High Alkaline Conditions Research Articles

Release Behavior of Pb(II) Ions on the Galena Surface: Dissolution Experiment, DFT Calculation, and MD Simulation

In this study, the release behavior of Pb(II) ions from the galena surface and their occurrence forms in the migration process under acid and alkaline conditions were investigated by dissolution experiment, the density functional theory (DFT) calculation, and molecular dynamics (MD) simulation. The dissolution experiments indicated that acidic and high alkaline conditions are more beneficial for the release of Pb(II) rather than neutral and weak alkaline conditions. The quantum chemical calculations indicated that under acidic conditions, H+ can destroy the surface structure of galena, leading to the dissolution of Pb2+ from the mineral surface into the liquid phase. OH− can also damage the galena surface to a certain extent under alkaline conditions. Additionally, MD simulations were further utilized to study the occurrence forms of Pb(II) ions in alkaline solutions. The results suggested that with a certain concentration of OH−, Pb2+ ions will form lead hydroxide aggregates, while excessive OH− could lead to the dispersion and dissolution of the lead hydroxo complexes. The surface morphological observation by SEM can well support the calculation and simulation results.

The effects of pH regulators on the flotation separation of sphalerite and dolomite and their interaction mechanism

pH regulators play a key role in mineral flotation. In the study, the effects of CaO, Na2CO3 and NaOH on the flotation separation of sphalerite and dolomite were investigated, and the interaction mechanisms were analyzed by flotation tests of mixed minerals, scanning electron microscope (SEM) and energy dispersion spectrum (EDS), turbidity, Zeta potential and the extended Derjaguin-Landau-Verwey-Overbeek (EDLVO) theory. The results indicated that Na2CO3 was favorable for flotation separation of sphalerite and dolomite, but NaOH had a negligible effect. CaO improved the flotation recovery of MgO to a maximum value of 9.29%, but it was unfavorable to the enriched sphalerite. SEM-EDS results revealed that dolomite was adsorbed on the sphalerite surface in the three systems, but the amounts of dolomite attached in the CaO system was higher than those of the other two systems. Turbidity tests indicated that the turbidity in the CaO system was less than that in Na2CO3 and NaOH systems. The sphalerite surface was negatively charged regardless of the pH regulators. Na2CO3 and NaOH hardly affected the surface potentials of dolomite. However, CaO changed the surface potential of dolomite from negative value to positive value under high alkaline condition. EDLVO theoretical calculations revealed that the electrostatic forces in CaO system were stronger than that in Na2CO3 and NaOH systems, leading to the slime coating.

Tapping into haloalkaliphilic bacteria for sustainable agriculture in treated wastewater: insights into genomic fitness and environmental adaptation.

The increasing salinity and alkalinity of soils pose a global challenge, particularly in arid regions such as Tunisia, where about 50% of lands are sensitive to soil salinization. Anthropogenic activities, including the use of treated wastewater (TWW) for irrigation, exacerbate these issues. Haloalkaliphilic bacteria, adapted to TWW conditions and exhibiting plant-growth promotion (PGP) and biocontrol traits, could offer solutions. In this study, 24 haloalkaliphilic bacterial strains were isolated from rhizosphere sample of olive tree irrigated with TWW for more than 20years. The bacterial identification using 16S rRNA gene sequencing showed that the haloalkaliphilic isolates, capable of thriving in high salinity and alkaline pH, were primarily affiliated to Bacillota (Oceanobacillus and Staphylococcus). Notably, these strains exhibited biofertilization and enzyme production under both normal and saline conditions. Traits such as phosphate solubilization, and the production of exopolysaccharide, siderophore, ammonia, and hydrogen cyanide were observed. The strains also demonstrated enzymatic activities, including protease, amylase, and esterase. Four selected haloalkaliphilic PGPR strains displayed antifungal activity against Alternaria terricola, with three showing tolerances to heavy metals and pesticides. The strain Oceanobacillus picturea M4W.A2 was selected for genome sequencing. Phylogenomic analyses indicated that the extreme environmental conditions probably influenced the development of specific adaptations in M4W.A2 strain, differentiating it from other Oceanobacillus picturae strains. The presence of the key genes associated with plant growth promotion, osmotic and oxidative stress tolerance, antibiotic and heavy metals resistance hinted the functional capabilities might help the strain M4W.A2 to thrive in TWW-irrigated soils. By demonstrating this connection, we aim to improve our understanding of genomic fitness to stressed environments. Moreover, the identification of gene duplication and horizontal gene transfer events through mobile genetic elements allow the comprehension of these adaptation dynamics. This study reveals that haloalkaliphilc bacteria from TWW-irrigated rhizosphere exhibit plant-growth promotion and biocontrol traits, with genomic adaptations enabling their survival in high salinity and alkaline conditions, offering potential solutions for soil salinization issues.

First approach of fractals nickel-copper dendrites on stainless steel electrodes for ammonia oxidation to nitrogen monitored in operando by differential electrochemical mass spectroscopy

Fractal nickel-copper dendrites were synthesized by electrochemical deposition (ECD) on a stainless steel electrode (SS/NiCu). The electrode surface was characterized using Field Emission Scanning Electron Microscopy (FE-SEM), X-ray diffractometry (XRD), and Raman spectroscopy. The Ni-Cu molar ratio and the time applied in the ECD method were studied, revealing that both are critical factors in modifying and controlling the surface morphology. The SS/NiCu electrodes show a higher density current response when exposed to ammonium hydroxide, reaching a limiting current density at concentrations above 0.050 M NH4OH. Ammonia oxidation reaction (AOR) was monitored in operando using differential electrochemical mass spectroscopy (DEMS). When a bias potential over +1.50 V (vs. RHE) was applied, the evolution of oxygen and NO was observed. However, N2 was the only oxidation product at a constant potential below +1.50 V (vs. RHE). Oxygen (O2) evolution was the main competitive reaction during the AOR. The results show that products are strongly dependent on the electrochemical perturbation applied. The study demonstrated that the SS/NiCu electrodes are suitable for AOR to N2 in high alkaline conditions.

Acetyl zingerone methyl ether protects hair against oxidative damage incurred during and after treatment with permanent dyes and helps extend longevity of newly developed hair colour.

Use of permanent hair dyes causes unintended oxidative damage during the short time frame of the dyeing process that leads to perceivable changes in the feel, manageability and appearance of hair. Moreover, after hair has been dyed, regular exposure to the sun as a key environmental stressor continues to stimulate additional oxidative damage and to induce newly developed hair colours to fade prematurely or undergo changes in colour quality. To document the utility of acetyl zingerone methyl ether (MAZ) as a newly designed haircare ingredient to afford extra protection against oxidative damage and safeguard the integrity of hair colour. We demonstrate that MAZ is compatible chemically with the high alkaline conditions required for the colouring process and from theoretical calculations preferentially binds Fe and Cu ions relative to Ca or Zn ions. In model Fenton reactions MAZ effectively chelated active redox metals (Fe and Cu ions) in the presence of excess Ca+2 ions to inhibit the production of hydroxyl radicals, and in separate studies, MAZ neutralized singlet oxygen with greater efficiency than α-tocopherol by a factor of 2.5. When mixed into permanent dyes prior to hair tress application, MAZ significantly reduced combing forces, and SEM images led to substantial reductions in visual signs of surface damage. In a 28-day clinical study, relative to controls, mixing MAZ into hair dyes prior to application interfered neither with colour development nor with ability to cover grey hair and led to significant improvements in perceived attributes associated with hair's condition immediately following the dyeing process. Over a 28-day maintenance phase, especially between Day 14 and Day 28, continued use of shampoo and conditioner containing MAZ significantly preserved gloss measurements and hair colour in terms of longevity and colour quality as remaining desired and fresh compared to use of control shampoo and conditioner. This work establishes MAZ as a next-generation hair care ingredient for use in permanent dyes to attenuate oxidative damage and in shampoos and conditioners to promote longevity of hair colour and to maintain overall health and appearance of hair on a daily basis.

Barley β-glucan bioactive films: Promising eco-friendly materials for wound healing

Mixtures containing β-glucans were extracted from barley, under both mild and high alkaline conditions, to prepare biodegradable films (MA and HA, respectively), as natural dressings with intrinsic therapeutic properties. An in-depth characterization was performed to evaluate the impact of mild and high alkaline conditions on chemical, physicochemical, and biological features for potential use in wound treatments. Both MA and HA films exhibited a good ability to absorb water and simulate wound fluid, which helps maintain optimal tissue hydration. Moreover, their oxygen permeability (147.6 and 16.4 cm3 × μm/m2 × 24 h × Pa × 107, respectively) appeared adequate for the intended application. Biocompatibility tests showed that the films do not harm human dermal fibroblasts. Impressively, they promote cell attachment and growth, with MA having a stronger effect due to its higher β-glucan content. Furthermore, MA films can modulate macrophage behaviour in an inflamed microenvironment, reducing oxidative stress and pro-inflammatory cytokines, while simultaneously increasing levels of anti-inflammatory cytokines. In a scratch test, HA films allowed for faster fibroblast migration within the first 16 h compared to MA.Overall, this study demonstrates that developing β-glucan based films from barley, through a sustainable and cost-effective process, holds great promise for skin applications. These films exhibit significant potential to promote wound healing and modulate inflammation.

Large-scale assessment of characteristic plant species on Eurasian saline and alkaline soda ecosystems

From an ecological standpoint, saline and alkaline habitats are considered as extreme environments for vascular plants because salinity and alkalinity serve as primary structuring factors that significantly influence the species richness of vegetation cover. The non-alkaline salinity stress on plants primarily results from interactions of NaCl, Na2SO4, and other neutral salts, whereas alkalinity stress is caused by NaHCO3 and Na2CO3, accompanied by an increase in pH. Some halophytes and salt-tolerant plants are well-adapted to such permanent abiotic stress. Surprisingly, they are able to survive and reproduce under environmental conditions of more than 200 mM NaCl concentration and are also able to live permanently in extreme conditions. The aim of this study was to identify characteristic and indicator plant species for permanently alkaline soda and non-alkaline saline wetland habitats, and to analyze the relationship between the chemical composition of water and the plant’s saturation index. Based on the obtained results we can conclude that plant species identified to live in high saline conditions may also grow under high alkaline conditions. Two groups were distinguished based on the salinity and alkalinity: “Saline group” includes all types of halophytes and halotolerant species, while “Soda group” includes obligate alkalophytes and alkalotolerant species. However, the diversity of plants in alkaline environment is bigger than in saline environment, and most of the halotolerant species grow in both alkaline soda and saline habitats. It is possible to identify three indicator species requiring alkaline soda habitats to live in (Aster tripolium, Puccinellia limosa, Suaeda pannonica) and three indicator species that dominantly grow in non-alkaline saline habitats (Juncus maritimus, Salicornia prostrata, Suaeda salsa). Different independent variables have been identified and analyzed to understand their influence on the species saturation index by calculating percentage of characteristic plant species of the entire region. It was identified that the plant saturation index has a significant positive relationship with the Mean Temperature of the Warmest Quarter, Topsoil Sand, and Clay fraction variables, and there is a significant negative relationship with the Solid Earth surface heat flow, as the heating can increase the extremity of the environment. Identification of indicator species of salinity and alkalization makes it possible to determine the type of soil, water bodies and habitats as a rapid biomonitoring method as a visual observation, without the use of expensive equipment and chemical laboratory tests.

Decolorization and detoxification of direct blue 5B by a Marinobacter-dominated halo-thermoalkalophilic consortium

Azo dye-containing sewage is commonly detected at high salinity, temperature and pH. In this study, a halo-thermoalkalophilic azo dye decolorization consortium was enriched and named “consortium HL”. Consortium HL which was dominated by Marinobacter (84.30%), Desulfocurvibacter (1.89%), and Pseudomonas (1.85%), was able to completely decolorize Direct Blue 5B (DB5) during incubation with the material at 5% salinity, 50 °C, and pH 9 for 30 h. The decolorization mechanism was proposed based on combined metagenomic analysis, GC‒MS, and enzymatic activity detection. The action of the consortium HL showed great tolerance to variations in salinity, temperature and pH. A phytotoxicity study indicated that the metabolic intermediates showed no significant toxicity to the generation of Cucumis sativus and Oryza sativa seeds. This study, in which azo dye decolorization and degradation under high-salt, high-temperature and high-alkalinity conditions were investigated and deeply analyzed by metagenomic information, is the first report regarding the ability of Marinobacter to decolorize azo dyes at high temperatures.

Hexane defatting effects on rapeseed protein extractability and properties at neutral and mild pH 8.5

Rapeseed is a promising plant protein source yet to be fully explored. Traditionally, rapeseed proteins are extracted from hexane-defatted press cake at high alkaline conditions to maximise protein recovery. Instead of the traditional approach, this study explored the effects of extracting proteins from the whole-kernel seed, focusing on assessing the hexane defatting process followed by gentle protein extraction at neutral pH compared with pH 8.5. Extraction at neutral pH resulted in a napin-rich protein extract, while alkaline conditions favoured cruciferin extraction as expected. Hexane defatting destroyed the oil bodies's structure while detaching the cell membrane from the cell wall, causing dehydration, and enabling interactions between the seed constituents. Increasing cycles of hexane treatment greatly reduced the total protein recovery by 9 g/100 g under neutral pH and >60 g/100 g under mild alkaline conditions which affected the protein structure, leading to a more rigid structure with a slightly higher melting temperature.

Preparation of N-halamine-based mesoporous composites for decontamination of formaldehyde and simultaneous deactivation of bacteria

Environmental contamination can cause serious problems in water cycling systems. In this study, mesoporous composite-supported N-halamines (MCSNs) were synthesized and characterized, where the surface area retention rate of the MCSNs was over 70 % higher than MCM-41. The reaction between organic N-halamines and formaldehyde was examined in aqueous phase. The monomeric N-halamines (MCDMH) rapidly reacted with formaldehyde (10 ppm, 10 mL), and finished completely within 10 min. The MCSNs only reacted with formaldehyde in the high molar ratio (Cl+ to formaldehyde, 40:1) and alkaline conditions (pH higher than 10), and approximately 60 % of formaldehyde can be degraded within 10 min. The reaction kinetics were studied and the kinetic parameters were investigated. The MCSNs were highly effective against S. aureus (7.94 logs) and E. coli O157:H7 (8.0 logs) with 1 min of contact time, demonstrating impressive antibacterial properties in aqueous conditions. As a type of antibacterial material, MCSNs introduce a new direction for the application of N-halamine-based materials in formaldehyde decontamination, indicating their potential to be utilized as novel water treatment materials.

Rational engineering of Halomonas salifodinae to enhance hydroxyectoine production under lower-salt conditions

Hydroxyectoine is an important compatible solute that holds potential for development into a high-value chemical with broad applications. However, the traditional high-salt fermentation for hydroxyectoine production presents challenges in treating the high-salt wastewater. Here, we report the rational engineering of Halomonas salifodinae to improve the bioproduction of hydroxyectoine under lower-salt conditions. The comparative transcriptomic analysis suggested that the increased expression of ectD gene encoding ectoine hydroxylase (EctD) and the decreased expressions of genes responsible for tricarboxylic acid (TCA) cycle contributed to the increased hydroxyectoine production in H. salifodinae IM328 grown under high-salt conditions. By blocking the degradation pathway of ectoine and hydroxyectoine, enhancing the expression of ectD, and increasing the supply of 2-oxoglutarate, the engineered H. salifodinae strain HS328-YNP15 (ΔdoeA::PUP119-ectD p-gdh) produced 8.3-fold higher hydroxyectoine production than the wild-type strain and finally achieved a hydroxyectoine titer of 4.9 g/L in fed-batch fermentation without any detailed process optimization. This study shows the potential to integrate hydroxyectoine production into open unsterile fermentation process that operates under low-salinity and high-alkalinity conditions, paving the way for next-generation industrial biotechnology.Key points• Hydroxyectoine production in H. salifodinae correlates with the salinity of medium• Transcriptomic analysis reveals the limiting factors for hydroxyectoine production• The engineered strain produced 8.3-fold more hydroxyectoine than the wild typeGraphical

CuFeS2/MXene-Modified Polyvinylidene Fluoride Membrane for Antibiotics Removal through Peroxymonosulfate Activation

In this research, the CuFeS2/MXene-modified polyvinylidene fluoride (PVDF) membrane was prepared to activate peroxymonosulfate (PMS) to remove moxifloxacin (MOX) and its morphology; surface functional groups and hydrophilicity were also studied. The parameters of the catalytic membrane/PMS system were optimized, with an optimal loading of 4 mg/cm2 and a PMS dosage of 0.20 mM. High filtration pressure, alkaline conditions, and impurities in water could inhibit MOX removal. After continuous filtration, the removal efficiency of MOX using the catalytic membrane/PMS system and PVDF membrane was 68.2% and 9.9%, respectively. Batch filtration could remove 87.8% MOX by the extra 10 min contact time between the catalytic membrane and solution. During the filtration process, CuFeS2/MXene on the surface of the catalytic membrane activated PMS to produce SO4•−, HO•, and 1O2, and MOX was removed through adsorption and degradation. Taking humic acid (HA) as the model foulant, reversible fouling resistance in the catalytic membrane/PMS system was 22.8% of the PVDF membrane. The catalytic membrane/PMS system weakened the formation of the cake layer by oxidizing HA into smaller pollutants and followed the intermediate blocking cake filtration model. The novelty of this research was to develop a CuFeS2/MXene–PVDF membrane-activated PMS system and explore its application in antibiotics removal.

Green Fabrication of Superhydrophilic/Underwater Superoleophobic Composite Membrane for High-Efficiency Oil/Water Separation in Harsh Environments.

Due to the high oil spill incidence and industrial wastewater discharge including oil and emulsified oil, designing and synthesizing oil-water separation materials which can maintain stability under harsh environmental conditions with high separation efficiencies remains a great challenge. The present work developed an easy, green, cost-effective, and easily scaled-up approach for fabricating cellulose-based membranes. First, we coated polydopamine (PDA) onto fibers of filter membrane (FM). Then, the PDA-FM membrane was immersed into the mixed solution of poly(vinyl alcohol)/poly(acrylic acid) (PVA/PAA) and further thermally cross-linked at 150 °C to create a superhydrophilic/underwater superoleophobic membrane (PVA/PAA@PDA-FM) to separate oil/water mixtures. The simple thermally cross-linking process promotes multiple covalent chemical bonds generation between cellulose filter membrane, PAA, PDA, and PVA, endowing membranes with excellent stability and resistance to acidity, alkalinity, and salinity. The PVA/PAA@PDA-FM membrane not only demonstrates great separation performance (>99.8%) and great flux (>1000 L m-2 h-1) in oil-water immiscible mixtures but also maintains high separation efficiency under conditions of high acidity, alkalinity, and salinity. Additionally, the PVA/PAA@PDA-FM membrane exhibits excellent separation capacity in oil-water emulsions, which can maintain the >99.6% separation efficiency even after 40 cycles in harsh environments, showing outstanding reusability. Thus, due to the multiple cross-linked networks in the membrane, the excellent performance makes the PVA/PAA@PDA-FM membrane a good application prospect in water purification and oily wastewater treatment.

Adsorption behavior and solidification mechanism of Pb(II) on synthetic C-A-S-H gels with different Ca/Si and Al/Si ratios in high alkaline conditions

Calcium silicate aluminate hydrate (C-A-S-H) is the main hydration product and its porous adsorption property can effectively inhibit Pb(II) leaching from alkaline pore solution of alkali-activated municipal solid waste incineration (MSWI) fly ash compacts. The study examines how different ratios of Ca/Si and Al/Si in C-(A)-S-H affect Pb(II) adsorption behavior and mechanism in high alkaline conditions. The results showed that Al-doped C-A-S-H gels have increased specific surface area and cumulative pore volume, and slightly decreased average pore size. Pb(OH)3- adsorption by C-A-S-H was mainly chemisorption with spontaneity. Temperature, pH value, Al/Si and Ca/Si ratios of C-A-S-H affected Pb(II) adsorption. Equilibrium adsorption capacity (Qe) initially increased then decreased with higher Al/Si for C-A-S-H with Ca/Si 0.60 but decreased with higher Al/Si for Ca/Si 1.20. Active Si-OH (Q1 or Q2b) and Al-OH (Q2(1Al)) in aluminosilicate tetrahedra chains dehydrate and condense with Pb(OH)3- to form Si-O-Pb or Al-O-Pb bonds. Higher interlayer water content in low Ca/Si and Al/Si C-A-S-H facilitated ion exchange during Pb(II) adsorption. After adsorption, aluminosilicate tetrahedra chain length increased while interlayer water content decreased. Ca(II) and Pb(II) in C-A-S-H underwent partial ion exchange during the adsorption process. Simulation results indicate Pb(OH)3- was more likely to polycondensate with silica tetrahedral bridging oxygen in Si2AlO2(OH)8 to form Si-O-Pb than Al-O-Pb bonds. These findings provide theoretical support for designing dosages of alkali activators and doped aluminosilicate minerals to improve the solidification efficiency of Pb(II) in alkali-activated MSWI fly ash compacts.

NiAlFe LTH /MoS2 p-n junction heterostructure composite as an effective visible-light-driven photocatalyst for enhanced degradation of organic dye under high alkaline conditions

Designing of an effectual heterostructure photocatalyst for catalytic organic pollutant exclusion has been the subject of rigorous research intended to resolve the related environmental aggravation. Fabricating p-n junctions is an effective strategy to promote electron-hole separation of semiconductor photocatalysts as well as enhance the organic toxin degradation performance. In this study, a series of n-type NiAlFe-layered triple hydroxide (LTH) loaded with various ratios of p-type MoS2 was synthesized for forming a heterostructure LTH/MoS2 (LMs) by an in situ hydrothermal strategy. The photocatalysts were characterized by XRD, SEM&EDX, TEM, FT-IR, XPS, as well as UV–vis DRS. The photoactivity of photocatalysts was tested by the degradation of Indigo Carmine (IC) dye. The optimized catalyst (LM1) degrades 100% of indigo dye in high alkaline pH under UV light for 100 min. Besides, the degradation rate of LM1 is 15 times higher than that of pristine NiAlFe-LTH. The enhanced photoactivity is attributed to the synergistic effect between NiAlFe-LTH and MoS2 as well as the p-n junction formation.

Optimization of a Rare Earth and Aluminum Leaching Process from Weathered Crust Elution-Deposited Rare Earth Ore with Surfactant CTAB

Ammonium sulfate is typically employed as a leaching agent in the in situ leaching of weathered crust elution-deposited rare earth ore. However, it is associated with challenges such as low efficiency in mass transfer for rare earth (RE) leaching, high usage of the leaching agent, and prolonged leaching duration. To address the issues mentioned above, the surfactant cetyltrimethyl ammonium bromide (CTAB) was compounded with 2% ammonium sulfate to form a leaching agent in this paper. The effects of CTAB concentration, temperature, pH, and leaching agent flow rate on the rare earth (RE) and aluminum (Al) leaching mass transfer process from RE ore were investigated using chromatographic plate theory. The results revealed that CTAB addition improved the RE mass transfer process while moderately inhibiting the Al mass transfer efficiency. Increasing the temperature and pH of the leaching solution led to higher theoretical plate numbers for RE and Al leaching, lowered theoretical plate height (HETP), and enhanced leaching mass transfer efficiency. However, under high temperature and alkaline conditions, the mass transfer efficiency begins to decrease, indicating that high temperature and alkaline conditions are not conducive to the synergistic enhancement of RE and Al leaching by CTAB. Considering that clay minerals have good pH buffering properties, adjusting the pH of the leaching solution during rare earth ore leaching operations was deemed unnecessary. The optimal mass transfer conditions for leaching RE and Al were identified as 2% ammonium sulfate concentration, 0.00103 mol/L CTAB concentration, pH range of 5.2–5.5 for the leaching solution, 0.6 mL/min leaching solution flow rate, and room temperature. The rare earth leaching mass transfer effect could be enhanced during summer operations.

Identification of Gene-Allele System Conferring Alkali-Tolerance at Seedling Stage in Northeast China Soybean Germplasm.

Salinization of cultivated soils may result in either high salt levels or alkaline conditions, both of which stress crops and reduce performance. We sampled genotypes included in the Northeast China soybean germplasm population (NECSGP) to identify possible genes that affect tolerance to alkaline soil conditions. In this study, 361 soybean accessions collected in Northeast China were tested under 220 mM NaHCO3:Na2CO3 = 9:1 (pH = 9.8) to evaluate the alkali-tolerance (ATI) at the seedling stage in Mudanjiang, Heilongjiang, China. The restricted two-stage multi-locus model genome-wide association study (RTM-GWAS) with gene-allele sequences as markers (6503 GASMs) based on simplified genome resequencing (RAD-sequencing) was accomplished. From this analysis, 132 main effect candidate genes with 359 alleles and 35 Gene × Environment genes with 103 alleles were identified, explaining 90.93% and 2.80% of the seedling alkali-tolerance phenotypic variation, respectively. Genetic variability of ATI in NECSGP was observed primarily within subpopulations, especially in ecoregion B, from which 80% of ATI-tolerant accessions were screened out. The biological functions of 132 candidate genes were classified into eight functional categories (defense response, substance transport, regulation, metabolism-related, substance synthesis, biological process, plant development, and unknown function). From the ATI gene-allele system, six key genes-alleles were identified as starting points for further study on understanding the ATI gene network.

Rh proteins and H+ transporters involved in ammonia excretion in Amur Ide (Leuciscus waleckii) under high alkali exposure

High alkaline environment can lead to respiratory alkalosis and ammonia toxification to freshwater fish. However, the Amur ide (Leuciscus waleckii), which inhabits an extremely alkaline lake in China with titratable alkalinity up to 53.57 mM (pH 9.6) has developed special physiological and molecular mechanisms to adapt to such an environment. Nevertheless, how the Amur ide can maintain acid-base balance and perform ammonia detoxification effectively remains unclear. Therefore, this study was designed to study the ammonia excretion rate (Tamm), total nitrogen accumulation in blood and tissues, including identification, expression, and localization of ammonia-related transporters in gills of both the alkali and freshwater forms of the Amur ide. The results showed that the freshwater form Amur ide does not have a perfect ammonia excretion mechanism exposed to high-alkaline condition. Nevertheless, the alkali form of Amur ide was able to excrete ammonia better than freshwater from Amur ide, which was facilitated by the ionocytes transporters (Rhbg, Rhcg1, Na+/H+ exchanger 2 (NHE2), and V-type H+ ATPase (VHA)) in the gills. Converting ammonia into urea served as an ammonia detoxication strategy to reduced endogenous ammonia accumulation under high-alkaline environment.

Isolation, screening and optimization of alkaliphilic cellulolytic fungi for production of cellulase

Abstract This study concerns with the production and partial characterization of alkaline cellulase from alkaliphilic cellulolytic (AC) fungi isolated fromsoil in Perlis, Malaysia. The best fungi strain was selected on the basis of producing the highest cellulase at high pH conditions. Cellulase from the selected fungi strain was further characterized under saccharification but varies in operating parameters. Finally, the kinetic model describing the growth of the AC fungi strain was studied by employing the logistic model. Among the tested fungi strains, Basidiomycetes strain (BK1) showed high potentiality for the production of maximum alkaline cellulase production at pH 9 after 72 h of incubation at 30°C containing 6 g·L−1 carboxyl methyl cellulose. The saccharification process showed that the enzyme favour high alkaline condition and proves thermotolerant properties, while 15% (v/v) enzyme loading and 1% substrate concentration recorded the highest glucose production at about 1.2–1.3 mg·mL−1. The novelty of the study is to identify and optimize a unique indigenous fungi that emit alkaliphilic cellulase as alternative usage in biotechnology industries due to its capacity to adapt to the extreme conditions of specific industrial processes. There are revolutionary options for use in biotechnological businesses that involve high pH and therefore have substantial biotechnological promise.

Optimized Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) Production by Moderately Haloalkaliphilic Bacterium Halomonas alkalicola Ext

Polyhydroxyalkanoates (PHAs) are biodegradable and biocompatible polymers that are produced by microorganisms as storage materials under limited nutrition and excess carbon. These PHAs have been found to be ideal for replacing synthetic plastics for use in packaging and biomedical applications. In this study, an alkaliphilic and moderately halophilic bacterium Halomonas alkalicola Ext was isolated from Lake Simbi Nyaima in western Kenya and investigated for PHA production. Sudan Black B and Nile Red A staining showed that bacterium had distinct ability for accumulation of PHAs. To optimize PHA production, the bacterium was grown in submerged fermentation under varying culture conditions and different sources and concentrations of carbon and nitrogen. With one-factor-at-a-time (OFTA) approach, optimal PHA yields were obtained after 72 hours at a pH of 10.0, temperature of 35°C, and 2.5% (w/v) NaCl. The bacterium yielded the highest biomass, and PHA amounts on 2% galactose and 0.1% ammonium sulfate as sources of carbon and nitrogen, respectively. A record PHA yield of 0.071 g g-1 with a titer of 1.419±0.09 g/L was achieved from 3.397 g/L of biomass, equivalent to 41.8% PHA content. Using response surface methodology, PHA titer was increased by 1.5% to 1.44 g/L, while PHA content was improved 1.1-fold to 45.57%. Polymer analysis revealed that the extracted PHA was a poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) (3−HB:3−HV=92:8) with two copolymer subunits of 3-hydroxyvaryrate (3-HB) and 3-hydroxybutyrate (3-HV). Halomonas alkalicola Ext attained efficient galactose conversion into PHBV under high salinity and alkalinity conditions.