Effect Of pH Research Articles

Effect of pH on the emulsifying performance of protein-polysaccharide complexes.

Protein-polysaccharide complexes have been successfully used for emulsion stabilization. However, it is unclear how the complex's surface charge influences aggregation stability and coalescence stability of emulsions, and whether a low charged interfacial film can still maintain the coalescence stability of oil droplets. In the present study, the effects of pH (around the pI of protein) on the aggregation and coalescence stability of emulsions were investigated. Whey protein isolate (WPI) and peach gum polysaccharides (PGP) complexes (WPI-PGP complexes) were synthesized at pH 3, 4 and 5. Their sizes were 598, 274 and 183 nm, respectively, and their ζ-potentials were +2.9, -8.6 and -22.8 mV, respectively. Interface rheological experiments showed that WPI-PGP complex at pH 3 had the lowest interfacial tension, and formed the softest film compared to the complexes at pH 4 and 5. Microfluidic experiments showed that all WPI-PGP complexes were able to stabilize droplets against coalescence within short timescales (milliseconds). At pH 3, no coalescence was observed even under conditions where the continuous phase flow influenced the shape of oil droplets (from spheres to ellipsoids). At pH 4 and 5, the model emulsions were stable over 16 days of storage, extensive aggregation and creaming occurred at pH 3 after 8 days. Importantly, no coalescence took place. The present study confirmed that the aggregation stability of the emulsions was mainly determined by the surface charge of the complex, whereas the coalescence stability of emulsions is expectedly determined by steric repulsion, providing new insights into how to prepare stable food emulsions. © 2024 Society of Chemical Industry.

Management of caffeine in wastewater using MOF and perovskite materials: optimization, kinetics, and adsorption isotherm modelling

AbstractPharmaceuticals and personal care products (PPCPs) have been increasingly used all over the world and they have been reported on water cycle and cause contamination. Among these pharmaceuticals is caffeine (CAF). In this work, CAF removal from aqueous samples by metal–organic framework (UIO-66) and perovskite (La0.7Sr0.3FeO3) was achieved. Detailed studies on the preparation of MOFs and perovskite oxides compounds have been presented. Extensive characterizations such as X-Ray diffraction (XRD), field emission scanning electron microscope (FESEM), Fourier transform infrared spectra (FT-IR), N2 adsorption–desorption isotherms were also carried out to assure proper formation and to better understand the physico-chemical behavior of the synthesized samples before and after adsorption. Batch experiments of CAF adsorption onto both MOFs and perovskite were performed to compare the effectiveness of both materials on the removal competence of the CAF residue at different conditions including the effect of pH, initial concentration, and contact time. It was observed that the adsorption capacity of CAF by MOF increased with increasing acidity. On the other hand, the adsorption capacity of perovskite is stable in pH 4–10. The maximum adsorption capacities of UiO-66 and perovskite toward CAF are high as 62.5 mg g−1 and 35.25 mg g−1, respectively. Equilibrium isotherms were investigated by numerous models: Langmuir, Freundlich, Temkin, Redlich-Peterson, Sips, Langmuir-Freundlich, Toth, Kahn, Baudu, and Fritz Schlunder. Moreover, the kinetics of the CAF@MOF and CAF@Perovskite systems have been studied by five kinetic models (Pseudo-1st -order (PFO), Pseudo-2nd -order (PSO), Mixed 1st, 2nd-order, Intraparticle diffusion and Avrami). The best model described the adsorption of CAF onto both of MOF and perovskite was the mixed 1st, 2nd-order model. The metal–organic framework and perovskite were applied to quickly extract CAF from water samples successfully. The maximum removal percentage obtained for MOF and perovskite was 0.89% and 0.94% respectively within 30 min contact time which suggests that these materials are considered as promising adsorbents for CAF.

An Incubation System for the Simulation of Ammonia Emissions from Soil Surface-Applied Slurry: Effect of pH and Acid Type

Acidification of slurry is a promising approach for reducing ammonia emissions during the application procedure. Since only a few studies have been conducted focusing on ammonia emissions during the application of liquid organic fertilizers on the soil surface, a suitable incubation system was developed to evaluate the effects of acidification under controlled conditions. This incubation system was used to measure the ammonia emissions of various liquid organic fertilizers. The substrates were acidified with sulfuric and citric acid to different pH values to determine both the influence of the pH value of the substrates and of the type of acid on the ammonia emissions. The emissions decreased with declining pH value, and the reduction in emissions compared to the initial pH of the substrate was over 86% for pH 6.5 and over 98% for pH 6.0 and below. At the same pH value, the ammonia emissions did not differ between substrates acidified with citric acid and sulfuric acid, although more than twice as much 50% citric acid was required compared to 96% sulfuric acid to achieve the same pH value. Overall, our results demonstrate that the incubation system used is suitable for measuring ammonia emissions from surface-applied liquid organic fertilizers. The system allows for the differentiation of emission levels at various pH levels and is therefore suitable for testing the effectiveness of additives for reducing ammonia emissions from liquid organic fertilizers.

Synthesis and characterisation of hydrogel based on propiolic acid

ABSTRACT In this study, using a propiolic acid monomer and ammonium persulphate as initiator and N,N’-methylenebisacrylamide as crosslink agent, poly propiolic acid hydrogel was designed and tested for water absorption. Also, to investigate the effect of pH on hydrogel’s efficiency, swelling was investigated at different pH levels. To obtain the optimal formula for hydrogel with maximum water absorption, the initiator and crosslink agent levels were changed. The obtained data showed that the highest conversion rate of monomer to polymer was observed for the S1 sample with an initiator concentration of 10% by weight and a crosslinking agent with a concentration of 2% by weight. It also has the highest water absorption for this sample and its swelling rate is 27.6 times that of dry hydrogel. Increasing the concentration of the crosslinking agent and reducing the amount of initiator resulted in the reduction of hydrogel swelling in water. Also, the swelling rate of samples at different pH shows that reducing pH to acidic environments or increasing it to basic environments led to a decrease in network swelling in all three samples. Finally, to investigate the structure and morphology of hydrogels, FTIR, SEM, and measuring the amount of hydrogel swelling at ambient temperature tests were used.

Preparation of geopolymer for in-situ pavement construction on the moon utilizing minimal additives and human urine in lunar regolith simulant

Constructing lunar pavements is of great significance for improving the transportation efficiency of materials and personnel transfer at lunar bases. Utilizing lunar regolith for the in-situ preparation of geopolymer is an effective means of supplying raw materials for lunar pavement construction. This present study prepared geopolymers for pavement material with lunar regolith simulant. The influence of NaOH on the compressive strength of geopolymers was understood by using different percentages of NaOH as alkaline activator. The effect of urine on the compressive strength of geopolymers by using artificial urine of different pH values as liquid phases. The results indicated that the addition of artificial urine slightly reduces the compressive strength of geopolymers, and the effects of pH and NaOH percentage are different. Microstructural analysis performed by Mercury Intrusion Porosimetry and Scanning Electron Microscope, indicated that choosing fine-particle lunar regolith simulant as precursor is more conducive to the preparation of high-strength geopolymers using human urine.

Role of Calcium Chloride on the Eluting Process of Residual Ammonium from Weathered Crust Elution-Deposited Rare Earth Ore Tailings

A large amount of ammonium salt leaching agent will remain in the leaching site of weathered crust elution-deposited rare earth ore (WREOs). The release of residual ammonium (RA) will seriously affect the water system ecology of the mining area, and it is urgent to control it. In this paper, column eluting was used to simulate the eluting process of RA in rare earth (RE) ore tailings, and the effects of calcium chloride concentration, eluting temperature, liquid-solid ratio, eluent pH and eluent flow rate on the eluting process of RA in rare earth ore tailings were discussed. It was found that calcium chloride could effectively elute the RA from ore tailings. Eluting agent pH almost had no effect on the eluting process of RA in the pH range of 4–6, and a greater impact on it at pH 8. The flow rate could effectively enhance the elution efficiency. The optimum conditions were calcium ion concentration of 0.1 mol/L, liquid-solid ratio of 2:1, pH 4–6, flow rate of 0.6 mL/min and elution at room temperature. At this time, the elution efficiency of RA was 91.85%. The eluting process of RA in ore tailings was controlled by the inner particle diffusing according to the kinetic analysis. The reaction order was 0.368, and the activation energy of the reaction is 12.450 kJ/mol. This will provide a theoretical basis and technical support for the efficient eluting process of residual ammonium in the leaching site of WREOs.

Modulating Nonlinear Acoustic Response of Phospholipid-Coated Microbubbles with pH for Ultrasound Imaging.

Activatable microbubble contrast agents for contrast-enhanced ultrasound have a potential role for measuring physiologic and pathologic states in deep tissues, including tumor acidosis. In this study, we describe a novel observation of increased harmonic oscillation of phosphatidylcholine microbubbles (PC-MBs) in response to lower ambient pH using a clinical ultrasound scanner. MB echogenicity and nonlinear echoes were monitored at neutral and acidic pH using B-mode and Cadence contrast pulse sequencing (CPS), a harmonic imaging technique at 7.0 and 1.5 MHz. A 3-fold increase in harmonic signal intensity was observed when the pH of PC-MB suspensions was decreased from 7.4 to 5.5 to mimic normal and pathophysiological levels that can be encountered in vivo. This pH-mediated activation is tunable based on the chemical structure and length of phospholipids composing the MB shell. It is also reliant on the presence of phosphate groups, as the use of lipids without phosphate instead of phospholipids completely abrogated this phenomenon. The increased harmonic signal likely is the result of increased MB oscillation caused by a decrease of the interfacial tension induced at a lower pH, altering the lipid conformation. While relative signal changes are interpreted clinically as mostly related to blood flow, pH effects could be significant contributors, particularly when imaging tumors. While our observation can be used clinically, it requires further research to isolate the effect of pH from other variables. These findings could pave the way toward for the development of new smart ultrasound contrast agents that expand the clinical utility of contrast-enhanced ultrasound.

Effect of Soil Acidification on Temperature Sensitivity of Soil Respiration

Soil pH significantly impacts microbial activity and community assembly, which in turn determines the temperature sensitivity (Q10) of soil respiration. Due to the high soil acidification in China, it is necessary to understand how soil acidification impacts Q10. Here, the Q10 of soil respiration was examined in a long-term field experiment (1982–present) with different soil pH caused by fertilization management. In this experiment, we selected treatments with neutral pH: (1) no crops and fertilization (CK); (2) crops without fertilization (NF); low pH with (3) crops with chemical fertilization (NPK); and (4) crops with chemical fertilization combined with wheat straw incorporation (WS). Under natural soil temperature changes, we observed that soil acidification lowered the Q10 value of soil respiration. Considering only temperature changes, the Q10 of soil respiration was strongly associated with microbial community composition, alpha diversity, and soil ammonium nitrogen. Considering the interaction between soil pH and temperature, warming strengthened the negative effect of soil pH on the Q10 of soil respiration, and the pathway through which soil pH mediated Q10 included not only microbial community composition, alpha diversity, and biomass but also the soil’s available phosphorus. This work enhanced our insights into the relationships between Q10, temperature, and soil pH by identifying important microbial properties and key soil environmental factors.

Improved Enzymatic Production of the Fucosylated Human Milk Oligosaccharide LNFP II with GH29B α-1,3/4-l-Fucosidases.

Five GH29B α-1,3/4-l-fucosidases (EC 3.2.1.111) were investigated for their ability to catalyze the formation of the human milk oligosaccharide lacto-N-fucopentaose II (LNFP II) from lacto-N-tetraose (LNT) and 3-fucosyllactose (3FL) via transglycosylation. We studied the effect of pH on transfucosylation and hydrolysis and explored the impact of specific mutations using molecular dynamics simulations. LNFP II yields of 91 and 65% were obtained for the wild-type SpGH29C and CpAfc2 enzymes, respectively, being the highest LNFP II transglycosylation yields reported to date. BbAfcB and BiAfcB are highly hydrolytic enzymes. The results indicate that the effects of pH and buffer systems are enzyme-dependent yet relevant to consider when designing transglycosylation reactions. Replacing Thr284 in BiAfcB with Val resulted in increased transglycosylation yields, while the opposite replacement of Val258 in SpGH29C and Val289 CpAfc2 with Thr decreased the transfucosylation, confirming a role of Thr and Val in controlling the flexibility of the acid/base loop in the enzymes, which in turn affects transglycosylation. The substitution of an Ala residue with His almost abolished secondary hydrolysis in CpAfc2 and BbAfcB. The results are directly applicable in the enhancement of transglycosylation and may have significant implications for manufacturing of LNFP II as a new infant formula ingredient.

Synthesis and characterization of Neurospora intermedia-based composite mycoprotein gel meat: Insight into the effect of pH and soluble starch on water-holding capacity and texture properties

Meat alternatives are in great demand in current situation to address the increasing human health and animal welfare issues. This study focuses on microbial protein meats, emphasizing the importance of sourcing structurally similar fungal strains and optimizing processing conditions. A new strain, Neurospora intermedia, was identified and evaluated for availability. The impact of pH (3, 5, and 7) and soluble starch (SS) addition (0, 3, and 6%) on the textural and water retention properties of composite mycoprotein gel meat (CMGM) developed by using N. intermedia was investigated. Zeta potential, dynamic rheology, SEM, and FTIR techniques were employed to elucidate the mechanism. CMGM at pH 7 exhibited the sparsest internal structure but demonstrated better elasticity and recovery properties due to strong electrostatic repulsion. Lowering pH enhanced material interaction, improving gel intensity and water-holding capacity after steaming. A 6% SS addition significantly enhanced CMGM's hardness and reduced internal porosity, which further enhanced the water retention, but also reduced fracture elongation. Thus a 3% SS addition was found to be moderate. The mycelium and gel in the system exhibited complementary characteristics. SPI and SS were dispersed under the guidance of the mycelial fiber framework before steaming. The materials were fully crosslinked after steaming and the mycelial fibers were fixed in the gel material, which conferred support to the gel material. As a result, the modulation of excipients can achieve CMGM with different properties—a systematic approach to producing high-quality microbial protein meat.

Thermodynamic and structural investigation of oily wastewater treatment using peach kernel and walnut shell based activated carbon.

Despite the many articles about activated carbon with different precursors in adsorption process, no in-depth research has been carried out to understand the causes of the difference in surface adsorption characteristics of activated carbon with different precursors and different activation processes. In this work, the ability of two active carbon adsorbents made of walnut shell and peach kernel by two chemical and physical methods (totally 4 different types of activated carbon) in treatment of oily wastewater including diesel, gasoline, used oil or engine lubricant has been compared. The results show that the chemical activated peach carbon active with 97% hardness has provided the highest hardness and physical activated walnut carbon active has obtained the lowest hardness value (87%). It is also found that peach activated carbon has a higher iodine number than walnut activated carbon, and this amount can be increased using chemical methods; Therefore, the highest amount of Iodine Number is related to Peach activated carbon that is made by chemical method (1230 mg/g), and the lowest amount of iodine number is seen in walnut activated carbon that is made by physical method (1020 mg/g). moreover, the pore diameter of physical activated carbon is lower than chemical activated carbon in all cases. So that the pore diameter of chemical activated peach carbon active is equal to 22.08 μm and the measured pore diameter of physical activated peach carbon active is equal to 20.42 μm. These values for walnut are obtained as 22.74 μm and 21.86 μm, respectively. Furthermore, the temperature and pH effects on the adsorption of different synthesized oily wastewater was studied and it was found that a decrease in adsorption can be seen with an increase in temperature or decreasing the pH value, which can be referred to this fact that the process of adsorption is an exothermic process. Finally, to analyze the compatibility of adsorption isotherms with experimental data and to predict the adsorption process, three different isotherms named Langmuir, Temkin, and Freundlich isotherms were applied and their parameters were correlated. The correlation results show that the Langmuir isotherm had the best correlation in all cases compared to the Freundlich and Temkin isotherms, based on the correlation coefficient, and the calculated R2 values which was greater than 0.99 in all the studied cases.

Bimolecular optimization of cellulase production by <i>Richoderma citrinoviride</i> and <i>Aspergillus niger</i> isolates on corn cob, rice bran and sorghum bran as biomass substrates

This work focuses on the assessment of the conditions relevant for the improvement of enzymes hydrolysis of pretreated corn cob, rice bran and sorghum bran by using Trichoderma Citrinoviride and Aspergillus niger. To achieve this, different fermentation conditions were applied to assess their effect in the optimization of cellulase production. Effects of fermentation duration, inoculation size, temperature and pH of fermentation on cellulase production were investigated. At 96 hrs of fermentation, maxim cellusale product was found to be at optimum in both organisms. Hence, 6% substrates concentration with 10 discs of 8mm inoculum size yielded maximum cellulase production in both A. niger and T. citrinoviride after 5 days of incubation. At 35ºC, A niger and T citrinoviride recorded maximum cellulase production 0.50 mg/ml in sorghum bran while 40ºC was optimum for maximum cellulase production for T, citrinoviride on corn cob. Whereas, pH 5.0 T. citrinoviride exhibits maximum cellulase production with sorghum bran 1.30 mg/ml compared to carboxymetyyl cellulose which served as control and sorghum bran 1.2mg/ml. These results highlight the potentials of T. citrinoviride as species of fungus for the industrial production of cellulase using Agricultural wastes as substrates. Cellulase yield was repressed in the presence of glucose and was induced in the presence of corn cob, rice bran and sorghum using T. citrinoviride. Cellulase yield from Corn cob, rice bran and sorghum bran differed significantly at (P<0.05) from glucose.

Aerobic Polishing of Liquid Digestate for Preparation of Hydroponic Fertiliser

Aerobic Polishing of Liquid Digestate for Preparation of Hydroponic Fertiliser

Effect of pH and salt on the protonation state of fatty aniline investigated by sum-frequency vibrational spectroscopy.

Langmuir monolayers of fatty aniline (C16-aniline) were investigated using sum-frequency vibrational spectroscopy at various pH levels and NaCl concentrations. To analyze the sum-frequency generation (SFG) spectra of aniline, a multi-peak Lorentzian model, in accordance with the theory of SFG for a charged interface, was applied. First, SFG spectra of C16-aniline from pH 2 to 6 at a constant ionic strength of 10mM (where the phase of the complex potential of the dc-induced signal was suppressed to a few degrees) were fitted with the above-mentioned method. The mean-field theory that considers the chemical equilibrium of the aniline headgroup was used to analyze the fitting results to find that the pKa of aniline is 4.4 ± 0.3. The protonation fraction of the aniline headgroup was estimated to be less than 5% at pH 6 and NaCl concentrations were up to 1M. The generalized Poisson-Boltzmann equation in the Gouy-Chapmann model effectively explained the observed SFG spectra in the OH region for fatty aniline at pH as low as 2, even for the systems without addition of any salt.

Investigation of ionic liquid adsorption and interfacial tension reduction using different crude oils; effects of salts, ionic liquid, and pH

The results revealed the significant effect of NaCl, KCl, CaCl2, MgCl2, CaSO4, MgSO4, and Na2SO4 and pH values of 3.5–11 on the interfacial tension (IFT) reduction using three types of neutral, acidic, and basic crude oils, especially for acidic crude oil (crude oil II) as the pH was changed from 3.5 to 11 (due to saponification process). The findings showed the highest impact of pH on the IFT of crude oil II with a reducing trend, especially for the pH 11 when no salts exist. The results revealed that the salts except MgCl2 and CaCl2 led to a similar IFT variation trend for the case of distilled water/crude oil II. For the MgCl2 and CaCl2 solutions, a shifting point for IFT values was inevitable. Besides, the dissolution of 1-dodecyl-3-methyl imidazolium chloride ([C12mim][Cl]) with a concentration of 100–1000 ppm eliminates the effect of pH on IFT which leads to a reducing trend for all the examined crude oils with minimum IFT of 0.08 mN/m. Finally, the [C12mim][Cl] adsorption (under pH values) for crude oils using only Na2SO4 was measured and the minimum adsorption of 0.41 mg surfactant/g Rock under the light of saponification process was obtained.

Heteroaggregation kinetics of nanoplastics and soot nanoparticles in aquatic environments

Heteroaggregation between polystyrene nanoplastics (PSNPs) and soot nanoparticles (STNPs) in aquatic environments may affect their fate and transport. This study investigated the effects of particle concentration ratio, electrolytes, pH, and humic acid on their heteroaggregation kinetics. The critical coagulation concentration (CCC) ranked CCCPSNPs > CCCPSNPs-STNPs > CCCSTNPs, indicating that heteroaggregation rates fell between homoaggregation rates. In NaCl solution, as the PSNPs/STNPs ratio decreased from 9/1 to 3/7, heteroaggregation rate decreased and CCCPSNPs-STNPs increased from 200 to 220 mM due to enhanced electrostatic repulsion. Outlier was observed at PSNPs/STNPs= 1/9, where CCCPSNPs-STNPs= 170 mM and homoaggregation of STNPs dominated. However, in CaCl2 solution where calcium bridged with STNPs, heteroaggregation rate increased and CCCPSNPs-STNPs decreased from 26 to 5 mM as the PSNPs/STNPs ratio decreasing from 9/1 to 1/9. In composite water samples, heteroaggregation occurred only at estuarine and marine salinities. Acidic condition promoted heteroaggregation via charge screening. Humic acid retarded or promoted heteroaggregation in NaCl or CaCl2 solutions by steric hindrance or calcium bridging, respectively. Other than van der Waals attraction and electrostatic repulsion, heteroaggregation was affected by steric hindrance, hydrophobic interactions, π − π interactions, and calcium bridging. The results highlight the role of black carbon on colloidal stability of PSNPs in aquatic environments.

Influence of pH on the formation of benzyl ester bonds between dehydrogenation polymer and cellulose

Generation of lignin-carbohydrate complex (LCC) between dehydrogenation polymer (DHP) and pulp fibers may have an important impact on the properties of pulp. In this work, the benzyl ester-type LCC was formed between oxidized cellulose and DHP. The effect of pH on the addition reaction of oxidized cellulose to quinone methide in the synthesis of DHP-cellulose complex (DHPCC) was investigated. The structure of the product was characterized by Fourier Transform Infrared (FTIR), Carbon 13-Nuclear Magnetic Resonance (13C-NMR), and 2-Dimensional Heteronuclear Single Quantum Coherence Nuclear Magnetic Resonance (2D HSQC NMR) analyses. The results indicated that cellulose was indeed oxidized and carboxyl groups were introduced into cellulose by the oxidation process. The formed DHPCC was connected by benzyl ester linkage. In addition, the pH of the reaction system had an important role in the formation of the benzyl ester bonds. The acidic condition (pH = 4.0) was conducive to the addition reaction of quinone methide with carboxyl groups of cellulose. Overall, this study provides helpful guidance for the generation of LCC between DHP and paper pulp fibers.

Synthesis, Spectral Characteristics, Sensing Properties and Microbiological Activity of New Water-Soluble 4-Sulfo-1,8-naphthalimides

A new water-soluble polyamidoamine (PAMAM) dendrimer modified with 4-sulfo-1,8-naphthalimide (DSNI) and its monomeric structural analogue (MSDI) were synthesized. Their photophysical properties were investigated in organic solvents of different polarities and aqueous solutions. The effect of pH on fluorescence intensity was determined. It was found that the dendrimer emits blue fluorescence in an acidic medium, which is quenched in an alkaline environment. This phenomenon is due to the possibility of suppression of nonradiative photoinduced electron transfer in acidic media. The influence of different metal ions (Cu2+, Pb2+, Sn2+, Sr2+, Mg2+, Ba2+, Co2+, Hg2+, Zn2+, Ni2+, Fe3+, Al3+) and anions (CN−, S2−, S2O52−, HPO42−, H2PO4−, F−, CH3COO−, NO2−, CO32−, SO42−) on the intensity of the emitted fluorescence was studied. Quenching was only found in the presence of Cu2+. This makes the dendrimer suitable for determining copper ions in water solutions in the presence of other metal ions and anions. Additionally, DSNI was used as a ligand to obtain a stable copper complex, the structure of which was investigated by electron paramagnetic resonance (EPR), infrared spectrum, and elemental analysis. Two copper ions were found to form a complex with one dendrimer. The in vitro microbiological activity of the new compounds against bacteria Pseudomonas aeruginosa and two viruses HRSV-2 and HAdV-5 was investigated. With a view to obtaining antibacterial and anti-viral textiles, cotton fabrics were treated with the three compounds, and then their activity against the same microbial strains was investigated. It was found that the microbiological activity was preserved after the application of the new compounds to the cotton fabrics.

PH Stabilized NH4+-Fed Nutrition Promotes Higher B Uptake and Plant Growth in Rapeseed (Brassica napus L.) by the Upregulation of B Transporters

AbstractRapeseed (Brassica napus L.) is a major oilseed crop with high boron (B) requirements. In hydroponic cultivation, B uptake is highly responsive to the media conditions (e.g., pH). Different N sources, such as NH4+ and NO3−, directly affect the media pH. To date, the underlying mechanisms, the role of the buffering at constant N-sources by separating the effects of pH and/or sources of N-form, for the uptake of B remain indistinct under hydroponic cultivation, particularly in rapeseed. Two identical experiments were conducted using (NH4)2SO4 and Ca(NO3)2 as sole N-sources each set were subjected to four treatments viz. non-buffered, buffered pH 5.0, 6.0, and 7.0 at low (1 µM) and high (100 µM) B for 5 days. The novelty of this study demonstrates that NH4+-fed plants prefer buffered pH (6 and 7) for promoting higher plant growth, which was in line with the B concentration, while NO3−-fed plants were not influenced. These aforesaid findings were further supported by the upregulation of BnaNIP5;1 and BnaBOR1;2 in the root and higher expression of BnaNIP5;1 in shoots with buffered pH in NH4+-fed plants. According to our findings, in NH4+-based buffering, B transport channel protein BnaNIP5;1 (through diffusion) facilitated B uptake and distribution from root to shoot while BnaBOR1;2 mediated active uptake of B was in root under low supply of B. In a nutshell, pH buffering in hydroponics is very important in NH4+-based but not in NO3−-based nutrition for the uptake of boron and growth of the rapeseed plants.

Impact of Peptide Length and Solution Conditions on Tetrameric Coiled Coil Formation.

Unlike naturally derived peptides, computationally designed sequences offer programmed self-assembly and charge display. Herein, new tetrameric, coiled coil-forming peptides were computationally designed ranging from 8 to 29 amino acids in length. Experimental investigations revealed that only the sequences having three or more heptads (i.e., 21 or more amino acids) exhibited coiled coil behavior. The shortest stable coiled coil sequence had a melting temperature (Tm) of approximately 58 ± 1 °C, making it ideal for thermoreversible assembly over moderate temperatures. Effects of pH and monovalent salt were examined, revealing structural stability over a pH range of 4 to 11 and an enhancement in Tm with the addition of salt. The incorporation of the coiled coil as a hydrogel cross-linker results in a thermally and mechanically reversible hydrogel. A subsequent demonstration of the hydrogel printed through a syringe illustrated one of many potential uses from 3D printing to injectable hydrogel drug delivery.