Degradation Rate Research Articles

Enhanced antibiotic degradation using rGO composites under visible light photocatalysis

A robust reduced graphene oxide (rGO), polyaniline (PANI) with calcium (Ca) and magnesium (Mg) bimetallic nanocomposite was successfully prepared using an in-situ chemical facial reducing method and named rGO@PANI-Ca:Mg. Various spectroscopic techniques, including XRD, SEM, TEM, XPS, and supplementary methods, were utilized to characterize the catalyst phase, microstructure, and optical attributes. The composite's photocatalytic efficiency was assessed by degrading antibiotics such as ciprofloxacin (CP) and tetracycline (TC) using calcium peroxide (CaO2) under visible light irradiation. The rGO@PANI-Ca:Mg composite demonstrates superior degradation efficiency for CP, 45 %, and for TC, 70 %, achieving a correlation coefficient R² of 0.94 and 0.991 respectively. This performance surpasses that of pristine GO, rGO, and rGO@PANI. The heightened photocatalytic activity is ascribed to forming a heterojunction, effectively mitigating electron-hole pair recombination. The incorporation of CaO2 promotes the generation of additional active reactive oxygen species (ROS), particularly OH·, ·O2−, e-, h+, as verified by radical scavenging experiments, indicating an enhancement in the degradation and a potential mechanism is also suggested. The degradation rate of TC, CP, and real wastewater (RW) is about 71 %, 45 %, and 40.98 %, respectively. The composite demonstrates stability and reusability for up to three catalytic cycles. Our experiments also showed that when bacteria were treated with a 2 mg catalyst, the minimum inhibitory concentration (MIC) was determined to be at a 10−3 dilution. This MIC value represents the lowest concentration at which the catalyst effectively inhibited bacterial growth, as evidenced by clear inhibition zones.

Hygrothermal aging behavior of C/GFRP hybrid rod with bundle‐by‐bundle dispersion

AbstractFiber hybrid with bundle‐by‐bundle dispersion can achieve the high performance of composites, fully understand the hybrothermal resistance of hybrid composites is the key to prove the applications in engineering structures. In the present paper, the hygrothermal resistance performances of new type carbon and glass fiber reinforced epoxy based hybrid rod with bundle‐by‐bundle dispersion produced by pultrusion technology is investigated experimentally. The tests of water absorption and desorption, thermal and mechanical performances are performed to obtain the evolution rules of hygrothermal aging. As a result, the water absorption of hybrid rod confirms to the Fick's diffusion behavior, the serious relaxation of resin matrix and the interfacial debonding of fiber‐resin exposed at high temperature provide more diffusion space for water molecules. Long‐term hydrothermal aging results in the recoverable plasticization of resin matrix and irrecoverable interfacial debonding of fiber‐resin, which brings about the degradation of 6.7%–15.0% for short beam shear strength (SBSS) retention. In addition, the plasticization effect reduces the cross‐linking density of resin matrix, which leads to the degradation of 3.3%–15.6% for glass transition temperature (Tg) retention. The life prediction results show that degradation rate of SBSS is gradually slow down and reached to a stable retention of 85.5%.Highlights Relaxation of resin matrix and interfacial debonding accelerate the diffusion of water molecules. Plasticization and interfacial debonding lead to the degradation of short beam shear strength retention and glass transition temperature. Long‐term life prediction shows that short beam shear strength e retention is 85.5%.

3D-printed artificial cornea featuring aligned fibrous structure and enhanced mechanical strength

The global shortage of donor eye bank tissue has significantly impeded advancements in biomaterial for corneal implantation. To address this issue, we have developed a 3D-printed artificial cornea using a composite hydrogel of sodium alginate (SA) and cellulose nanofibers (CNF), crosslinked with poly-L-lysine-co-L-glutamic acid (PLL80GA20, PG) and calcium chloride (CaCl2, CC). The 2 wt% SA/CNF composite hydrogel offers several advantages, including low toxicity, cost-effectiveness, excellent printability, and high mechanical strength, even with low crosslinker concentrations. The PG was synthesized via ring-opening polymerization of L-glutamate N-carboxyl anhydride (BGNCA) and L-lysine N-carboxyl anhydride (CBZNCA). The purity of the monomers was verified through DSC analysis, revealing a melting point of 97 ℃. The molecular weight of the synthesized PG was determined to be 47 kDa. A dual crosslinking strategy was employed, starting with electrostatic crosslinking, followed by ionic crosslinking using varying concentrations of PG and CC at different effective charge concentrations of 6.25 mM, 12.25 mM, and 25 mM. The hydrogel and 3D-printed cornea were comprehensively evaluated for chemical structure, surface functional groups, water content, mechanical strength, orientation, cytotoxicity, biocompatibility, and transparency. Notably, the inclusion of PG significantly enhanced the mechanical properties of the 3D-printed cornea, with the hydrogel achieving a storage modulus of 2,360 kPa at 6.25 mM of PG/CC, while maintaining over 95% water content. The artificial cornea demonstrated 86% transparency, and the cell viability showed 96% viable on Day 7 with degradation rate of 35.9% in 28 days. The superior hydrophilicity, transparency, and mechanical strength of the printed hydrogel highlights its potential for the development of full-thickness corneal structures, making it a promising candidate for future corneal implants.

Spatiotemporal distribution of sedimentary chloropigments and organic carbon in a shelf sea ecosystem, with a focus on the cold water mass

The Yellow Sea is one of the most thoroughly studied shelf seas in the northwestern Pacific. However, many aspects of the northern Yellow Sea sediments remain poorly understood. Sedimentary chloropigments and total organic carbon (TOC) are crucial components that indicate benthic primary productivity and ecosystem functioning in the marginal sea system. The present study investigated the temporal and spatial variations of sediment chloroplastic pigments (Chl-a and Pha-a) and TOC contents in relation to seasons and the northern Yellow Sea Cold Water Mass (NYSCWM). Decadal trends were also examined using linear regression on time-series data from 12 cruises conducted over a nine-year period (2006–2014). The correlations between sedimentary Chorophy-a (Chl-a), Pheophorbide-a (Pha-a), TOC, and their ratios with other abiotic and biotic factors were analyzed to detect any effects of the NYSCWM on the spatiotemporal distribution of sediment Chl-a, Pha-a, TOC contents, as well as the ecological relevance of their ratios as indicators of food quality (freshness) in the benthic system. The NYSCWM substantially influences the spatial and seasonal distribution of sedimentary Chl-a, Pha-a, and TOC contents. High values of Pha-a, TOC, and the ratios of Pha-a/(Chl-a + Pha-a) and TOC/Chl-a were often observed in the central region of the NYSCWM, where Chl-a showed clear seasonal fluctuations while Pha-a and TOC remained relatively constant. While sedimentary TOC appears to negatively mirror the spatial pattern of primary productivity in the water column, the spatial pattern of sedimentary Chl-a in relation to NYSCWM is less evident. However, the contents of Pha-a and TOC in the central NYSCWM sediments were higher than those at surrounding NYSCWM stations. Surface sediment Pha-a/(Chl-a + Pha-a) ratio was negatively correlated with meiofauna abundance and biomass and positively correlated with nematode/copepod ratio. This finding indicates that the quality of sediment organic matter is important to meiofauna. Conversely, the lower organic degradation rate at the lower bottom temperature of the NYSCWM may explain the observed higher Pha-a and TOC contents in its central area. Time-series data collected over nine years at the NYSCWM stations showed a decreasing trend for Chl-a, while TOC and the ratio of Pha-a/(Chl-a + Pha-a) exhibited increasing tendencies. This trend may imply a reduced quality of food supply to the benthic food web in the shelf sea system, along with degraded ecosystem functioning and service under the impacts of global change and anthropogenic disturbances.

Synthesis and Evaluation of Starch-Grafted-Poly[(Acrylic Acid)-Co-Acrylamide] Based Nanoclay Polymer Composite Fertilizers for Slow Release of Nitrogen in Soil.

Nitrogen (N) losses from conventional N fertilizers contribute to environmental degradation and low N use efficiency. Highlighting the need for slow-release fertilizers (SRFs) to mitigate these problems, this study aims to develop slow-release N fertilizers using starch-grafted-poly[(acrylic acid)-co-acrylamide] based nanoclay polymer composites (NCPCs) and investigate their efficacy for slow N delivery in soil. Three types of NCPCs, NCPC(A) (poly [(acrylic acid)-co-acrylamide]), NCPC(W) (wheat starch-grafted-poly[(acrylic acid)-co-acrylamide), and NCPC(M) (maize starch-grafted-poly[(acrylic acid)-co-acrylamide) were prepared and characterized using FTIR spectroscopy and X-ray diffraction techniques. N-release behaviour of the products was assessed under two distinct soils, i.e., Assam (Typic Hapludults, pH 4.2) and Delhi (Typic Haplustepts, pH 7.9) soils. Additionally, the effects of varying soil moisture and temperature levels on N release were studied in the Assam soil. The N-release kinetics of the synthesized fertilizers were assessed using zero-order, first-order, Higuchi, and Korsmeyer-Peppas models. Degradability of the NCPCs was evaluated by measuring evolved CO2-C under various soil conditions as an indicator of microbial degradation. The results indicated that NCPC fertilizers significantly slowed down the release of N compared to urea. According to the R2 values obtained, it was evident that the first-order kinetic model most accurately describes the N release from both urea and NCPC-based N fertilizers in the studied soils. Among the formulations, NCPC(A) exhibited the lowest N release (42.94-53.76%), followed by NCPC(M) (51.05-61.70%), NCPC(W) (54.86-67.75%), and urea (74.33-84.27%) after 21 days of incubation. The rate of N release was lower in the Assam soil compared to the Delhi soil, with higher soil moisture and temperature levels accelerating the release. Starch addition improved the biodegradability of the NCPCs, with NCPC(W) showing the highest cumulative CO2-C evolution (18.18-22.62 mg g-1), followed by NCPC(M) (15.54-20.97 mg g-1) and NCPC(A) (10.89-19.53 mg g-1). In conclusion, NCPC-based slow-release fertilizers demonstrated a more gradual N release compared to conventional urea and the inclusion of starch enhanced their degradability in the soil, which confirms their potential for sustainable agricultural applications. However, soil properties and environmental factors influenced the N release and degradation rates of NCPCs.

Performance of Dye-Containing Wastewater Treatment Using MnxOy-Catalyzed Persulfate Oxidation

Dye wastewater is characterized by high salinity, intense coloration, difficulty in degradation, and complex organic compositions, posing significant environmental risks. Manganese oxide (MnxOy)-based materials have been widely used for the removal of recalcitrant organic pollutants in water environments. In this study, various MnxOy polymorphs were prepared, and their catalytic activities for persulfate (PS) activation were evaluated using Orange II (AO7) as a model molecule. After 50 min treatment, the degradation efficiency of AO7 ranked as α-MnO2/PS > γ-MnO2/PS > β-MnO2/PS > Mn2O3/PS, with α-MnO2/PS achieving the highest efficiency of 98.6%. XPS, XRD, and electrochemical analyses indicated that α-MnO2 exhibited an exceptional crystal structure and performance. The α-MnO2/PS system exhibited a strong pH adaptability across a wide pH range of 3.0–9.0. The presence of coexisting anions at 0.1 mM, including Cl−, NO3−, CO32−, and SO42−, slightly reduced the degradation rate of AO7. The reactive oxygen species, mainly SO4•− and 1O2, predominantly destroyed the naphthalene ring structure of AO7. Furthermore, α-MnO2 exhibited an excellent stability, allowing for multiple reuse cycles without interference from common anions in water, highlighting its strong potential for practical applications. These results provided insights into the environmental fates of AO7 in the α-MnO2/PS system.

Synergistic effects of bacteriophage cocktail and antibiotics combinations against extensively drug-resistant Acinetobacter baumannii

BackgroundThe extensively drug-resistant (XDR) strains of Acinetobacter baumannii have become a major cause of nosocomial infections, increasing morbidity and mortality worldwide. Many different treatments, including phage therapy, are attractive ways to overcome the challenges of antibiotic resistance.MethodsThis study investigates the biofilm formation ability of 30 XDR A. baumannii isolates and the efficacy of a cocktail of four tempetate bacteriophages (SA1, Eve, Ftm, and Gln) and different antibiotics (ampicillin/sulbactam, meropenem, and colistin) in inhibiting and degrading the biofilms of these strains.ResultsThe majority (83.3%) of the strains exhibited strong biofilm formation. The bacteriophage cocktail showed varying degrees of effectiveness against A. baumannii biofilms, with higher concentrations generally leading to more significant inhibition and degradation rates. The antibiotics-bacteriophage cocktail combinations also enhanced the inhibition and degradation of biofilms.ConclusionThe findings suggested that the bacteriophage cocktail is an effective tool in combating A. baumannii biofilms, with its efficacy depending on the concentration. Combining antibiotics with the bacteriophage cocktail improved the inhibition and removal of biofilms, indicating a promising strategy for managing A. baumannii infections. These results contribute to our understanding of biofilm dynamics and the potential of bacteriophage cocktails as a novel therapeutic approach to combat antibiotic-resistant bacteria.

Enhancing PET degradation efficiency through fusing carbohydrate-binding modules in LCC-ICCG

Polyethylene terephthalate (PET) is a largely-produced polymer worldwide. However, its extensive waste generation and resistance to degradation pose significant environmental concerns. Consequently, there is considerable interest in researching enzymatic degradation of PET. Relevant studies have shown that the addition of a carbohydrate binding module (CBM) can increase the affinity between the enzyme and the substrate, enhancing the enzyme's degradation ability. In order to develop more efficient PET hydrolytic enzymes, this study introduced carbohydrate binding domains (CBMs) from different families with different substrate affinities into the PET-degrading enzyme LCC-ICCG. High crystallinity PET powder and amorphous PET film were used as substrates to characterize the degradation efficiency of the modified enzymes, aiming to explore the enzyme with the optimal degradation ability. The results showed that the fusion of type B CBM reduced the degradation rate and Tm value of the enzyme towards PET, while the introduction of type A and type C CBMs significantly improved the degradation rate of the enzyme towards the film-like substrate. The degradation rate and Tm value of PET were also enhanced, especially with the fusion enzyme LCC-ICCG-CBM9-2, which showed an over 10-fold increase in the degradation rate compared to the original enzyme LCC-ICCG. Therefore, this study demonstrates that by introducing type A and type C CBMs, the degradation rate and thermal stability of LCC-ICCG towards film-like PET can be improved, addressing the issue of its low activity and enabling more effective PET degradation. This research provides support for plastic degradation technology and contributes to environmental conservation efforts.

A Review of Advanced Hydrogel Applications for Tissue Engineering and Drug Delivery Systems as Biomaterials

Hydrogels are known for their high water retention capacity and biocompatibility and have become essential materials in tissue engineering and drug delivery systems. This review explores recent advancements in hydrogel technology, focusing on innovative types such as self-healing, tough, smart, and hybrid hydrogels, each engineered to overcome the limitations of conventional hydrogels. Self-healing hydrogels can autonomously repair structural damage, making them well-suited for applications in dynamic biomedical environments. Tough hydrogels are designed with enhanced mechanical properties, enabling their use in load-bearing applications such as cartilage regeneration. Smart hydrogels respond to external stimuli, including changes in pH, temperature, and electromagnetic fields, making them ideal for controlled drug release tailored to specific medical needs. Hybrid hydrogels, made from both natural and synthetic polymers, combine bioactivity and mechanical resilience, which is particularly valuable in engineering complex tissues. Despite these innovations, challenges such as optimizing biocompatibility, adjusting degradation rates, and scaling up production remain. This review provides an in-depth analysis of these emerging hydrogel technologies, highlighting their transformative potential in both tissue engineering and drug delivery while outlining future directions for their development in biomedical applications.

Isolation and degradation characterization of a 1, 4-dioxane-degrading bacterial strain

To address the potential pollution caused by the carcinogen 1, 4-dioxane in aquatic environments, we isolated a highly efficient 1, 4-dioxane-degrading bacterial strain, designated as DXTK-010, from the groundwater contaminated by 1, 4-dioxane. According to the morphological characteristics, the phylogenetic tree established based on the 16S rRNA gene sequence, and the whole genome sequence, we identified DXTK-010 as Aminobacter aminovorans. This strain demonstrated robust degradation capacity within a temperature range of 20 ℃ to 37 ℃ and a pH range of 5.0 to 8.0. Furthermore, single-factor experiments indicated the optimal degradation conditions at 30 ℃ and pH 7.5. Under the optimal conditions, the strain completely degraded 200 mg/L of 1, 4-dioxane within 24 h, achieving a maximum degradation rate of 9.367 mg/(L·h). The Monod equation was adopted to fit the degradation kinetics of 1, 4-dioxane at different initial concentrations, which revealed a maximum specific degradation rate of 0.224 mg 1, 4-dioxane/(mg protein·h), a half-saturation constant (Ks) of 41.350 mg/L, and a cell yield of 0.130 mg protein/(mg 1, 4-dioxane). Whole genome sequencing revealed a circular chromosome and three plasmids within DXTK-010. Functional gene annotation and analysis underscored the significance of the propane monooxygenase gene cluster and alcohol dehydrogenase gene in facilitating the efficient degradation of 1, 4-dioxane by this strain. DXTK-010 outperformed the existing degraders for 1, 4-dioxane, expanding the strain resources for the bioremediation of 1, 4-dioxane pollution. This study provides a theoretical basis for the practical application of DXTK-010 in the remediation of 1, 4-dioxane pollution.

Establishing the green algae Chlamydomonas incerta as a platform for recombinant protein production.

Chlamydomonas incerta, a genetically close relative of the model green alga Chlamydomonas reinhardtii, shows significant potential as a host for recombinant protein expression. Because of the close genetic relationship between C. incerta and C. reinhardtii, this species offers an additional reference point for advancing our understanding of photosynthetic organisms, and also provides a potential new candidate for biotechnological applications. This study investigates C. incerta's capacity to express three recombinant proteins: the fluorescent protein mCherry, the hemicellulose-degrading enzyme xylanase, and the plastic-degrading enzyme PHL7. We have also examined the capacity to target protein expression to various cellular compartments in this alga, including the cytosol, secretory pathway, cytoplasmic membrane, and cell wall. When compared directly with C. reinhardtii, C. incerta exhibited a distinct but notable capacity for recombinant protein production. Cellular transformation with a vector encoding mCherry revealed that C. incerta produced approximately 3.5 times higher fluorescence levels and a 3.7-fold increase in immunoblot intensity compared to C. reinhardtii. For xylanase expression and secretion, both C. incerta and C. reinhardtii showed similar secretion capacities and enzymatic activities, with comparable xylan degradation rates, highlighting the industrial applicability of xylanase expression in microalgae. Finally, C. incerta showed comparable PHL7 activity levels to C. reinhardtii, as demonstrated by the in vitro degradation of a polyester polyurethane suspension, Impranil® DLN. Finally, we also explored the potential of cellular fusion for the generation of genetic hybrids between C. incerta and C. reinhardtii as a means to enhance phenotypic diversity and augment genetic variation. We were able to generate genetic fusion that could exchange both the recombinant protein genes, as well as associated selectable marker genes into recombinant offspring. These findings emphasize C. incerta's potential as a robust platform for recombinant protein production, and as a powerful tool for gaining a better understanding of microalgal biology.

Development of an assay for the detection of the federally threatened Florida eastern indigo snake (Drymarchon couperi) using soil eDNA

AbstractAccurate information on species range contraction is the cornerstone of effective biodiversity conservation. The eastern indigo snake (Drymarchon couperi) is an apex predator in Florida and, similar to many species native to Florida, is threatened by widespread habitat destruction. Environmental deoxyribonucleic acid (eDNA) monitoring of this elusive snake would provide a non‐invasive approach to improve our knowledge of the species' range and distribution. We designed and tested an eDNA assay that can detect the presence of D. couperi from soil samples from their natural scrub habitat in Florida. We validated our assay in silico, in vitro, and in situ. Furthermore, we investigated the influence of temperature and humidity on the degradation rate of eDNA over time. We successfully amplified the cytochrome b gene for D. couperi at concentrations as low as 3 × 10−3 ng/μL and successfully detected the presence of D. couperi in 2 of 30 in situ field soil samples. The degradation experiment resulted in detectable DNA for 10 days. Interestingly, temperature and humidity had no effect on the degradation rate of eDNA in our experimental conditions. This study provides support for soil eDNA applications to detect the presence of a federally threatened species in their natural environment bolstering our ability to monitor the conservation and management of imperiled species. Environmental DNA provides an additional conservation tool to quickly and effectively monitor species range shifts driven by multiple anthropogenic stressors to promote the persistence of imperiled species.

Improvement of Saline–Alkali Soil and Straw Degradation Efficiency in Cold and Arid Areas Using Klebsiella sp. and Pseudomonas sp.

Corn straw is an important renewable resource, which could improve the quality of saline–alkali cultivated land. However, the slow decomposition of crop residues in cold, arid, and saline–alkali soils can lead to serious resource waste and ecological crises. The use of beneficial microorganisms with degradation functions could solve these problems. In this study, three types of saline–alkali soil with low, medium, and high salinity levels were used in the straw-returning experiment. The experiment was conducted with four treatments: GF2 (Klebsiella sp.), GF7 (Pseudomonas sp.), GF2+GF7, and CK (control without bacteria). Microbial characteristics, straw degradation efficiency, element release rate, and soil factors were compared, and random forest linear regression and partial least squares path modeling analysis methods were utilized. The results indicated that the degradation of bacterial metabolites, the efficiency of corn stover degradation, the efficiency of component degradation, and the release rates of elements (C, N, P, and K) initially increased and then decreased with the increase in salinity. At the maximum value of moderately saline–alkali soil, the effect of GF2+GF7 treatment was significantly better than that of other treatments (p < 0.05). Given the interactive effects of saline–alkali soil and microbial factors, the application of exogenous degrading bacteria could significantly increase soil enzyme activity and soil available nutrients, as well as regulate the salt–alkali ion balance in soil. The cation exchange capacity (9.13%, p < 0.01) was the primary driving force for the degradation rate of straw in saline–alkali soil with different degrees of salinization under the influence of exogenous degrading bacteria. Straw decomposition directly affected the soil chemical properties and indirectly affected soil enzyme activity. The results of this study would provide new strategies and insights into the utilization of microbial resources to promote straw degradation.

Evaluation of photocatalytic efficiency of TiO2 applied over cement plaster for mitigating urban air pollutant: TVOC

Photocatalysis emerged as a prominent method for mitigating air pollution stemming from emissions of total volatile organic compounds (TVOCs) in both indoor and outdoor environments. Given the slow degradation rate of certain TVOCs, which pose health risks, including carcinogenicity, there is a pressing need for effective air purification strategies, particularly within built environments where individuals spend substantial amounts of time. This study delves into the efficacy of TiO2 photocatalysis in reducing air pollutants when applied to building surfaces. Cement mortar samples, incorporating varied doses of TiO2 ranging from 7.83E-03 g/cm2 to 4.92E-02 g/cm2, were prepared and examined within batch reactors, both under sunlight exposure and in the absence thereof, to gauge their degradation rates towards TVOCs. Furthermore, surface characterization techniques were employed to explicate the microstructural properties of TiO2-coated plastered samples. The results obtained demonstrated the variation in the rate of degradation from 1.09E-04±0.1 % to 3.1E-4 ± 1.13 % min−1cm−2 for various initial concentrations of total volatile organic compounds (TVOCs) in the range of 600 ppm to 2900 ppm over a period of 100 min. The selected approach demonstrated the maximum degradation rate constant of 5.2E-04 min−1cm−2 corresponding to 15 % of TiO2 dose by weight of cement. These findings underscore the promise of TiO2 in purifying polluted air and advocate for its widespread implementation on building surfaces to enhance air quality.

Catalytic Degradation of Bisphenol A in Water by Non-Thermal Plasma Coupled with Persulfate

Bisphenol A (BPA) has become prevalent in the environment due to its extensive use in industrial materials, thus raising significant concerns regarding its potential toxicity and health effects. In this study, an efficient and eco-friendly non-thermal plasma (NTP) was used to catalyze persulfate (PS) for BPA decomposition, and the results showed that the integrated system could effectively degrade BPA. The best performance was attained at a PS to BPA mass ratio of 5:1, with a degradation rate of 91.3% following a 30 min treatment. The degradation rate of BPA increased with increasing input voltage and frequency; conversely, it decreased with an increase in BPA’s initial concentration. Higher BPA degradation rates could be achieved in alkaline environments. Radical quenching experiments revealed that SO4−•, OH•, O2−• and 1O2 were important active substances involved in BPA degradation. Nine intermediate products were identified by liquid chromatography–mass spectrometry (LC-MS), and four degradation pathways were deduced. Additionally, a toxicity analysis of intermediate products was performed. The significant decrease in chemical oxygen demand (COD) during the actual wastewater treatment suggested that the NTP/PS system has good applicability in actual wastewater treatment.

Photocatalytic degradation of methylene blue using a Cu2+-modified bimetallic titanium-based metal organic framework (MIL-125) photocatalyst with enhanced visible light activity.

Cu-modified TiO2 nanoparticles derived from MIL-125 were prepared by solvothermal method for the photocatalytic degradation of methylene blue under visible light illumination. For boosting the photocatalytic performance as well as the physicochemical properties of bare sample, 2 wt % Cu2+ ions were integrated into the nodes of the MIL-125 framework. The results showed that incorporation of 2 wt % Cu2+ ions into the MOF framework had significant effects on the crystallographic structure and morphological and optical properties of photocatalytic samples, as well as catalytic activity for the methylene blue degradation reaction. The high activity profile of Cu-modified TiO2 nanoparticles derived from MIL-125 might be attributed to the increased thermal stability, lower band gap energy, and smaller crystallite size of the sample. Activity tests were carried out at five varying MB initial concentrations and four different pH values. According to the findings, an increase in initial dye concentration resulted in a decrease in degradation efficiency. It was observed that increasing the pH value in the range of 3-11 initially led to higher degradation rates until pH 7, after which the degradation rate began to decline.

Exploring the photocatalytic breakdown of organic pollutants using intercalated ZnO/SiO2 nanocomposites

The increasing prevalence of organic pollutants in water sources necessitates the development of efficient and cost-effective photocatalysts for their degradation. ZnO nanoparticles (NPs) have been widely studied for their photocatalytic properties; however, their application is hindered by low photocatalytic efficiency and high recombination rates of photogenerated carriers. This manuscript explores the enhanced photocatalytic performance of intercalated ZnO/SiO2 nanocomposites (NCs), synthesized through a combination of co-precipitation and Stöber methods, as a solution to these challenges. A comprehensive analysis of the structural, optical elemental and Morphological properties of both ZnO NPs and ZnO/SiO2 NCs was conducted using various characterization techniques, including X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV–Vis spectrometry and Brunauer-Emmett-Teller (BET) analysis. Through, XRD analysis, the calculated crystallite sizes of ZnO NPs and ZnO/SiO₂ NCs were found to be 36 nm and 39 nm respectively. TEM images illustrated that the ZnO NPs and ZnO/SiO₂ NCs have crystallized in elongated spherical morphology. XPS and FTIR analyses provided the signature band details the presence of Cu and Si in their Zn2⁺ and Si⁴⁺ oxidation states. The optical bandgap energies were calculated to be 3.38 eV for ZnO NPs and 3.22 eV for ZnO/SiO₂ NCs. The enhanced photocatalytic efficiency of the ZnO/SiO2 NCs achieved an impressive degradation rate of 92 % for Rhodamine B (RhB), compared to a relatively lower rate of 81 % for pure ZnO NPs for the degradation of RhB under visible light due to its lower bandgap, high surface area, and lower electron-hole recombination rate. BET surface area measurements revealed that ZnO nanoparticles have a surface area of 11.234 m2/g, while ZnO/SiO₂ NCs show 57.118 m2/g, highlighting SiO₂'s enhancement. The NCs demonstrated exceptional reusability for degradation, sustaining high efficiency across multiple cycles. Its ability to scavenge superoxide radicals highlighted the effectiveness of the ZnO/SiO₂ NCs in environmental remediation, especially for wastewater treatment.

Codon optimality influences homeostatic gene expression in zebrafish.

The ribosome plays a crucial role in translating mRNA into protein; however, the genetic code extends beyond merely specifying amino acids. Upon translation, codons, the three-nucleotide sequences interpreted by ribosomes, have regulatory properties affecting mRNA stability, a phenomenon known as codon optimality. Codon optimality has been previously observed in vertebrates during embryogenesis, where specific codons can influence the stability and degradation rates of mRNA transcripts. In our previous work, we demonstrated that codon optimality impacts mRNA stability in human cell lines. However, the extent to which codon content influences vertebrate gene expression in vivo remained unclear. In this study, we expand on our previous findings by demonstrating that codon optimality has a robust effect on homeostatic mRNA and protein levels in whole zebrafish during normal physiological conditions. Using reporters with nearly identical nucleotide sequences but different codon compositions, all expressed from the same genomic locus, we show that codon composition can significantly influence gene expression. This study provides new insights into the regulatory roles of codon usage in vertebrate gene expression and underscores the importance of considering codon optimality in genetic and translational research. These findings have broad implications for understanding the complexities of gene regulation and could inform the design of synthetic genes and therapeutic strategies targeting mRNA stability.

MgO nanofiller reinforced biodegradable, flexible, tunable energy gap HPMC polymer composites for eco-friendly electronic applications

This study explores the development and characterization of eco-friendly Magnesium Oxide (MgO) nanofiller reinforced hydroxypropyl methylcellulose (HPMC) polymer composites for eco-friendly electronic applications. The prepared nanocomposites are biodegradable and flexible without any additional plasticizer. MgO nanoparticles were synthesized using the solution combustion method and incorporated into HPMC matrix through solution casting method. The structural, mechanical, optical, AC and DC electrical, and degradation properties of the prepared nanocomposites were systematically investigated. X-ray diffraction (XRD) confirmed the successful integration of MgO nanoparticles into the HPMC matrix, with noticeable interactions affecting the crystallinity. Mechanical testing revealed an optimal MgO concentration of 0.2 g, which provided the best balance of strength and ductility, while higher concentrations led to increased brittleness. UV–Vis spectroscopy results evident that the energy gap of nanocomposites can be tuneable with MgO incorporation. The photoresponsivity study indicated that higher MgO content reduce the photocurrent due to agglomeration and defect states. Dielectric studies showed a typical frequency-dependent behaviour, with enhanced dielectric constants at lower frequencies attributed to interfacial polarization. However, increasing MgO content decreased the dielectric constant and loss due to reduced polymer chain mobility and increased resistive pathways. Current-Voltage (I-V) characteristics demonstrated a non-ohmic conduction behaviour with Poole-Frenkel emission identified as the predominant conduction mechanism. Degradation tests in both tap water and soil, demonstrated that the MgO incorporation significantly slowed the degradation rate of the composites, enhancing their durability. These findings suggest that MgO-HPMC nanocomposites hold promise for sustainable and flexible eco-friendly electronic applications.

Identification and characterization of Morganella morganii strain YC12-C3 and Enterococcus faecalis strain YC12-C10 and elucidation of its deoxynivalenol-degrading potential.

Deoxynivalenol ( DON) is one of the most harmful mycotoxins in food or feed or Traditional Chinese Medicine. An efficient and applicable method for the detoxification of DON is urgently developed. 1152 strains were isolated from the intestinal contents of crucian. Morganella morganii YC12-C3 and Enterococcus faecalis YC12-C10 were screened with the highest degradation rate of DON via HPLC methods. The optimal degradation condition of YC12-C3 and YC12-C10 is co-cultured 24 h and 36 h at 28 ℃ in LB medium with pH 7 and 1.0% inoculation dosage, respectively. LC-MS/MS and 1H NMR results show that YC12-C10 and YC12-C3 can transform DON to 3-deoxy-6-demethanol-DON, a new metabolite biotransformed from DON, by deoxidization at C3 hydroxy and de-methanal reaction at methanol moiety of C6. In addition, the DON-degradation in agricultural material assay showed that YC12-C10 and YC12-C3 can degrade 150 μg·kg-1 DON in Coix lacryma-jobi, with a degradation rate of 68.89% and 59.94%, respectively. This result shows that YC12-C10 and YC12-C3 have a sound efficiency in removing DON ability in Coix lacryma-jobi, providing a new strain resource and application technique for biological detoxification of DON in food or feed or TCM industry.