Anticyanobacterial effect of p-coumaric acid on Limnothrix sp. determined by proteomic and metabolomic analysis.

Regulating photosynthetic machinery is a powerful but challenging strategy for selectively inhibiting bloom-forming cyanobacteria, in which photosynthesis mainly occurs in thylakoids. P-coumaric acid (p-CA) has several biological properties, including free radical scavenging and antibacterial effects, and studies have shown that it can damage bacterial cell membranes, reduce chlorophyll a in cyanobacteria, and effectively inhibit algal growth at concentrations exceeding 0.127 g/L. Allelochemicals typically inhibit cyanobacteria by inhibiting photosynthesis; however, research on inhibiting harmful algae using phenolic acids has focused mainly on their inhibitory and toxic effects and metabolite levels, and the molecular mechanism by which p-CA inhibits photosynthesis remains unclear. Thus, we examined the effect of p-CA on the photosynthesis of Limnothrix sp. in detail. We found that p-CA inhibits algal growth and damages photosynthesis-related proteins in Limnothrix sp., reduces carotenoid and allophycocyanin levels, and diminishes the actual quantum yield of Photosystem II (PSII). Moreover, p-CA significantly altered algal cell membrane protein systems, and PSII loss resulting from p-CA exposure promoted reactive oxygen species production. It significantly altered algae cell membrane protein systems. Finally, p-CA was found to be environmentally nontoxic; 80 % of 48-h-old Daphnia magna larvae survived when exposed to 0.15 g/L p-CA. These findings provide insight into the mechanism of cyanobacterial inhibition by p-CA, providing a more practical approach to controlling harmful algal blooms.

Quantitative relationship between soil pH and electrical conductivity values and cadmium phytoavailability for Chinese cabbage under simulated conditions.

Pot experiments were conducted to investigate the impacts of continuous addition of different concentrations of calcium chloride (CaCl2) and/or low-molecular-weight organic acids (LMWOAs) on soil pH, electrical conductivity (EC), and cadmium (Cd) transformation. These factors subsequently affected Cd phytoavailability in a system consisting of Cd-contaminated soil and Chinese cabbage (Brassica chinensis L.). The results indicate that CaCl2 addition had a greater impact on reducing soil pH value, increasing soil EC value, and enhancing Cd phytoaccumulation in Chinese cabbage compared to LMWOAs. When soil pH dropped by 0.3 unit and the soil EC increased by 500 µS cm-1, the Cd concentration in the Chinese cabbage shoots was 3 times higher than that in the control group. Throughout two planting terms of Chinese cabbage, the addition of CaCl2 (1.6-3.2 g kg-1) and LMWOAs (≤ 1.0 g kg-1) led to phytoextracted Cd concentration exceeding exchangeable Cd concentration in soil samples before the pot experiment. Regarding phytoextracted Cd, desorption from carbonate-bound Cd contributes more than desorption from bound to organic matter Cd and adsorption to Fe/Mn oxide Cd. This study underscores the influence of soil pH and EC value variations and Cd transformation on Cd phytoavailability. Special attention should be given to leafy vegetables grown in Cd-contaminated soil, as the phytoavailable Cd concentration reaches approximately 2.0 µg kg-1, which may lead to Cd levels surpassing acceptable limits for Chinese cabbage.

Identification of cadmium phytoavailability in response to cadmium transformation and changes in soil pH and electrical conductivity.

Owing to complex changes in the soil environment, determining cadmium (Cd) phytoavailability is challenging. We devised a soil-wheat system to monitor alterations in soil pH, electrical conductivity (EC), and Cd transformation under various rates of calcium chloride and/or low-molecular-weight organic acids (LMWOAs) addition. The findings indicate that decreasing soil pH value, increasing soil EC value, and Cd transformation affect the phytoextraction of Cd. The exchangeable Cd and transformation of Cd under shifts in soil pH and EC contribute differentially to the phytoextracted Cd. The level of potentially phytoavailable Cd was identified through complete wheat cultivation in which the soil pH decreased by 0.47 unit and soil EC increased by 600-1000 µS cm-1, resembling the concentration of 0.01 M LMWOAs extractable Cd, when transitioning from paddy to dryland soil. Based on considering the phytoextracted Cd as the phytoavailable Cd throughout a complete wheat growth term, the threshold for phytoavailable Cd in soil, ensuring the safety of wheat grain (limit: 0.1 mg kg-1), is determined to be 2.90 µg kg-1. Maintaining control over Cd phytoavailability in soil emerges as the key factor in ensuring the safety of wheat grain cultivation.

Plant Gravitropism and Signal Conversion under a Stress Environment of Altered Gravity.

Humans have been committed to space exploration and to find the next planet suitable for human survival. The construction of an ecosystem that adapts to the long-term survival of human beings in space stations or other planets would be the first step. The space plant cultivation system is the key component of an ecosystem, which will produce food, fiber, edible oil and oxygen for future space inhabitants. Many plant experiments have been carried out under a stimulated or real environment of altered gravity, including at microgravity (0 g), Moon gravity (0.17 g) and Mars gravity (0.38 g). How plants sense gravity and change under stress environment of altered gravity were summarized in this review. However, many challenges remain regarding human missions to the Moon or Mars. Our group conducted the first plant experiment under real Moon gravity (0.17 g) in 2019. One of the cotton seeds successfully germinated and produced a green seedling, which represents the first green leaf produced by mankind on the Moon.

Doping and facet effects synergistically mediated interfacial reaction mechanism and selectivity in photocatalytic NO abatement.

The surface atomic coordination and arrangement largely determine photocatalytic properties. Whereas, the intrinsic impact of surface microstructures on the reaction mechanism and pathway is still unclear. Herein, via constructing N-doped Bi2O2CO3 photocatalysts with diverse exposed facets, (1 1 0) and (0 0 1) facet, we testify that the pivotal roles of crystal facet and doping effect on the intermediate production and reactivity for photocatalytic nitric oxide (NO) abatement. The photoreactivity of N-doped Bi2O2CO3 is documented to be higher than that of the pure samples because of the enhanced light absorption and charge transfer. Further in situ probing experiments and theoretical calculations verify that the unique adsorption patterns and activated intermediates on the (1 1 0) facet facilitate the formation of final products and inhibit the generation of toxic NO2 by-product in terms of thermodynamics. More importantly, we found that the selective and nonselective oxidation processes are emerged over (1 1 0) and (0 0 1) facets of Bi2O2CO3, respectively.

Spatiotemporal variability and environmental factors of harmful algal blooms (HABs) over western Lake Erie.

Over the past decades, numerous studies have been carried out in understanding causes of Harmful Algal Blooms (HABs) and their dynamics, yielding great knowledge in this field. Lake Erie, the fourth-largest lake of the five Great Lake, is among those highly vulnerable to the impacts of HABs and has received substantial attention from the public, water management sectors, and academic field. Building upon previous work, this study aims to characterize spatiotemporal variability of Chlorophyll a (Chl-a), which is an important indicator of HABs, and to explore relative importance of environmental factors associated with HABs in the west Lake Erie. Ten years of biweekly Chl-a information over western Lake Erie were derived from MERIS data at the pixel scale. Based on the MERIS-derived information high concentrations of Chl-a were observed in the south near shore area in spring and fall and in the west corner area of western Lake Erie in all three seasons except winter. Wavelet analysis suggested that the 0.5- and 1-year periods were dominant modes for the Chl-a series. The Multivariate Adaptive Regression Splines (MARS) analysis was performed to explore factors associated with the dynamics of Chl-a. The results suggested that overall both phenological (e.g. wind) and ecological (e.g. nutrient levels) factors exhibited significant correlations with the remotely-sensed imagery based observations of Chl-a despite spatial and temporal variations. The important phenological and ecological factors include solar radiation and wind speed in spring, water temperature, solar radiation, and total Kjeldahl nitrogen concentration in summer, wind speed in fall, and water temperature and streamflow in winter. Both consistency and differences of findings of the study with others in the region may suggest strengths and limitations of the remotely sensed imagery-based analysis, offering valuable information for future work.

Tomato FK506 Binding Protein 12KD (FKBP12) Mediates the Interaction between Rapamycin and Target of Rapamycin (TOR).

Target of Rapamycin (TOR) signaling is an important regulator in multiple organisms including yeast, plants, and animals. However, the TOR signaling in plants is much less understood as compared to that in yeast and animals. TOR kinase can be efficiently suppressed by rapamycin in the presence of functional FK506 Binding Protein 12 KD (FKBP12) in yeast and animals. In most examined higher plants rapamycin fails to inhibit TOR kinase due to the non-functional FKBP12. Here we find that tomato plants showed obvious growth inhibition when treated with rapamycin and the inhibitory phenotype is similar to suppression of TOR causing by active-site TOR inhibitors (asTORis) such as KU63794, AZD8055, and Torin1. The chemical genetic assays using TOR inhibitors and heterologous expressing SlFKBP12 in Arabidopsis indicated that the TOR signaling is functional in tomato. The protein gel shifting and TOR inhibitors combination assays showed that SlFKBP12 can mediate the interaction between rapamycin and TOR. Furthermore, comparative expression profile analysis between treatments with rapamycin and KU63794 identified highly overlapped Differentially Expressed Genes (DEGs) which are involved in many anabolic and catabolic processes, such as photosynthesis, cell wall restructuring, and senescence in tomato. These observations suggest that SlFFBP12 is functional in tomato. The results provided basic information of TOR signaling in tomato, and also some new insights into how TOR controls plant growth and development through reprogramming the transcription profiles.

Enzyme-substrate binding landscapes in the process of nitrile biodegradation mediated by nitrile hydratase and amidase.

The continuing discharge of nitriles in various industrial processes has caused serious environmental consequences of nitrile pollution. Microorganisms possess several nitrile-degrading pathways by direct interactions of nitriles with nitrile-degrading enzymes. However, these interactions are largely unknown and difficult to experimentally determine but important for interpretation of nitrile metabolisms and design of nitrile-degrading enzymes with better nitrile-converting activity. Here, we undertook a molecular modeling study of enzyme-substrate binding modes in the bi-enzyme pathway for degradation of nitrile to acid. Docking results showed that the top substrates having favorable interactions with nitrile hydratase from Rhodococcus erythropolis AJ270 (ReNHase), nitrile hydratase from Pseudonocardia thermophila JCM 3095 (PtNHase), and amidase from Rhodococcus sp. N-771 (RhAmidase) were benzonitrile, 3-cyanopyridine, and L-methioninamide, respectively. We further analyzed the interactional profiles of these top poses with corresponding enzymes, showing that specific residues within the enzyme's binding pockets formed diverse contacts with substrates. This information on binding landscapes and interactional profiles is of great importance for the design of nitrile-degrading enzyme mutants with better oxidation activity toward nitriles or amides in the process of pollutant treatments.

Effect of Triton X-100 on the removal of aqueous phenol by laccase analyzed with a combined approach of experiments and molecular docking.

Effects of Triton X-100 on the removal of aqueous phenol catalyzed by laccase were studied. The optimal concentration of Triton X-100 was 155 µM to improve phenol removal when the concentrations of phenol and laccase were 50 mg/L and 0.05 mg/mL, respectively. Laccase activity was increased with Triton X-100 at concentrations from 31 to 930 µM and the highest increase was about 17% by 930 µM Triton X-100. The removal efficiencies of phenol with 155 µM Triton X-100 were 1.2, 1.6, 3.4, 4.5, and 5.7 fold those of the control after 6h when the initial concentrations of phenol were 50, 100, 200, 400 and 600 mg/L, respectively. Molecular docking method was used to analyze the interactions between laccase and substrates. Docking results showed that phenol formed hydrogen bonds and hydrophobic interactions with laccase, whereas Triton X-100 formed hydrophobic interactions with laccase, which may increase the laccase activity and enhance phenol removal. The reaction of phenol removal was also characterized using UV spectra. The results indicated that the presence of low concentrations of Triton X-100 for phenol removal catalyzed by enzymes may be an alternative to the present phenol removal processes in water treatment or remediation.

Influence of rhamnolipids and Triton X-100 on adsorption of phenol by Penicillium simplicissimum.

The effects of rhamnolipids and Triton X-100 on phenol adsorption by Penicillium simplicissimum were studied. The optimum pH was 7 for phenol adsorption by all the test biomasses. The adsorption of phenol at pH 7 by biomass pre-treated with 0.05% Triton X-100, 0.2% Triton X-100, 0.05% rhamnolipids and 0.005% rhamnolipids was 3.4, 2.7, 2.4, and 1.8-fold, respectively, that of untreated biomass. The pseudo-second-order model and the Freundlich isotherms described the adsorption processes better than the pseudo-first-order model and the Langmuir isotherms, respectively. The pre-treatments by surfactants increased the zeta potential and hydrophobicity of P. simplicissimum. Analysis of the cell surface by Fourier transform infrared spectrometry, energy dispersive X-ray, and environmental scanning electron microscopy indicated that the pre-treatments by surfactants changed the cell surface functional groups, element concentrations and micrographs. The results indicated that surfactants can be potentially used to increase phenol adsorption.

Immobilization of laccase on magnetic bimodal mesoporous carbon and the application in the removal of phenolic compounds.

A novel magnetically separable laccase immobilized system was constructed by adsorbing laccase into bimodal carbon-based mesoporous magnetic composites (CMMC). A large adsorption capacity (491.7 mg g(-1)), excellent activity recovery (91.0%) and broader pH and temperature profiles than free laccase have been exhibited by the immobilized laccase. Thermal stability was enhanced to a great extent and operational stability was increased to a certain extent. The shift of kinetic parameters indicated affinity change between enzyme and substrate. Application of the immobilized system in phenol and p-chlorophenol removal was investigated in a batch system. Adsorption effects of the support were responsible for the quick removal rate in the first hour, and up to 78% and 84% of phenol and p-chlorophenol were removed in the end of the reaction, respectively, indicating that the magnetic bimodal mesoporous carbon is a promising carrier for both immobilization of laccase and further application in phenol removal.

Spectroscopic studies of dye-surfactant interactions with the co-existence of heavy metal ions for foam fractionation.

The interaction between a cationic dye Methylene Blue (MB) and an anionic surfactant sodium dodecyl sulfate (SDS) with the presence of Cd2+ was investigated spectrophotometrically in a certain concentration range. The spectrophotometric measurements of dye-metal ion-surfactant system were carried out. The results indicated that the SDS concentration had a significant influence on the dye spectrum, while the addition of Cd2+ hardly caused change of the maximum value of absorbance. According to this observation, we concluded that electrostatic and hydrophobic interaction between dye and surfactant occurred up to a certain level, and the homo-ions Cd2+ almost exerted no effect on the dye-surfactant complexation, establishing a theoretical foundation for simultaneous removal of organic dye and heavy metal using foam fractionation. Meanwhile, the effects of their interaction on foam performance were investigated. The results showed that the addition of Cd2+ favored the tendency to ameliorate foam properties just contrary to MB. The feasibility of foam separation for dye and heavy metal removal from simulated wastewater was also confirmed using a continuous foam fractionator. In the simultaneous removal process, with the initial SDS concentration ranging from 0.5 to 5.0 mmol/L, the maximum removal efficiencies of MB and Cd2+ were obtained as 99.69% and 99.61%, respectively. The enrichment ratios were reduced from 24.34 to 7.65 for MB and from 22.01 to 3.35 for Cd2+.

Removal and recovery of Zn2+ and Pb2+ by imine-functionalized magnetic nanoparticles with tunable selectivity.

This research investigated the adsorption of zinc and lead from binary metal solution with tunable selectivity. A nano adsorbent was prepared by introducing imine groups onto the surface of stability enhanced magnetic nanoparticles and then characterized by TEM and FTIR. Binary metal components adsorption was carried out in different concentration of metal and EDTA solution. Due to the interaction between metals and adsorbent in the presence of EDTA, the selective adsorption of zinc and lead could be achieved with 100% selectivity. To only remove zinc from binary metals, the solution condition was [EDTA]/[M(2+)] = 0.7 with pH of 6, and its saturated adsorption capacity was 1.25 mmol/g. For selective adsorption of lead, an equilibrium adsorption capacity of 0.81 mmol/g was obtained under the condition of [EDTA]/[M(2+)] = 0.7 and pH of 2. The exhausted adsorbent could be regenerated by simple acid or alkali wash, and high purity lead and zinc salt solutions were recovered and concentrated.

Understanding lignin-degrading reactions of ligninolytic enzymes: binding affinity and interactional profile.

Previous works have demonstrated that ligninolytic enzymes mediated effective degradation of lignin wastes. The degrading ability greatly relied on the interactions of ligninolytic enzymes with lignin. Ligninolytic enzymes mainly contain laccase (Lac), lignin peroxidase (LiP) and manganese peroxidase (MnP). In the present study, the binding modes of lignin to Lac, LiP and MnP were systematically determined, respectively. Robustness of these modes was further verified by molecular dynamics (MD) simulations. Residues GLU460, PRO346 and SER113 in Lac, residues ARG43, ALA180 and ASP183 in LiP and residues ARG42, HIS173 and ARG177 in MnP were most crucial in binding of lignin, respectively. Interactional analyses showed hydrophobic contacts were most abundant, playing an important role in the determination of substrate specificity. This information is an important contribution to the details of enzyme-catalyzed reactions in the process of lignin biodegradation, which can be used as references for designing enzyme mutants with a better lignin-degrading activity.

Oxalate production at different initial Pb²+ concentrations and the influence of oxalate during solid-state fermentation of straw with Phanerochaete chrysosporium.

The production of oxalate at different initial Pb(2+) concentrations during solid-state fermentation of straw with Phanerochaete chrysosporium was investigated. It was found that the maximal peak value of oxalate concentration (22.84 mM) was detected at the initial Pb(2+) concentration of 200 mg kg(-1) dry straw, while the minimum (15.89 mM) at the concentration of 600 mg Pb(2+)kg(-1) dry straw, and at moderate concentration of Pb(2+) the capability of oxalic acid secretion was enhanced. In addition, it was also found that more oxalic acid accumulation went together with better Pb(2+) passivation effect and higher manganese peroxidase (MnP) activity. The present findings will improve the understandings of the interactions of heavy metals with white-rot fungi and the role of oxalate in lignin degradation system, which could provide useful references for more efficient treatment of Pb-contaminated lignocellulosic waste.

Biosorption of zinc(II) from aqueous solution by dried activated sludge.

The biosorption potential of dried activated sludge as a biosorbent for zinc(II) removal from aqueous solution was investigated. The effects of initial pH, contact time, initial zinc ion concentration, and adsorbent dosage on the biosorption processes were determined, and the equilibrium data were modeled by the Langmuir and Freundlich isotherms. The Langmuir isotherm model (R2 = 0.999) was proved to fit the equilibrium data much better than the Freundlich isotherm model (R2 = 0.918). The monolayer adsorption capacity of dried activated sludge for zinc(II) was found to be 17.86 mg/g at pH of 5 and 25 degrees C. The kinetic data were tested using pseudo first- and second-order models. The results suggested that the pseudo second-order model (R2 > 0.999) was better for the description of the adsorption behavior of zinc(II) onto the dried activated sludge. Fourier transform infrared spectral analysis showed that the dominant mechanism of zinc(II) biosorption onto the dried activated sludge was the binding between amide groups and zinc ions.

[Performance of desulfurizing absorbent of roasted navajoite].

An innovative flue gas desulfurization (FGD) coupling process was proposed in this study to overcome the problems in wet-type limestone/lime processes which include fouling, clogging, and difficulty of selling the by-products and the problems in traditional process for vanadium extraction from navajoite ore such as excessive consumption of sulfuric acid and emissions of pollutants. The performance of a jet bubbling reactor (JBR) at pilot-scale was evaluated using navajoite ore produced in the process of extracting vanadium pentoxide as desulfurization absorbent. Results showed that navajoite ore slurry achieved better desulfurization performance than limestone slurry. When the inlet flue gas pressure drop was 3.0 kPa, the gas flow was about 2350 m3 x h(-1) and the pH of the navajoite ore slurry was higher than 4.5, the desulfurization efficiency was stable about 90%. The SO2 removal efficiency appeared to increase along with the increasing of absorbent cycle-index. The efficiency of the second circulation was improved 3.5% compared to the first circulation. After an operating duration of 40 minutes, the leaching rate of vanadium pentoxide was about 20%, and reached 60% when the by-products were leached with 5% dilute sulfuric acid for 10 hours. The by-product from this process not only could be used to produce vanadium pentoxide which is a valuable industrial product, but also could significantly overcome the pollution problem existing in the traditional refining process of vanadium pentoxide when navajoite ore is used as the feed material. This FGD process using roasted navajoite slurry as absorbent is environmental sound and cost-effective, and shows the potential for application in the field of flue gas desulfurization as well as hydrometallurgy.

Effects of surfactants and salt on Henry's constant of n-hexane.

n-Hexane biological removal is intrinsically limited by its hydrophobic nature and low bioavailability. The addition of surfactants could enhance the transport of volatile organic compounds (VOCs) and change the gas-liquid equilibrium of VOCs. In this paper, the effects of four surfactants, sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), tert-octylphenoxypoly-ethoxyethanol (Triton X-100), polyoxyethylene (20) sorbitan monooleate (Tween 80), and sodium nitrate on apparent Henry's constant of n-hexane in surfactant solutions were investigated. The apparent Henry's constants were significantly reduced when surfactants concentrations exceeded their critical micelle concentrations (cmc's). On a cmc basis, the anionic surfactant SDS was found to have the greatest effect on the apparent Henry's constant with CTAB succeeding, then followed by Triton X-100 and Tween 80. However, the apparent Henry's constant of n-hexane decreased even more rapidly when Triton X-100, a nonionic surfactant, was added than when the ionic surfactant of SDS or CTAB was applied under identical mass concentration and other conditions. These results suggest that Triton X-100 have the biggest solubilization of n-hexane among the four surfactants. Sodium nitrate slightly decreased the apparent Henry's constant of n-hexane in surfactant solutions, and could be considered as a cosolvent in the surfactant-(n-hexane) solution. In addition, the relationship between apparent Henry's constant and surfactant concentration was further developed.

[Research and application of producing laccase by Phanerochaete chrysosporium in solid-state fermentation system].

The potential of banana skin and corn cob as a support-substrate for the production of extracellular laccase by the white-rot fungus Phanerochaete chrysosporium (BKMF-1767) was investigated. The results indicate that laccase showed a maximum activity of 12.68 U/g when the proportion of banana skin and corn cob is 1:2 and the inducer is 0.4 mmol/L CuSO4. In addition, crude laccase enzyme shows degradation activity to pentachlorophenol (PCP) without redox mediator or with the redox mediator (ABTS) at a concentration of 5 mmol/L, and the degradation rates of PCP were 37.8% and 97% respectively after 6 h. The crude laccase was purified by treatment of (NH4)2SO4, and the purified laccase could make the degradation rate of PCP to 81.8% within 6 h.