pH Variation Research Articles

Cryosphere and land cover influence on stream water quality in Central Asia's glacierized catchments

This work helps address recent calls for systematic water quality assessment in Central Asia and considers how nutrient and salinity sources, and transport, affect water quality along the continuum from the cryosphere to the lowland plains. Spatial and, for the first time, temporal variations in stream water pH, temperature, electrical conductivity, and nitrate and phosphate concentrations are presented for four catchments (485–13,500 km2), all with glaciers and major urban areas. The catchments studied were: Kaskelen (Kazakhstan), Ala-Archa (Kyrgyzstan), Chirchik (Uzbekistan) and the Kofarnihon (Tajikistan). Measurements were made in cryosphere, stream water, groundwater, reservoir and lake samples over a 22-month period at fortnightly intervals from 35 sites. The results highlight that glacier, permafrost and rock glacier outflows were primary and secondary nitrate sources (>1 mg N L−1) to the headwaters, and there were major increases in salinity and nitrate concentrations where rivers receive inputs from agriculture and settlements. Overall, the water quality complied with national and World Health Organization standards, however there were pollution hot-spots with shallow urban groundwaters contaminated with nitrate (>11 mg N L−1) and stream electrical conductivity above 800 μS cm−1 in some agricultural areas indicative of high salinity. Phosphate concentrations were generally low (<0.06 mg P L−1) throughout the catchments, though elevated (>0.2 mg P L−1) in urban areas due to effluent contamination. A melt water dilution effect along the main river channels was discernible, in the electrical conductivity and nitrate concentration seasonal dynamics, 100 s of km from the headwaters. Thus, the input of relatively clean water from the cryosphere is an important regulator of main channel water quality in the urban and farmed lowland plains adjacent to the Tien Shan and Pamir. Improved sewage treatment is needed in urban areas.

Study of ISFET sensitivity to pH variations using Silvaco TCAD

Study of ISFET sensitivity to pH variations using Silvaco TCAD

Thermophilic-mesophilic temperature phase anaerobic co-digestion compared with single phase co-digestion of sewage sludge and food waste

Anaerobic co-digestion is an effective method for addressing the issue of a single substrate not being able to achieve optimal conditions for anaerobic digestion. By adjusting the mixture ratio of sewage sludge and food waste to achieve the optimal carbon to nitrogen ratio, the effectiveness of thermophilic–mesophilic temperature phase anaerobic co-digestion (TPAcD) was evaluated in comparison to single phase mesophilic anaerobic co-digestion (MAcD) and thermophilic anaerobic co-digestion (TAcD). The results indicated that TPAcD increased methane yield by 50.3% and 32.7% compared to MAcD and TAcD, respectively. The variation in VFA, pH, and ammonia nitrogen levels demonstrated that TPAcD combines the advantages of both MAcD and TAcD, with a higher hydrolysis rate in the early stage under thermophilic conditions (55 °C) and a suitable environment in the later stage under mesophilic conditions (35 °C). The kinetic parameters of anaerobic co-digestions also demonstrated that TPAcD performs better. Therefore, further research on TPAcD of sewage sludge and food waste is warranted due to its significant improvements in methane production rate, total methane yield, and system stability. Additionally, TPAcD contributes to reducing carbon emissions and supports the realization of “carbon neutrality”.

Synthesis and dual sensing of vanadium and copper ions using protein capped selenium nanoparticles

Highly homogenous and spherical shaped Selenium nanoparticles with an average size of 20 nm were synthesized from an eco-friendly and environmentally safe approach using bovine milk protein casein as stabilizing agent (named as CasSeNPs). Protein functionalization provided excellent stability at variable temperatures (25–60 °C), pH (8–10), ionic strength (0.05–2 M), and storage period for more than five months. Synthesized CasSeNPs were extensively characterized using various spectroscopic (UV–visible, Fourier transform infrared (FTIR), circular dichroism (CD), intrinsic fluorescence spectroscopy), particle sizing (dynamic light scattering (DLS) and zeta potential), microscopic (scanning electron microscopy, energy dispersive X-ray spectroscopy (SEM/EDS), atomic force microscopy (AFM)), and X-ray diffraction (XRD) measurements. Moreover, CasSeNPs was established as highly sensitive and selective sensor for the simultaneous detection of vanadium (V+2) and copper (Cu+2) ions with significant linearity (0.5–10 and 0.1–1.0 µM, respectively), detection limits (LOD = 0.03 and 0.067 µM, respectively), and percent recoveries (94–105 %) in real environmental (tap water) and biological (human plasma and urine) samples with adequate test performance. Cumulatively, obtained results revealed that the established very simple, biocompatible and economical nanosensor has great potential for applications in analytical chemistry as well as for biological investigations.

Heterologous expression of frog antimicrobial peptide Odorranain-C1 in Pichia pastoris: Biological characteristics and its application in food preservation

To reduce food spoilage and deterioration caused by microbial contamination, antimicrobial peptides (AMPs) have gradually gained attention as a biological preservative. Odorranain-C1 is an α-helical cationic antimicrobial peptide extracted from the skin of frogs with broad-spectrum antimicrobial activity. In this study, we achieved the expression of Odorranain-C1 in Pichia pastoris (P. pastoris) (also known as Komagataella phaffii) by employing DNA recombination technology. The recombinant Odorranain-C1 showed broad-spectrum antibacterial activity and displayed a minimum inhibitory concentration within the range of 8–12 μg.mL-1. Meanwhile, Odorranain-C1 exhibited superior stability and lower hemolytic activity. Mechanistically, Odorranain-C1 disrupted the bacterial membrane's integrity, ultimately causing membrane rupture and subsequent cell death. In tilapia fillets preservation, Odorranain-C1 inhibited the total colony growth and pH variations, while also reducing the production of total volatile basic nitrogen (TVB-N) and thiobarbituric acid (TBA). In conclusion, these studies demonstrated the efficient recombinant expression of Odorranain-C1 in P. pastoris, highlighting its promising utilization in food preservation.

Enzymic Deactivation in Tender Coconut Water by Supercritical Carbon Dioxide

Polyphenol oxidase (PPO) and peroxidase (POD) are target enzymes in the processing of tender coconut water (TCW). This study primarily evaluated the combined effect of supercritical carbon dioxide (SC-CO2) and mild temperatures on the PPO and POD deactivation of TCW. A factorial design was performed to investigate the effect of temperature (in the range of 35 to 85 °C), pressure (75 to 370 bar), and holding time (13 to 47 min) on the enzymic deactivation, physicochemical parameters, and color of the TCW. The percentages of reduction in PPO activity ranged from 3.7 to 100%, and POD ranged from 43.4 to 100%. The pH values of the freshly extracted and processed TCW were 5.09 and 4.90, and the soluble solids content were 5.5 and 5.4 °Brix, respectively. The holding time (t) had a significant effect (p ≤ 0.1) on the total color variation. As for the reduction of PPO activity, the temperature (T) and the interaction between pressure (P) and t had a significant effect. None of variables (P, T, or t) affected (p &gt; 0.1) the POD reduction, pH, and soluble solids variation. The combination of SC-CO2 and mild temperatures is a promising intervention in the enzymic stabilization of TCW.

Comprehensive investigation of pollution levels and potential bioavailable risks of 7 potentially toxic elements in Qinghai-Tibet soils by using diffusive gradients in thin-films (DGT)

ABSTRACT Seven potentially toxic elements (PTEs) including Cr, Ni, Cd, Zn, Cu, Pb and As of soil samples from Qinghai-Tibet Plateau (QTP) were measured to assess the degree of contaminations. To have a comprehensive understanding of PTEs’ risks in QTP, the single-step nitric acid extraction and diffusive gradients in thin-films (DGT) technique were employed in this study for the determination of PTEs’ total amount as well as bioavailable content, respectively. Haibei state of Qinghai province was the most contaminated sites by PTEs. Behaviors of PTEs should be highly concerned as they can produce continuous bioavailable effects to ecological systems. High DGT concentrations of Zn and Cr showed their remarkable available risks in soils. In the environment with insufficient organic matter and slight pH variations, phosphorus level was the main contributor to affect the mobility of labile PTEs, especially for Pb and Ni. Concentration ratio between DGT measurement and soil solution and correlation analysis confirmed the high bioavailability of Pb, Zn and Cr, leading to short-term mixture effects on ecological systems, while the long-term release dynamics were found for As and Cu. Results from road-side and river-side soils of QTP evidenced the short-term bioavailable risks were possibly attributed to intensive anthropogenic activities including traveling industries and vehicle driving, whereas long-term bioavailable risks was from the natural transportation and deposition.

Potential application of curcumin nanoemulsions to preserve properties of refrigerated cheese

The current study focused on employing curcumin nanoemulsions (CRNEs) to maintain their quality and prolong shelf life. The three tested CRNE ratios (1.0, 1.5, and 2.00 mg/ml) passed the stability test at 40 °C, indicating that all samples were stable for 4 weeks. The pH values ranged from 5.74 to 5.75, the droplet size from 63.05 to 64.55 d nm, and the polydispersity index PDI from 0.457 to 0.494. The spherical shape of (CRNEs) formulations is demonstrated by a TEM micrograph. The zeta potentials of CRNEs ranged between −3.82 and −2.72 mV. The physicochemical parameters of Kareish cheese (KCh) and KCh-CRNEs revealed no significant protein, fat, moisture, and pH variations. Kareish cheese has a poor antioxidant activity of 19.23%, compared to 42.31% in KCh-CRNE3 (2 mg/g). Except for color, the sensory parameters results revealed no significant difference between kareish cheese and KCh-CRNEs. CRNE3 had greater efficacy as an antibacterial agent (MIC values 150 and 250) than natural Curcumin (MIC values 800 and 1000) against Staphylococcus aureus and Bacillus cereus, respectively. In vivo study of KCh-CRNEs against Bacillus cereus, the activity was reduced by (55.5 × 104 cfu/g) in KCh-CRNE3, after 12 days of storage at 4 °C. The antioxidant values were (38.02%) in KCh-CRNE3 at the end of storage with no significant change of protein content or pH for all KCh-CRNEs treatments. The findings suggest that curcumin nanoemulsions can enhance antimicrobial protection in Kareish cheese preservation, extending shelf life, and promoting healthier, more sustainable food products, benefiting both the food industry and public health.

Partial denitrification in rope-type biofilm reactors: Performance, kinetics, and microflora using internal vs. external carbon sources

Stable nitrite accumulation through partial denitrification (PDN) represents an efficient pathway to support the anammox process, but limited studies explored the internal wastewater carbon sources and biofilm processes. This study assessed the viability of the PDN process, biofilm community evolution, and functional enzyme formation in rope-type biofilm media reactors using primary effluent (PE) and anaerobically pretreated wastewater carbon sources for the first time. Comparison was made with external carbon (acetate) under varied pH and biofilm thicknesses, maintaining a favourable sCOD: NO3-N ratio of 3. The wastewater’s internal carbon resulted in thinner biofilms; nevertheless, modest nitrite accumulation (0.24 g/m2/d) occurred only at elevated pH. The highest nitrite accumulation (0.79 g/m2/d) was exhibited in the biofilm thickness-controlled acetate-fed reactor, featuring porous biofilms dominated by denitrifier Thauera (10.24 %) and imbalance between Nar, Nap, and Nir reductases. Using internal wastewater carbon sources offers a sustainable avenue for adopting the PDN process in full-scale application.

Spin Crossover and Exchange Effects on Oxygen Evolution Reaction Catalyzed by Bimetallic Metal Organic Frameworks.

Bimetallic metal-organic frameworks (BMOFs) have shown a superior oxygen evolution reaction (OER) performance, attributed to the synergistic effects of dual metal sites. However, the significant role of these dual-metal synergies in the OER is not yet fully understood. In this study, we employed density functional theory to systematically investigate the OER performance of NiAl- and NiFe-based BMOFs by examining all possible spin states of each intermediate across diverse external potentials and pH environments. We found that the spin state featuring a shallow hole trap state and Ni ions with a higher oxidation state serve as strong oxidizing agents, promoting the OER. An external potential-induced spin crossover was observed in each intermediate, resulting in significant changes in the overall reaction and activation energies due to altered energy levels. Combining the constant potential method and the electrochemical nudged elastic band method, we mapped the minimum free energy barriers of the OER under varied external potential and pH by considering the spin crossover effect for both NiAl and NiFe BMOFs. The results showed that NiFe exhibits better OER thermodynamics and kinetics, which is in good agreement with experimentally measured OER polarization curves and Tafel plots. Moreover, we found that the improved OER kinetics of NiFe not only is attributed to lower barriers but also is a result of improved electrical conductivity arising from the synergistic effects of Ni-Fe dual-metal sites. Specifically, replacing the second metal Al with Fe leads to two significant outcomes: a reduction in both the band gap and the effective hole mass compared to NiAl, and the initiation of super- and double-exchange interactions within the Ni-F-Fe chain, thereby enhancing electron transfer and hopping and leading to the improved OER kinetics.

Performance and mechanism of lanthanum-modified MnO2 for defluoridation from water: The role of MnO2 crystal forms

MnO2 has a large potential for defluoridation, however, the influences of its crystal forms on the performance and mechanism of defluoridation are unknown. The research systematically investigated the defluoridation performance and mechanism of a total of eight materials with different crystal forms of MnO2 (α, β, γ, δ) before and after lanthanum modification, separately. It was indicated that the largest Langmuir adsorption of α-MnO2 and La-γ-MnO2 for fluoride achieved 5.04 mg/g and 42.39 mg/g, correspondingly. The surface hydroxyl group and lanthanum loading of the material proved to be the major contributors to defluoridation. For the adsorption performance of eight materials on fluoride, pH was a significant influencing factor, with the highest adsorption performance at pH 5 ∼ 6. The eight materials showed consistent selectivity for fluoride adsorption in the existence of different anions, with the order of influence on the removal efficiency: CO32–> NO3–> SO42–> Cl–. The studies of FTIR, XPS, and variation of solution pH further illustrated that the adsorption mechanism of the eight materials on fluoride was the ion-exchange interaction and the complexation reaction. In addition, the effect of crystal forms on the adsorption of fluoride ions was further elaborated by DFT analysis. Finally, this study provided an in-depth discussion of the parameters of the dynamic process as well as the nature of the penetration curves by applying the Thomas, Clark, and BDST models.

Characterization of a Food‐Safe Colorimetric Indicator Based on Black Rice Anthocyanin/PET Films for Visual Analysis of Fish Spoilage

ABSTRACTThe safety of food products is of prime importance for consumers and manufacturers. Many means can be used to validate a food product's safety before it is consumed. This study is about the preparation, characterization and evaluation of a generally recognized as safe (GRAS) sensitive colorimetric sensor that detects volatile gases (TVB‐N) resulting from fish spoilage, thus indicating the pH variation of packaged fish products. This is performed by coating a thin layer of ink sensors on the surface of the supporting matrix (corona‐treated PET). Various visual pH indicators were prepared based on black rice anthocyanin as an FDA‐approved dye. Black rice, which contains more than 80% cyanidin‐3‐glucoside, is the most prevalent anthocyanin component. Because of its low toxicity and high concentration, it can be utilized as a natural food colourant. pH indicators based on black rice can show distinct colours in various pH: from red (low pH) to violet (4–6) and deep purple/blue (6–7), blue (7–9) to yellowish/light brown (9–13) throughout the acid–base reaction by the analyte. The ink formulation was prepared by incorporating a binder system (PVOH‐PEG) for higher surface wettability, a crosslinking agent (citric acid) for higher adhesion, an antifoaming agent (natural vanillin) and acetic acid as a pH fixing agent. Corona treatments affected substrate surface chemistry in this study. The samples with thermal treatment passed the ASTM D3330 tape test, the 8000 passages for dry sponge and the 25 passages for wet sponge through the abrasion method. Anthocyanin concentration in formulated ink based on calculation by UV–vis spectra is 0.240 mg/100 g. Sensitivity tests towards TVB‐N gases were carried out at a temperature of 4°C to evaluate the performance of colorimetric films with formulated ink along with thermal treatment (temperature: 165°C, time: 5 min) using the volatile gases emitted by the fish sample inside the package.

Ligand Dissociation of Metal-Complex Photocatalysts toward pH-Photomanipulation in Dynamic Covalent Hydrogels for Printing Reprocessable and Recyclable Devices.

Dynamic covalent hydrogels are gaining attention for their potential in smart materials, soft devices, electronics, and more thanks to their impressive mechanical properties, biomimetic structures, and dynamic behavior. However, a significant challenge lies in designing precise and efficient dynamic photochemistry for their preparation, allowing for complex structures and control over the dynamic process. Herein, we propose a general and straightforward orthogonal dynamic covalent photochemistry strategy for preparing high-performance printable dynamic covalent hydrogels, thereby broadening their advanced applications. This photochemical strategy uses a bifunctional photocatalyst to initiate radical polymerization and release ligands through a rapid light-mediated dissociation mechanism. This process leads to a controlled increase in system pH from mildly acidic to alkaline conditions within one hundred seconds, which in turn triggers the pH-sensitive model reactions of boronic acid/diol complexation and Knoevenagel condensation. The orthogonal photochemistry enables the formation of interpenetrated and conjoined networks, significantly enhancing the mechanical properties of the hydrogels. The reversible bonds formed during the process, i.e., boronic ester and unsaturated ketone bonds, confer excellent self-healing, reprocessable, and recyclable properties on the hydrogels through photochemical pH variations. Furthermore, this rapid, controlled fabrication process and dynamic behavior are highly compatible with printing techniques, enabling the design of adaptive and recyclable sensors with different structures. These advancements are promising for various material science, medicine, and engineering applications.

Removal of Metribuzin and Bentazon by LDH-HA Modified Material: Kinetic and Equilibrium Study

ABSTRACT This study investigates the adsorption behavior of herbicides Metribuzin and Bentazon using a soil model incorporating Layered Double Hydroxide (LDH) and humic acid. Mg3AlCl-LDH, synthesized at pH 10, was combined with humic acid to produce two distinct materials: Mg3–5%HA and Mg3–10%HA. These materials were characterized using FTIR, XRD, and SEM techniques. The research confirms that humic acid adsorbs onto the LDH surface without altering its structure, resulting in negatively charged materials. While both materials fully adsorb Metribuzin at 20 mg/L, their adsorption capacities diverge at higher concentrations, with Mg3–10%HA exhibiting a higher capacity than Mg3–5%HA. In contrast, Bentazon’s adsorption is unaffected by humic acid content, displaying identical adsorption capacities in both materials at different concentrations. Both herbicides exhibit rapid adsorption kinetics, reaching equilibrium in 15 minutes. The Avrami model accurately predicts equilibrium adsorption capacities, with Metribuzin primarily adsorbed through electrostatic attraction and hydrogen bonding, while Bentazon’s adsorption is limited due to electrostatic repulsion. The adsorption of both herbicides by Mg3-HA materials is not influenced by pH variations, likely due to the surface charge of the materials. Metribuzin retention in soil containing LDH and humic acid is effective, increasing with higher humic acid concentrations, whereas Bentazon demonstrates greater mobility and resistance. These findings provide valuable insights for developing efficient water decontamination techniques, with implications for environmental protection and public health. Policymakers, researchers, and professionals in water management and pollution control should consider these findings to enhance current practices and technologies.

PH-responsive anti-corrosion activity of gallic acid-intercalated MgAl LDH in acidic, neutral, and alkaline environments

Undoubtedly, designing pH-responsive particles is one of the most fascinating aims for corrosion experts. Local pH variations can occur through the corrosion process (chemical and electrochemical reactions), accelerating the corrosion rate. However, by designing this class of modern inhibitors, a significant part of the effects of pH variation during corrosion disappears. Herein, a novel layer double hydroxide-based (LDH) nanocomposite, which is filled by gallic acid (GA) molecules, was designed. To prove the composite inhibition proficiency, EIS tests were conducted in acid, neutral and alkaline atmospheres and then surface morphology of the protected and unprotected samples are visualized by FE-SEM images. Simultaneously, the EDS-Mapping technique was applied to predict the elemental composition of the generated inhibitive layer. The results of the EIS test indicated an increase in corrosion resistance after using nanoparticles in all three acidic, neutral and alkaline environments. In addition, the potentiodynamic polarization test confirmed the mixed-protection mechanism in these three media. Furthermore, FE-SEM approach demonstrated the formation of a protective film on metal surfaces, and the EDS-Mapping evaluation confirmed these results in line with the element recognition.

Characteristics, physicochemical stability and in vitro release of curcumin-loaded glycated bovine serum albumin nanofibrils: Effects of molecular weight of saccharide

The goal of this study is to fabricate glycated bovine serum albumin nanofibrils as efficient curcumin nano-delivery systems to enhance its water solubility, storage stability against environmental stress, chemical stability and in vitro antioxidant activity, which can widely be applied in real food products. Glycosylation exhibited almost no impacts on the morphology of bovine serum albumin nanofibril as revealed by atomic force microscopy, regardless of saccharide types. Glycated bovine serum albumin nanofibrils possessed nanometric diameter (less than 15 nm) and micrometric length (1–1.5 μm). Glycation further enhanced the surface hydrophobicity of bovine serum albumin nanofibrils and its curcumin binding capacity. Water solubility of curcumin was sharply enhanced with bovine serum albumin nanofibril-based nanocarriers and curcumin-bovine serum albumin nanofibrils-glucose exhibited the highest aqueous solubility (50.2%). There was a strong positive proportion between curcumin solubility and surface hydrophobicity of bovine serum albumin nanofibril-based nanocarriers. Fluorescence data demonstrated that the formation of curcumin-glycated bovine serum albumin nanofibril nanocomposites was mainly through hydrophobic interactions. All three glycated bovine serum albumin nanofibrils were resistant to pH variation, high salt and heating. The chemical stability of curcumin was remarkably enhanced through glycation and there was a negative correlation between the chemical stability of curcumin and molecular weight of saccharides. Antioxidant capacities (2,2-diphenyl-1-picrylhydrazyl radical scavenging activity and reducing power) of curcumin were dramatically soared through complexation with three glycated bovine serum albumin nanofibrils and the antioxidant activity of glycated bovine serum albumin nanofibril was negatively correlated with the molecular weight of saccharides. The release of curcumin in bovine serum albumin nanofibril nanocomposites could be controlled through glycation. Generally, this research indicates that the glycated bovine serum albumin nanofibril would be employed to load, stabilize, and deliver hydrophobic nutraceuticals and expand the food application.

High internal phase emulsions stabilized by physically modified mung bean protein isolates under different pHs

This research explored the impact of modified mung bean protein isolates (MBPIs) on the physicochemical, rheological, and structural properties of 70% oil-containing high internal phase emulsions (HIPEs). MBPIs (4% protein concentration) were subjected to heating (90 °C for 2 h) or sequential heating/ultrasonication (20 kHz, 120 W for 10 min) at different pHs (2, 7, and 10). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of modified MBPIs confirmed heat treatment at pH 2 hydrolyzed MBPI, unlike MBPIs heated at pH 7 and 10. Sequential heating/ultrasonication significantly reduced particle size, improved solubility and surface hydrophobicity of MBPIs, resulting in smaller droplet size and enhanced gel-like properties of HIPEs. Transmission electron microscopy revealed that sequentially heated/ultrasonicated MBPIs in the oil–water interface existed in a fibrillar or randomly aggregated structure at pH 2, a randomly aggregated structure at pH 7, and a particulate aggregated structure at pH 10. Overall, these structural modifications at varied pH conditions influenced MBPI adsorption at the HIPE droplet interface, impacting rheological features and promoting the potential use of protein-stabilized HIPEs across diverse applications.

Formation of the calpain-1/calpastatin complex promotes activation of calpain-1 under oxidizing conditions.

Calpains are cysteine proteinases responsible for many biological roles in muscle, including protein degradation, muscle growth, and myoblast fusion. Calpains are inhibited by calpastatin, an endogenous inhibitor. Other factors, such as variations in pH, ionic strength, and oxidation influence calpain activity. This study aimed to determine the extent to which oxidation influences calpastatin inhibition of calpain-1. A series of order of addition assays were used to determine calpain-1 calcium activation and autolysis after exposure to an oxidizing agent (n-ethylmaleimide [NEM] or hydrogen peroxide [H2O2]. In the first series, purified calpastatin was added to the assay before or after oxidizing exposure at 165mM NaCl, pH 6.5. In the second series, incubation buffer ionic strength (165mM or 295mM NaCl) was evaluated. The inhibitory activities of purified porcine calpastatin, purified human calpastatin domain I, or a subdomain B inhibitor peptide were evaluated in the third series. In the fourth series, a maleimide-polyethylene glycol molecule (MAL-PEG; MW = 5,000 Dalton) was used to evaluate the accessibility of free sulfhydryl groups and tagging of calpain-1 under each condition through a molecular weight shift assay. Results from this study indicate that autolysis of calpain-1, when used as an indicator of activation, occurred when the calpain-1/calpastatin complex was exposed to an oxidant or cysteine modifier such as NEM. However, when calpain-1 was exposed to the cysteine modifier before calpastatin, autolysis of calpain-1 did not occur or was significantly decreased (P < 0.05). Irreversible modification of cysteine residues by NEM prevented activation of calpain-1 in the absence of calpastatin, but if the cysteine modification is potentially reversible (H2O2), calpain-1 activity can be recovered. Results from this study indicate that when calpastatin is bound to calpain-1, calpain-1 activation can occur even after being exposed to a cysteine modifier (NEM) or hydrogen peroxide (H2O2). Calpain-1 is not tagged with maleimide-polyethylene glycol (MAL-PEG) in the presence of calpastatin, indicating that calpastatin blocks or covers free cysteines on calpain-1 from modification. Moreover, exposure to calpain-1/calpastatin complex with a cysteine modifier allows activation of calpain-1, indicating that the inhibitory action of calpastatin is compromised. These results indicate a regulatory role for calpastatin that is not inhibitory but protective for calpain-1.

Innovative smart colorimetric sensor for nitrite detection in poultry packaging

Detecting nitrite ions is crucial for environmental and health monitoring, given the prevalence of nitrites in water sources and meat. Colorimetric methods provide a cost-effective, rapid, and straightforward means of nitrite ion detection. This study focuses on monitoring nitrite levels in meat to ensure its safe consumption. Three different dyes—Bromophenol blue (B.P.B.), Eriochrome Black T (E.B.T.), and Potassium permanganate (KMnO4)—were employed to identify and quantify nitrite ions under various experimental conditions such as variable pH, temperature, concentration, and selectivity. UV–visible studies revealed low average detection limits of 0.2054 mM for E.B.T. dye, 0.218 mM for B.P.B., and 3.317 mM for KMnO4 dye solution. An Internet of Things (IoT)-based, portable, and cost-effective device for colorimetric nitrite ion detection was also developed. This innovative system integrates a connected detection mechanism within a smart device, enabling swift acquisition of red, green, and blue (RGB) readings for real-time applications in nitrite ion detection. This development has the potential to offer an economical, precise, and easily transportable method for monitoring nitrite ions, presenting a promising approach to creating accessible tools in this field.

The potential of durum wheat-chickpea intercropping to improve the soil available phosphorus status and biomass production in a subtropical climate.

The intercropping system is a promising approach to augmenting the soil nutrient status and promoting sustainable crop production. However, it is not known whether intercropping improves the soil phosphorus (P) status in alluvial soils with low P under subtropical climates. Over two growing seasons--2019-2020 and 2020-2021--two experimental fields were employed to explore the effect of durum wheat (Dw) and chickpea (Cp) cropping systems on the soil available P. A randomized complete block design was used in this experiment, with three blocks each divided into three plots. Each plot was used for one of the following three treatments with three replications: Dw monocrop (Dw-MC), Cp monocrop (Cp-MC), and Dw + Cp intercrop (CpDw-InC), with bulk soil (BS) used as a control. A reduction in the rhizosphere soil pH (-0.44 and -0.11 unit) was observed in the (Cp-MC) and (CpDw-InC) treatments over BS, occurring concomitantly with a significant increase in available P in the rhizosphere soil of around 28.45% for CpDw-InC and 24.9% for Cp-MC over BS. Conversely, the rhizosphere soil pH was significantly higher (+0.12 units) in the Dw-MC treatments. In addition, intercropping enhanced the soil microbial biomass P, with strong positive correlations observed between the biomass P and available P in the Cp-MC treatment, whereas this correlation was negative in the CpDw-InC and Dw-MC treatments. These findings suggested that Cp intercropped with Dw could be a viable approach in enhancing the available P through improved pH variation and biomass P when cultivated on alluvial soil under a subtropical climate.