High Activity Research Articles

Conversion of Isopropanol to Diisopropyl Ether over Cobalt Phosphate Modified Natural Zeolite Catalyst

This study aims to produce diisopropyl ether (DIPE) via isopropanol dehydration using cobalt-phosphate-supported natural zeolite catalysts. The catalytic activities of the zeolite/CoO and zeolite/Co(H2PO4)2 were compared. The as-prepared catalysts were assessed using X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared (FTIR) spectroscopy, and N2 adsorption-desorption. Surface acidity was determined using the gravimetric method with pyridine as the probe. The results of this study showed that natural zeolite was favorably impregnated by CoO and Co(H2PO4)2 species. The impregnation process affected the textural and acidic features of the catalysts. The zeolite/Co(H2PO4)2 catalyst with a loading of 8 mEq.g-1 exhibited the highest surface acidity of 1.827 mmol.g-1. This catalyst also promoted the highest catalytic activity towards isopropanol dehydration, with an isopropanol conversion of 66.19%, DIPE selectivity, and yield of 46.72% and 34.99%, respectively. The cobalt phosphate species promoted higher catalytic activity for isopropanol dehydration than the CoO species. This study demonstrated the potential of cobalt phosphate-supported natural zeolite catalysts for DIPE production with adequate performance. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Recombinant expression and characterization of the endochitinase Chit36-TA from Trichoderma asperellum in Komagataella phaffii for chitin degradation of black soldier fly exuviae.

The natural polymer chitin is an abundant source for valuableN-acetylchitooligosaccharides and N-acetylglucosamine applicable in several industries. The endochitinase Chit36-TA from Trichoderma asperellum was recombinantly expressed in Komagataella phaffii for the enzymatic degradation of chitin from unused insect exuviae into N-acetylchitooligosaccharides. Chit36-TA was purified by Ni-NTA affinity chromatography and subsequently biochemically characterized. After deglycosylation, the endochitinase had a molecular weight of 36kDa. The optimum pH for Chit36-TA was 4.5. The temperature maximum of Chit36-TA was determined to be 50°C, while it maintained > 93% activity up to 60°C. The chitinase was thermostable up to 45°C and exhibited ~ 50% activity after a 15min incubation at 57°C. Chit36-TA had a maximum specific enzyme activity of 50 nkat/mg with a Km value of 289µM with 4-methylumbelliferyl-N,N',N″-triacetyl-β-chitotrioside as substrate. Most tested cations, organic solvents and reagents were well-tolerated by the endochitinase, except for SDS (1mM), Cu2+ (10mM) and Mn2+ (10mM), which had stronger inhibitory effects with residual activities of 3, 41 and 28%, respectively. With a degree of hydrolysis of 32% applying colloidal shrimp chitin (1% (w/v)) and 12% on insect larvae (1% (w/v)) after 24h, the endochitinase was found to be suitable for the conversion of colloidal chitin as well as chitin from black soldier fly larvae into water-soluble N-acetylchitooligosaccharides. To prove scalability, a bioreactor process was developed in which a 55-fold higher enzyme activity of 49µkat/l and a tenfold higher protein expression of 1258mg/l were achieved.

Novel Insight into the Synergistic Mechanism for Pd and Rh Promoting the Hydro-Defluorination of 4-Fluorophenol over Bimetallic Rh-Pd/C Catalysts.

This study explores the synergistic effect between the Rh and Pd of bimetallic Rh-Pd/C catalysts for the catalytic hydro-defluorination (HDF) of 4-fluorophenol (4-FP). It was found that 4-FP could not be efficiently hydro-defluorinated over 6% Pd/C and 6% Rh/C due to the inherent properties of Pd and Rh species in the dissociation of H2 and the activation of C-F bonds. Compared with 6% Pd/C and 6% Rh/C, bimetallic Rh-Pd/C catalysts, especially 1% Rh-5% Pd/C, exhibited much higher catalytic activity in the HDF of 4-FP, suggesting that the synergistic effect between the Rh and Pd of the catalyst was much more positive. Catalyst characterizations (BET, XRD, TEM, and XPS) were introduced to clarify the mechanism for the synergistic effect between the Rh and Pd of the catalyst in the HDF reaction and revealed that it was mainly attributed to the bifunctional mechanism: Pd species were favorable for the dissociation of H2, and Rh species were beneficial to the activation of C-F bonds in the HDF reaction. Meanwhile, the interaction between Rh and Pd species enabled Rh and Pd to exhibit a more positive synergistic effect, which promoted the migration of atomic H* from Pd to Rh species and thus enhanced the HDF of 4-FP. Furthermore, 1% Rh-5% Pd/C prepared using 20-40 equiv NaBH4 exhibited the best performance in the catalytic HDF of 4-FP. Catalysis characterizations suggested that appropriate Rh3+/Rh0 and Pd2+/Pd0 ratios were beneficial to the dissociation of H2 and the activation of C-F bonds, which caused the more positive synergistic effect between the Rh and Pd of Rh-Pd/C in the HDF reaction. This work offers a valuable strategy for enhancing the performance of catalytic HDF catalysts via promoting synergistic effects.

Investigating the treatment shortening potential of a combination of bedaquiline, delamanid and moxifloxacin with and without sutezolid, in a murine tuberculosis model with confirmed drug exposures.

New and shorter regimens against multi-drug resistant tuberculosis (TB) remain urgently needed. To inform treatment duration in clinical trials, this study aimed to identify human pharmacokinetic equivalent doses, antimycobacterial and sterilizing activity of a novel regimen, containing bedaquiline, delamanid, moxifloxacin and sutezolid (BDMU), in the standard mouse model (BALB/c) of Mycobacterium tuberculosis (Mtb) infection. Treatment of mice with B25D0.6M200U200, B25D0.6M200, B25D0.6M200(U2003) or H10R10Z150E100 (isoniazid, rifampicin, pyrazinamide, ethambutol, HRZE), started 3 weeks after Mtb infection. Bactericidal activity was assessed after 1, 2, 3 and 4 months of treatment and relapse rates were assessed 3 months after completing treatment durations of 2, 3 and 4 months. B25D0.6M200U200 generated human equivalent exposures in uninfected BALB/c mice. After 1 month of treatment, a higher bactericidal activity was observed for the B25D0.6M200U200 and the B25D0.6M200 regimen compared to the standard H10R10Z150E100 regimen. Furthermore, 3 months of therapy with both BDM-based regimens resulted in negative lung cultures, whereas all H10R10Z150E100 treated mice were still culture positive. After 3 months of therapy 7% and 13% of mice relapsed receiving B25D0.6M200U200 and B25D0.6M200, respectively, compared to 40% for H10R10Z150E100 treatment showing an increased sterilizing activity of both BDM-based regimens. BDM-based regimens, with and without sutezolid, have a higher efficacy than the HRZE regimen in the BALB/c model of TB, with some improvement by adding sutezolid. By translating these results to TB patients, this novel BDMU regimen should be able to reduce treatment duration by 25% compared to HRZE therapy.

Increased nitrogen accumulation in mulberry trees due to the secretion of glomalin-related soil protein induced by arbuscular mycorrhizal fungi

In the initial stages of restoring areas affected by rocky desertification, plant survival is strongly influenced by nitrogen nutrition. Mycorrhization is a unique type of inter-root engineering that improves nitrogen acquisition efficiency by plant roots. We selected potted mulberry trees inoculated, two dominant arbuscular mycorrhizal fungi (AMF) with Funneliformis mosseae (Fm) and Rhizophagus intraradices (Ri), to clarify the effects of AMF on the root nitrogen content of mulberry trees. Meanwhile, the key factors of soil nitrogen changes caused by AMF were analyzed, based on the primary role of soil nitrogen as the source of root nitrogen. Simultaneously, the potential of AMF to promote the acquisition of different forms of nitrogen by mulberry roots was investigated. Our findings indicate that the inoculation of mulberry plants with Fm and Ri, improved plant height and increased nitrogen accumulation in the roots and shoots. Additionally, AMF regulates nitrogen transformation, significantly increasing soil nitrate nitrogen (NO3−-N) and dissolved organic nitrogen (DON) levels. The results indicated that soil NH4+-N, NO3−-N, and DON contributed to the observed changes in root nitrogen accumulation. The largest contribution (22.0 %) to the overall effect size was made by NO3−-N. AMF stimulated soil microbial activity and significantly increased soil glomalin-related soil protein (GRSP), enzyme activity, and soil microbial biomass (SMB). Urease activity and microbial biomass carbon (MBC) both increased exponentially by 118.7 % and 115.2 %, respectively. Higher GRSP, enzyme activity, and SMB were positively correlated with changes in soil nitrogen patterns, and GRSP had the most significant effect on changes in the soil nitrogen dynamics. Our study confirmed that inoculation with AMF not only regulates soil nitrogen dynamics but also diversifies plant nitrogen sources. This is achieved by increasing plant growth and enhancing soil microbial activity. Ultimately, this enhances plant root nitrogen nutrition. Therefore, AMF promote root nitrogen accumulation and enhance root nitrogen uptake through GRSP-regulated soil nitrogen, providing a theoretical basis for the management of rocky desertification.

Production of antioxidant hydrolysates from bovine caseinate and soy protein using three non-commercial bacterial proteases

The release of bioactive peptides from proteins can be achieved by enzymatic hydrolysis, whereby mainly commercial enzymes are applied, although increasing attention is focused on alternative proteases. Hence, crude proteases from Bacillus sp. CL14, CL18, and CL33A were investigated to obtain antioxidant hydrolysates from bovine sodium caseinate (NaCAS) and soy protein isolate (SPI). The proteases were able to hydrolyze both substrates. Hydrolysis improved the radical-scavenging, Fe2+-chelating, and reducing power abilities of NaCAS and SPI. Higher antioxidant activities were commonly achieved at 2–3 h of hydrolysis. Overall antioxidant activities were higher for NaCAS hydrolysates produced with CL14 > CL18 > CL33 protease, and for SPI hydrolysates obtained with CL14 > CL33A ∼ CL18 protease. Generation of antioxidant protein hydrolysates suggest applications of enzymes and hydrolysates in food/feed (bio)technology.

Coupled Ni─Co Dual-Atom Catalyst for Guiding Sulfur and Lithium Evolutions in Lithium-Sulfur Batteries.

The kinetically retarded sulfur evolution reactions and notorious lithium dendrites as the major obstacles hamper the practical implementation of lithium-sulfur batteries (LSBs). Dual metal atom catalysts as a new model are expected to show higher activity by their rational coupling. Herein, the dual-atom catalyst with coupled Ni─Co atom pairs (Ni/Co-DAC) is designed successfully by programmed approaches. The Ni─Co atom pairs alter the local electron structure and optimize the coordination configuration of Ni/Co-DAC, leading to the coupling effect for promoting the interconversion of sulfur and guiding lithium plating/striping. The LSB delivers a remarkable capacity of 818mA h g-1 at 3.0 C and a low degeneration rate of 0.053% per cycle over 500 cycles. Moreover, the LSB with a high sulfur mass loading of 6.1mg cm-2 and lean electrolyte dosage of 6.0µL mgS -1 shows a remarkable areal capacity of 5.7mA h cm-2.

Isolation, Identification, and Characterization of L-asparaginase-Producing Human Commensal Bacterial Strains: A Promising Next-Gen Probiotics.

L-asparaginase is an FDA-approved drug for treating blood cancer, but its inherent antigenicity and L-glutaminase activity are associated with hypersensitivity and organ toxicity. Extracellularly produced glutaminase-free L-asparaginase from human commensal bacteria may be a good alternative to reduce the side effects of therapeutic L-asparaginase. Here, we report the isolation and characterization of fourteen L-asparaginase-producing bacterial strains belonging to the genera Acinetobacter, Escherichia, Klebsiella, and Pseudomonas from human stool and saliva samples. To the best of our knowledge, this is the first report of L-asparaginase-producing human commensal bacterial strains isolated from healthy individuals. L-asparaginase produced by fecal and salivary isolates exhibited significantly higher activity (3.64 to 16.96 U/ml) toward L-asparagine than L-glutamine. Interestingly, L-asparaginase from fecal isolates, Escherichia coli strains 3F1 and 3F2 and salivary isolate Klebsiella pneumoniae 3S3, exhibited no L-glutaminase activity. These isolates were also sensitive to all tested antibiotics. Additionally, these three isolates demonstrated tolerance to pH 3.0 (≥ 88% survival) and 0.3% bile (≥ 95% survival), indicating their potential as probiotics. Among these isolates, L-asparaginase from the highest-producing K. pneumoniae 3S3 strain was found to be a homodimer, with native and subunit molecular weights of 110kDa and 55kDa, respectively. The purified enzyme can be further explored for its antitumor and immunomodulatory properties. Overall, future research can be expanded to include the use of a pool of human commensal bacteria as genuine and alternative sources of L-asparaginase for effective cancer treatments and cutting-edge next-generation probiotics.

In Vitro Antiprotozoal Activity of Schinus molle Extract, Partitions, and Fractions against Trypanosoma cruzi

Chagas disease, caused by the protozoan Trypanosoma cruzi, represents an important and worldwide public health issue, particularly in Latin America. Limitations of conventional treatment with benznidazole and nifurtimox underscore the urgent need for new therapeutic strategies for this disease. Schinus molle, a tree used in traditional medicine for various ailments, has demonstrated promising antiparasitic activity. The in vitro anti-T. cruzi activity of Schinus molle crude methanol extract, partitions, and fractions, as well as their cytotoxicity in Vero cells and Artemia salina, and hemolytic activity in human erythrocytes were assessed. Most of the extracts possessed anti-T. cruzi effects, with Sm-CF3 being the fraction with the highest activity (IC50 = 19 µg/mL; SI = 6.8). Gas chromatography–mass spectrometry analysis identified 20 compounds, with fatty acyls comprising the predominant chemical class (55%). We also identified the antiparasitic compounds cis-5,8,11,14,17-eicosapentaenoic acid and trans-Z-α-bisabolene epoxide, suggesting their potential contribution to the observed anti-T. cruzi activity. In conclusion, our findings support the therapeutic potential of S. molle as a source of novel antiparasitic agents against T. cruzi.

Interfacial Enrichment of Lauric Acid Assisted by Long-Chain Fatty Acids, Acidity and Salinity at Sea Spray Aerosol Surfaces.

Surfactant monolayers at sea spray aerosol (SSA) surfaces regulate various atmospheric processes including gas transfer, cloud interactions, and radiative properties. Most experimental studies of SSA employ a simplified surfactant mixture of long-chain fatty acids (LCFAs) as a proxy for the sea surface microlayer or SSA surface. However, medium-chain fatty acids (MCFAs) make up nearly 30% of the FA fraction in nascent SSA. Given that LCFA monolayers are easily disrupted upon the introduction of chemical heterogeneity (such as mixed chain lengths), simple FA proxies are unlikely to represent realistic SSA interfaces. Integrating experimental and computational techniques, we characterize the impact that partially soluble MCFAs have on the properties of atmospherically relevant LCFA mixtures. We explore the extent to which the MCFA lauric acid (LA) is surface stabilized by varying acidity, salinity, and monolayer composition. We also discuss the impacts of pH on LCFA-assisted LA retention, where the presence of LCFAs may shift the surface-adsorption equilibria of laurate─the conjugate base─toward higher surface activities. Molecular dynamic simulations suggest a mechanism for the enhanced surface retention of laurate. We conclude that increased FA heterogeneity at SSA surfaces promotes surface activity of soluble FA species, altering monolayer phase behavior and impacting climate-relevant atmospheric processes.

Comparative Study on Silver Nanoparticle Synthesis Using Male and Female Pistacia Khinjuk Leaf Extracts: Enhanced Efficacy of Female Leaf Extracts

AbstractThis study aims to uncover the potential differences in bioactive compounds present in leaf extracts obtained from female and male individuals of Pistacia khinjuk, abundantly found in the Southeast Anatolia region of Turkey, and their roles in influencing the properties of synthesized silver nanoparticles (AgNPs). Results obtained through TEM and SEM imaging techniques determined the morphology and size of AgNPs synthesized from female (FL‐AgNPs) and male (ML‐AgNPs) leaf extracts. Additionally, FTIR spectrum analysis demonstrated the chemical composition of the FL‐AgNPs, ML‐AgNPs, and the extracts. Zeta potential and zeta sizer analyses revealed differences between nanoparticles obtained from female and male plants. The total phenolic content of leaf extracts from female plants is significantly higher than that obtained from male plants (female plants: 30.68±0.26 mg GAE/g, male plants: 24.22±0.37 mg GAE/g). Furthermore, FL‐AgNPs (43.2±2.64 mg GAE/g) exhibit higher antioxidant activity compared to ML‐AgNPs (31.7±1.16 mg GAE/g). ICP‐MS analyses indicate that FL‐AgNPs are synthesized with higher efficiency compared to ML‐AgNPs (FL‐AgNPs: 99.90±0.106 %, ML‐AgNPs: 94.99±0.079 %). Finally, the antibacterial efficacy of FL‐AgNPs and ML‐AgNPs nanoparticles was evaluated agar well diffusion method against the pathogen Escherichia coli (E.Coli) and Staphylococcus aureus (S. Aureus]

Effective Immobilization of Novel Antimicrobial Peptides via Conjugation onto Activated Silicon Catheter Surfaces

Antibiotic-resistant microorganisms have become a serious threat to public health, resulting in hospital infections, the majority of which are caused by commonly used urinary tract catheters. Strategies for preventing bacterial adhesion to the catheters’ surfaces have been potentially shown as effective methods, such as coating thesurface with antimicrobial biomolecules. Here, novel antimicrobial peptides (AMPs) were designed as potential biomolecules to prevent antibiotic-resistant bacteria from binding to catheter surfaces. Thiolated AMPs were synthesized using solid-phase peptide synthesis (SPPS), and prep-HPLC was used to obtain AMPs with purity greater than 90%. On the other side, the silicone catheter surface was activated by UV/ozone treatment, followed by functionalization with allyl moieties for conjugation to the free thiol group of cystein in AMPs using thiol-ene click chemistry. Peptide-immobilized surfaces were found to become more resistant to bacterial adhesion while remaining biocompatible with mammalian cells. The presence and site of conjugation of peptide molecules were investigated by immobilizing them to catheter surfaces from both ends (C-Pep and Pep-C). It was clearly demonstrated that AMPs conjugated to the surface via theirN terminus have a higher antimicrobial activity. This strategy stands out for its effective conjugation of AMPs to silicone-based implant surfaces for the elimination of bacterial infections.

Dietary habits in Italian children with inflammatory bowel disease: A case-control multicenter study.

Patients with inflammatory bowel disease (IBD) tend to self-modify their dietary habits according to disease activity and symptoms. This study aimed to assess the adequacy of the usual diet in Italian children with IBD in comparison to a control group and to the recommended dietary allowances (RDA). Dietary habits of IBD children and age- and gender-matched healthy controls were investigated using a validated Food Frequency Questionnaire in five Italian pediatric IBD centers. Adherence to the Mediterranean diet (MD) was assessed using the KID-MED test. Energy (EI), macro, and micronutrients intakes were compared between the two groups, to the RDA and the predicted total energy expenditure (EI/total energy expenditure [TEE]%). IBD subjects (n = 110) reported a lower EI, EI/RDA%, and EI/TEE% compared to controls (n = 110) (p = 0.012, p < 0.0002, and p = 0.014), lower total protein and fat intakes (p = 0.017, p < 0.0001) and lower minerals/RDA, vitamins/RDA and micronutrients/RDA ratio (%). Poor adherence to the MD was more frequent in IBD children compared to controls (p = 0.013). The total EI and carbohydrate intake were inversely correlated with higher disease activity. Italian children with IBD report an inadequate diet in terms of energy, macro, and micronutrients and have a low adherence to a high-quality MD pattern.

Evaluation of In Vitro Antihypertensive and Anti-Inflammatory Properties of Dairy By-Products

Sweet whey (SW) and yogurt acid whey (YAW) are dairy by-products of the cheese-making process and Greek-style yogurt production, respectively. Both of them are considered pollutants with huge volumes of SW and YAW produced due to the growing demand for dairy products worldwide. Moreover, whey-derived peptides, resulting from fermentation as well as from further hydrolysis during digestion, have been associated with various biological activities. In the present study, the angiotensin-converting enzyme (ACE)-inhibitory activity of 48 SW samples and 33 YAW samples from bovine, ovine, caprine, and ovine/caprine milk obtained were evaluated. Additionally, the SW and YAW digestates and two of their fractions (smaller than 10 kDa, SW-D-P10 and YAW-D-P10, and smaller than 3 kDa, SW-D-P3 and YAW-D-P3), which were obtained after in vitro digestion and subsequent ultrafiltration, were also subjected to evaluation. Our data indicated that the D-P10 and D-P3 fractions exhibited higher ACE-inhibitory activity compared to the corresponding values before digestion. The ACE-inhibitory capacity after in vitro digestion was higher for the ovine SW samples compared to their bovine and caprine counterparts. The effect of the D-P3 fraction on the inhibition of nitric oxide (NO) production and the expression of a selected panel of immune-response-related genes in LPS-stimulated RAW 264.7 macrophages was also evaluated. Fractions from both dairy by-products inhibited NO production in LPS-stimulated RAW 264.7 cells. Especially, ovine SW-D-P3 showed a strong NO inhibitory activity and suppressed inducible nitric oxide synthase (Nos2) mRNA levels. However, YAW-D-P3 could not trigger neither the gene expression of inflammatory macrophage mediators Nos2 and cyclooxygenase-2 (Ptgs2) nor tumor necrosis factor-α (Tnf) and interleukin 6 (Il6) in LPS-stimulated murine macrophages regardless of animal origin. These findings suggest that in vitro digestion could enhance the production of ACE-inhibitory peptides in both dairy by-products, while SW from ovine origin displays higher potential as an anti-inflammatory agent, effectively preventing excessive NO production.

Genetic Variation Affects the Anti-Melanogenic Efficacy of Platycodon grandiflorus Flowers

This study investigated the utilization of by-products from Platycodon grandiflorus and the role of genetic diversity in their anti-melanogenic properties, focusing on the purple-flower (PF) and white-flower (WF) varieties. Our results show that the WF variety exhibited significantly higher anti-melanogenic activity, attributed to higher concentrations of key saponins such as platycodin D3 and platycodin D. These saponins demonstrated strong tyrosinase inhibitory effects as confirmed by molecular docking analysis. Further, the WF variety showed increased expression of genes involved in saponin biosynthesis, highlighting the role of genetic diversity in determining phytochemical composition and pharmacological efficacy. The superior anti-melanogenic activity of WF suggests its potential as a valuable ingredient in the cosmetic industry for skin-whitening products. Our findings emphasize the importance of utilizing by-products and selecting specific genotypes to enhance the quality and efficacy of plant-derived products. Future research should explore the full spectrum of bioactive compounds in P. grandiflorus, investigate sustainable extraction methods, and conduct clinical trials to validate the safety and effectiveness of these compounds in cosmetic and therapeutic applications.

P-CNN: Percept-CNN for semantic segmentation

ABSTRACT The task of image segmentation remains a fundamental challenge, in the field of computer vision. Convolutional Neural Networks (CNNs) have achieved significant success in this field, yet there are some limitations in the conventional approach. The process of accurate, pixel-wise image annotation is time-consuming, as well as requires more human effort. These problems are addressed by the proposed method called as Percept-CNN (P-CNN), which extracts the power of percepts, pixels responsible for the higher activations at each level. From each layer, percepts are extracted during the forward propagation. These percepts are then passed onto the subsequent layers, enabling the model to focus only on the useful visual information. The proposed method with Percept Convolution can potentially eliminate the complex and time-consuming task of image annotation without affecting the segmentation accuracy. Since the model focuses only on the useful salient visual information, it tends to reduce the extraction of the redundant features, which doesn’t really contribute towards the final goal. This makes the model to be more robust, accurate and efficient. The proposed model was able to perform semantic segmentation without pixelwise annotations with an accuracy of 67% when tested on Oxford IIIT pet dataset.

Development of Dual Cooperative Multi‐Urea Catalysts for Henry Reaction

AbstractA dual cooperative multi‐urea catalyst for Henry reaction was developed in which four urea groups were introduced into a rigid and rotatable framework. The tetraurea catalyst 1 showed higher activity for Henry reaction than its analogues, close‐bisurea 2 or distal‐bisurea 3 with two urea units, demonstrating additional cooperativity between the two substrate‐pinching catalytic sites of tetraurea 1. Addition of the reaction product to the reaction system resulted in a small amount of further activation. This work would provide a basis for new cooperative molecular catalysts, leading to a high degree of regulation based on allosteric cooperativity, e.g. with a distinct ON/OFF threshold for reactivity, or feedback activation by using the product as a reaction template.

Exploring microbial dynamics in a reactive magnetised Casson-Maxwell-Oldroyd-B nanofluid on a slanted elongated cylinder: entropy assessment

Biological fluids often have complex properties due to the presence of tiny particles, cells, microbes, or large molecules. The Casson-Maxwell-Oldroyd-B (CMO) fluid model is a key tool for understanding the effects of non-Newtonian behaviour in biological processes like microbe movement, blood flow, and mucus transport. This research focuses on how microbes move in a reactive magnetised CMO nanofluid on a slanted elongated cylinder, considering entropy generation effects. It explores how factors like Arrhenius activation energy and specific boundary conditions influence this process. The CMO model helps clarify how non-Newtonian nanofluids behave in microbial migration. The study converts the model equations to a dimensionless form using similarity methods. The results are calculated using a combination of a shooting method and a fourth-order Runge-Kutta scheme in MATLAB, and presented in graphs and tables. The results show the impact of various factors: Lorentz force and porosity slow down the fluid, while higher temperatures speed it up. Higher activation energy increases concentration. The Casson-Oldroyd-B (CO) nanofluid has a lower Nusselt number than the Casson-Maxwell (CM) nanofluid. The presence and movement of microorganisms greatly affect entropy generation. This research is valuable for understanding biological fluids, which is essential in medical research, diagnostics, and the development of healthcare products.

Promotion of CO2 Electroreduction on Bismuth Nanosheets with Cerium Oxide nanoparticles.

Formic acid (HCOOH) is a highly energy efficient product of the electrochemical CO2 reduction reaction (CO2RR). Bismuth-based catalysts have shown promise in the conversion of CO2 to formic acid, but there is still a great need for further improvement in selectivity and activity. Herein, we report the preparation of Bi nanosheets decorated by cerium oxide nanoparticles (CeOx) with high Ce3+/Ce4+ ratio and rich oxygen vacancies. The CeOx nanoparticles affect the electronic structures of bismuth, enhance CO2 adsorption, and thus promote the CO2RR properties of Bi nanosheets. Compared with elemental Bi nanosheets, the hetero-structured CeOx/Bi nanosheets exhibit much higher activity over a wide potential window, showing a current density of 16.1 mA cm-2 with a Faradaic efficiency of 91.1% at -0.9 V vs. reversible hydrogen electrode.

Repurposing NAMPT inhibitors for germinal center B-cell-like diffuse large B-cell lymphoma.

Diffuse Large B-cell lymphoma (DLBCL) includes the Activated B-cell-like (ABC) and Germinal Center B-cell-like (GCB) subtypes, which differ in cell-of-origin, genetics and clinical response. By screening the subtype-specific activity of 211 drugs approved or in active clinical development for other diseases, we identified inhibitors of nicotinamide phosphoribosyl transferase (NAMPTi) as active in a subset of GCB-DLBCLs in vitro and in vivo. We validated three chemically distinct NAMPTi for their on-target activity based on biochemical and genetic rescue approaches, and found the ratio between NAMPT:PARP1 RNA levels was predictive of NAMPTi sensitivity across DLBCL subtypes. Notably, the NAMPT:PARP1 transcript ratio predicts higher anti-tumor activity in BCL2-translocated GCB-DLBCL. Accordingly, pharmacological and genetic inhibition of BCL2 was potently synergistic with NAMPT blockade. These data support the inhibition of NAMPT as a therapeutically relevant strategy for BCL2-translocated DLBCLs.