MW Fraction Research Articles

Evaluation of in vitro simulated digestion and fermentation characteristics of the crude exopolysaccharide from Levilactobacillus brevis M-14.

The present study employed an in vitro static digestion model to simulate the saliva-gastrointestinal digestion and fecal fermentation of exopolysaccharides (EPSs) extracted from Levilactobacillus brevis M-14, aiming to understand the dynamic changes in physicochemical properties, biological potential of EPS, as well as their impact on the human enteric microorganism. EPS was mainly composed of polysaccharides. The molecular weight (Mw) showed that EPS comprised two parts with a high Mw and a low Mw fraction of 42.81 × 104 and 1.23 × 104 Da, respectively. EPSs mainly consisted of mannose, rhamnose, galacturonic acid, glucose, and galactose in a molar ratio of 0.42∶0.13∶0.21∶0.13∶0.11. In the simulated digestion process, EPS was relatively stable. Furthermore, simulated digestion increased the antioxidant and hypoglycemic capacities of EPS. During the fermentation stage, the total carbohydrate contents of EPS decreased by 20.19%. The Mw of the two components of EPS decreased by 16.37% and 61.67%, respectively, and accompanied by the production of free monosaccharides. EPS had the potential to modulate the composition of gut microbiota, increasing the relative abundance of Enterococcus and Parabacteroides, while decreasing the relative abundance of Bacteroides. The pH decreased and total short-chain fatty acids contents increased, especially acetic acid and propionic acid. This research provided valuable insights into the potential application of EPS as a prebiotic agent.

Associating structural characteristics to immunomodulating properties of carrot rhamnogalacturonan-I fractions

Carrot rhamnogalacturonan-I (cRG-I) is a polydisperse polysaccharide with molecular weights of 7–250 kDa. Using size exclusion chromatography cRG-I was fractionated and pooled in fractions (PF1–6). All fractions contained the same RG-I monosaccharides and similar glycosidic linkages although in varying relative amounts. The main differences were in rhamnose substitution, arabinan- and galactan side chain length and in levels of acetylation and methyl esterification. Atomic force microscopy showed either spheric or elongated structures for cRG-I and its derived fractions. To gain insight in the structure-function relationship of cRG-I, the immunomodulatory effect of the six fractions and their saponified derivatives was assessed in vitro. All fractions, except PF2, dose-dependently stimulated TNFα, IL-6, IL-1β, IL-8 and IL-10 production in peripheral blood mononuclear cells (PBMCs) of three healthy donors. Cytokine levels were largely influenced by the Mw and degree of esterification of the individual fractions. Notably, the highest Mw fraction (100 kDa) displayed the most potent activity, which was strongly reduced after the removal of ester residues by saponification. In contrast, the 75 kDa Mw population (PF2) proved inactive while its saponified counterpart exhibited substantial immunomodulatory activity. This confirmed the role of ester residues on the immune profile of RG-I subpopulations.

Molecular weight fraction-specific transformation of natural organic matter during hydroxyl radical and sulfate radical oxidation

Aquatic natural organic matter (NOM) is one of the main scavengers of reactive species (e.g., •OH and SO4•−) during oxidation processes and undergoes complex transformations. Here, the organic content, optical properties, and redox state in various MW fractions and bulk Suwannee River NOM (SRNOM) were simultaneously evaluated during •OH and SO4•− oxidation processes for the first time. The SRNOM transformation pathways were specific to radical species and MW fractions, which was evidenced by a proportional decrease in electron-donating moieties and chromophores during •OH oxidation but a higher decrease in electron-donating moieties than chromophores during SO4•− oxidation, particularly in lower MW fractions (<3 kDa). The •OH decomposed reactive moieties mainly via aromatic ring opening or depolymerization in all MW fractions. SO4•− oxidation followed a similar pathway in higher MW fractions (>3 kDa) but mainly formed compounds with UV-absorbing properties (e.g., quinones) in lower MW fractions (<3 kDa). With competitive kinetics and depolymerization model, •OH was quantified as approximately 10 times more reactive towards MW fractions than SO4•−. However, the SO4•− concentrations were approximately 10 times those of •OH, resulting in comparable performance to •OH oxidation. SRNOM depolymerization by •OH and SO4•− resulted in formation of more precursors of disinfection byproducts than the parent constituents, especially for •OH. This work improves our understanding of the transformation of specific SRNOM fractions during radical oxidation processes.

Ultrafiltration fractionation of potentially inhibitory substances of hydrothermal liquefaction aqueous phase derived from municipal sludge

Hydrothermal liquefaction (HTL) is a promising thermo-chemical technology for municipal sludge treatment due to its potential for biocrude oil recovery and minimizing biosolids management costs. However, the process generates a high volume of an aqueous byproduct that needs to be treated due to its high chemical oxygen demand (COD) and various organic and inorganic compounds. Although the aqueous phase is known to contain recalcitrant and potentially inhibitory substances that may affect its biological treatment, their molecular weight distribution (MwD) and its impact on anaerobic biodegradability are poorly understood. Ultrafiltration (UF) was conducted to fractionate HTL aqueous into different molecular weight (Mw) fractions using 300, 100, 10, and 1 kDa membranes. Mesophilic biochemical methane potential (BMP) assays were conducted to assess the anaerobic biodegradability of each fraction, and the first-order model was used to calculate the degradation kinetics of potential inhibitory compounds. The highest percentage of organics (65 %) was found in the Mw<1 kDa range, whereas the 10>Mw>1 kDa had the lowest percentage (8 %). There was no significant difference in the cumulative specific methane produced from various Mw fractions (p>0.05). The Mw<1 kDa fraction had the highest first-order specific methane production rate (0.53 day−1), whereas the unfiltered HTL had the lowest (0.38 day−1). Although UF fractionation increased the rate of anaerobic degradation of HTL aqueous for the Mw<1 kDa fraction, the observed methane potential was only 55 % of the theoretical value. This implies that 45 % of COD remains undegraded even after permeation through the lowest Mw cut-off membrane. Therefore, further characterization of HTL aqueous is needed for compounds with molecular weights below 1 kDa to fully understand the nature of inhibitory organics and their impact on anaerobic digestion. Furthermore, pretreatments utilizing techniques such as adsorption and advanced oxidation may be necessary to enhance the specific methane yields from various HTL aqueous fractions, thereby bringing them closer to the theoretical yield.

Biological properties of LMW-peptide fractions from apricot kernel protein: Nutritional, antibacterial and ACE-inhibitory activities

In this study, angiotensin-converting enzyme (ACE) inhibitory, antioxidant and antibacterial activities, and nutritional quality of low molecular weights (LMWs) peptide fractions (PFs) from apricot-kernel (Prunus armeniaca cv. Tabarzeh) with PFs <3, 3–10, 10–30 and 30–100 kDa were investigated. The ratio of essential to total (E/T) amino acids (∼34.5 %) and PER value (1.8–1.9) indicated the high nutritional and digestibility of peptide fractions. Antioxidant indices were affected by enzymatic hydrolysis, molecular weight (Mw) and concentration of peptides. In general, the highest inhibition of DPPH− (89.2 %), ABTS+ (93.1 %), TEAC (2.52 mM), OH• (78.1 %), NO• (70.4 %), total antioxidant activity (2.01), reducing power (1.27), ACE inhibitory (75.1 %), chelation of Fe2+ (90.2 %) and Cu2+ (40.2 %) metal-ions were related to low Mw fractions (PF-3 and PF-10). The hydrolysates and primary protein showed enhanced antibacterial effects against Escherichia coli and Bacillus cereus with diameter of inhibition zones of 17 and 14 mm, respectively. Overall, apricot-kernel peptides can be considered as a nutrient source, natural antioxidant and preservative with ACE-inhibitory effect in dietary supplements and food formulations.

Glucoregulatory Properties of a Protein Hydrolysate from Atlantic Salmon (Salmo salar): Preliminary Characterization and Evaluation of DPP-IV Inhibition and Direct Glucose Uptake In Vitro.

Metabolic disorders are increasingly prevalent conditions that manifest pathophysiologically along a continuum. Among reported metabolic risk factors, elevated fasting serum glucose (FSG) levels have shown the most substantial increase in risk exposure. Ultimately leading to insulin resistance (IR), this condition is associated with notable deteriorations in the prognostic outlook for major diseases, including neurodegenerative diseases, cancer risk, and mortality related to cardiovascular disease. Tackling metabolic dysfunction, with a focus on prevention, is a critically important aspect for human health. In this study, an investigation into the potential antidiabetic properties of a salmon protein hydrolysate (SPH) was conducted, focusing on its potential dipeptidyl peptidase-IV (DPP-IV) inhibition and direct glucose uptake in vitro. Characterization of the SPH utilized a bioassay-guided fractionation approach to identify potent glucoregulatory peptide fractions. Low-molecular-weight (MW) fractions prepared by membrane filtration (MWCO = 3 kDa) showed significant DPP-IV inhibition (IC50 = 1.01 ± 0.12 mg/mL) and glucose uptake in vitro (p ≤ 0.0001 at 1 mg/mL). Further fractionation of the lowest MW fractions (<3 kDa) derived from the permeate resulted in three peptide subfractions. The subfraction with the lowest molecular weight demonstrated the most significant glucose uptake activity (p ≤ 0.0001), maintaining its potency even at a dilution of 1:500 (p ≤ 0.01).

Conventional extraction of fucoidan from Irish brown seaweed Fucus vesiculosus followed by ultrasound-assisted depolymerization

Fucoidan has attracted considerable attention from scientists and pharmaceutical companies due to its antioxidant, anticoagulant, anti-inflammatory, anti-tumor, and health-enhancing properties. However, the extraction of fucoidan from seaweeds often involves the use of harsh chemicals, which necessitates the search for alternative solvents. Additionally, the high viscosity and low cell permeability of high molecular weight (Mw) fucoidan can limit its effectiveness in drug action, while lower Mw fractions exhibit increased biological activity and are also utilized as dietary supplements. The study aimed to (1) extract fucoidan from the seaweed Fucus vesiculosus (FV) using an environmentally friendly solvent and compare it with the most commonly used extraction solvent, hydrochloric acid, and (2) assess the impact of ultrasound-assisted depolymerization on reducing the molecular weight of the fucoidan extracts and examine the cytotoxic effect of different molecular weight fractions. The findings indicated that the green depolymerization solvent, in conjunction with a brief ultrasound treatment, effectively reduced the molecular weight. Moreover, a significant decrease in cell viability was observed in selected samples, indicating potential anticancer properties. As a result, ultrasound was determined to be an effective method for depolymerizing crude fucoidan from Fucus Vesiculosus seaweed.

Fractionation and purification of a high-impurity, alkaline-pretreated, corn stover lignin with simple renewable solvents

Corn stover has been identified as a key resource in the transition from petrochemicals to sustainably sourced energy and materials; however, the as-recovered lignin from alkaline pretreatment contains unusually high levels of residual impurities, which must be removed to maximize potential application. Thus, the Aqueous Lignin Purification using Hot Agents (ALPHA) process was applied to a corn stover lignin containing ∼10 % carbohydrates and ∼3 % ash. Lignin fractions ∼100 times cleaner than the feed lignin and of controlled molecular weight (i.e., as low as one-fifth and as high as triple the absolute molecular weight (Mw) of the feed) were obtained. The ALPHA solvent was a hot (60 or 75 °C) solution of 80 % ethanol combined with the feed lignin at an unusually low, 3:1 solvent-to-feed lignin ratio – conditions that create the liquid–liquid equilibrium (LLE) phase split needed to practice ALPHA. Lignin fractionation then commenced by adding water to the original solution, decreasing the ethanol content in increments of 3–4 wt%. Surprisingly, the highest Mw fractions did not precipitate until the solution contained just below 50 % ethanol, by which point almost half of the starting lignin of near-average Mw had already precipitated. Another unexpected result was that the lignin waste stream from the initial purification step could be increased from 40 to 98 % lignin in a single equilibrium stage simply by re-processing that waste with another 80 % ethanol solution at the conditions given above. In summary, the efficacy of ALPHA for purifying and fractionating an impurities-laden corn stover lignin to ultraclean levels in a scalable manner requiring only aqueous bioethanol solutions has been demonstrated.

Molecular insights into the bonding mechanisms between selenium and dissolved organic matter

Natural organic matter (NOM) plays a critical role in the mobilization and bioavailability of metals and metalloids in the aquatic environment. Selenium (Se), an environmental contaminant of aquatic systems, has drawn increasing attention over the years. While Se is a vital micronutrient to human beings, animals and plants, excess Se intake may pose serious long-term risks. However, the interaction between Se and dissolved organic matter (DOM) remains relatively unexplored, especially the reaction mechanisms and interactions of specific NOM components of certain molecular weight and the corresponding functional group change. Herein, we report an investigation on the interactions between Se and DOM by focusing on the mass distribution profile change of operationally defined molecular weight fractions of humic acid (HA) and fulvic acid (FA). The results showed that across all molecular weights studied, HA fractions were more prone to enhanced aggregation upon introduction of Se into the system. For FA, the presence of Se species results in aggregation, dissociation, and redox reactions with the first two being the major mechanisms. Total organic carbon analysis (TOC), UV–vis spectroscopy (UV–vis), and Orbitrap MS data showed that [10, 30] kDa MW fraction had the largest aromatic decrease (CRAM-like, lignin-like and tannin-like) upon addition of SeO2 via dissociation as the dominant mechanism. Fourier transform infrared spectroscopy (FT-IR) revealed that Se based bridging or chelation of functional groups from individual DOM components through hydrogen bonding in the form of SeO⋯H and possibly Se⋯H and/or attractive electrostatic interactions lead to aggregated DOM1⋯Se⋯DOM2. It was concluded from two-dimensional correlation analyses of excitation emission matrix (EEM) and FT-IR that the preferred Se-binding follows lipid ➔ peptide ➔ tannin ➔ aromatic functionalities. These results provide new understanding of Se interactions with various NOM components in aquatic environments and provide insight for Se assessing health risk and/or treatment of Se contaminated water.

Unmasking the efficacy of Skipjack Tuna (Katsuwonus Pelamis) dark muscle hydrolyzate in lipid regulation: a promising component for functional food

ABSTRACT To effectively utilize the by-products of skipjack tuna (Katsuwonus Pelamis) for the preparation of peptides with lipid-lowering activity, alkaline proteinase was selected from six commercial proteases to hydrolyze dark muscle. An L16 (54) orthogonal design was employed to optimize the hydrolysis conditions, resulting in the production of a high-peptide-content hydrolyzate named KPHs-AL. This hydrolyzate exhibited the ability to significantly reduce TG content. KPHs-AL also showed higher persuasive pancreatic lipase (PL) and cholesterol esterase (CEase) inhibitory potential than various molecular weight (Mw) fractions and other enzymatic hydrolyzates, with IC50 values of 5.14 and 8.51 mg/mL, respectively. Furthermore, KPHs-AL exerted a combined effect of regulating lipid accumulation in FAA-induced steatosis HepG2 cells, leading to decreased total cholesterol (TC) and total triglyceride (TG). Based on the high binding likelihood and interaction with specific binding sites predicted by Pepsite2, 38 peptide sequences were identified as potential PL and CEase inhibitors. Hence, KPHs-AL holds promise as a beneficial component of functional food and exhibits the potential for anti-obesity effects through the alleviation of lipid accumulation

Composition, structural properties and immunomodulatory activity of several aqueous Pleurotus β-glucan-rich extracts

In this work, aqueous extracts from six different Pleurotus species were obtained and their yield, gross composition, β-glucan content, monosaccharide profile, thermal stability, molecular weight distribution, and FT-IR were analyzed before and after purification through ethanol precipitation of the carbohydrate-rich fractions. The bioactivity (anti-inflammatory and immunomodulatory activity) of the various fractions obtained was also analyzed in three different cell cultures and compared with a lentinan control. The trend observed after purification of the aqueous fractions was an increase in the concentration of polysaccharides (especially β-glucans), a decrease in ash, glucosamine and protein content and the elimination of low molecular weight (Mw) compounds, thus leaving in the purified samples high Mw populations with increased thermal stability. Interestingly, all these purified fractions displayed immunomodulatory capacity when tested in THP-1 macrophages and most of them also showed significant activity in HEK-hTLR4 cells, highlighting the bioactivity observed for Pleurotus ostreatus (both the extracts obtained from the whole mushroom and from the stipes). This specific species was richer in heteropolysaccharides, having moderate β-glucan content and being enriched upon purification in a high Mw fraction with good thermal stability.

6-deoxy-6-amino chitosan: a preventative treatment in the tomato/Botrytis cinerea pathosystem.

6-deoxy-6-amino chitosan (aminochitosan) is a water-soluble chitosan derivative with an additional amine group at the C-6 position. This modification has improved aqueous solubility, in vitro antifungal activity and is hypothesized to have enhanced in vivo antifungal activity compared to native chitosan. Gray mold disease in tomatoes is caused by the fungus, Botrytis cinerea, and poses a severe threat both pre- and post-harvest. To investigate the optimal concentration of aminochitosan and its lower molecular weight fractions for antifungal and priming properties in the tomato/B. cinerea pathosystem, different concentrations of aminochitosan were tested in vitro on B. cinerea growth and sporulation and in vivo as a foliar pre-treatment in tomato leaves. The leaves were monitored for photosynthetic changes using multispectral imaging and hydrogen peroxide accumulation using DAB. Despite batch-to-batch variations in aminochitosan, it displayed significantly greater inhibition of B. cinerea in vitro than native chitosan at a minimum concentration of 1 mg/mL. A concentration-dependent increase in the in vitro antifungal activities was observed for radial growth, sporulation, and germination with maximum in vitro inhibition for all the biopolymer batches and lower MW fractions at 2.5 and 5 mg/mL, respectively. However, the inhibition threshold for aminochitosan was identified as 1 mg/mL for spores germinating in vivo, compared to the 2.5 mg/mL threshold in vitro. The pre-treatment of leaves displayed efficacy in priming direct and systemic resistance to B. cinerea infection at 4, 6 and 30 days post-inoculation by maintaining elevated Fv/Fm activity and chlorophyll content due to a stronger and more rapid elicitation of the defense systems at earlier time points. Moreover, these defense systems appear to be ROS-independent at higher concentrations (1 and 2.5 mg/mL). In addition, aminochitosan accumulates in the cell membrane and therefore acts to increase the membrane permeability of cells after foliar spray. These observations corroborate the notion that aminochitosan biopolymers can exert their effects through both direct mechanisms of action and indirect immunostimulatory mechanisms. The contrast between in vitro and in vivo efficacy highlights the bimodal mechanisms of action of aminochitosan and the advantageous role of primed plant defense systems.

P14.03.A DO GLIOMA PATIENTS PRODUCE AUTO-ANTIBODIES FOR GLIOMA-SPECIFIC PHOSPHO-PROTEIN MODIFICATIONS

Abstract BACKGROUND Many studies have shown that dysregulation of protein phosphorylation plays an important role in the development of cancer. Aberrantly phosphorylated peptides can be derived from dysregulated cell signaling pathways in various cancers and may serve as tumor-specific antigens and might be promising targets for cancer immunotherapy. Several techniques are available to purify immunoglobulins (IgG) from plasma or other body fluids using affinity to immobilized binders In contrast, Melon Gel resin retains non-IgG proteins and hence allows enrichment of IgG directly from the sample without affinity binding. We have developed a technique for the detection of auto-antibodies in HGG. MATERIAL AND METHODS To perform an Ab-peptide binding assay, we used a phospho-peptide library (a mixture of phospho-peptides obtained after phospho-enrichment of enzymatically digested fresh-frozen GBM tissue) and three plasma samples from HGG patients and a healthy donor as source of IgG. After mixing of the plasma samples with the phospho-peptide library the IgG purification was performed using the Melon Gel resin. We separated possible unbound peptides using a 30 kDa-molecular-weight (MW) filter device. The high MW fraction, containing IgGs and IgG-peptide complexes were acidified and precipitated to release Ab-bound peptides. Subsequently, the IgG-bound peptides were measured and identified in a mass spectrometer. RESULTS Performing the developed Ab-peptide binding assay using the HGG and healthy plasma samples combined with the GBM phospho-peptide library, we detected EGFR phospho-peptide GSHQIS[+80]LDNPDYQQDFFPK (S1166) in three of four IgG-bound fractions of samples incubated with HGG plasma and not in the corresponding unbound fractions. This result indicates the presence of auto-antibodies against EGFR phospho-peptide S1166 in the plasma of the three HGG patients. A contrasting result was obtained in the donor sample, where the EGFR peptide was detected almost exclusively in the unbound fraction. With the use of Avastin as negative control instead of plasma, the EGFR peptide S1166 was solely found in the unbound fraction. CONCLUSION An antibody-peptide-antigen complex enrichment with Melon Gel was successfully applied to find auto-antibodies that recognize disease-related phospho-peptides. This method has the potential to detect the putative presence of auto-antibodies without knowledge of the antigen. We demonstrated in a proof of concept the presence of auto-antibodies against an EGFR phospho-peptide in plasma of HGG patients. This antibody-peptide binding assay could potentially be further applied to other types of cancer to find targets for therapeutic interventions.

Physicochemical characteristics and antioxidant stability of spray-dried soy peptide fractions.

The direct addition of health-promoting peptides to food products is limited due to their physicochemical instability and bitter taste as well as their bio-functionality may be influenced by MW. In this study, SPI hydrolysate (SPIH) was Alcalase-prepared, size-fractionated (<10, 10-30, and 30-100 kD), and the amino acid composition of peptide fractions determined. The physicochemical properties, morphology, and antioxidant stability of the fractions were also investigated after spray-drying encapsulation in maltodextrin-WPC carrier. The two low MW peptide fractions (especially, PF < 10) were more active than intact SPI, SPIH, and high MW peptide fraction in scavenging free radicals and chelating transition metal ions. As compared to the particles containing SPIH, those containing the smallest peptide fraction (PF < 10) had higher solubility and hygroscopicity, lower production yield and wettability, and more wrinkles, indentations and surface roughness. The highest antioxidant stability during spray-drying was observed for the two low MW peptide fractions, which examined by scavenging of free radicals of DPPH (88%), ABTS (97%), OH (93%) and NO (80%), chelating of iron (88%) and copper (87-90%) ions, reducing power (93%), and total antioxidant activity (90%). This finding reflects more structural and biological stability of the low MW fractions to shear stress and dehydration during spray-drying, as compared with SPIH. The spray-drying encapsulated soy peptide fractions may be used as nutraceuticals for the development of functional foods.

Advanced Processing of Giant Kelp (Macrocystis pyrifera) for Protein Extraction and Generation of Hydrolysates with Anti-Hypertensive and Antioxidant Activities In Vitro and the Thermal/Ionic Stability of These Compounds.

In this study, giant kelp was explored under various conventional and ultrasound-assisted extraction (UAE) conditions for the extraction of protein, its hydrolysis, and ultrafiltration to generate multiple fractions. The amino acid composition of all the fractions and their biological activities in vitro, including angiotensin-converting enzyme I (ACE) inhibitory activity and antioxidant activities (2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, reducing power (RP), and ferrous chelating (FC) activities) were tested by storing the compounds for 2 weeks at various temperatures (-20-60 °C) and pHs (2-11) to elucidate their thermal and ionic stability, respectively. The yield of protein extraction using the conventional method was lower (≈39%) compared to the use of UAE (150 W, 15 min), which achieved protein recoveries of approximately 60%. After enzymatic hydrolysis and ultrafiltration, low-molecular-weight (MW) hydrolysates had the highest levels of ACE inhibitory (80%), DPPH (84%), RP (0.71 mM trolox equivalents), and FC (81%) activities. Amino acids associated with peptides of high biological activities, such as Val, Ala, Asx, Gly, Lys, Met, Leu, and His, were at higher levels in the low MW fraction compared to any other sample. The biological activities in vitro of all the samples fluctuated under the multiple storage conditions studied, with the highest stability of all the samples appreciated at -20 °C and pH 7. This study shows for the first time the use of giant kelp as a promising source of bioactive peptides and indicates the optimum processing and storing conditions for the use of these compounds as nutraceuticals or functional foods that could help in the prevention of cardiovascular disorders and multiple chronic diseases associated with oxidative damage.

Characterization and Disinfection by Product Formation of Dissolved Organic Matter in Anaerobic–Anoxic–Oxic Membrane Bioreactor (AAO-MBR) Process

In the process of sewage treatment, the characteristics of dissolved organic matter (DOM) are always changed during chemical and biological processes, affecting the generation of disinfection by-products (DBPs) compositions at the following disinfection stage. The present study systematically investigated the effect of DOM characterization on C- and N-DBPs formation at AAO-MBR reactor when treating wastewater. The results showed that the AAO-MBR treatment process could efficiently eliminate dissolved organic carbon (DOC) and ammonium nitrogen (NH4+-N) from wastewater with an elimination rate of 89% and 98%, respectively. Most of the precursors (i.e., 56.8% C-DBPs and 78.1% N-DBPs) were removed at the MBR unit, while AGC and AAO units promoted the formation of DBPs precursors. More specifically, soluble microbial products (SMPs) and humus acid were increased, which led to improved C- and N-DBPs via aerated grit chamber (AGC) treatment. At the AAO treatment unit, the content of low MW hydrophobic SMPs, humus acid, and polysaccharides was increased, indicating low MW and HPO fractions dominating the C- and N-DBPs. MBR treatment improved C-DBPs in high MW and HPO fractions and N-DBPs in low MW and HPO fractions, which is explained by higher MW hydrophobic SMPs and humus acids, compared to the AAO unit. The present study provided deep insight into the linkage of DOM characteristics and C- and N-DBPs formation at each treatment unit during the AAO-MBR process.

Cationic Tantalum Hydrides Catalyze Hydrogenolysis and Alkane Metathesis Reactions of Paraffins and Polyethylene.

Sulfated aluminum oxide (SAO), a high surface area material containing sulfate anions that behave like weakly coordinating anions, reacts with Ta(═CHtBu)(CH2tBu)3 to form [Ta(CH2tBu)2(O-)2][SAO] (1). Subsequent treatment with H2 forms Ta-H+ sites supported on SAO that are active in hydrogenolysis and alkane metathesis reactions. In both reactions Ta-H+ is more active than related neutral Ta-H sites supported on silica. This reaction chemistry extends to melts of high-density polyethylene (HDPE), where Ta-H+ converts 30% of a low molecular weight HDPE (Mn = 2.5 kg mol-1; Đ = 3.6) to low molecular weight paraffins under hydrogenolysis conditions. Under alkane metathesis conditions Ta-H+ converts this HDPE to a high MW fraction (Mn = 6.2 kDa; Đ = 2.3) and low molecular weight alkane products (C13-C32). These results show that incorporating charge as a design element in supported d0 metal hydrides is a viable strategy to increase the reaction rate in challenging reactions involving reorganization of C-C bonds in alkanes.

Effect of fermentation modification on the physicochemical characteristics and anti-aging related activities of Polygonatum kingianum polysaccharides

In order to fully investigate the anti-aging value of the plants polysaccharides, the fermentation method was applied to modify the Polygonatum kingianum polysaccharides (PKPS), and the ultra-filtration was used to further segment the hydrolyzed polysaccharides. It was found that the fermentation induced an increase in the in vitro anti-aging-related activities of PKPS including antioxidant, hypoglycemic and hypolipidemic activity, and cellular aging-delaying ability. In particular, the low Mw fraction PS2-4 (10-50 kDa) separated from the fermented polysaccharide exhibited superior anti-aging activity on experimental animals. PS2-4 extended the Caenorhabditis elegans lifespan by 20.70 %, with an increased effect of 10.09 % compared to the original polysaccharide; it was also more effective than the original one in improving movement ability and reducing lipofuscin accumulation of worms. This fraction was screened as the optimal anti-aging active polysaccharide. After fermentation, the main molecular weight distribution of PKPS changed from 50–650 kDa to 2–100 kDa, and the chemical composition and monosaccharide composition also changed; the initial rough and porous microtopography turned into smooth state. These alterations in physicochemical characteristics suggest that fermentation exerted an influence on the structure of PKPS, which contributed to the enhanced anti-aging activity, indicating that fermentation was promising in the structural modification of polysaccharides.

Improving the Photovoltaic Performance of Dithienobenzodithiophene-Based Polymers via Addition of an Additional Eluent in the Soxhlet Extraction Process.

Dithieno[2,3-d;2',3'-d']benzo[1,2-b;4,5-b']dithiophene (DTBDT) is a kind of pentacyclic aromatic electron-donating unit with unique optoelectronic properties, but it has received less attention in the design of photovoltaic polymers. In this work, we copolymerized DTBDT with the electron-deficient unit of dithieno[3',2':3,4;2″,3″:5,6]benzo[1,2-c][1,2,5]thiadiazole (DTBT) and obtained two polymers, PE55 and PE56, with a synergistic heteroatom substitution strategy. When blended with the classic nonfullerene acceptor Y6, PE55 and PE56 achieve power conversion efficiencies (PCEs) of 13.78% and 14.49%, respectively, which indicates that the introduction of sulfur atoms on the conjugated side chain of the D unit is a promising method to enhance the performance of DTBDT-based polymers. Besides, we utilize dichloromethane and chloroform to separate the low molecular weight (Mw) fractions in the solvent extraction process to obtain PE55-CF and PE56-CB, and the PCEs are further improved to 15.00% and 16.11%, respectively. The stronger π-π stacking, optimized blend film morphology, and higher charge mobilities contribute to the enhanced PCEs for polymers with higher Mw obtained via the multistep solvent extraction strategy. Our results not only provide a simple and effective way to improve the photovoltaic performance of conjugated polymers but also imply that some reported polymers purified from the traditional one-step solvent extraction method might be seriously underestimated.

Effects of molecular weight on intestinal anti-inflammatory activities of β-D-glucan from Ganoderma lucidum.

To investigate the influence of molecular weight (Mw) on the anti-inflammatory activity of β-D-glucan from Ganoderma lucidum, ultrasonic irradiation was applied to treat the β-D-glucan (GLP, 2.42 × 106 g/mol) solution to obtain two degraded fractions with molecular weight of 6.53 × 105 g/mol (GLPC) and 3.49 × 104 g/mol (GLPN). Structural analysis proved that the degraded fractions possessed similar repeated units with the original β-D-glucan. The in vitro anti-inflammatory activity studies showed that all fractions could significantly inhibit LPS-induced expression of cytokines including TNF-α, IL-8, MIF and MCP-1 in Caco-2 cells at certain concentrations. Moreover, GLPC and GLPN exhibited better anti-inflammatory activity than GLPC. The intestinal anti-inflammatory activity evaluated by dextran sulfate sodium (DSS)—induced colitis mice model showed that intragastric administration of GLPN (lower Mw fraction) could significantly recover inflamed tissues of mice. Compared with GLP and GLPC, GLPN exhibited stronger ability to inhibit the secretion of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6). The results revealed that Mw of β-D-glucan influenced its anti-inflammatory activity and decreasing of Mw would improve the activity, which provided evidence for the potential use of β-D-glucan from G. lucidum as anti-colitis ingredients.