Molecular Weight Research Articles

Preparation and characterization of cysteine-rich collagen peptide and its antagonistic effect on microplastic induced damage to HK-2 cells

Cysteine (Cys) plays a significant role in the stability and antioxidant capacity of peptide. This study was to prepare Cys-rich collagen peptide and evaluate its preventive effect on microparticle (MPs)-induced HK-2 cell damage. The results showed that the Cys-rich peptides (AMP-C) were successfully prepared from collagen hydrolysate by plastein reaction in the presence of exogenous Cys. The scavenging activities of 2,2-Diphenyl-1-picrylhydrazyl and hydroxyl radical of AMP-C were significantly higher than those of original peptides without Cys. The fraction with molecular weight < 3 kDa (AMP-CA) significantly improved MPs-induced damage and apoptosis of HK-2 cells. Compared with the same fractions lacking Cys (AMP-A), AMP-CA showed better performance in reducing reactive oxygen species and increasing the total superoxide dismutase and glutathione peroxidase levels, which may be related to its down-regulation of Kelch-like ECH-associated protein 1 (Keap1) expression. In addition, AMP-CA showed strong effects on inhibiting interleukin-6, tumor necrosis factor-α, monocyte chemoattractant protein-1, kidney injury molecule-1, and nuclear factor kappa-B levels. Finally, 330 Cys-containing peptides were isolated from AMP-CA, among which Leucine-Glycine-Asparagine-Glycine-Cysteine-Proline (LGNGCP) showed the lowest binding energy with Keap1 protein. In conclusion, the Cys-rich collagen peptide with higher antioxidant activity was successfully prepared by plastein reaction, which alleviated the HK-2 cells damage induced by MPs through antioxidant and anti-inflammatory. Our findings suggested that Cys-rich collagen peptide might be used as a functional food to mitigate health hazards associated with MPs accumulation.

A novel deep eutectic solvent-based green extraction and purification of DPP-IV inhibitory peptides from tilapia (Oreochromis niloticus) viscera hydrolysate

The use of green and low-cost techniques to produce bioactive peptides with anti-diabetic properties from protein-rich fish waste is a sustainable way to manage agro-fishery and food industrial waste. This study investigated a novel ultrasound (UL) assisted deep eutectic solvent (DES) based extraction approach to recover bioactive protein-rich extracts from tilapia fish viscera waste under optimized conditions (52.52% ultrasound amplitude, 1:4 DES molar ratio, 25 min extraction time). The aqueous two-phase system (ATPS) method successfully concentrated the crude proteins in the top phase and back-extracted proteins to the bottom phase with a high recovery yield. Hydrolysis by Alcalase produced tilapia viscera protein hydrolysate (TVPH) with low molecular weight (MW) peptides and low dipeptidyl peptidase (DPP)-IV half-maximal inhibitory concentration (IC50) value of 1.57 ±0.16 mg/mL. Notably, TVPH-3 fraction and TVPH-3-2 sub-fraction exhibited appreciable DPP-IV IC50 values of 1.36 ±0.08 mg/mL and 0.42 ±0.01 mg/mL, respectively. Ultrafiltration combined with RP-HPLC enriched the DPP-IV inhibitory concentration of the individual protein fractions. TVPH-3-2 sub-fraction contained hydrophobic amino acids and peptide sequences with typical DPP-IV inhibitory peptide sequence motifs. The results presented in this study indicate that tilapia viscera biomass is a potential source for protein recovery aided with a green extraction approach, and tilapia viscera protein-derived hydrolysates have potential applications as a potent functional food ingredient for the management of metabolic diseases like type-2 diabetes.

Retrospective study evaluating safety, clinical effect, and dosing of dalteparin for the treatment of venous thromboembolism in term neonates.

There is an increased risk of venous thromboembolism (VTE) among neonates due to their unique hemostatic system. However, there is lack of approved treatment options for VTE in neonatal population. Importantly, dalteparin, a low molecular weight heparin approved for pediatric VTE in children ≥1month of age, has also been used for the treatment of neonatal VTE. Based on the request from the Food and Drug Administration, this retrospective study aimed to characterize the safety, clinical effects, and dosing of dalteparin for treatment of VTE among neonates. Data from electronic medical records for neonates (born ≥35weeks of gestation) treated with dalteparin for VTE between January 2010 and December 2021 were collected. The data assessed included bleeding and deterioration in hematological biomarkers among other adverse events, changes in relevant factor antifactor Xa (anti-Xa) levels and VTE status, and dosing of dalteparin and corresponding anti-Xa assay levels. Sixteen neonates from five participating sites in the United Kingdom were included. There were no bleeding events or deaths. Only one serious adverse event of hypoglycemic brain injury (unrelated to dalteparin) was documented in a patient with a history of hyperinsulinism. Median (range) daily dose of dalteparin at initiation was 309 (297-314)IU/kg. Eight of 16 neonates achieved therapeutic anti-Xa level, including two patients who did so after the first dose. Dalteparin treatment in neonates raised no major safety concerns. Larger cohort studies may help provide further insights on clinical effects of dalteparin for neonatal VTE.

Aldehyde End-Capped Degradable Polyethylenes from Hydrogen-Controlled Ethylene/CO Copolymerization.

To access degradable polyolefin plastic, non-alternating copolymerization of ethylene (E) and carbon monoxide (CO) for producing polyethylene (PE) with in-chain ketones is particularly appealing; however, it still presents significant challenges such as molecular weight modulation (hydrogen response) and chain endgroup control (functional terminal). In this study, we achieved hydrogen-controlled E/CO non-alternating copolymerization using late transition metal catalysts. This process results in linear PEs containing the desired non-alternating in-chain keto groups (1.0-9.3 mol%) and with tunable molecular weights ranging from 43 to 195 kDa. In this reaction, H2 serves as a chain transfer agent, modulating the polymer's molecular weight, forming unique aldehyde endgroups and eliminating usual olefinic endgroups; CO undergoes non-alternating insertion into the PE chain, resulting in a strictly non-alternating structure (> 99%) for the keto-PE. The dispersed incorporation of in-chain keto groups retains bulk properties of PE and makes PE susceptible to photodegradation, which produces significantly lower molecular weight polymers and oligomers with unambiguous vinyl and acetyl terminals.

Effects of Dissolved Organic Matter with Different Molecular Weights on Antimony Mobilization in Shallow Groundwater at the World’s Largest Antimony Mine, China

Effects of Dissolved Organic Matter with Different Molecular Weights on Antimony Mobilization in Shallow Groundwater at the World’s Largest Antimony Mine, China

Identification of New Angiotensin-Converting Enzyme Inhibitory Peptides Isolated from the Hydrolysate of the Venom of Nemopilema nomurai Jellyfish

Recently, jellyfish venom has gained attention as a promising reservoir of pharmacologically active compounds, with potential applications in new drug development. In this investigation, novel peptides, isolated from the hydrolysates of Nemopilema nomurai jellyfish venom (NnV), demonstrate potent inhibitory activities against angiotensin-converting enzyme (ACE). Proteolytic enzymes—specifically, papain and protamex—were utilized for the hydrolysis under optimized enzymatic conditions, determined by assessing the degree of hydrolysis through the ninhydrin test. Comparative analyses revealed that papain treatment exhibited a notably higher degree of NnV hydrolysis compared to protamex treatment. ACE inhibitory activity was quantified using ACE kit-WST, indicating a substantial inhibitory effect of 76.31% for the papain-digested NnV crude hydrolysate, which was validated by captopril as a positive control. The separation of the NnV-hydrolysate using DEAE sepharose weak-anion-exchange chromatography revealed nine peaks under a 0–1 M NaCl stepwise gradient, with peak no. 3 displaying the highest ACE inhibition of 96%. The further purification of peak no. 3 through ODS-C18 column reverse-phase high-performance liquid chromatography resulted in five sub-peaks (3.1, 3.2, 3.3, 3.4, and 3.5), among which 3.2 exhibited the most significant inhibitory activity of 95.74%. The subsequent analysis of the active peak (3.2) using MALDI–TOF/MS identified two peptides with distinct molecular weights of 896.48 and 1227.651. The peptide sequence determined by MS/MS analysis revealed them as IVGRPLANG and IGDEPRHQYL. The docking studies of the two ACE-inhibitory peptides for ACE molecule demonstrated a binding affinity of −51.4 ± 2.5 and −62.3 ± 3.3 using the HADDOCK scoring function.

The Catalytic Effect of Low Molecular Weight Acids on the Physicochemical and Dielectric Properties of Oil-Paper Insulation Systems

In most industrialized countries, power transformers built several decades ago are approaching the end of their operational lifespan. The ongoing energy transition, focused on developing 100% renewable energy sources and accelerating global transportation electrification, further exacerbates these assets. Combined with rising electricity demand, there is an increasing risk of critical transformers’ degradation acceleration. In this context, understanding the aging mechanisms of the insulation system inside these essential assets, which form the core of every energy network, becomes paramount for today’s managers and engineers responsible for their operations. The acids generated through oil oxidation can be classified into two categories: low molecular weight acids (LMAs), which are inherently more hydrophilic and consequently have a greater impact on the degradation rate of solid insulation through hydrolysis, and high molecular weight acids (HMAs), which do not significantly contribute to the degradation of paper insulation. This study specifically addresses the impact of acids generated through oil oxidation—focusing on LMAs. New oil samples were infused with different ratios of LMAs before impregnation. The impregnated paper samples underwent thermal aging at 115 °C. Different physicochemical and dielectric properties were investigated. The investigations revealed that oils blended with formic acid exhibited more adverse effects on the insulation system compared to other LMAs. This information is essential for industry professionals seeking to mitigate the risks associated with transformer degradation and extend the lifespan of these critical assets during the energy transition.

Efficient Synthesis of Ultrahigh Molecular Weight Poly(methyl methacrylate) via Visible Light-Induced RAFT Polymerization in Deep Eutectic Solvent

Efficient Synthesis of Ultrahigh Molecular Weight Poly(methyl methacrylate) via Visible Light-Induced RAFT Polymerization in Deep Eutectic Solvent

Thermoplastic Elastomers and Their Physical Gels Electrospun into Tunable Microfibrous Nonwoven Mats: Structure Formation and Property Enhancement

AbstractThermoplastic elastomers (TPEs) based on styrenic block copolymers constitute excellent examples of self‐networking macromolecules that are employed in a wide range of contemporary technologies as molded parts. In such applications, these TPEs exist as dense (nonporous) films or other shapes. Here, it is first demonstrated that a series of commercial TPEs possessing comparable compositions can be electrospun from solution to form microfibers that are arranged into nonwoven mats that are breathable. An important consideration for microfiber formation is the copolymer molecular weight, which regulates i) the viscosity of the parent solution prior to electrospinning, ii) the ability of these copolymers to self‐assemble during electrospinning, iii) the microfiber morphology, and iv) the mechanical properties of the resultant microfibers. The addition of a midblock‐selective aliphatic oil to these TPEs yields thermoplastic elastomer gels (TPEGs), wherein the copolymer morphology and mechanical properties become highly composition‐tunable. Electrospinning TPEGs from a binary oil+solvent solution introduces a micelle inversion mechanism that begins with an oil‐rich micellar core and ends with a styrene‐rich micellar core, required for network stabilization, as the solvent dries during microfiber solidification. This work has implications for the production of controllably low‐modulus microfibrous materials possessing modestly improved toughness but exceptional extensibility and enhanced optical transparency.

Investigating the immunological activity of the Hsp70-P113 fusion protein for Mycoplasma ovipneumoniae detection: a groundbreaking study

BackgroundMycoplasmal pneumonia of sheep and goats (MPSG) is an important infectious disease that threatens sheep and goat production worldwide, and Mycoplasma ovipneumoniae (Movi) is one of the major aetiological agents causing MPSG. The aim of this study was to investigate the immunological activity of the Hsp70‒P113 fusion protein derived from Movi and to develop a serological assay for the detection of Movi.MethodsThis study involved codon optimization of the dominant antigenic regions of Movi heat shock protein 70 (Hsp70) and adhesin P113. Afterwards, the optimized sequences were inserted into the prokaryotic expression vector pET-30a( +) through tandem linking with the aid of a linker. Once a positive recombinant plasmid (pET-30a-rHsp70-P113) was successfully generated, the expression conditions were further refined. The resulting double gene fusion target protein (rHsp70‒P113) was subsequently purified using ProteinIso® Ni–NTA resin, and the reactivity of the protein was confirmed via SDS‒PAGE and Western blot analysis. An indirect enzyme-linked immunosorbent assay (i-ELISA) technique was developed to detect Movi utilizing the fusion protein as the coating antigen. The specificity, sensitivity, and reproducibility of all methods were assessed after each reaction parameter was optimized.ResultsThe resulting rHsp70-P113 protein had a molecular weight of approximately 51 kDa and was predominantly expressed in the supernatant. Western blot analysis demonstrated its favourable reactivity. The optimal parameters for the i-ELISA technique were as follows: the rHsp70-P113 protein was encapsulated at a concentration of 5 μg/mL; the serum was diluted at a ratio of 1:50; the HRP-labelled donkey anti-goat IgG was diluted at a ratio of 1:6,000. The results of the cross-reactivity assays revealed that the i-ELISA was not cross-reactive with other goat-positive sera against Mycoplasma mycodies subsp. capri (Mmc), Mycoplasma capricolum subsp. capripneumoniae (Mccp), Mycoplasma arginini (Marg), orf virus (ORFV) or enzootic nasal tumour virus of goats (ENTV-2). The sensitivity of this method is high, with a maximum dilution of up to 1:640. The results of the intra- and inter-batch replication tests revealed that the coefficients of variation were both less than 10%, indicating excellent reproducibility. The analysis of 108 clinical serum samples via i-ELISA and indirect haemagglutination techniques yielded significant findings. Among these samples, 43 displayed positive results, whereas 65 presented negative results, resulting in a positivity rate of 39.8% for the i-ELISA method. In contrast, the indirect haemagglutination technique identified 20 positive samples and 88 negative samples, resulting in a positivity rate of 18.5%. Moreover, a comparison between the two methods revealed a conformity rate of 78.7%.ConclusionThe results obtained in this study lay the groundwork for advancements in the use of an Movi antibody detection kit, epidemiological inquiry, and subunit vaccines.

Natural Rubber Films Reinforced with Cellulose and Chitosan Prepared by Latex Aqueous Microdispersion

In this paper, green composite films comprising natural rubber (NR), cellulose (CE), and chitosan (CS) were successfully fabricated through a simple, facile, cost-effective method in order to improve mechanical, chemical, and antimicrobial properties of NR composite films. Chitosan with a low molecular weight of 30,000–50,000 g/mol (CS-L) and a medium molecular weight of 300,000–500,000 g/mol (CS-M) was used for the fabrication. The composite films were prepared via a latex aqueous microdispersion method with different weight ratios of NR:CE:CS-L/CS-M. Fourier transform infrared spectroscopy (FTIR) results demonstrated strong interactions of hydrogen bonds between CE and CS-L/CS-M in the composite films. The tensile strength and the modulus of the composite films in dried form were found to significantly increase with the reinforcement of CE and CS-L/CS-M. The maximum tensile strength (13.8 MPa) and Young’s modulus (12.7 MPa) were obtained from the composite films reinforced with CE at 10 wt.% and CS-L at 10 wt.%. The high elongation of 500–526% was obtained from the composite films reinforced with CE at 10 wt.% and CS (CS-L or CS-M) at 5.0 wt.%. The modification could also significantly promote antimicrobial activities and chemical resistance against non-polar solvents in the composite films. The NR composite films have potential uses as flexible films for sustainable green packaging.

Ecological and Geochemical Assessment of the State of Soils in the City of Baikalsk According to the Content of Polycyclic Aromatic Hydrocarbons

The pollution of the topsoils of the city of Baikalsk (Irkutsk region) under the influence of industrial emissions and wastes of the Baikal Pulp and Paper Mill (BPPM) was studied. The content of 16 individual PAH structures in samples of urban and background soils taken during the soil geochemical survey in the summer of 2019 was analyzed. Relatively low levels of PAH content were found in the lignin sludge from the BPPM and СHP ash. The concentration of total PAHs in CHP ash reaches 46 mg/ kg with a predominance of low molecular weight compounds (the proportion of naphthalene and its homologues is 24% and 34% of the total PAHs, respectively), among high molecular weight PAHs, 5-nuclear benzo(b)fluoranthene dominates (16%). In lignin sludge, the amount of PAHs is 7.16 mg/kg with the predominance of benzo(b)fluoranthene (83%). In the soils of Baikalsk, the average total content of PAHs (38.4 mg/kg) is 5 times higher than the background content. In urban soils, 4–5-nuclear fluoranthene (61.1%) and benzo(b)fluoranthene (29.4%) prevail. This makes it possible to attribute soil pollution to the fluoranthene type. The soils of the motor transport (total PAH 105 mg/kg) and industrial (59.5 mg/ kg) zones are the most polluted, where the most contrasting PAH anomalies were formed. In descending order of the amount of PAHs, the land use zones of the city form a series: motor transport industrial residential one-storey railway transport residential multi-storey recreational zone. Several local anomalies in the amount of PAHs are distinguished, forming two large pollution halos in the western and eastern parts of the city. The leading factors in the accumulation of high molecular weight PAHs in soils are acid-alkaline conditions and soil organic matter, while the accumulation of low molecular weight polyarenes is mainly controlled by pH. The environmental hazard of pollution of Baikalsk soils with polyarenes is due to benzo(b)fluoranthene, its contribution is 83.5%.

Calculated hydration free energies become less accurate with increases in molecular weight

In order for computer-aided drug design to fulfil its long held promise of delivering new medicines faster and cheaper, extensive development and validation work must be done first. This pertains particularly to molecular dynamics force fields where one important aspect–the hydration free energy (HFE) of small molecules–is often insufficiently analyzed. While most benchmarking studies report excellent accuracies of calculated hydration free energies–usually within 2 kcal/mol of experimental values–we find that deeper analysis reveals significant shortcomings. Herein, we report a dependence of HFE prediction errors on ligand molecular weight–the higher the weight, the bigger the prediction error and the higher the probability the calculated result is erroneous by a large amount. We show that in the drug-like molecular weight region, HFE predictions can easily be off by 5 kcal/mol or more. This is likely to be highly problematic in a drug discovery and development setting. We make our HFE results and molecular descriptors freely and fully available in order to encourage deeper analysis of future molecular dynamics results and facilitate development of the next generation of force fields.

Hypolipidemic Effects of Mesona chinensis Benth Polysaccharides with Different Structures and Molecular Weights.

Four novelMesona chinensis Benth polysaccharideswere isolated usingaqueous alcohol precipitation. Their molecular weights were determined using high-performancegel permeation chromatography: MA1 (2.3 kDa), MA2 (80.5 kDa), MA3 (180.9 kDa), and MA4 (635.2 kDa), and their compositionswere analyzed using GC-MS. The polysaccharides were mainlyD-glucose, D-galactose, L-Rhamnose,D-arabinose, D-xylose, and D-mannose.The structural characteristics were further analyzed usinginfrared spectrophotometryand were identified as a typeof pyrrhicsugar.An insulin-induced insulin resistance model of HepG2 cells and oleic acid-induced fat accumulation model of insulin were established to evaluate the hypolipidemic effects. Three Bacteroidesspp. [Bacteroides thetaiotaomicron(BT), B. ovatus(BO), and B. cellulosilyticus(BC)] that werenegatively correlated with lipid-lowering activity were used to evaluate the lipid-lowering activity of polysaccharides.The Bacteroidesmetabolites of MA1 and MA2exhibited hypolipidemic effects andantioxidant activities and could potentially be used as lipid-lowering supplements.

Development of a carboxymethyl chitosan functionalized slide for small molecule detection using oblique-incidence reflectivity difference technology

Label-free optical biosensors have become powerful tools in the study of biomolecular interactions without the need for labels. High throughput and low detection limit are desirable for rapid and accurate biomolecule detection. The oblique-incidence reflectivity difference (OI-RD) technique is capable of detecting thousands of biomolecular interactions in a high-throughput mode, specifically for biomolecules larger than 1000 Da. In order to enhance the detection capability of OI-RD for small molecules (typically &lt; 500 Da), we have developed a three-dimensional biochip that utilized carboxymethyl chitosan (CMCS) functionalized slides. By investigating various factors such as sonication time, protein immobilization time, CMCS molecular weight, and glutaraldehyde (GA) functionalization time, we have achieved a detection limit of 6.8 pM for avidin (68 kDa). Furthermore, accurate detection of D-biotin with a molecular weight of 244 Da has also been achieved. This paper presents an effective solution for achieving both high throughput and low detection limits using the OI-RD technique in the field of biomolecular interaction detection.

Organic–Inorganic Fertilization Shifts Dissolved Organic Matter Chemodiversity in Runoff From Tropical Cropland: Roles of Soil Nutrient Stoichiometry

ABSTRACTDissolved organic matter (DOM) is a crucial quality indicator for water health. However, it remains unknown how organic–inorganic fertilization differently shifts the DOM chemodiversity in cropland‐impacted runoff, especially the roles of terrestrial nutrient stoichiometry. Here, a field experiment subjected to 7‐year history of four fertilization regimes, that is, unfertilized (CK), chemical fertilization (NPK), straw return (SR), and NPK + SR, was conducted to examine the quantity and chemodiversity of runoff DOM in tropical China. Moreover, the ecological relationships between runoff DOM properties and soil C:N:P stoichiometry were evaluated. Relative to the control treatment, the carbon content (DOC) of runoff DOM increased by 29.20% and 48.82% under SR and NPK + SR treatments, but remained unchanged in NPK treatment. Conversely, the DOM nitrogen content (TDN) only elevated in NPK treatment (262.58%). For DOM chemodiversity, SR treatment was rich in methyl carbon and protein‐like substances, but lacked fulvic‐/humic‐like compounds. NPK treatment increased the hydrophilic compounds like amino acids and polysaccharides, while reducing aromaticity. NPK + SR treatment enhanced DOM's aromaticity, molecular weight and humification due to the enrichment of quinone, ketone and fulvic‐like substances, possibly shaping an oligotrophic aquatic microbial community. Further study revealed that the occurrence of aromatic DOM was positively correlated with soil moisture content, TK (total potassium), total organic carbon and stoichiometric N:P ratio, indicating the contribution of terrestrial straw‐decomposed products. Inversely, the accumulation of hydrophilic substances (e.g., TDN) correlated positively with soil NO3‐N and C:P ratio, indicating the contribution of endogenous DOM.

Large-scale floating polyacrylonitrile hybrid micro-/nanofiber membrane achieves efficient H/D isotope separation via photocatalytic proton transport

Advancements in isotope separation are both essential and challenging. The separation of water isotopes is vital in industrial production, biopharmaceuticals, and healthcare applications. This process is energy-intensive and complex due to the similarity of the isotopes. Pure polyacrylonitrile (PAN) is resistant to proton permeability, but neutral hydrogen radicals are capable of penetration. In this study, we report a novel approach using PAN macroscopic hybrid micro-/nanofibers in combination with a photocatalyst to separate hydrogen ion isotopes. Application of photocatalytic water splitting to generate protons results in significantly slower deuteron permeation in these fibers relative to protons, resulting in a separation factor of approximately 15 at room temperature. The composite PAN fibers exhibit a conductivity of 17.5 mS cm−1 at 25 °C and 95 % relative humidity. Our approach not only converts sunlight directly into storable hydrogen, but also enriches heavy water from H₂O/D₂O by H/D isotope separation. This study provides new insights into proton transport mechanisms in acidic media and demonstrates the significant potential of high molecular weight polymers for hydrogen isotope separation.

Potential Bioactivities, Chemical Composition, and Conformation Studies of Exopolysaccharide-Derived Aspergillus sp. Strain GAD7

This research identified a marine fungal isolate, Aspergillus sp. strain GAD7, which produces an acidic and sulfated extracellular polysaccharide (EPS) with notable anticoagulant and antioxidant properties. Six fungal strains from the Egyptian Mediterranean Sea were screened for EPS production, with Aspergillus sp. strain GAD7 (EPS-AG7) being the most potent, yielding ~5.19 ± 0.017 g/L. EPS-AG7 was characterized using UV-Vis and FTIR analyses, revealing high carbohydrate (87.5%) and sulfate (24%) contents. HPLC and GC-MS analyses determined that EPS-AG7 is a heterogeneous acidic polysaccharide with an average molecular weight (Mw¯) of ~7.34 × 103 Da, composed of mannose, glucose, arabinose, galacturonic acid, galactose, and lyxose in a molar ratio of 6.6:3.9:1.8:1.3:1.1:1.0, linked through α- and β-glycosidic linkages as confirmed by NMR analysis. EPS-AG7 adopted a triple helix-like conformation, as evidenced by UV-Vis (Congo Red experiment) and circular dichroism (CD) studies. This helical arrangement demonstrated stability under various experimental conditions, including concentration, ionic strength, temperature, and lipid interactions. EPS-AG7 exhibited significant anticoagulant activity, doubling blood coagulation time at a concentration of 3.0 mg/mL, and showed significant antioxidant activity, with scavenging activities reaching up to 85.90% and 58.64% in DPPH and ABTS+ assays at 5.0 mg/mL, and EC50 values of 1.40 mg/mL and 3.80 mg/mL, respectively. These findings highlight the potential of EPS-AG7 for therapeutic applications due to its potent biological activities.

Humic acid: A promising bio-organic catalyst for green synthesis of phenol in aqueous medium at room temperature

A simple and mild catalytic protocol has been described using humic acid as a reusable catalyst for the synthesis of phenol in aqueous medium. Humic acid is an inexpensive, non-toxic and easily available high molecular weight polymer. The mentioned catalytic protocol utilizes hydrogen peroxide as a green oxidant and water: isopropanol as solvent which has several advantages like commercially available, cheap and reusable catalyst, high percentage yield, short reaction time, room temperature etc.

Various steaming durations alter digestion, absorption, and fermentation by human gut microbiota outcomes of Polygonatum cyrtonema Hua polysaccharides

IntroductionDifferent steaming durations dramatically alter the structure of Polygonatum cyrtonema polysaccharides (PCPs). This study aimed to compare characteristics of digestion, absorption, and fermentation by gut microbiota across four representative PCPs from different steaming durations (0, 4, 8, and 12 h), each with unique molecular weights and monosaccharide profiles.MethodsChemical composition of the four PCPs was analyzed. Digestibility was evaluated using an in vitro saliva-gastrointestinal digestion model. Absorption characteristics were assessed with a Caco-2 monolayer model, and impacts on gut microbiota composition and short chain fatty acid (SCFA) levels were analyzed using in vitro fermentation with human gut microbiota.ResultsLonger steaming durations altered the chemical profiles of PCPs, reducing carbohydrate content (84.87–49.58%) and increasing levels of uronic acid (13.99–19.61%), protein (1.07–5.43%), and polyphenols (0.05–2.75%). Four PCPs were unaffected by saliva digestion but showed enhanced gastrointestinal digestibility, with reducing sugar content rising from 4.06% (P0) to 38.5% (P12). The four PCPs showed varying absorption characteristics, with P0 having the highest permeability coefficient value of 9.59 × 10−8 cm/s. However, all PCPs exhibited poor permeability, favoring gut microbiota fermentation. The four PCPs altered gut microbiota composition and elevated SCFA production, but levels declined progressively with longer steaming durations. All PCPs significantly increased the abundance of Bacteroidota, Firmicutes, and Actinobacteriota, making them the dominant bacterial phyla. Additionally, all PCPs significantly increased the abundance of Bifidobacterium, Prevotella, and Faecalibacterium compared to the control group, which, along with Bacteroides, became the dominant microbiota. Increasing the steaming duration led to a reduction in Prevotella levels, with PCPs from raw rhizomes showing the highest relative abundance at 24.90%. PCPs from moderately steamed rhizomes (4 h) led to a significant rise in Faecalibacterium (7.73%) among four PCPs. P8 and P12, derived from extensively steamed rhizomes (≥8 h), exhibited similar gut microbiota compositions, with significantly higher relative abundances of Bacteroides (20.23–20.30%) and Bifidobacterium (21.05–21.51%) compared to P0 and P4.DiscussionThis research highlights the importance of adjusting steaming durations to maximize the probiotic potential of P. cyrtonema polysaccharides, enhancing their effectiveness in modulating gut microbiota and SCFA levels.