwave-assisted extraction combined with acidic natural deep eutectic solvents (NaDESs) for efficient lignin recovery, evaluating three different NaDES formulations. The results indicate that choline chloride–lactic acid (ChCl-LA), a NaDES with superior thermal stability as confirmed via thermogravimetric analysis (TGA), is an ideal solvent for lignin extraction at 150 °C and 15 min, achieving a balance of high yield and quality. ChCl-LA also demonstrated good solubility and cell disruption capabilities, while microwaves significantly reduced processing time and severity. Under optimal conditions, i.e., 150 °C, 15 min, in the presence of ChCl-LA NaDES, the extracted lignin achieved a purity of up to 79% and demonstrated an IC50 (inhibitory concentration 50%) of approximately 0.022 mg/L, indicating a relatively strong antioxidant activity. Fourier transform infrared (FTIR) and 2D-HSQC NMR (heteronuclear single quantum coherence nuclear magnetic resonance) spectroscopy confirmed the successful isolation and preservation of its structural integrity. This study highlights the potential of BSG as a valuable lignocellulosic resource and underscores the effectiveness of acidic NaDESs combined with microwave extraction for lignin recovery. [ABSTRACT FROM AUTHOR]

Conventional synthetic sorbents for oil spill cleanup are the most widely employed materials, although a major drawback is the extensive chemical modification that they have undergone, making them economically and environmentally nonsustainable. The use of inexpensive, abundant, nontoxic, biodegradable, and reusable lignocellulosic materials might be an alternative to conventional sorbents, with obvious positive impact on sustainability and circular economy. The present study subsequently utilizes the well‐established process, of converting grape molasses—a byproduct of the winemaking industry that represents a typical and abundant source of biomass—into a laser‐assisted graphene‐like product (LA‐B). Comparative experiments were carried out with two additional materials that are similarly produced by the same laser‐assisted method, yet use synthetic polyimide foil and tape polymers as precursors, namely LA‐F and LA‐T. The results showed that diesel oil adsorption capacity of LA‐B was 33.5 g/g, while the ultraoleophilic LA‐T adsorbed 57 g/g and LA‐F adsorbed 41 g/g. Furthermore, the crude oil uptake was 31.1, 56.0, and 38.6 g/g for LA‐B, LA‐T, and LA‐F, respectively. The adsorption of oil on the used materials could be well‐described by pseudo‐second‐order kinetics, showing that over 80% of oil was removed from the water within 15 min. [ABSTRACT FROM AUTHOR]

Forestry residues (FR) and medicinal-aromatic plant waste (MAPW) are considered potential resources for energy recovery. In this context, we explore the bioethanol production potential of three microbial strains Aspergillus niger, Zymomonas mobilis, and Trichoderma longibrachiatum using this lignocellulosic hydrolysate as a substrate. The blend of FR and MAPW was pretreated by different methods like acid sulfuric (AS), steam explosion (SE), and enzymatic (E). The ethanol yield was measured by gas chromatography (GC). Zymomonas mobilis demonstrated the highest ethanol yield of 5.95% on untreated substrate. Conversely, Aspergillus niger exhibited peak performance with an ethanol yield of 10.78% following AS, SE and E combined pretreatment. Trichoderma longibrachiatum, yielded ethanol ranging from 1.27% to 2.47%. Furthermore, the use of immobilized d' Aspergillus niger strains revealed a small decrease in ethanol yield from 11.34% in the first cycle to only 5.02% in the sixth cycle. In conclusion, Aspergillus niger emerges as a promising candidate due to its dual functionality in pretreatment and ethanol fermentation, offering pathways for advancing sustainable biofuel technologies. [ABSTRACT FROM AUTHOR]

Globally escalating ethanol demand necessitates the use of hybrid technologies integrating first- and second-generation biofuel feedstocks for achieving the futuristic targets of gasoline replacement with bioethanol. In present study, an optimized two-step sequential pre-treatment (first dilute alkali, then dilute acid) of Pine forest litter (PFL) was developed. Furthermore, the saccharification of pre-treated PFL was optimized through Response Surface Methodology using Box-Behnken Design, wherein 0.558 g/g of reducing sugar was released under the optimized conditions (12.5% w/v of biomass loading, 10 FPU/g of PFL enzyme loading, 0.15% v/v Tween-80 and 48 h incubation time). Moreover, during hydrolysate fermentation using Saccharomyces cerevisiae NCIM 3288 strain, 22.51 ± 1.02 g/L ethanol was produced. Remarkably, hydrophobic resin (XAD-4) treatment of PFL hydrolysate, significantly removed inhibitors (Furfural, 5-hydroxymethylfurfural and phenolics) and increased ethanol production to 27.38 ± 1.18 g/L. Furthermore, during fermentation of molasses supplemented PFL hydrolysate (total initial sugar: 100 ± 3.27 g/L), a maximum of 46.02 ± 2.08 g/L ethanol was produced with 0.482 g/g yield and 1.92 g/l/h productivity. These findings indicated that the integration of molasses to lignocellulosic hydrolysate, would be a promising hybrid technology for industrial ethanol production within existing bio-refinery infrastructure. [ABSTRACT FROM AUTHOR]

Xylooligosaccharides (XOS) are considered a potent source of prebiotics for humans. The global prebiotic market is expanding in size, was valued at USD 6.05 billion in 2021, and is expected to grow at a 14.9% compound annual growth rate between 2022 and 2030, indicating a huge demand. These XOS are non‐digestible pentose sugar oligomers comprising mainly xylose. Xylose is naturally present in the lignocellulosic biomass (LCB), fruits and vegetables. Apart from the prebiotic effect, these XOS have been reported to reduce blood cholesterol, possess antioxidant effects, increase calcium absorption, reduce colon cancer risk, and benefit diabetic patients. The primary use of XOS is reported in the feed industry followed by health, medical use, food and drinks. LCB mainly contains glucan, xylan and lignin. After glucan, xylan is the second‐highest available sugar on the globe composed of xylose. Therefore, the xylan fraction of LCB has great significance in producing food, feed and energy. Glucan has been exploited for the commercial production of ethanol, xylitol, furfural, hydroxymethyl furfural and glucose. As of now, xylan has limited applications. Therefore, xylan can be exploited to convert to XOS. The production of XOS from LCB fraction not only helps to produce these at a very low price, but also helps in the reduction of greenhouse gases. Its use in food and drinks is increasing as it can be derived from the abundantly and cheaply available LCB. The article provides a review on the production, purification and characterization of XOS in view of their use as nutraceuticals. © 2024 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Herbivorax saccincola A7 is an anaerobic alkali-thermophilic lignocellulolytic bacterium that possesses a cellulosome and high xylan degradation ability. To understand the expression profile of extracellular enzymes by carbon sources, quantitative real-time PCR was performed on all cellulosomal and non-cellulosomal enzyme genes of H. saccincola A7 using cellulose and xylan as carbon sources. The results confirmed that the scaffolding proteins of H. saccincola A7 were expressed. In general, the cellulosomal genes belonging to the glycoside hydrolase families 9, 10, 11, and 48 were repressed when xylan was the sole carbon source, but these genes were significantly induced in the presence of cellulose. These results indicate that cellulose, not xylan, is a key inducer of cellulosomal genes in H. saccincola A7. The RsgI-like proteins, which regulate a carbohydrate-sensing mechanism in Clostridium thermocellum, were also found to be encoded in the H. saccincola A7 genome. To confirm the regulation by RsgI-like proteins, the relative expression of σI1–σI4 factors was analyzed on both carbon sources. The expression of alternative σI1 and σI2 factors was enhanced by the presence of cellulose. By contrast, the expression of σI3 and σI4 factors was activated by both cellulose and xylan. Taken together, the results reveal that the cellulosomal and non-cellulosomal genes of H. saccincola A7 are regulated through a carbohydrate-sensing mechanism involving anti-σ regulator RsgI-like proteins. Key points: • qRT-PCR performed on cellulosomal and non-cellulosomal genes of H. saccincola A7 • Cellulose is a key inducer of the cellulosome of H. saccincola A7 • H. saccincola A7 possesses a similar system of anti-σ regulator RsgI-like proteins [ABSTRACT FROM AUTHOR]

Biopurification system (BPS) or biobeds are low-cost system for decontamination of on-farm generated pesticide waste. A biobed contains a mixture of soil, lignocellulosic biomass and organic matter source (compost/peat) and works on the principal of retention of pesticide in high organic matter matrix and its subsequent degradation by microbes. Bioaugmentation, a green technology, is defined as the improvement of the degradative capacity of biobeds by augmenting specific microorganisms. During last 20 years, several studies have evaluated pesticide degradation in biobeds augmented with bacterial and fungal species and prominent microorganism include genus Pseudomonas, Sphingomonas, Arthrobacter, Phanerochaete, Stereum, Delftia, Trametes, Streptomyces etc. Degradation of pesticides belonging to major classes have been studied in the bioaugmented biobeds. Studies suggested that some pesticides were degraded faster in the bioaugmented biobeds subject to survival and proliferation of degrading microbe. However, no effect of bioaugmentation was observed on degradation of some pesticides and no clear reason for the same was evident. Bioaugmentation with pesticide degrading microorganisms/consortium in combination with rhizosphere-assisted biodegradation could be an optimal strategy for accelerating the degradation of pesticides in biobeds. [ABSTRACT FROM AUTHOR]

Enzymatic degradation of biomass is preferred over chemical methods for environmental protection. However, in most cases, a chemical pretreatment is still required to help improve enzyme accessibility of the biomass. Therefore, it is necessary to develop highly efficient enzymes for those reasons and to save costs accordingly. Costs can be further reduced if the enzymes are recycled. XynR8(N58D) is an engineered and highly active xylanase originating from the rumen fungus Neocallimastix patriciarum. In this study, XynR8(N58D) was extracellularly over-expressed by Pichia pastoris. The resulting crude enzyme solution, with a purity of XynR8(N58D) of over 80%, was used to prepare the cross-linked enzyme aggregates (CLEA) of XynR8(N58D). Specific activity of the crude enzyme solution was 11,599.39 IU/mg, and that of CLEA was 6129.42 IU/mg. The immobilization yield and the immobilization efficiency were 62.68 ± 16.20% and 84.31 ± 3.11%, respectively. The thermostability, stress tolerance, and shelf life of CLEA were significantly better than those of the free enzyme. The free enzyme and CLEA both effectively decomposed insoluble xylan and autoclaved corncob powders. Therefore, XynR8(N58D) made into CLEA not only maintained high activity, but also improved its stability and permitted its reuse or recyclability. Both forms of the enzyme can effectively degrade lignocellulosic biomass without relying on chemical pretreatment to reduce recalcitrance of the biomass structure. The application of XynR8(N58D) and its CLEA to biomass degradation can help establish an eco-friendly and more cost-effective process. [ABSTRACT FROM AUTHOR]

This research involved conducting continuous adsorption experiments to assess fluoride elimination from drinking water achieved by utilizing biocomposites created from the peels of oranges and apples, which were impregnated with zirconium (Zr), to form BOP-Zr and BAP-Zr, respectively. The findings from the experimental data indicate that BOP-Zr and BAP-Zr are effective biosorbents with a solid ability to remove fluoride selectively. Additionally, these biosorbents were found to be stable, as they do not release Zr into the treated water. Notably, these environmentally friendly biosorbents are derived from renewable sources and enhance the value of waste materials. The study employed various empirical models, including Bohart-Adamas, Thomas, Yoon-Nelson, BDST, Clark, Yan, and Woolborska, to elucidate the mechanisms and crucial parameters involved in fluoride adsorption within packed bed columns. The Yan model demonstrated the highest correlation among these models, indicating a chemical adsorption process with kinetics following a pseudo-second-order pattern. BOP-Zr and BAP-Zr exhibited a maximum adsorption capacity of 59.3 and 47.5 mg/g, respectively, under a flow rate of 4 mL/min and an inlet fluoride concentration of 25 mg/L. The analysis of mass transfer coefficients revealed that the primary step governing the adsorption procedure was diffusion through pores. Consequently, the study conclusively establishes that BOP-Zr and BAP-Zr biocomposites, originating from lignocellulosic biomass remains, present a practical and competitive choice for eliminating fluoride from water. These materials surpass waste materials in performance and rival more expensive options in efficiency and performance. [ABSTRACT FROM AUTHOR]

Biowaste management is one of the major concerns for the effective processing of the production of toxic and value-added products. Biowaste is generally either by-products or end products of numerous bioprocess industries, including agriculture, food, dairy, textile, paper, pulp, or biopharma industries. They may not only consist of numerous varieties of toxic substances but also contain the most useful energy sources, especially celluloses, which are abundant energy-rich derivatives from agricultural waste. This biowaste mismanaged, especially in agriculture bases countries like India and Asian countries by either burning or dumping, may cause severe environmental pollution. Microbial degradation of waste will be the best appreciable, cost-effective, and eco-friendly process, and the majority of biowaste can be easily degraded by several microbial communities, and biowaste can be effectively converted into less toxic or nontoxic. Among them, certain bacteria target plant-based celluloses which are acting as the main structural component of the majority parts of plant cells by producing cellulases. As this process results in diverse energy-rich derivatives such as cellobiohydrolase and glucose, further, these can be used for bioethanol production. To hydrolyse the polymeric structure of glucose that is abundant in most plant-based wastes, the enzyme cellulases are the most essential and categorised into four classes:exoglucanase, endoglucanase, cellobiohydrolases, and glucosidases. These will act at different sites of the cellulose for further degradation into glucose, a chief source for bioethanol production. There are numerous natural bacterial communities with higher potentials for the degradation of biowaste, especially cellulosic waste into energy-rich sugars highlighted besides other waste decomposition. It would be a futuristic approach to enhance the catalytic activity of microbial enzymes that convert cellulose into glucose for biofuel production. Similarly, there are other bacteria with protease activity on biowastes like soya, whey, and other food and dairy waste. This study emphasised on a natural isolate with multipotent efficiency in the degradation of numerous waste materials and optimisation for the degradation of numerous raw materials. This attempt will be contributing to the best biowaste utilisation and management of various production of biofuel. This study will emphasise the versatile activities of bacterial enzymes of a novel isolate, Bacillus which can lead to futuristic applications for the conversion of domestic waste into energy sources. [ABSTRACT FROM AUTHOR]

The country's first tubular microfiltration membranes for water purification from various contaminants, made from an alternative natural material—wood,—was developed at the Dumansky Institute of Colloid and Water Chemistry of the National Academy of Sciences of Ukraine. The proposed procedure cuts significantly the costs of manufacturing membranes. They studied the main patterns of the defluoridation process of water using these lignocellulosic (wooden) membranes, which were modified with a dynamic layer of hydrophilic A-300 aerosil. The modification of the lignocellulosic membranes involved the preliminary formation of an additional retentive layer on their surface, due to the steric mechanism, in the form of a dynamic membrane. The research demonstrated the high efficiency of the water defluoridation process using a dynamic membrane made of SiO2 particles, which retained fluoride ions (F–) ions due to the electrostatic mechanism of their interaction. Specific conditions for forming the dynamic membrane included concentrations of modifying and membrane-supporting aerosil additives at 500 and 100 mg/dm3, respectively, with an operating pressure of 1.0 MPa and a formation duration of 120 min. The concentration of suspended SiO2 particles in the permeate (turbidity) did not exceed the maximum permissible concentration (0.3 mg/dm3) in water. The modified lignocellulosic membrane could decrease the fluoride concentration in water to the permissible level for drinking water (0.7–1.5 mg/dm3) from an initial concentration of up to 7.5 mg/dm3 and a neutral pH at an operating pressure of 1.0 MPa. The membrane's specific productivity was 0.024 m3/(m2 h), due to significant pore blockage by SiO2 particles. [ABSTRACT FROM AUTHOR]

Levulinic acid (LA) was produced from oil palm empty fruit bunch (OPEFB) pretreated in two different ways: (1) a two-step treatment with peracetic acid (PA) and alkaline peroxide (AP); and (2) an ammonia soak pretreatment. The pretreated material was subjected to acid hydrolysis (5% w/v sulfuric acid, 125 °C to 175 °C, 120 min) to produce LA. Compared to the ammonia treatment, the two-step PA–AP pretreatment was better in removing lignin from OPEFB, and resulted in a higher LA yield based on the mass of the pretreated OPEFB. On a mass basis, the LA yield was 31.1% on pretreated OPEFB, that had been pretreated using the PA–AP process, but only 16.7% from the biomass treated using the ammonia process. The kinetics of acid-catalyzed production of LA from the pretreated OPEFB were investigated to develop a mathematical model for predicting the conversion of cellulose to the intermediates (glucose, 5-hydroxymethylfurfural), and the final product, LA. The hydrolysis of cellulose to glucose was found to be the rate-controlling step in acid-catalyzed production of LA, confirming the importance of the delignification pretreatment in making cellulose more amenable to hydrolysis. During the two-stage acid hydrolysis, the reaction at 175 °C for 15 min in the first stage, followed by 125 °C for 105 min in the second stage, resulted in LA molar yield (based on cellulose) of ∼40%. This was comparable to the yield obtained if both steps were performed at 150 °C for a total of 120 min. [ABSTRACT FROM AUTHOR]

Water contamination is a major health issue that can be addressed by using carbonaceous materials to adsorb and filter pollutants, yet adsorption mechanisms need to be better understood to improve the adsorption efficiency. Here we review the models that are used to study the mechanisms of adsorption of drugs, dyes and metal ions on carbonaceous materials, with emphasis on classical and advanced isotherms. We discuss the fitting frequency, lignocellulosic and fossil fuel-derived adsorbents, biomass composition, activating agents, surface functions, the carbonization temperature, the medium temperature effect and the use of several isotherms to explain the same mechanism. The adsorption capacity can reach up to 2651 mg of contaminant per g of lignocellulosic materials and 1274 mg of contaminant per g of fossil materials. Isotherm validation commonly depends on several parameters. The adsorption on lignocellulosic carbonaceous materials is best described by the Langmuir isotherm. In contrast, adsorption on fossil materials is best described by the Redlich-Peterson isotherm. Advanced and classical isotherms are in good agreement in 44% of reports. [ABSTRACT FROM AUTHOR]

Vegetable trimmings can be used to stabilize edible O/W Pickering emulsions. The lignocellulosic biomass (LCB) from the leek trimmings was mechanically treated to produce high-yield lignocellulose micro and nanofibrils (LCF) using a high-pressure homogenizer (HPH). Different O/W phase ratios (20/80, 30/70, and 40/60 wt.%) were studied. The use of the micro/nano cellulosic fibers increased the stabilization of the Pickering emulsions by 30–40%. In all cases, stable emulsions were obtained, with emulsification indexes > 92%. The respective stabilization mechanism was thoroughly analysed from confocal laser scanning, and cryo-scanning electron microscopy, which showed the fibers are not coating the droplets but forming a network that traps the droplets and prevents coalescence. The most stable batch formulations, O/W 30/70 wt.% (LCB 4.2 wt.%) and O/W 40/60 wt.% (LCB 3.6 wt.%), were also studied in continuous mode using NETmix technology. Results show the scale-up feasibility of the production of Pickering emulsions containing LCF. Most significantly, this work proposes a continuous process to produce Pickering emulsions stabilized with a natural biopolymer extracted from leek trimmings, which is suitable to industrial manufacturing processes. This valorizes the vegetable trimmings that are usually tossed away as waste, creating new market niches and business models based on circular economy concepts. [ABSTRACT FROM AUTHOR]

Hydrothermal pretreatments are commonly employed prior to the biotechnological conversion of lignocellulosic biomass (LCB) into value-added products, such as fuels and chemicals. However, the by-products of this pretreatment, including furaldehydes, lignin-derived phenolics, and carboxylic acids, can inhibit the enzymes and microbes used in the biotechnological process. In this study, LCB degrading enzymes of endophytic and litter fungi were screened for their tolerance to potential pretreatment-derived inhibitors. Several fungi produced endo- and exoglucanases that remained functional in the presence of lignocellulose-derived phenolics. Some were also active in the presence of tannic acid. Additionally, thermostable endoglucanase activity was observed in some fungi. The ability of some of these fungi to utilize furaldehyde inhibitors as a sole carbon source was also noted. The culture supernatants of the fungal strains were tested in hydrolysis experiments using microcrystalline cellulose as a substrate, in the presence of lignocellulose phenolics and tannic acid. With some strains, higher sugar yields were obtained in the hydrolysis of cellulose when phenolics were added. Our results highlight the need for more intensive exploration of endophytic and plant litter fungi for novel inhibitor-resistant cellulases for biofuel production. [ABSTRACT FROM AUTHOR]

Utilization of lignocellulosic biomass as a renewable resource to produce liquid fuels/fuel additives and commodity chemicals offer solutions to minimize the exhaustion of nonrenewable carbon‐based fossil resources and mitigate environmental problems. Cellulose and hemicellulose derived from lignocellulose can be converted into several important platform molecules like glucose, fructose, xylose, 5‐hydroxymethylfurfural, furfural, levulinic acid, etc. which subsequently can be transformed into fuels/fuel additives and value‐added chemicals using heterogeneous catalytic processes. Aluminophosphates (AlPO‐n) are zeotype materials with tunable physicochemical properties like acidity and porosity, and this have promoted their wide use as versatile catalysts for several acid‐catalyzed reactions, including hydrolysis, dehydration, isomerization, transfer hydrogenation, reductive etherification, acetalization and aldol condensation. This review summarizes the design and synthetic advances of AlPO‐n catalysts as well as their application in the valorization of lignocellulose and derivatives to platform chemicals and fuel compounds. Perspectives for future design strategies are finally outlined. [ABSTRACT FROM AUTHOR]

Background: The ability of lignocellulose degradation for filamentous fungi is always attributed to their efficient CAZymes system with broader applications in bioenergy development. ADP-ribosylation factor GTPase-activating proteins (Arf-GAPs), pivotal in fungal morphogenesis, lack comprehensive studies on their regulatory mechanisms in lignocellulose utilization. Results: Here, the orthologs (TgGlo3 and TgGcs1) of Arf-GAPs in S. cerevisiae were characterized in Trichoderma guizhouense NJAU4742. The results indicated that overexpression of Tggcs1 (OE-Tggcs1) enhanced the lignocellulose utilization, whereas increased expression of Tgglo3 (OE-Tgglo3) elicited antithetical responses. On the fourth day of fermentation with rice straw as the sole carbon source, the activities of endoglucanase, cellobiohydrolase, xylanase, and filter paper of the wild-type strain (WT) reached 8.20 U mL−1, 4.42 U mL−1, 14.10 U mL−1, and 3.56 U mL−1, respectively. Compared to WT, the four enzymes activities of OE-Tggcs1 increased by 7.93%, 6.11%, 9.08%, and 12.92%, respectively, while those decreased to varying degrees of OE-Tgglo3. During the nutritional growth, OE-Tgglo3 resulted in the hyphal morphology characterized by sparsity and constriction, while OE-Tggcs1 led to a notable increase in vacuole volume. In addition, OE-Tggcs1 exhibited higher transport efficiencies for glucose and cellobiose thereby sustaining robust cellular metabolic rates. Further investigations revealed that Tgglo3 and Tggcs1 differentially regulated the transcription level of a dynamin-like GTPase gene (Tggtp), eliciting distinct redox states and apoptotic reaction, thus orchestrating the cellular response to lignocellulose utilization. Conclusions: Overall, these findings underscored the significance of TgArf-GAPs as pivotal regulators in lignocellulose utilization and provided initial insights into their differential modulation of downstream targets. [ABSTRACT FROM AUTHOR]

This work explored whether partial cellulose bioconversion with fungal mycelium can improve the properties of cellulose fibre-based materials. We demonstrate an efficient approach for producing cellulose-mycelium composites utilizing several cellulosic matrices and show that these materials can match fossil-derived polymeric foams on water contact angle, compression strength, thermal conductivity, and exhibit selective antimicrobial properties. Fossil-based polymeric foams commonly used for these applications are highly carbon positive, persist in soils and water, and are challenging to recycle. Bio-based alternatives to synthetic polymers could reduce GHG emissions, store carbon, and decrease plastic pollution. We explored several fungal species for the biofabrication of three kinds of cellulosic-mycelium composites and characterized the resulting materials for density, microstructure, compression strength, thermal conductivity, water contact angle, and antimicrobial properties. Foamed mycelium-cellulose samples had low densities (0.058 – 0.077 g/cm3), low thermal conductivity (0.03 – 0.06 W/m∙K at + 10 °C), and high water contact angle (118 – 140°). The recovery from compression of all samples was not affected by the mycelium addition and varied between 70 and 85%. In addition, an antiviral property against active MS-2 viruses was observed. These findings show that the biofabrication process using mycelium can provide water repellency and antiviral properties to cellulose foam materials while retaining their low density and good thermal insulation properties. [ABSTRACT FROM AUTHOR]

The use of food‐based biomass and arable land for bio‐oil and biofuel production could compromise global food security. Therefore, renewable and environmentally friendly oils for biofuels from oleaginous microorganisms such as yeasts and microalgae (heterotrophic and mixotrophic) are gaining interest within the scientific community. These microorganisms have shorter cultivation times and higher lipid productivity when compared to higher plants/food crops/autotrophic microorganisms. Despite many advantages, the high carbon requirements and production cost are limiting factors that hinder their deployment at a commercial scale. Lignocellulosic waste substrates are abundant and inexpensive materials that are rich in organic carbon in the form of cellulose and hemicellulose, which release bioavailable forms of sugars upon hydrolysis. Recent studies have shown the tremendous potential of the hydrolysates of these substrates to be utilized as carbon sources for biomass production and the accumulation of lipids in oleaginous hetero‐/mixotrophic microorganisms. Therefore, this review highlights the potential use of lignocellulosic biomass as a low‐cost carbon substrate for the cultivation of hetero‐/mixotrophic microalgae and yeast for microbial oil production for commercial applications. It also examines the current status, challenges, and future prospects for the utilization of lignocellulose biomass. [ABSTRACT FROM AUTHOR]

One method of preparing sludge for management and use is solar drying. To intensify the drying process, natural lignocellulosic additives can be used to alter the structure of the sludge and accelerate water evaporation. Light, hard materials with low absorption capacity are best suited for this purpose, e.g., walnut shells, which are unused waste. The aim of the study was to determine the impact of the evaluation of walnut shells on the sludge drying process and to assess the impact of the drying process on the chemical, physical, and fuel properties of the additive. The moisture content, crushing strength, chemical composition, and physical and fuel properties of mixtures were determined. A small addition of walnut shells (25%) was found to accelerate the drying process even in winter and spring (up to 30 days) compared to sludge without additives. Walnut shells retain their chemical composition and strength despite unfavourable conditions and a chemically aggressive environment, indicating they may be reused. The mixture containing sewage sludge and walnut shells has a calorific value of 15.6 MJ/kg, which is similar to wood; it is also fully biodegradable and suitable as a fertiliser to improve soil structure, as it contains approx. 80–90% DM (including approx. 40% carbon, 3% nitrogen, and other elements, such as phosphorus and potassium.) [ABSTRACT FROM AUTHOR]

This review analyzes in detail the topic of supercapacitors based on biochar technologies, including their advantages, disadvantages, and development potential. The main topic is the formation of precursors in the process of pyrolysis and activation, and the possibility of the application of biochar itself in various fields is brought closer. The structure, division, and principle of operation of supercondensates are discussed, where their good and bad sides are pointed out. The current state of the scientific and legal knowledge on the topic of biocarbon and its applications is verified, and the results of many authors are compared to examine the current level of the research on supercapacitors based on biochar electrodes created from lignocellulosic biomass. Current application sites for supercapacitors in transportation, electronics, and power generation (conventional and unconventional) are also examined, as is the potential for further development of the technology under discussion. [ABSTRACT FROM AUTHOR]

Lignin is the main component of plant cell walls, conferring upon lignocellulosic biomass both excellent mechanical and barrier properties. At the same time, the considerable number of unsaturated groups and conjugated structures present in lignin render it a promising candidate for applications in the optical domain. In recent years, the development of the optical properties of lignin and lignin-derived optical materials has paved the way for a novel avenue of lignin valorization. This review is concerned with the mechanisms of lignin-derived optical materials, with particular emphasis on the physical and chemical structures that are linked to their optical performance, including UV absorption, photothermal conversion, and photoluminescence. Additionally, the potential applications of these materials in energy storage, bioimaging, structural materials, and photonic crystal are also presented, demonstrating the unique optical properties of lignin. Finally, the challenges and future directions of lignin as an optical material are presented, with the objective of developing lignin into a polymer biobased raw material that can serve advanced emerging industries. [ABSTRACT FROM AUTHOR]

Converting lignin into aromatic chemicals is a promising strategy for the high‐value utilization of lignocellulosic feedstock. However, the inherent heterogeneity of lignin poses a significant obstacle to achieving efficient conversion and optimal product yields within bio‐refinery systems. Herein, we employed a one‐step fractionation method to enhance lignin homogeneity and utilized the THF/DMSO‐EtONa (tetrahydrofuran/dimethyl sulfoxide‐sodium ethoxide) system to depolymerize the fractionated lignin. Three protic and three aprotic solvents were used for fractionation. The impact of the solvent properties on the structure and the depolymerization efficiency of the fractionated lignin was investigated. Methanol‐fractionated lignin generated the benzoic acid compounds with a yield of 30 wt%, 50 % higher than that of the unfractionated lignin. The polarities (δP), hydrogen bonding abilities (δH), and viscosities (η) of selected protic solvents showed strong linear correlation with molecular weight (Mw), polymer dispersity index (PDI), and syringyl/guaiacyl ratio (S/G ratio) of the fractionated lignin, as well as the total yield of benzoic acid compounds derived from the β‐O‐4 bond cleavage. This study elucidates the relationship between solvent properties and lignin structure and proposes a promising approach for refining lignin to enhance utilization efficiency, thereby presenting a potential strategy for value‐added application of complex lignin polymers. [ABSTRACT FROM AUTHOR]

Anaerobic fungi are known to migrate and establish a 3D network of biofilms (microbiomes) and live invisible in the rumen and terrestrial subsurface, deep-sea - marine, and anoxic environment. They deserve our attention to understand anoxic fungal ecology and functions and develop new products and solutions. Such fungi activate unique genes to produce various polysaccharidases deemed essential for degrading plants' lignocellulosic materials. Nutrient release, recycling, and physical support by anaerobic fungi are crucial for microbiome formation. Multiple reports point to the ability of strictly anaerobic and facultative fungi to adapt and live in anoxic subsurface. Deep-sea sediments and natural anoxic methane-emitting salty waters of sulfidic springs offer suitable habitats for developing prokaryotic-fungal microbiomes. Researchers found a billion-year-old fossil of the fungus-prokaryotic sulfate-reducing consortium buried in deep-sea biospheres. Fungal spores' ability to migrate, even after germination, through sandy layers demonstrates their potential to move up and down porous geological layers or rock fissures. Selective fungal affinity to specific wood in wood chip arrays might help differentiate viable anaerobic fungi from an anoxic environment for their rapid collection and investigation. New collection methods, cultivation, gene expression, and drug and enzyme activity analyses can boost anaerobic fungal research. [ABSTRACT FROM AUTHOR]

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The environmental impacts of the postindustrial era, which rely on fossil fuels, have compelled a reconsideration of the future of energy and chemical industries. Fungi are a valuable resource for improving a circular economy through the enhanced valorization of biomass and plant waste. They harbor a great diversity of oxidative enzymes, especially in their secretome. Enzymatic breakdown of the plant cell wall complex and lignocellulosic biomass yields sugars for fermentation and biofuel production, as well as aromatic compounds from lignin that can serve as raw materials for the chemical industry. To harness the biocatalytic potential, it is essential to identify and explore wild-type fungi and their secretomes. This study successfully combined genome mining and activity screening to uncover the oxidative potential of a collection of underexploited ascomycetes and basidiomycetes. The heme peroxidase and laccase activities of four promising candidates, Bipolaris victoriae, Colletotrichum sublineola, Neofusicoccum parvum and Moesziomyces antarcticus, were investigated to gain a deeper insight into their enzyme secretion. Furthermore, a plant-based medium screening with the phytopathogen C. sublineola revealed that soybean meal is a beneficial component to trigger the production and secretion of enzymes that catalyze H2O2-dependent oxidations. These results demonstrate that understanding fungal secretomes and their enzymatic potential opens exciting avenues for sustainable biotechnological applications across various industries. [ABSTRACT FROM AUTHOR]

Highlights: The lignin in paddy and wheat straws is highly resistant to degradation, and burning the same is a global warming issue. Dye degrading ability and expression of three vp genes were studied in Pleurotus ostreatus and Fusarium sp. cultures. High enzymatic activity and the vp2 gene were observed in the Fusarium sp. culture, which makes it an alternate fungal species for lignin degradation. Lignocellulosic biomass is contemplated to be an inexpensive and copious feedstock that can be used for numerous industrial applications. However, lignin forms the lignin sheath and provides a physical barrier to enzymatic hydrolysis. In addition, lignin physically blocks cellulase, preventing it from being combined with the substrate in a process known as non-productive binding. Therefore, the depletion of lignin is a crucial method for obtaining fermentable sugars from the lignocellulosic biomass. Different white-rot fungi secrete different sets of lignin-mineralizing enzymes and each fungus secretes one or more of the three enzymes essential for lignin degradation. Among efficient redox enzymes, versatile peroxidase is extensively studied for its ability to degrade aromatics without the need for a mediator or polyvalent catalytic site. However, the presence of versatile peroxidase in F. spp. has not been studied. This study was planned with the objective of screening and comparing the production of versatile peroxidase enzymes from F. spp. and a standard culture of Pleurotus ostreatus MTCC-142. These fungal strains were first screened on solid media containing tannic acid, malachite green, or bromocresol green. The potency index for the tannic acid, malachite green, and bromocresol green on the 16th day of incubation was reported to be 1.28, 1.07, 1.09, and 1.10, respectively. Versatile peroxidase production patterns were investigated under solid state fermentation conditions for a period of 25 days at different temperatures ranging from 10 to 35 °C. The highest versatile peroxidase activity (592 UL−1) in F. sp. was observed at 30 °C after the 7th day of incubation. The molecular confirmation showed the presence of the vp gene in F. sp. along with Pleurotus ostreatus MTCC-142. The results determined that F. sp. possesses a versatile peroxidase enzyme and is able to degrade lignin efficiently, and thus it could be utilized as an alternative to other ligninolytic enzyme-producing fungi. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Efforts are ongoing to utilise agricultural waste to achieve a full resource use approach. Bambara groundnut is an important crop widely grown in the sub-Saharan Africa with potential future importance because of its resilience to thrive under heightened weather uncertainty and widespread droughts that have challenged food security. After harvesting, the edible nuts are separated from the shells which are discarded as waste. Therefore, this research is aimed at characterising the chemical composition and the structural properties of Bambara groundnut shells (BGS) in view of their potential application as a biomass for different bio-products. The chemical composition of BGS was found to be 42.4% cellulose, 27.8% hemicellulose, 13% lignin and 16.8% extractives. Proximate analysis showed a high amount of volatile matter (69.1%) and low moisture (4.4%). XRD analysis confirmed crystallinity of cellulose I polymer and FTIR analysis observed functional groups of lignocellulosic compounds. Thermal stability, maximum degradation temperature and activation energy were found to be 178.5 °C, 305.7 °C and 49.4 kJ/mol, respectively. Compared to other nutshells, BGS were found to have a relatively high amount of cellulose and crystallinity that may result in biocomposites with improved mechanical properties. [ABSTRACT FROM AUTHOR]

Lignocellulosic biomass, the most abundant natural resource on earth, can be used for cellulosic ethanol production but requires a pretreatment to improve enzyme access to the polymeric sugars while obtaining value from the other components. γ‐Valerolactone (GVL) is a promising candidate for biomass pretreatment since it is renewable and bio‐based. In the present work, the effect of a pretreatment based on GVL on the enzymatic saccharification of white birch was evaluated at a laboratory scale and the importance of the washing procedure for the subsequent saccharification was demonstrated. Both the saccharification yield and the production of cellulosic ethanol were higher using a noncommercial enzyme crude from Talaromyces amestolkiae than with the commercial cocktail Cellic CTec2 from Novozymes. Furthermore, the production of extracellular cellulases by T. amestolkiae has been optimized in 2 L bioreactors, with improvements ranging from 40% to 75%. Finally, it was corroborated by isoelectric focus that optimization of cellulase secretion by T. amestolkiae did not affect the pattern production of the main β‐glucosidases and endoglucanases secreted by this fungus. [ABSTRACT FROM AUTHOR]

This study investigates the correlation between both the chemical compositions and physicochemical properties of pretreated oil palm empty fruit bunch (OPEFB) fibre and their enzymatic saccharification/total glucose yield (TGY). Twenty OPEFB samples, pretreated with various aqueous pretreatments, with diverse cellulose (25.63–44.23%), hemicellulose (0.01–42.49%), and lignin (3.7–47.1%) levels, were examined for their correlation with TGY (8.5–40%). The quadratic regression model was verified significant (p-value = 0.0006, R2 = 0.8006). It was found that the pre-refined OPEFB experienced greater cellulose loss (35%) compared to unrefined ones (9%), adversely affecting TGY. Among physicochemical properties analysed using SEM, FTIR, XRD, Py-GCMS, and XPS, only crystallinity index (CrI) was significantly correlated with TGY based on theoretical glucose concentration (TGC) (R2 = 0.77, 0.91). Other characteristics (morphology, functional groups, crystallite size, S/G ratio, and O/C ratio) exhibited no significant correlation to saccharification efficiency, exhibiting random trends (R2 < 0.5). OPEFB fibres with CrI of 30–40 could achieve 100% TGY based on TGC. In conclusion, regardless of pretreatments, chemical compositions predominantly affected TGY in the enzymatic saccharification of biomass. Among commonly used physicochemical analytical methods, CrI is most significant in this evaluation and OPEFB should be unrefined before treatment to avoid cellulose loss. [ABSTRACT FROM AUTHOR]

The purpose of this research was to develop an integrated biorefinery process of solid-state anaerobic digestion (SS-AD) and hydrothermal carbonization (HTC) for the co-production of methane and hydrochar using elephant dung (ED) as substrate. With a leachate recirculation rate of 4 times/day, the SS-AD presented the highest cumulative methane yield of 83.2 ± 1.7 NmL/g volatile solid (VS)added and VS removal efficiency of 53.9 ± 0.3%. In subsequent HTC, the maximum higher heating value (HHV) of 10,078.5 ± 288.5 MJ/ton dry wt. was achieved for the digested ED without leachate recirculation under HTC temperature of 170 °C. In addition, the maximum mass and energy yields were 76.3 ± 0.8% and 84.1 ± 0.3%, respectively. The produced hydrochar had higher HHV compared to the raw digestate. Moreover, the HHV of the hydrochar was higher, and ash content was identical to conventional coal (lignite). An assessment of a full-scale elephant-sanctuary waste management scheme integrating SS-AD and HTC indicates that more than 10,078.5 ± 288.5 MJ of energy and 563.0 ± 5.2 kg dry weight of hydrochar could be recovered per ton dry weight of ED. The developed elephant dung management platform could enhance energy yield from ED while addressing environmental issues. [ABSTRACT FROM AUTHOR]