Peroxidase Activity Research Articles

"Moringa leaf extract alleviates salt stress in tomato (Solanum lycopersicum L.) by activating antioxidant defenses, reducing osmolyte accumulation, improving water status, and enhancing yield."

Salt stress poses a significant threat to crop productivity, prompting investigations into mitigation strategies. This study assessed the efficacy of foliar spraying with moringa leaf extract (MLE) to alleviate salt stress at concentrations of 50, 100, 150, and 200 mM, alongside a control (0 mM), in tomato plants. Salt stress-induced marked significant reductions in vegetative parameters (shoot height, root length, stem diameter, and number of leaves plant-1), yet MLE-treated plants exhibited enhanced growth compared to the untreated and control plants. Salinity adversely affected chlorophyll content, relative water content, and membrane stability index, all of which were significantly ameliorated by MLE application. Additionally, MLE treatment bolstered the activity of catalase, peroxidase, superoxide dismutase, and proline accumulation, contributing to improved plant resilience. Notably, MLE-treated plants demonstrated significantly increased yields compared to untreated counterparts. These findings underscore the potential of MLE as a bioresource for mitigating salt stress in tomato plants, offering promising avenues for sustainable crop management in the highly saline soil in a region like Qatar.

Mechanism of antimony oxidation and adsorption using immobilized Klebsiella aerogenes HC10 in soil

Klebsiella aerogenes HC10 is one of the few strains isolated from contaminated soil that efficiently oxidizes Sb. However, the sensitivity of microorganisms to environmental conditions limits Sb-oxidizing bacteria applications in soil remediation. Immobilizing Sb-oxidizing bacteria is a promising strategy to improve colonization rates and microorganism inefficiencies and to strengthen bioremediation in Sb-contaminated soil. This study evaluated the feasibility of an immobilization approach to enhance Sb oxidation and the remediation performance of strain HC10 in soil. The results indicated that a mixed matrix of polyvinyl alcohol and sodium alginate as fixed carriers provided a porous microstructural environment conducive to HC10 colonization and proliferation. Sb(III) concentration was reduced by 9.8 mg/L. The total Sb decreased by 3.8 mg/L by immobilized HC10 after 7 d. Key metabolites involved in Sb oxidation and adsorption were significantly upregulated. In soil, immobilized HC10 removed 48.68 % and 61.74 % of water-extractable and citric acid-extractable Sb(III), respectively. Some well-crystallized (hydr)oxide Sb fractions binding to the mineral surface were transformed into the mineral lattice form, creating an inner-sphere complex that effectively immobilized Sb. Immobilized HC10 enhanced hydrogen peroxidase, urease, and sucrase activities related to soil antioxidants and nutrient cycling. Immobilized HC10 promoted the proliferation of indigenous bacteria, which emerged as the dominant bacterial community with the potential for Sb oxidation. The ars operon genes associated with Sb resistance and transport were significantly expressed in HC10 treatments, providing a crucial basis for colonization in the soil. These results highlight the potential of immobilized Sb-oxidizing bacteria for enhanced bioremediation of Sb-contaminated soil.

Colonization of phthalate-degrading endophytic bacterial consortium altered bacterial community and enzyme activity in plants

Phthalates (PAEs) are widely distributed hazardous organic compounds that pose threats to ecosystems and human health. Endophytic bacteria can effectively eliminate PAEs contamination risk. However, limited information is available regarding the impact of endophytic bacterial colonization on bacterial communities within plants. In this study, the endophytic bacterial consortium EN was colonized in lettuce by seed soaking, root irrigation, leaf spraying, and combined spraying-irrigation, resulting in a marked improvement in plant growth. The findings revealed that consortium EN colonization through combined spraying-irrigation exhibited superior degradation capability with 40.54% PAEs removal from soil. Meanwhile, the residual PAEs in lettuce decreased by 94.05% compared with the uninoculated treatment. High-throughput sequencing analysis indicated that colonization of consortium EN altered the bacterial community in lettuce. Specifically, the relative abundance of the dominant genus Pseudomonas was significantly higher than that in the uninoculated control (P < 0.01). Additionally, colonization enhanced the activities of peroxidase and catalase in lettuce, thereby improving plant resistance. This work offers a theoretical foundation for comprehending the mechanism underlying the bioremediation of PAEs contamination by endophytic bacteria in soil-plant system.

LncRNA HOXA11-AS intercepts the POU2F2-mediated downregulation of SLC3A2 in osteoarthritis to suppress ferroptosis

BackgroundOsteoarthritis (OA) is a prevalent ailment characterized by the gradual degradation of joints, resulting in discomfort and restricted movement. The recently proposed mechanism of ferroptosis is intricately associated with the initiation and progression of OA. Our study found that the long non-coding RNA HOXA11-AS reduces ferroptosis by increasing the expression of SLC3A2 through the transcription factor POU2F2. Materials and methodsHOXA11-AS was identified through lncRNA microarray analysis, and its impact on chondrocytes and extracellular matrix was assessed using real-time quantitative PCR, western blotting, and CCK8 assays. Subsequently, overexpression of HOXA11-AS in the knee joints of mice confirmed its protective efficacy on chondrocyte phenotype in the OA model. The involvement of HOXA11-AS in regulating ferroptosis via SLC3A2 was further validated through RNA sequencing analysis of mouse cartilage and the assessment of malondialdehyde levels and glutathione peroxidase activity. Finally, a combination of RNA sequencing, pull-down assays, mass spectrometry (MS), and chromatin immunoprecipitation (ChIP) techniques was employed to identify POU2F2 as the crucial transcription factor responsible for repressing the expression of SLC3A2, which can be effectively inhibited by HOXA11-AS. ResultsOur study demonstrated that HOXA11-AS effectively enhanced the metabolic homeostasis of chondrocytes, and alleviated the progression of OA in vitro and in vivo experiments. Furthermore, HOXA11-AS was found to enhance SLC3A2 expression, a key regulator of ferroptosis, by interacting with the transcriptional repressor POU2F2. ConclusionsHOXA11-AS promotes SLC3A2 expression and inhibits chondrocyte ferroptosis, by binding to the transcriptional repressor POU2F2, offering a promising and innovative therapeutic approach for OA.

Abstract A016: Targeting metabolic vulnerability of non-small cell lung cancer with annonacin and 2-deoxy-d-glucose in individual and combination modality

Abstract Non-small cell lung cancer (NSCLC) is a primary type of lung cancer and a leading cause of cancer-related mortality worldwide. The Warburg effect, characterized by increased glycolysis and reduced oxidative phosphorylation, is a hallmark of NSCLC and presents a therapeutic target. Annonacin, a natural compound found in fruits from the Annonaceae family, interferes with oxidative phosphorylation by inhibiting mitochondrial complex I. 2-deoxy-d-glucose (2DG), a glucose analog, disrupts glycolysis. This study examines the effects of Annonacin and 2DG on NSCLC A549 cells, both individually and in combination, with the hypothesis that inhibiting both metabolic pathways simultaneously will lead to more effective cancer treatment. In addition, we explored how these treatments might alter the tumor microenvironment, oxidative stress, and effects on normal epithelial bronchial cells. A549 NSCLC cells were exposed to different concentrations of Annonacin (0, 1, 2, 4, 6 µM) and 2DG (0,1.25, 2.5, 5, 10 mM), separately and together. Cell viability was measured using the MTT assay. Genotoxicity was assessed through the Comet Assay, and oxidative stress was evaluated by measuring superoxide dismutase and glutathione peroxidase activities. The long-term ability of the cells to proliferate was tested using colony-forming assays. The NL20 bronchial epithelial cell line was tested as a parallel control. Both Annonacin and 2DG showed a dose-dependent ability to kill A549 cells. However, when used together, these substances had a stronger effect, significantly lowering the number of surviving cells compared to when each was used alone. The response of this combination treatment on genotoxicity using Comet Assay is being pursued. Changes in oxidative stress responses were found, as shown by the altered superoxide dismutase and glutathione peroxidase enzyme activities. The ability of A549 cells to form colonies was greatly reduced following combination treatment, indicating a reduction in their long-term proliferative capacity. The combination of Annonacin and 2DG effectively inhibits the growth of NSCLC A549 cells by targeting their metabolic weaknesses, which may lead to increased DNA damage and oxidative stress. These results suggest simultaneous targeting glycolysis and oxidative phosphorylation could be a promising new approach for treating NSCLC. Future in vivo studies will evaluate this combination in live models and can offer insights into efficacy and possible translation to clinical application. Citation Format: Bhoj Raj Bhattarai, Cora Teets, Avinash Tope. Targeting metabolic vulnerability of non-small cell lung cancer with annonacin and 2-deoxy-d-glucose in individual and combination modality [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Tumor-body Interactions: The Roles of Micro- and Macroenvironment in Cancer; 2024 Nov 17-20; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2024;84(22_Suppl):Abstract nr A016.

ZnO‐CuS/F127 Hydrogels with Multienzyme Properties for Implant‐Related Infection Therapy by Inhibiting Bacterial Arginine Biosynthesis and Promoting Tissue Repair

AbstractImplant‐related infections are characterized by the formation of bacterial biofilms. Current treatments have various drawbacks. Nanozymes with enzyme‐like activity can produce highly toxic substances to kill bacteria and remove biofilms without inducing drug resistance. However, it is difficult for current monometallic nanozymes to function well in complex biofilm environments. Therefore, the development of multimetallic nanozymes with efficient multienzyme activities is crucial. In the present study, bimetallic nanozyme, ZnO‐CuS nanoflowers with peroxidase (POD), glutathione oxidase (GSH‐Px), and catalase (CAT) activity are successfully synthesized via calcination and loaded into F127 hydrogels for the treatment of implant‐related infections. The ability of ZnO‐CuS nanoflowers to bind bacteria is key for efficient antimicrobial activity. In addition, ZnO‐CuS nanoflowers with H2O2 disrupt the metabolism of MRSA, including arginine synthesis, nucleotide excision repair, energy metabolism, and protein synthesis. ZnO‐CuS/F127 hydrogel in combination with H2O2 has been demonstrated to be effective in clearing biofilm infection and facilitating the switch of M1 macrophages to M2‐repairative phenotype macrophages for the treatment of implant infections in mice. Furthermore, ZnO‐CuS/F127 hydrogels have favorable biosafety, and their toxicity is negligible. ZnO‐CuS/F127 hydrogel has provided a promising biomedical strategy for the healing of implant‐related infections, highlighting the potential of bimetallic nanozymes for clinical applications.

Machine Learning Insights into Ascorbic Acid-Enhanced Germination of Black Cumin (Nigella sativa L.) under Cadmium Stress

AbstractThe objective of the present work is to study the impact of seed priming with varying concentrations of ascorbic acid (vitamin C) on the germination process of black cumin (Nigella sativa) under cadmium (Cd) stress. As expected, Cd had a great effect on germination rates and seedling growth. However, the application of ascorbic acid during seed priming effectively alleviated Cd stress and significantly increased seed vigor. Primed seeds exhibited markedly elevated final germination percentage, germination index, mean germination time, seedling length, seedling vigor index, and reduced abnormal seedling percentage. Additionally, vitamin priming reduced membrane lipid peroxidation, in treated seeds. Moreover, seed priming elicited a considerable increase in peroxidase and catalase activity, thus mitigating stress effects and augmenting seed vitality. Our experimental data allowed us to establish 100–150 mg/L as the optimal concentration range for ascorbic acid in seed priming of black cumin. These insights were further corroborated through modeling techniques based on supervised machine learning. Notably, XGBoost emerged as a proficient tool for predicting final germination percentage, mean germination time, seedling vigor index, abnormal seedling percentage, and peroxidase activity, while SVR demonstrated aptitude in forecasting catalase activity and germination index. The Gaussian method exhibited superior performance in predicting malondialdehyde content. These comprehensive findings substantiate the premise that vitamin priming with ascorbic acid serves as a promising strategy to ameliorate germination outcomes under Cd-induced stress conditions.

Combined Transcriptomic and Metabolomic Analyses Reveal the Mechanisms by Which the Interaction Between Sulfur and Nitrogen Affects Garlic Yield and Quality

Nitrogen and sulfur are essential macronutrients in plant growth and development, and their interaction profoundly influences gene expression, metabolic activities, and adaptability in plants, directly affecting plant growth and yield. Garlic (Allium sativum L.) is a crop of significant economic and medicinal value. However, despite the critical role of the nitrogen–sulfur interaction in garlic’s adaptability, yield, and quality, the specific mechanisms underlying these effects remain unclear. In this study, transcriptomic and metabolomic analyses were employed to investigate the effects of combined sulfur and nitrogen application on garlic bulb tissues. The results show that the combined application of sulfur and nitrogen significantly increased the diameter and weight of garlic bulbs by 14.96% and 35.47%, respectively. The content of alliin increased by 28.48%, while the levels of abscisic acid (ABA), jasmonic acid (JA), salicylic acid (SA), and gibberellin (GA) increased by 15.82%, 12.94%, 32.34%, and 48.13%, respectively. Additionally, the activities of alliinase, superoxide dismutase (SOD), and catalase (CAT) were enhanced by 7.93%, 4.48%, and 19.74%, respectively. Moreover, the application of sulfur and nitrogen significantly reduced the malondialdehyde (MDA) content and peroxidase (POD) activity in garlic bulbs by 29.66% and 9.42%, respectively, thereby improving garlic’s adaptability and growth potential. Transcriptomic analysis revealed differentially expressed genes in several key pathways, including plant hormone signal transduction, RNA degradation, glutathione metabolism, amino acid biosynthesis, and glycerophospholipid metabolism. Metabolomic analysis identified 80 differentially abundant metabolites primarily consisting of amino acids, indole carboxylic acids, and fatty acids. The integrated transcriptomic and metabolomic analyses highlighted the pivotal roles of glutathione metabolism, glycerophospholipid metabolism, and amino acid biosynthesis pathways in the synergistic effects of sulfur and nitrogen. This study not only provides critical scientific evidence for understanding the mechanisms underlying the nitrogen–sulfur interaction’s impact on the yield and quality of garlic but also offers a scientific basis for optimizing nutrient management strategies to enhance garlic yield and quality.

Close correlation between sugarcane ratoon decline and rhizosphere ecological factors.

Rhizosphere ecological factors that affect sugarcane ratoons are crucial components in the feedback mechanisms between the sugarcane plant and soil environment. However, systematic investigations on these dynamics are lacking. Therefore, this study investigated the relationship between sugarcane ratoon decline and rhizosphere ecological factors. In first-year sugarcane ratoons, ecological factors such as soil available potassium content, soil nitrogen fixation, and soil peroxidase activity were significantly positively correlated with sugarcane growth (P < 0.05) compared to that of third-year sugarcane ratoons. Significant intergroup disparities in the rhizosphere soil microbial community structure were observed based on different ratoon ages (P < 0.01), while highly significant intergroup differences in endophytic microbial community structure were observed based on a Jaccard distance analysis (P < 0.01). Generalised additive model analysis revealed a significant positive correlation (P < 0.05) between sugarcane growth properties and the alpha diversity of rhizosphere soil bacteria and endophytic bacteria but a predominantly negative correlation (P > 0.05) between the alpha diversity of endophytic fungi and key sugarcane growth indicators. The deterioration of mainly non-microbial ecological factors in rhizosphere soil (P < 0.05) with increasing ratoon age may represent a significant factor contributing to sugarcane ratoon decline. The fungal community significantly impacted soil enzyme activity, while the microbial community indirectly influenced sugarcane yield through its effect on soil enzyme activity. Therefore, endophytic fungi, particularly Ascomycota species, may play a crucial role in sugarcane diseases.

SNP alleviates ferric and salt stress in Phaseolus vulgaris seeds

Seed germination and early development are delicate events often influenced by various environmental factors. Among these factors, the accumulation of salts and heavy metals in the soil is noteworthy. This study aimed to observe the effect of priming with solutions of sodium nitroprusside, polyethylene glycol 6000, and potassium nitrate on the germination of Phaseolus vulgaris seeds exposed to toxic conditions of iron and sodium chloride. Seeds were germinated on plates placed in a growth chamber at a constant temperature of 25°C and a 12-hour photoperiod. The percentage of germination, germination speed, root and shoot lengths, catalase, peroxidase activities, and malondialdehyde content were evaluated. Exposure to high concentrations of sodium chloride and iron reduced germination percentage, germination speed, root and shoot lengths of treated plants. Only sodium nitroprusside treatment mitigated the effects of stressors. No increase in malondialdehyde content was observed in any treatment, suggesting no lipid peroxidation of membranes. However, all treatments showed increased catalase activity, possibly indicating oxidative stress and metabolic damage. Sodium nitroprusside stands out as a stress alleviator for sodium chloride and iron accumulation during the germination phase.

Two‐Phase Extraction, Structural Characterization of the Polysaccharide from Raspberry Pomace and Its Protection Effects against Erythrocyte Hemolysis

AbstractIn present study, a new polysaccharide (RPP) from raspberry pomace is prepared through ultrasound‐assisted aqueous two‐phase extraction (UAATPE) and purification using two‐step column chromatography, the extraction conditions are optimized by response surface method (RSM). Under the optimal parameters: liquid to material ratio of 80 mL g−1, ultrasonic power of 340 W, and ultrasonic time of 39 min, the yield of the polysaccharides is 11.72 ± 0.05%. RPP with average molecular weight (Mw) of 59 300 Da is composed of six monosaccharides. Nuclear magnetic resonance (NMR) analyses confirmed that RPP contains six main glycosidic linkages including α‐l‐Araf‐(1→, →2)‐α‐l‐Rhap‐(1→, →4)‐β‐d‐Manp‐(1→, →4)‐α‐d‐GalAp‐(1→, →3)‐β‐d‐Galp‐(1→, →4)‐β‐d‐Glcp‐(1→. RPP exhibits remarkable protective effects against H2O2‐induced erythrocyte hemolysis, the generations of reactive oxygen species, and malondialdehyde are inhibited, and the activities of glutathione peroxidase and catalase are effectively enhanced. The current findings proved that UAATPE is an effective method to extract the polysaccharide from raspberry pomace and provides a new idea for the utilization of nutrient‐rich raspberry fruit residue.

The effect of long term astaxanthin supplementation on the antioxidant status of racing Arabian horses - preliminary study.

Astaxanthin due to its strong antioxidant activity is believed to reduce oxidative stress and therefore is considered as feed additive in pathological conditions and also for the athletes. It is promoted by several equine web portals, however, data supporting that concept in horses is limited. Thus, the aim of this study was to evaluate the effect of astaxanthin supplementation on the parameters of oxidative status in 3 years old, racing Arabian horses during long term observation and the changes related to a single training session of high intensity. Six horses were supplemented with astaxanthin at a dose of 0.52-0.58mg/kg BW and 7 received no supplementation. Astaxanthin supplementation resulted in the increase in total antioxidant status by 31.5%, accompanied by decreases in the amount of total thiobarbituric acid-reactive substances -TBARS and glutathione reductases - GR values by 34.5% and 45.4%, respectively, after 1 month and this effect persisted until the end of the observation. After individual training session the activities of glutathione peroxidases and GR were lower by 69% and 46%, respectively, and TBARS lower by 38% in supplemented horses. These results directly confirmed the beneficial effects of astaxanthin supplementation on the antioxidant status of race horses. Astaxanthin partially counterbalance the training-related oxidative stress, save the horse natural antioxidant defense, and shift the redox status towards a more reducing environment. At the same time, exercise-induced reactive oxygen species production at certain level was maintained and so that contributed to training progress.

The Effect of Pomegranate Peel Extract on the Oxidative and Inflammatory Status in the Spleens of Rats with Metabolic Syndrome

Polyphenols have antioxidant and anti-inflammatory properties and maintain the immune system in balance; therefore, the aim of the study was to investigate the effect of polyphenols present in pomegranate peel extract on the spleens of rats with metabolic syndrome. The study objects were adult male Zucker Diabetic Fatty (ZDF-Leprfa/Crl, fa/fa) rats. The rats were divided into a control group (MetS) consisting of rats with metabolic syndrome and four study groups consisting of rats with metabolic syndrome (MetS + 100 mg and MetS + 200 mg) or healthy animals (H + 100 mg and H + 200 mg) receiving polyphenol extract at a dose of 100 mg or 200 mg/kg, respectively. Concentrations of IL-6, NF-κB, NFATc1, Cyt-C, TNFα, MMP-2, ROS/RNS, and MDA were measured; the activities of GPX, SOD, CAT, MMP-2, and MMP-9 were assessed; and the expression of the BAX and BCL-2 genes was evaluated in homogenized spleens. In conclusion, pomegranate extract may lead to an increase in catalase and glutathione peroxidase activity. Additionally, it may have a reducing effect on the ROS/RNS level, leading to a reduction in the activity of SOD in the MetS groups with PPE administration. Moreover, the BCL-2 gene showed lower expression in the MetS + 100 mg group compared to the H + 100 mg group, indicating that the balance between pro- and antiapoptotic factors of the BCL-2 family may be disrupted by the metabolic syndrome promoting the proapoptotic pathway.

Effects of Inoculation of Thermotolerant Bacillus Strains on Lignocellulose Degradation

Thise study investigated the effect of three lignocellulolytic thermophilic Bacillus strains (F11, Q1, and FP4) on lignocellulose degradation, enzymatic activities, and microbial community structure in composting. The lignin degradation rate reached 36% in the presence of the inoculant, the hemicellulose degradation rate ranged from 43% (F11) to 51% (Q1), and cellulose degradation rates reached 57% in F11 and in FP4, which were significantly higher than the control (CK). The inoculation treatment could explain 28% of the lignin degradation for all three strains. The contribution of FP4 to hemicellulose and cellulose degradation was 30% and 20%, respectively. Compared to CK, lignin peroxidase activity in the water extract of the compost had increased by 66~145% for inoculation treatments, and manganese peroxidase and laccase activity increased by 114% and 78% for Q1. The inoculation stimulated the growth of indigenous bacteria with stronger lignocellulolytic enzyme-producing ability; such shifts in microbial communities were most likely responsible for the improved lignocellulose degradation.

Biochemical and proteomic approaches to investigating effects of IAA-aspartate in pea (Pisum sativum L.) seedlings during osmotic shock.

Osmotic shock is the first step of high salt or drought action that involves biochemical and molecular changes during plant response to these unfavorable conditions. Indole-3-acetyl-aspartate (IAA-aspartate, IAA-Asp) is the main amide conjugate of auxin in pea (Pisum sativum L.) tissues. Although the exact molecular mechanism of the IAA-Asp action is unknown, this conjugate's indole-3-acetic acid (IAA)-independent biological activity has been observed during physiological and stress conditions. In this work, we investigated the effect of IAA-Asp alone, as well as in combination with NaCl or polyethylene glycol (PEG) (osmotic shock) on reduced/oxidized glutathione (GSH/GSSG) ratio, activities of enzymes modulating glutathione concentration, protein S-glutathionylation, and IAA homeostasis. We did not observe the hydrolysis of IAA-Asp to IAA in pea seedlings, which, together with other results, suggests that IAA-Asp modulates plant response to abiotic stimuli independently of IAA. Moreover, despite the effect of IAA-Asp on the enzymes responsible for IAA conjugation, no changes in this phytohormone level were visible. Furthermore, 3h plant treatment with IAA-Asp increased the activity of glutathione reductase (GR), which correlates with an elevated GSH/GSSG ratio. On the contrary, more extended (48h) incubation with IAA-Asp diminished the GSH/GSSG ratio and increased the activity of glutathione peroxidase (GPX). IAA-Asp reduced GR activity during salt treatment but did not affect the GSH/GSSG ratio. Similarly, under plant incubation with PEG, IAA-Asp did not change the GSH/GSSG ratio but increased glutathione S-transferase (GST) activity. We also analyzed the effect of IAA-Asp on pea protein S-glutathionylation. Increased S-glutathionylation of heat shock 70 kDa protein (HSP70) was observed after plant treatment with IAA-Asp, PEG, or IAA-Asp combined with PEG. The proteomic analysis also revealed that IAA-Asp diminished S-glutathionylation of lipoxygenase during plant incubation with PEG. Thus, we suggest that IAA-Asp modulates redox status in pea during oxidative stress and under normal physiological conditions.

Effects of hap2 deletion on mnp/vp transcription in Pleurotus ostreatus grown on lignocellulosic substrates.

The regulatory mechanisms governing expression of genes encoding lignin-modifying enzymes (LME) in white-rot fungi remain largely unexplored. Although molecular cloning has identified CCAAT-boxes frequently located 5'-upstream of these genes, their role in transcriptional regulation is not well understood. This study examines the function of hap2, a gene encoding a hypothetical protein homologous to a component of the CCAAT-binding Hap complex, in the white-rot fungus Pleurotus ostreatus. Deletion of hap2 resulted in significantly reduced Mn2+-dependent peroxidase activity and lignin-degrading capacity compared to the parental strain 20b grown on beech wood sawdust (BWS) medium. Real-time PCR revealed that vp2 transcript levels were significantly lower in hap2 deletants than in 20b grown when cultured on the three solid media consisting of BWS, holocellulose, or Avicel, but not on yeast-malt-glucose (YMG) agar plates. Additionally, glutathione S-transferase (GST) pulldown and electrophoretic mobility shift assays demonstrated that recombinant P. ostreatus Hap2, Hap3, and Hap5 expressed in Escherichia coli form a complex capable of binding to the CCAAT sequence 5'-upstream of vp2 in vitro. These results suggest that Hap2, as part of the CCAAT-binding complex, is essential for transcriptional upregulation of vp2 in P. ostreatus growing on lignocellulosic substrates. KEY POINTS: • P. ostreatus hap2 deletants were generated. • Lignin-degrading capacity was significantly reduced in the hap2 deletants. • vp2 was significantly downregulated upon hap2 deletion.

Protective role of short-chain fatty acids on intestinal oxidative stress induced by TNF-α.

Inflammatory bowel diseases (IBD) are driven by an exaggerated inflammatory response, which leads to a marked increase in oxidative stress. This, in turn, exacerbates the inflammatory process and causes significant cellular and tissue damage. Intestinal dysbiosis, a common observation in IBD patients, alters the production of bacterial metabolites, including short-chain fatty acids (SCFAs), which are key by-products of dietary fiber fermentation. While the role of SCFAs in intestinal physiology is still being elucidated, this study aimed to investigate their effects on intestinal oxidative stress, particularly under inflammatory conditions induced by the proinflammatory mediator tumour necrosis factor alpha (TNF-α). The Caco-2/TC7 cell line was employed as an in vitro model of the intestinal epithelium, and the cells were treated with a range of SCFAs, including acetate, propionate, and butyrate. The levels of protein and lipid oxidation were quantified, as well as the activity of antioxidant enzymes. Our findings demonstrate that microbiota-derived SCFAs can effectively mitigate TNF-α-induced oxidative stress by modulating antioxidant enzyme activity. The proinflammatory mediator TNF-α induces lipid peroxidation by inhibiting catalase and glutathione peroxidase activities. SCFAs are able to upregulate antioxidant enzyme activity to restore lipid oxidative levels. These results underscore the critical role of the gut microbiota in maintaining intestinal homeostasis and highlight the therapeutic potential of SCFAs in managing oxidative stress-related pathologies.

Physiological changes in shrub species due to different sources of dust pollution in an urban environment.

Plants effectively filter ambient air by adsorbing particulate matter. The correct selection of landscape plants can exert greater dust retention benefits in different polluted areas. However, few studies have focused on the dust retention ability and related physiological responses of plants under continuous dust pollution from different dust sources. Here, we assessed the particle retention dynamics and plant physiology (chlorophyll content, soluble protein content, soluble sugar content, and peroxidase activity) of six shrubs (Berberis thunbergii var. atropurpurea, Ligustrum vicaryi, Rosa multiflora, Sorbaria sorbifolia, Swida alba, and Syzyga oblata) under continuous dust pollution from different dust sources (industrial sources: area below the direction of the coal-fired thermal power plant in Chengyang District, Qingdao, China; traffic sources: both sides of the road in each direction at the intersection of Great Wall Road and Zhengyang Road, Chengyang District, Qingdao, China; clean sources: Qingdao Agricultural University Campus, Qingdao Olympic Sculpture Park). The results showed that R. multiflora had the highest dust retention per unit leaf area of 3.27 ± 0.018g·m-2 and 2.886 ± 0.02g·m-2 in the experimental treatments of fuel source dust and clean source dust, respectively. The chlorophyll content of the tested shrubs significantly decreased due to the influence of dust treatment time, the range of cellular osmoregulatory substances (soluble sugars, soluble proteins, proline) tended to first increase and then decrease, and the antioxidant enzyme activities (superoxide dismutase, peroxidase) tended to increase and then decrease after continuous dust treatment. The greatest physiological changes were observed in plants within the industrial dust treatment area. The peroxidase activity and chlorophyll could be used as sensitive indicators of dust pollution in plants. R. multiflora showed better resistance to dust and had a greater dust retention capacity than other shrubs, making it more suitable for planting as a greening tree in industrial and traffic-polluted areas. S. alba and S. sorbifolia are sensitive to dust pollution, so they can be used as sensitive tree species to indicate atmospheric dust pollution. Our results may help design a feasible approach for urban shrub greening.

Fungi Preference of Fungivorous Nematode Aphelenchus avenae (Aphelenchida: Aphelenchidae) and Its Impact on Strawberry (Fragaria ananassa Duch.) Root

In continuously cropped strawberry soil, a large population of the fungivorous nematode, Aphelenchus avenae, was observed to increase significantly over time. This nematode, which feeds on pathogenic fungi affecting strawberries, has significant potential as a biocontrol agent. The purpose of this article is to discuss the nematode’s preference for fungi associated with strawberries and its impact on the growth of strawberry roots. With the exception of Trichoderma harzianum, most of the pathogenic fungi commonly found in strawberry soil, such as Fusarium oxysporum, Rhizoctonia solani, Verticillium, Phytophthora infestans, and Botrytis cinerea Pers. attracted A. avenae and supported their propagation. All treatments with A. avenae and the non-nematode control showed a consistent trend throughout strawberry development, indicating that a moderate amount of A. avenae does not adversely affect strawberry roots. Moderate and low levels of A. avenae significantly increased the activity of antioxidant enzymes, superoxide dismutase (SOD), and peroxidase (POD) in strawberry roots in all treatments during the entire growth stages. Also, the malondialdehyde (MDA) content of strawberry roots in all nematode treatments was lower than that in the no-nematode control. Despite an overabundance of A. avenae, which negatively affected the redox system balance of strawberry roots, A. avenae can protect the roots from pathogenic fungi by preventing infection and damage. These results lay the foundation for the potential use of A. avenae as a biological agent to control these pathogenic fungi in strawberry soil, in combination with the biological fungi (T. harzianum).

Response of various cultivars of Egyptian wheat (Triticum aestivum L.) to infection by Stemphylium vesicarium

AbstractA new fungal disease affecting wheat in Egypt, known as Stemphylium leaf spot, caused by Stemphylium vesicarium Wallr (Simmons) is reported. From all symptomatic wheat leaves, S. vesicarium was the most frequently isolated fungus (71.9%). The isolated pathogen was identified based on morphological characteristics together with molecular diagnosis. The Stemphylium isolate AUMC 15115 in this study was clustered at the same branch as Stemphylium mali CBS 122640, ex-type material (Synonym = Stemphylium vesicarium). At the Smart Agriculture Clinic Project, Sids Agricultural Research Station, Agricultural Research Centre, Beni Suef governorate, 12 cultivars of wheat were assessed in pot experiments for their resistance to Stemphylium leaf spot during the 2020 and 2021 growing seasons. Overall, distinct variations were observed in all examined cultivars in response to S. vesicarium infection. The Sakha 95 cultivar exhibited a minimal infection rate (disease incidence was 6.7, 3.3% and disease severity being, 0.7, 0.5%, respectively in the two growing seasons) and was classified as resistant. In contrast, Beni Suef 5 had the highest percent of infection (63.3, 66.7%), disease severity (38.5, 40.3%) and was classified as susceptible. In resistant cultivars, there was an increase in total phenol content, polyphenol oxidase (PPO), peroxidase (POD), and superoxide dismutase (SOD) activities. Conversely, there was a reduction in electrolyte leakage percentage and hydrogen peroxide (H2O2) accumulation. However, the number of protein bands in resistant wheat cultivars exhibited a more significant increase than susceptible ones, particularly in the Sakha 95, which displayed the highest number of proteins.