High Xylose Research Articles

Cascade fractionation of bamboo shoot shells into high-yield xylose, easily digestible cellulose and high-quality lignin nanoparticles by tailored catalytic hydrothermal–hydrated alkaline deep eutectic solvents pretreatment

The high complexity and compactness of inherent structure in lignocellulosic materials (LCM) leads to the difficulty of fractionation and conversion of its major component, which is the key obstacle limiting the value-added utilization of LCM. In this work, a cascade fractionation strategy, coupling catalytic hydrothermal pretreatment (CHTP, choline chloride: ethylene glycol: AlCl3, ChCl/ EG/ AlCl3) with hydrated alkaline deep eutectic solvent (HADES, triethylbenzyl ammonium chloride/ethanolamine, TEBAC/EM) treatment, was proposed to fractionate dendrocalamus latiftorus munro shoot shells (DLMSS). The results showed that considerably high hemicelluloses removal (94.57 %) and xylose yield (90.73 %) were achieved by the first step (CHTP, 160 °C, 1 h, 2 % of catalyst loading). The cascaded HADES treatment realized 90.25 % delignification ratio under the optimal conditions (120 °C, 3 h, 75 % of ADES loading), and the obtained residue could be easily converted into high-yield (93.35 %) of glucose via enzymatic saccharification. In addition, multiple enrichment cycle strategy (MECS) was performed to facilitate the recyclability of the HADES. The results showed that the enriched lignin recovered by MECS was activated by in-situ demethoxylation reaction. And such lignin fraction could be easily assembled into homogeneous lignin nanoparticles (LNPs, ∼31.51 nm in diameter) by simple sonication. Meanwhile, the MECS signally energized the antioxidant activity of the enriched lignin. Based on the high-efficiency cascade fractionation with the coupled CHTP-HADES fractionation strategy, it will observably boost the effectiveness and scalability of the advanced biorefinery strategy.

Exploring hemp seed hull biomass for an integrated C-5 biorefinery: Xylose and activated carbon

Large quantities of hemp hulls can be completely utilized for creation of value-added products (cost effective biofuels and biochemicals) through a biorefinery approach. A sustainable approach in making xylose, a low calorie sweetener and high surface area activated carbons (AC) for super capacitors, attracts interest. The AC when leveraged as a co-product from biorefinery process makes it more cost effective and, in this paper, we discuss the production of xylose and AC from hemp seed hull with methane sulphonic acid (MSA) hydrolysis. Xylose recovery with MSA hydrolysis was 25.15 g/L when compared to the traditional sulphuric acid (SA) hydrolysis of 19.96 g/L at the same acid loading of 1.8 %. The scanning electron microscope (SEM) images and Fourier transform infrared (FT-IR) spectra indicate partial delignification along with hemicellulose hydrolysis responsible for high xylose recovery. Post hydrolysis fibers were KOH activated and carbonized to make AC. The MSA hydrolyzed and KOH activated fiber produced pure, fluffier and finer particle AC with a drastic increase in surface area 1 452 m2/g when compared to SA hydrolyzed of 977 m2/g. These results indicate the potential of MSA in dilute acid hydrolysis of biomass for xylose recovery and production of high surface area activated carbon. From a production standpoint this can lead to increased use of sustainable low-cost agricultural biomass for making high surface area AC as components in supercapacitors.

Exploration of a two-stage polymerization mechanism in construction of dense polyester membranes for drinking water treatment

Due to the relatively low reactivity of hydroxyls with acyl chloride groups, the synthesized polyester (PE) membranes commonly have loose structures, only capable of removing large-molecule organics with low rejection of inorganic salts. In this study, the pore size reduction of the synthesized PE membrane was successfully achieved by optimizing the interfacial polymerization (IP) reaction between erythritol and trimesoyl chloride (TMC). The optimized membrane was able to maintain a high xylose rejection (∼60 %) and acceptable water permeance (7.85 L m−2 h−1 bar−1), which was suitable for drinking water treatment. Through comprehensive characterizations, a two-stage membrane formation process was demonstrated regarding the reaction between aqueous monomers with different reactive functional groups and TMC. The highly reactive primary hydroxyls more preferentially participated in the initial reaction stage, leading to a linear cross-linking pattern of polyester. When the molecular diffusion was inhibited, the participation of secondary hydroxyls made the reaction proceed toward partial or full cross-linking. The distinct roles of the two kinds of hydroxyl groups were further verified by the energy barrier differences obtained by density functional theory (DFT) calculation. The exploration of membrane-optimized preparation and formation mechanisms can promote the structural regulation and tailored synthesis of PE membranes for various applications.

Enhancement of Liquid Hot Water Pretreatment on Corn Stover with Ball Milling to Improve Total Sugar Yields

Conversion of the lignocellulosic biomass to bioethanol contributes to the reduction of greenhouse gas emissions, enhancement of energy security, utilization of waste materials, and the promotion of sustainable agricultural practices. In this study, we report the effect of combining ball milling followed by liquid hot water (LHW) pretreatment of corn stover to lower the amount of enzyme required while also greatly increasing the recovery of xylose in fermentable form compared to either pretreatment alone. Short-duration ball milling for 60 min reduces the particle size of corn stover to 37.3 μm; however, the glucose only increased to 47% compared to 32% for unpretreated corn stover. In contrast, liquid hot water pretreatment alone can achieve increasing enzyme hydrolysis yields of cellulose from 49% to 93% as the pretreatment severity factor is increased from 3.24 to 4.41. However, the xylose yield decreased to 36% due to the fact that a considerable part of the xylose was degraded into furfural and humins. Surprisingly, the combination of mild ball milling (30 min) followed by mild liquid hot water pretreatment (190 °C, 15 min) could achieve both high glucose (83%) and xylose (72%) yields for a total sugar yield of 79%, theoretically. Thus, combining ball milling with liquid hot water pretreatment allows for milder conditions for both processes that lead to enhanced cellulose conversion without sacrificing xylose to degradation, which hinders enzymatic hydrolysis.

Expression of β-xylosidase An-xyl from Aspergillus niger and characterization of its xylose tolerance

The hydrolysis of xylo-oligosaccharides catalyzed by β-xylosidase plays an important role in the degradation of lignocellulose. However, the enzyme is easily inhibited by its catalytic product xylose, which severely limits its application. Based on molecular docking, this paper studied the xylose affinity of Aspergillus niger β-xylosidase An-xyl, which was significantly differentially expressed in the fermentation medium of tea stalks, through cloning, expression and characterization. The synergistic degradation effect of this enzyme and cellulase on lignocellulose in tea stems was investigated. Molecular docking showed that the affinity of An-xyl to xylose was lower than that of Aspergillus oryzae β-xylosidase with poor xylose tolerance. The Ki value of xylose inhibition constant of recombinant-expressed An-xyl was 433.2 mmol/L, higher than that of most β-xylosidases of the GH3 family. The Km and Vmax towards pNPX were 3.6 mmol/L and 10 000 μmol/(min·mL), respectively. The optimum temperature of An-xyl was 65 ℃, the optimum pH was 4.0, 61% of the An-xyl activity could be retained upon treatment at 65 ℃ for 300 min, and 80% of the An-xyl activity could be retained upon treatment at pH 2.0-8.0 for 24 h. The hydrolysis of tea stem by An-xyl and cellulase produced 19.3% and 38.6% higher reducing sugar content at 2 h and 4 h, respectively, than that of using cellulase alone. This study showed that the An-xyl mined from differential expression exhibited high xylose tolerance and higher catalytic activity and stability, and could hydrolyze tea stem lignocellulose synergistically, which enriched the resource of β-xylosidase with high xylose tolerance, thus may facilitate the advanced experimental research and its application.

Isolation of xylose-utilizing yeasts from oil palm waste for xylitol and ethanol production

The energy crisis triggers the use of energy sources that are renewable, such as biomass made from lignocellulosic materials, to produce various chemical compounds for food ingredients and biofuel. The efficient conversion of lignocellulosic biomass into products with added value involves the activity of microorganisms, such as yeasts. For the conversion, microorganisms must be able to use various sugars in lignocellulosic biomass, including pentose sugars, especially xylose. This study aims to isolate xylose-utilizing yeasts and analyze their fermentation activity to produce xylitol and ethanol, as well as their ability to grow in liquid hydrolysate produced from pretreated lignocellulosic biomass. Nineteen yeast isolates could grow on solid and liquid media using solely xylose as a carbon source. All isolates can grow in a xylose medium with incubation at 30 °C, 37 °C, 42 °C, and 45 °C. Six isolates, namely SLI (1), SL3, SL6, SL7, R5, and OPT4B, were chosen based on their considerable growth and high xylose consumption rate in a medium with 50 g/L xylose with incubation at 30 °C for 48 h. Four isolates tested, namely SLI (1), SL6, SL7, and R5, can produce xylitol in media containing xylose carbon sources. The concentration of xylitol produced was determined using high-pressure liquid chromatography (HPLC), and the results ranged from 5.0 to 6.0 g/L. Five isolates tested, namely SLI (1), SL6, SL3, R5, and OPT4B, can produce ethanol. The ethanol content produced was determined using gas chromatography (GC), with concentrations ranging from 0.85 to 1.34 g/L. Three isolates, namely SL1(1), R5, and SL6, were able to produce xylitol and ethanol from xylose as carbon sources and were also able to grow on liquid hydrolyzate from pretreated oil palm trunk waste with the subcritical water method. The three isolates were further analyzed using the 18S rDNA sequence to identify the species and confirm their phylogenetic position. Identification based on DNA sequence analysis revealed that isolates SL1(1) and R5 were Pichia kudriavzevii, while isolate SL6 was Candida xylopsoci. The yeast strains isolated from this study could potentially be used for the bioconversion process of lignocellulosic biomass waste to produce value-added derivative products.Graphical

Phytochemical characterization and bioactivities of different fruit parts of Tunisian barbary fig (Opuntia ficus-indica)

The valorization of bio-waste to acquire products with high added value presents a great profit for the pharmaceutical, medicinal and food industries. Thus, seeds, peels, and pulps obtained from green (GFI), orange (OFI), and purple (PFI) Tunisian pear fruit (Opuntia ficus-indica L.) were evaluated in terms of phytochemical composition and biological activities. The peel part of the purple fruit contained the highest content of K, Ca, and Mg. While the seed possessed the highest P and Fe amounts. Moreover, the total carbohydrate contents in the different pear fruit parts ranged from 43.41% in the seeds (GFI) to 68.12% in pulp parts (OFI) and were significantly different from each other. The pulp parts showed much higher xylose and fructose contents, averaging 3.38 and 119.17 g/L. The seeds of the three varieties were characterized by higher levels of polyunsaturated fatty acids and mostly predominated by oleic acid that varied from 43.51 to 47.84% for the green and orange colored fruit seeds, followed by linoleic acid (32.76—37.1%). The seeds and peels parts contained higher levels of phenolic compounds with a total of 37 compounds compared to pulp extracts. The seeds of the three studied fruits possessed high repellency potentials against the red flour beetle (Tribolium castaneum). The greatest repellency activities were recorded in the purple (53.33%) and the orange (46.66%) fruit seeds at the concentration of 5 μL/cm2 and after 1h of exposure. The fruit parts showed considerable antibacterial and antifungal effects against Erwinia amylovora and Botrytis cinerea. The prickly pear fruit could be used as natural ingredients with potential biological activities.

Physicochemical characterization and microbiota modulatory potential of brewer’s spent grain and arabinoxylan-derived fractions: A valorization study

Brewer’s spent grain (BSG), one of the largest by-products generated by brewing industries, holds a wealthy nutritional value due to its content in proteins and fibres. Although some initiatives have explored alternatives for leveraging the nutritional value of BSG, it mostly remains an underexploited source of valuable ingredients for human nutrition, being mainly dedicated to animal feed and landfilling. BSG is rich in hemicellulosic material, composed of arabinoxylans (AX), which have been postulated as emergent prebiotics, capable to confer health benefits through modulating the gut microbiome. In this work we comprehensively investigated in vitro the composition and gut microbiome modulatory potential of BSG and AX fractions on human microbiota of two population groups by means of fecal batch fermentations and 16S rRNA gene sequencing. The gut microbiome modulatory effects was influenced by the specific BSG/AX fraction; the population group (healthy or Crohn’s disease (CD) patients) and by interindividual variation. For instance, Dorea and Eubacterium halli which include well-known fibre degrading, and health promoting bacteria, were only stimulated in fermentations of fractions with high arabinose and xylose contents. This work demonstrates diverse modulatory capacity of distinct AX fractions, diversifying alternative BSG valorization strategies through exploitation of novel prebiotics tailored to specific groups.

Production of sugars from mixed hardwoods for use in the synthesis of sugar fatty acid esters catalyzed by immobilized‐stabilized derivatives of Candida antarctica lipase B

AbstractThe synthesis of sugar fatty acid esters (SFAEs) from lignocellulosic biomass and oleic acid (C18:1) was catalyzed by immobilized‐stabilized derivatives of Candida antarctica lipase B in a methyl ethyl ketone medium. After steam‐explosion pretreatment of mixed hardwoods and enzymatic hydrolysis at 15%wt solids, xylose and glucose were purified/concentrated to a mass ratio of ~3 to 1. These lignocellulosic sugars were superior to commercial sugars as the carbohydrate source for the esterification reaction in terms of sugar conversions. The highest conversions were obtained using 1.5% w/v of Novozyme 435 (N435, uncoated) as the biocatalyst for the synthesis of SFAEs. Coating the N435 with polyethyleneimine (PEI) prevented enzyme leakage into the reaction medium and produced 35% and 50% higher xylose and glucose conversions to SFAEs, respectively, at the same enzyme loading. After six 24 h reuse cycles with the PEI‐coated N435, xylose conversion decreased by 44%, while a 65% reduction in xylose conversion was observed with the uncoated lipase. Mass spectrometry analysis confirmed the production of xylose and glucose mono‐ and di‐esters. Our purified product presented an emulsion capacity (EC) close to that of a commercial sugar ester and the ECs of the xylose oleate, laurate, and palmitate synthesized in previous studies. © 2023 The Authors. Biofuels, Bioproducts and Biorefining published by Society of Industrial Chemistry and John Wiley & Sons Ltd.

Lignin Recovery Using Alkaline Pretreatment of Walnut Shells

The effects of alkaline pretreatment of walnut shells (WS) utilizing NaOH, Ca(OH)2, or KOH were studied. The highest lignin recovery was obtained from WS pretreated with NaOH-glycerol. The optimum lignin recovery after pretreatment could be achieved when the NaOH/solid value was 20:1 (mL g−1). CaCl2 loading could enhance lignin flocculation, which improved the lignin recovery. Also, the efficiency of enzymatic hydrolysis was determined when xylanase and cellulase were added to the pretreated residue. WS pretreated in NaOH-water and NaOH-glycerol solutions were found to result in the highest xylose and glucose concentrations. This study indicates the broad application prospects of alkaline pretreatment of lignocellulosic biomass in agriculture and industry.

Solid feeding and co-culture strategies for an efficient enzymatic hydrolysis and ethanol production from sugarcane bagasse

The feasibility of second-generation (2G) processes still highly depends on improvements in the hydrolysis and fermentation steps, ensuring the whole use of biomass sugars in an integrated approach. The main bottlenecks are the differences between the optimal conditions for both steps, limitations for high solid load (HSL) hydrolysis, and hexoses and pentose co-fermentation. To overcome these problems, the present work explored a feeding strategy to improve HSL enzymatic hydrolysis of hydrothermally pretreated sugarcane bagasse (PSB), at optimal and suboptimal temperatures, further integrated with a non-recombinant yeast co-culture (Saccharomyces cerevisiae and Kluyveromyces marxianus) for sugar co-fermentation. The entire PSB fraction was used without conditioning. Efficient enzymatic hydrolysis was achieved using a feeding strategy in a helical stirred bioreactor (64 and 75% cellulose conversion with 22.5% of solids, 72 h at 35 and 50 °C, respectively), obtaining hydrolysates with high glucose and xylose concentrations (100 g/L). Simultaneous saccharification and co-fermentation (SSCF) provided high glucose (98%) and xylose (52%) conversion in 24 deep-well plates, with ethanol yield of 0.23 getOH/gS, but faced problems of cell viability loss in the bioreactor. Sequential SCF (SqSCF) co-culture stood out as a promising strategy for the use of biomass sugars. The results of this study provide significant contribution to the intensification and feasibility of 2G production, in addition to highlighting the difficulties faced for process integration aiming at the full conversion of sugars coming from high solid load enzymatic hydrolysis.

Using a Novel Pervaporative Sequential-Co-immobilized Two-Sectional Bioreactor with an Ultralow Fouling–Biofouling Superhydrophobic Silicallite-1/PDMS Membrane to Enhance Bioethanol Production

This study is on the efficient fermentation of high glucose (G) and xylose (X) levels (G/X ratio of 1.5:1), simulating the hydrolysate of lignocellulosic wastes, via an innovative integrated two-stage fermentation–pervaporation process. Immobilized Zymomonas mobilis (Z) and Pichia stipitis (P) were exploited in a sequential-co-immobilized culture (Z in the first stage and Z and P in second stage) to simultaneously increase bioethanol productivity and lessen the inhibitions. The threshold inhibition was evaluated in 100 mL shake flasks by raising the initial total sugar concentration from 50 to 200 g/L where complete inhibition was observed at 200 g/L. Subsequently, fermentation (G: 120 g/L, X: 80 g/L) was examined in a sequential-co-immobilized two-sectional bioreactor (ITB-2L) during 200 h. ITB resulted in 100% glucose and 16% xylose conversion, showing ethanol productivity of 0.26 g/L·h and yield of 0.4 ge/gs. To investigate the effect of reducing inhibitions, a tubular superhydrophobic silicalite-1/PDMS pervaporative (TSP) autoclavable membrane with antiswelling properties was fabricated. The pervaporative sequential-co-immobilized two-sectional bioreactor (PITB) using TSP enhanced xylose conversion (57%), ethanol productivity (0.39 g/L·h), and yield (0.47 ge/gs). The membrane surface was probed after 161 h of usage, and the limited presence of only negative ions on its surface proved its superior ultralow fouling–biofouling formation. PITB proved itself as a robust integrated process for the second-generation bioethanol production.

Crabtree Effect on Rhodosporidium toruloides Using Wood Hydrolysate as a Culture Media

The interest in microorganisms to produce microbial lipids at large-scale processes has increased during the last decades. Rhodosporidium toruloides-1588 could be an efficient option for its ability to simultaneously utilize five- and six-carbon sugars. Nevertheless, one of the most important characteristics that any strain needs to be considered or used at an industrial scale is its capacity to grow in substrates with high sugar concentrations. In this study, the effect of high sugar concentrations and the effect of ammonium sulfate were tested on R. toruloides-1588 and its capacity to grow and accumulate lipids using undetoxified wood hydrolysates. Batch fermentations showed a catabolic repression effect on R. toruloides-1588 growth at sugar concentrations of 120 g/L. The maximum lipid accumulation was 8.2 g/L with palmitic, stearic, oleic, linoleic, and lignoceric acids as predominant fatty acids in the produced lipids. Furthermore, R. toruloides-1588 was able to utilize up to 80% of the total xylose content. Additionally, this study is the first to report the effect of using high xylose concentrations on the growth, sugar utilization, and lipid accumulation by R. toruloides-1588.

Preparation, Characterization, and Anti-Adhesive Activity of Sulfate Polysaccharide from Caulerpa lentillifera against Helicobacter pylori.

In the gastric mucosa, chronic inflammation due to Helicobacter pylori infection promotes gastrocarcinogenesis. Polysaccharides of Caulerpa lentillifera are well-characterized by broad antimicrobial activity and anti-inflammatory potentials. The present study was undertaken to investigate whether the low molecular sulfate polysaccharides of C. lentillifera (CLCP) exhibit any anti-adhesive activity against H. pylori. After a hot water extraction and purification process, two purified polysaccharide fractions (CLCP-1 and CLCP2) were studied based on structural characterization and bioactivity determination. The results implied that except for the molar ratio, CLCP-1 and CLCP-2 contain high sulfate, mannose, galactose, xylose, glucose levels, and low protein levels. The molecular weight and Fourier transform infrared spectroscopy (FT-IR) assays confirmed that CLCP-1 and CLCP-2 are sulfate polysaccharides with an average molecular weight (Mw) of 963.15 and 648.42 kDa, respectively. In addition, CLCP-1 and CLCP-2 exhibited stronger antibacterial activity against H. pylori. CLCP-1 and CLCP-2 could significantly promote macrophage proliferation and decrease the production of nitric oxide (NO) through downregulated expression of inducible nitric oxide synthase (iNOS). Meanwhile, CLCP-1 and CLCP-2 in this study showed efficiently protected gastric adenocarcinoma (AGS) cells against H. pylori with the inhibition of the IL-8/NF-κB axis. These findings suggested the effect of Caulerpa lentillifera polysaccharides on H. pylori adhesion, a potential supply of nutrients for eradication therapy through the reduction of cell count and inflammation.

A multi-product strategy for the fractionation of corn stover based on peracetic acid and maleic acid processing

As an efficient lignocellulose fractionation process, peracetic acid and maleic acid (PAM) pretreatment is integrated into a multi-product platform for the simultaneous manufacture of cellulose, lignin, and xylose. Employing such strategy, 100 g corn stover (dry basis) yielded 39.63 g cellulose-rich solids along with 11.88 g xylose and 12.00 g lignin recovered from the pretreatment liquor. The recovery of xylose and lignin was assessed with various organic solvents, of which 2-methyltetrahydrofuran (2-MeTHF) showed superior performance, giving high lignin yield (75.23%) and xylose yield (67.32%). The recovered lignin (2-MeTHF-L) was characterized by high purity, relatively low molecular weight, and large numbers of carboxyl group. Besides, 2D-HSQC NMR analysis revealed that the 2-MeTHF-L was esterified with maleic acid during PAM pretreatment, partly responsible for its enhanced antioxidant ability. This strategy maximizes feedstock utilization and improves the processability in downstream valorization, offering a prospect for sustainable and efficient biorefineries.

High-level production of xylose from agricultural wastes using GH11 endo-xylanase and GH43 β-xylosidase from Bacillus sp.

As a promising feedstock, alkali-extracted xylan from lignocellulosic biomass is desired for producing xylose, which can be used for renewable biofuels production. In this study, an efficient pathway has been established for low-cost and high-yield production of xylose by hydrolysis of alkali-extracted xylan from agricultural wastes using an endo-1,4-xylanase (XYLA) from Bacillus safensis TCCC 111022 and a β-xylosidase (XYLO) from B. pumilus TCCC 11573. The optimum activities of recombinant XYLA (rXYLA) and XYLO (rXYLO) were 60℃ and pH 8.0, and 30℃ and pH 7.0, respectively. They were stable over a broad pH range (pH 6.0-11.0 and 7.0-10.0). rXYLO showed a relatively high xylose tolerance up to 100mM. Furthermore, the yield of xylose from wheat straw, rice straw, corn stover, corncob and sugarcane bagasse by rXYLA and rXYLO was 63.77%, 71.76%, 68.55%, 53.81%, and 58.58%, respectively. This study demonstrated a strategy to produce xylose from agricultural wastes by integrating alkali-extracted xylan and enzymatic hydrolysis.

Integrated bioinformatics, modelling, and gene expression analysis of the putative pentose transporter from Candida tropicalis during xylose fermentation with and without glucose addition

The transport of substrates across the cell membrane plays an essential role in nutrient assimilation by yeasts. The establishment of an efficient microbial cell factory, based on the maximum use of available carbon sources, can generate new technologies that allow the full use of lignocellulosic constituents. These technologies are of interest because they could promote the formation of added-value products with economic feasibility. In silico analyses were performed to investigate gene sequences capable of encoding xylose transporter proteins in the Candida tropicalis genome. The current study identified 11 putative transport proteins that have not yet been functionally characterized. A phylogenetic tree highlighted the potential C. tropicalis xylose-transporter proteins CtXUT1, CtXUT4, CtSTL1, CtSTL2, and CtGXT2, which were homologous to previously characterized and reported xylose transporters. Their expression was quantified through real-time qPCR at defined times, determined through a kinetic analysis of the microbial growth curve in the absence/presence of glucose supplemented with xylose as the main carbon source. The results indicated different mRNA expression levels for each gene. CtXUT1 mRNA expression was only found in the absence of glucose in the medium. Maximum CtXUT1 expression was observed in intervals of the highest xylose consumption (21 to 36h) that corresponded to consumption rates of 1.02 and 0.82g/L/h in the formulated media, with xylose as the only carbon source and with glucose addition. These observations indicate that CtXUT1 is an important xylose transporter in C. tropicalis. KEY POINTS: • Putative xylose transporter proteins were identified in Candida tropicalis; • The glucose concentration in the cultivation medium plays a key role in xylose transporter regulation; • The transporter gene CtXUT1 has an important role in xylose consumption by Candida tropicalis.

Insights into the mechanism for the high-alkaline activity of a novel GH43 β-xylosidase from Bacillus clausii with a promising application to produce xylose

Nowadays, alkali-tolerant β-xylosidases and their molecular mechanism of pH adaptability have been poorly studied. Here, a novel GH43 β-xylosidase (XYLO) was isolated from Bacillus clausii TCCC 11004, and the recombinant β-xylosidase (rXYLO) was most active at pH 8.0 and stable in a broad pH range (7.0–11.0), exhibiting superior alkali tolerance. Molecular dynamics simulation indicated that XYLO showed a notable overall structural stability and an enlargement of substrate binding pocket under alkaline condition, resulting in the formation of a new hydrogen bond between substrate and Arg286 of XYLO, and the tight binding played a key role in improving the XYLO activity with the increasing pH. Moreover, rXYLO with an endo-xylanase resulted in high xylose yields by hydrolyzing alkali-extracted xylan from agricultural wastes. This work would provide an alkali-tolerant β-xylosidase, enhance the understanding for the relationship of structure and activity adapted to the high-alkaline environment, and promote its application in xylose production.

Effects of ultrasonic-assisted alkaline pretreatment on xylose production from pineapple peel waste

The pineapple industry generates large amounts of unusable waste (peel and core) with adverse environmental impacts. This experimental study aims to systemize the potential of ultrasonic-assisted alkaline pretreatment for xylose production from pineapple peel waste. The best condition for single alkaline pretreatment (1 % NaOH w/v, 100 °C, 60 min) has obtained hemicellulose, cellulose, and lignin composition at 34.80 %, 32.16 %, and 8.66 %, respectively, retained in the biomass. Meanwhile, a combination of alkaline (1 % NaOH, w/v) and ultrasonic (frequency 40 kHz, 45 min) pretreatment has obtained the percentage yield of hemicellulose and lignin at 51.15 % and 7.15 %, respectively. Both single alkaline and ultrasonic-assisted alkaline pretreated samples were subsequently hydrolyzed with 2 % H2SO4 (w/v). After acid hydrolysis for 30 min, the maximum xylose concentration of 48.85 g.L-1 was achieved by using ultrasonic-assisted alkaline pretreatment, while single alkaline pretreatment contributed to the lowest yield of xylose (37.11 g.L-1). It is shown that the ultrasonic-assisted alkaline treatment is more favorable than single alkaline pretreatment as it can produce high xylose concentration after the subsequent hydrolysis. These results indicated that ultrasonic-assisted alkaline pretreatment and its subsequent acid hydrolysis were appropriate for producing xylose from pineapple peel waste.

Structure of corn bran hemicelluloses isolated with aqueous ethanol solutions and their potential to produce furfural

The alkali-soluble hemicelluloses extracted with 10% KOH solution from corn bran were further isolated with different concentrations of aqueous ethanol solutions. Herein 92.2% of the original hemicelluloses can be obtained and the cellulase enzymatic hydrolysis rate of the alkali treated corn bran can reach to 97.2%. The corn bran hemicelluloses were mainly glucuronoarabinoxylan, in which xylose (48.4–53.8%) and arabinose (27.8–33.2%) were the main components. More linear hemicelluloses with high molecular weight tended to be precipitated in low concentration aqueous ethanol solutions. Furthermore, the relationship between the structural features of these alkali-soluble corn bran hemicelluloses and their furfural yield was investigated in MIBK (methyl isobutyl ketone)/H2O biphasic system. Results showed that the hemicelluloses with high xylose content are benefit to the furfural production, and the highest furfural yield of 67.7% was obtained.