Inhibition Of Electron Transfer Research Articles

Golden 2-like Transcription Factors Regulate Photosynthesis under UV-B Stress by Regulating the Calvin Cycle.

UV-B stress can affect plant growth at different levels, and although there is a multitude of evidence confirming the effects of UV-B radiation on plant photosynthesis, there are fewer studies using physiological assays in combination with multi-omics to investigate photosynthesis in alpine plants under stressful environments. Golden 2-like (G2-like/GLK) transcription factors (TFs) are highly conserved during evolution and may be associated with abiotic stress. In this paper, we used Handy-PEA and Imaging-PAM Maxi to detect chlorophyll fluorescence in leaves of Rhododendron chrysanthum Pall. (R. chrysanthum) after UV-B stress, and we also investigated the effect of abscisic acid (ABA) on photosynthesis in plants under stress environments. We used a combination of proteomics, widely targeted metabolomics, and transcriptomics to study the changes of photosynthesis-related substances after UV-B stress. The results showed that UV-B stress was able to impair the donor side of photosystem II (PSII), inhibit electron transfer and weaken photosynthesis, and abscisic acid was able to alleviate the damage caused by UV-B stress to the photosynthetic apparatus. Significant changes in G2-like transcription factors occurred in R. chrysanthum after UV-B stress, and differentially expressed genes localized in the Calvin cycle were strongly correlated with members of the G2-like TF family. Multi-omics assays and physiological measurements together revealed that G2-like TFs can influence photosynthesis in R. chrysanthum under UV-B stress by regulating the Calvin cycle. This paper provides insights into the study of photosynthesis in plants under stress, and is conducive to the adoption of measures to improve photosynthesis in plants under stress to increase yield.

Flavodiiron proteins prevent the Mehler reaction in Chlamydomonas reinhardtii

Regulation of photosynthetic electron transfer is fundamental for energetic efficiency and coping with changing environmental factors. All plant groups, except angiosperms, use flavodiiron proteins (FDPs) on the acceptor side of photosystem I (PSI), putatively protecting from PSI photoinhibition under fluctuating light. An alternative electron flow during photosynthesis is the direct reduction of O2 with consequential production of reactive oxygen species (ROS; the Mehler reaction), but to what extent FDPs prevent this is unknown. Here, we quantified O2-dependent electron flow, photosystem activity and the Mehler reaction in Chlamydomonas reinhardtii. Near-infra red absorbance measurement of PSI reaction centre (P700) showed that FDPs remain active long after a dark-to-light transition and their activity increased under hyperoxia. Light-induced hydrogen peroxide (H2O2) production, as a marker of the Mehler reaction, was influenced by O2 concentration, and was up to 67 % higher in an FDP-deficient mutant (flvb) than in the wild-type under saturating constant light. In cultures kept under sub-saturating constant light, flvb produced 315 % more H2O2 and had lower PSII efficiency than wild-type. Inhibiting electron transfer out of photosystem II (PSII) with 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) only partially blocked H2O2 production, particularly under hyperoxia, indicating that PSII was an additional ROS source. P700+ reduction in the dark in the presence of DCMU was faster in flvb than wild-type, revealing enhanced cyclic electron flow, which may also have led to PSI mediated Mehler reaction. We conclude that FDPs remain active in constant light and can prevent PSI mediated Mehler reaction, with relevance to PSII photoinhibition.

Chemical composition of Artemisia argyi essential oil and its antifungal activity against dermatophytes by inhibiting oxidative phosphorylation and causing oxidative damage

Ethnopharmacological relevanceDermatophytes are notorious pathogens capable of infecting various mammals skin, posing serious threats to human health and overall life quality worldwide. Artemisia argyi has been recorded and applied for over a thousand years to treat skin itching. Although it has the potential to be developed as a plant-based antifungal agent, it’s antifungal activity and action mechanism of active ingredients are still unclear. Aim of the studyThe aim of this study was to investigate the chemical composition, antifungal activity against skin fungi, and potential mechanisms of Artemisia argyi essential oil (AEO). Materials and methodsThe chemical composition of AEO was analyzed by gas chromatography-mass spectrometry (GC-MS) firstly. Flat growth restraint and double half dilution tests was performed to evaluate AEO antifungal activity against Microsporum gypseum, Trichophyton mentagrophytes, and Trichophyton rubrum. And then, the physiological mechanism of AEO inhibiting dermatophytes was systematically explored through scanning electron microscopy, relative conductivity, membrane leakage, ROS content, and antioxidant enzyme activity. Finally, the main pathways were screened through transcriptome sequencing, while the related genes expression levels and enzyme activity were validated. ResultsMonoterpenes and sesquiterpenoids were the most highly representative class of AEO. AEO had powerful antifungal activity against M. gypseum, T. mentagrophytes, and T. rubrum, with minimum inhibitory concentration (MIC) values of 0.6, 1.2, and 1.2 μL/mL, respectively. Moreover, AEO can also damage the cell membrane integrity of T. mentagrophytes, resulting in cellular extravasation of intracellular substances. Transcriptome analysis revealed that the main target of AEO is to inhibit electron transfer and oxidative phosphorylation during respiration, ultimately leading to obstruction of normal ATP synthesis and energy metabolism in mitochondria. And a large amount of ROS will generate due to the incompletely catalysis of oxygen under mitochondrial complexes. Coupled with the decrease of antioxidant enzyme (SOD, POD) activity, excessive accumulation of ROS will cause serious oxidative damage to cells and eventually exhibiting antifungal activity against dermatophytes. ConclusionsThe present study demonstrated that Artemisia argyi was a valuable source of active compounds with antifungal activity. These findings support AEO as a potential agent to inhibit dermatophytes and prevent related dermatophytoses.

A novel target-site mutation (H146Q) outside the ubiquinone binding site of succinate dehydrogenase confers high levels of resistance to cyflumetofen and pyflubumide in Tetranychus urticae

Mitochondrial electron transfer inhibitors at complex II (METI-II), also referred to as succinate dehydrogenase inhibitors (SDHI), represent a recently developed class of acaricides encompassing cyflumetofen, cyenopyrafen, pyflubumide and cyetpyrafen. Despite their novelty, resistance has already developed in the target pest, Tetranychus urticae. In this study a new mutation, H146Q in a highly conserved region of subunit B of complex II, was identified in a T. urticae population resistant to all METI-IIs. In contrast to previously described mutations, H146Q is located outside the ubiquinone binding site of complex II. Marker-assisted backcrossing of this mutation in a susceptible genetic background validated its association with resistance to cyflumetofen and pyflubumide, but not cyenopyrafen or cyetpyrafen. Biochemical assays and the construction of inhibition curves with isolated mitochondria corroborated this selectivity. In addition, phenotypic effects of H146Q, together with the previously described H258L, were further examined via CRISPR/Cas9 gene editing. Although both mutations were successfully introduced into a susceptible T. urticae population, the H146Q gene editing event was only recovered in individuals already harboring the I260V mutation, known to confer resistance towards cyflumetofen. The combination of H146Q + I260V conferred high resistance levels to all METI-II acaricides with LC50 values over 5000 mg a.i./L for cyflumetofen and pyflubumide. Similarly, the introduction of H258L via gene editing resulted in high resistance levels to all tested acaricides, with extreme LC50 values (>5000 mg a.i./L) for cyenopyrafen and cyetpyrafen, but lower resistance levels for pyflubumide and cyflumetofen. Together, these findings indicate that different mutations result in a different cross-resistance spectrum, probably also reflecting subtle differences in the binding mode of complex II acaricides.

Freezing treatment under light conditions leads to a dramatic enhancement of freezing tolerance in cold-acclimated Arabidopsis.

Overwintering plants survive subzero temperatures by cold acclimation (CA), wherein they acquire freezing tolerance through short-term exposure to low temperatures above 0°C. The freezing tolerance of CA plants increases when they are subsequently exposed to mild subzero temperatures, a phenomenon known as second-phase cold hardening (2PH). Here, we explored the molecular mechanism and physiological conditions of 2PH. The results show that, compared with supercooling, a freezing treatment during 2PH after CA enhanced the freezing tolerance of Arabidopsis. This required CA as a pretreatment, and was designated as second-phase freezing acclimation (2PFA). Light increased the effect of 2PFA to enhance freezing tolerance after CA. C-repeat binding factor and cold-regulatedgenes were downregulated by light during the 2PFA treatment, a different transcription profile from that during CA. The freezing tolerance of 2PFA plants was decreased by the presence of the photosynthetic electron transfer inhibitor 3-(3,4-dichlorophenyl)-1,1-dimethylureaduring the 2PFA treatment. Compared with wild-type plants, phototropin1,2 and phyb mutants showed lower freezing tolerance after 2PFA treatment. These results show that exposure to freezing after CA increases freezing tolerance as a secondary process, and that freezing under light conditions further increases freezing tolerance via pathways involving photoreceptors and photosynthetic electron transfer.

An impedance labeling free electrochemical aptamer sensor based on tetrahedral DNA nanostructures for doxorubicin determination.

Based on the electrochemical impedance method, a marker-free biosensor with aptamer as a biometric element was developed for the determination of doxorubicin (DOX). By combining aptamer with rigid tetrahedral DNA nanostructures (TDNs) and fixing them on the surface of gold electrode (GE) as biometric elements, the density and directivity of surface nanoprobes improved, and DOX was captured with high sensitivity and specificity. DOX was captured by immobilized aptamers on the GE, which inhibited electron transfer between the GE and [Fe(CN)6]3-/4- in solution, resulting in a change in electrochemical impedance. When the DOX concentration was between 10.0 and 100.0nM, the aptasensor showed a linear relationship with charge transfer resistance, the relative standard deviation (RSD) ranged from 3.6 to 5.9%, and the detection limit (LOD) was 3.0nM. This technique offered a successful performance for the determination of the target analyte in serum samples with recovery in the range 97.0 to 99.6% and RSD ranged from 4.8 to 6.5%. This method displayed the advantages of fast response speed, good selectivity, and simple sensor structure and showed potential application in therapeutic drug monitoring.

An AuNPs-based electrochemical aptasensor for the detection of 25-hydroxy vitamin D3.

Vitamin D3 (VD3) is the main form of vitamin D and an essential nutrient for maintaining human life. Currently, traditional methods for detecting 25-hydroxyvitamin D3(25(OH)D3) are complex and expensive. In this study, we constructed an accurate, sensitive, simple, and cost-effective label-free biosensor based on an aptamer for the detection of 25(OH)D3. The aptamer-modified sulfhydryl adopted self-assembly as a way to stably immobilize at the glassy carbon electrode (GCE) surface modified by gold nanoparticles (AuNPs). Upon 25(OH)D3 binding to the aptamer, the complexes inhibit electron transfer at the electrode surface, leading to reduced [Fe(CN)6]3-/4- redox peak current. Consequently, the quantity of 25(OH)D3 that interacts with the electrode-bound aptamer correlates with the observed electric current response values. The Aptamer/AuNPs/GCE aptasensor achieved direct and highly sensitive detection of 25(OH)D3 over a wide concentration range (1.0-1000nM), with a limit of detection of 1.0nM. At the same time, other molecules with a similar structure, such as 25(OH)D2, Vitamin D3, and Vitamin D2, had lower response interference than 25(OH)D3. Therefore, this biosensor has great potential to become a portable diagnostic device for 25(OH)D3.

Unraveling the impact of SO2 on electron transfer and oxygen vacancy over MnOx-CeO2 for ozone decomposition

Mn-based catalysts for O3 decomposition (deO3) in industrial flue gas suffer from serious deactivation due to SO2, especially its impact on surface electron transfer and oxygen vacancy remains unclear. Herein, irreversible deactivation over MnOx-CeO2 in presence of SO2 and H2O was mainly attributed to the decrease of surface area, low-temperature reducibility and oxygen vacancies (Vo). SO2 was easily adsorbed on MnOx-CeO2 and further oxidized into SO42− under the aid of O3. Electron transfer from SO2 to Mn4+ and Ce4+ produced stable and inactive metal sulfates, which inhibited electron transfer in the redox cycles between Mn and O in O3 and between Mn and Ce. Moreover, metal sulfates occupied Vo, while Vo generation became difficult and its recovery from desorption of adsorbed oxygen intermediates was restricted, hence less O3 could be adsorbed and decomposed. Metal Ce protected active Mn species by reacting with SO2 preferentially. H2O generated active hydroxyl groups on Vo to react with O3 and hindered the contact of SO2 with Mn species, increasing deO3 activity under SO2 atmosphere. This study offers new insights into the poisoning mechanism of SO2 on electron transfer and oxygen vacancy in deO3 process, and sheds light on rational design of anti-SO2 deO3 catalysts.

Possible Contribution of Corticular Photosynthesis to Grapevine Winter Hardiness

Numerous studies show that photosynthesis in non-foliar tissues contributes to plant productivity. Here, we demonstrate that in chlorenchyma tissues of lignified branches of grape vines, photosynthetic activity is maintained during winter and provide evidence that corticular photosynthesis could contribute to the plant’s freeze tolerance. In a collection of grape varieties that varied noticeably in freeze tolerance, a positive correlation between the maximum quantum yield of photosystem II in the wintering vines and the ability to survive harsh winter temperatures was observed. A more detailed comparison of two grapevine varieties differing in freeze tolerance showed that the vines of the more tolerant variety have more abundant corticular chlorenchyma with chloroplasts containing a better developed network of photosynthetic membranes, characterized by a higher photosynthetic pigments content, higher efficiency of both photosystems, and higher mobility of antennae complexes under the changing light intensity. In addition, we found that freezing temperatures induced more damage in vine samples when they were preliminarily treated with a specific inhibitor of photosynthetic electron transfer. The data obtained could be useful in the generation of freeze-tolerant grape varieties.

Photoinduced electron transfer from spinach chloroplasts to carbon paste electrodes through an exogenous electron acceptor

The photocurrent generated from chloroplasts of spinach is investigated using a carbon paste electrode. Chloroplasts extracted from spinach are shown to interact with a carbon paste electrode through five types of redox mediators. Among these mediators, 2,5-dichloro-1,4-benzoquinone (2,5-DCBQ) is found to be the best electron-transfer mediator, generating the highest photocurrent of approximately 310 nA cm−2 per μg chlorophyll. In addition, the photocurrent density is investigated as a function of the photon flux density, concentration of 2,5-DCBQ, and the amount of chloroplasts deposited onto the surface of the electrode. Photoreduction of 2,5-DCBQ exhibited Michaelis–Menten-like kinetics, and the reduction rates were dependent on the amount of 2,5-DCBQ and the light intensity. Even 10 days after the chloroplasts were extracted, the electrodes with the extracted spinach chloroplasts exhibited ∼90% of the photoinduced current that they exhibited immediately after the chloroplast extraction. The source of photocurrent was confirmed in experiments using 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), an inhibitor of electron transfer from primary quinone electron acceptor QA to secondary quinone electron acceptor QB in photosystem II, and KCN, an inhibitor of electron transfer from cytochrome b6f complex to photosystem I.

Photoelectrochemical aptasensor based on PTCDA/TiO2 efficient sensitization effect for sensitive protein analysis

Herein, a photoelectrochemical (PEC) aptasensor for sensitive detection of C-reactive protein (CRP) was designed based on the efficient sensitization effect of 3,4,9,10-Perylene tetracarboxylic dianhydride (PTCDA) towards titanium dioxide (TiO2). Initially, TiO2 and PTCDA were continuously incubated on electrode surface to produce a strong PEC signal owing to the PTCDA/TiO2 sensitization structure. Subsequently, electrodeposition of gold nanoparticles (dep Au) was performed to connect with the incubated CRP aptamer (S1) via AuN bonds. After that, 1-hexanethiol (HT) was added on the surface of the modified electrode to block the non-specific adsorption sites. Eventually, with the addition of CRP, the PEC signal decreased significantly because the CRP-S1 complexes generated by the specific recognition of CRP and S1 resulted in high steric hindrance effect and inhibited electron transfer. Under optimal conditions, the proposed PEC aptasensor was applied successfully for sensitive CRP detection with a wide linear range from 10 pg/mL to 10 μg/mL and a low detection limit of 3.33 pg/mL. Moreover, the designed PEC aptasensor based on PTCDA/TiO2 sensitized structure might be a versatile tool that provides a powerful alternative to traditional proteins, ions and RNAs detection methods by changing the corresponding recognition sequences.

Effect of Phosphorus, Iron, Zinc, and Their Combined Deficiencies on Photosynthetic Characteristics of Rice (Oryza sativa L.) Seedlings

Combined elemental deficiencies are more complex and insidious physiological metabolic responses than single elemental stresses. To determine the effects of phosphorus (P), iron (Fe), zinc (Zn), and their deficient combinations on photosynthetic characteristics of rice seedlings, we investigated their effects on dry weight, chlorophyll (Chl) content, rapid photosynthetic carbon assimilation CO2 responses, and Chl fluorescence in four-week-old rice (CB9 and BJ1 cultivars) seedlings. The results showed that the dry matter, maximum carboxylation efficiency (Vc,max), and maximum electron transfer efficiency (Jmax) of seedlings were all reduced to different degrees under the element deficiency treatments. JIP-test analysis showed that the decrease in the concentration of active PSII reaction centers (RC/ABS) under -Zn treatment was the main reason for the inhibition of performance index PIABS. The -P treatment reduced RC/ABS and inhibited electron transfer (ψEo). Primary photochemical reactions (φPo) of -P-Zn treated seedlings were also inhibited compared to the -P treatment. The -Fe and -Fe-Zn treatments inhibited photosynthesis most severely, which not only reduced RC/ABS but also severely inhibited φPo and ψEo. Notably, the -P-Fe and -P-Fe-Zn treatments of the CB9 improved the RC/ABS, alleviating the limitation of Fe deficiency. These results help enhance the understanding of the complex relationship between nutrient balance and photosynthesis, especially for P, Fe, Zn, and their combined deficiency.

Ionic accelerator based on metal–semiconductor contact for fast electrode kinetics and durable Zn-metal anode

The development of Zn metal anodes with high reversibility and fast kinetics is critical for achieving high-performance aqueous Zn-metal batteries. Herein, we report a Zn@SiC electrode with an Ohmic contact that exhibits excellent durability and enhanced electrode process kinetics. The Ohmic contact barrier (Φb) inhibited electron transfer from the metal to the SiC passivation layer and effectively regulated Zn deposition under the passivation layer, thus suppressing dendrite growth. The built-in potential (Vbi) accelerated the Zn transfer and reaction kinetics and decreased the nucleation energy, thereby enhancing the charge–discharge platform potential (∼40 mV) in full cells. Coupled with the good anti-side reaction ability of the SiC layer, the Zn@SiC electrode successfully delivered a highly reversible stripping/plating process after 3770 h under a 1.0 mA cm−2 current density with a low overpotential of 33.7 mV. Furthermore, by analyzing the energy band structure of the Ohmic contacts, the critical current density was quantitatively determined. This clarified the relationship between the deposition position and the current density, thus providing a standard for practical semiconductor design.

A predicted structure of NADPH Oxidase 1 identifies key components of ROS generation and strategies for inhibition.

NADPH oxidase 1 (NOX1) is primarily expressed in epithelial cells and responsible for local generation of reactive oxygen species (ROS). By specifically manipulating the local redox microenvironment, NOX1 actively engages in epithelial immunity, especially in colorectal and pulmonary epithelia. To unravel the structural basis of NOX1 engaged epithelial immune processes, a predicted structure model was established using RaptorX deep learning models. The predicted structure model illustrates a 6-transmembrane domain structure, a FAD binding domain, and an NADPH binding/NOXO1 interacting region. The substrate/cofactor binding scheme with respect to this proposed model highly correlates with published reports and is verified in our site-directed mutagenesis assays. An electron transport chain, from NADPH to FAD and the two heme groups, was well supported by the predicted model. Through molecular docking analysis of various small molecule NOX1 inhibitors and subsequent experimental validation, we identified pronounced active sites for potent NOX1 inhibition. Specifically, LEU60, VAL71, MET181, LEU185, HIS208, PHE211, TYR214, and TYR280 in the transmembrane domain form an active pocket for insertion of the small molecule inhibitors to inhibit electron transfer between the heme groups, thus affecting extracellular ROS generation. Altogether, our study provides structural information to help elucidate the role of NOX1 in epithelial generation of ROS and sheds light on the development of therapeutics for NOX1 related illnesses.

Effects and mechanisms of Al substitution on the catalytic ability of ferrihydrite for Mn(II) oxidation and the subsequent oxidation and immobilization of coexisting Cr(III)

Al(III)-substituted ferrihydrite existing in natural soils is more common than pure ferrihydrite; however, the effects of Al(III) incorporation on the interaction between ferrihydrite, Mn(II) catalytic oxidation, and coexisting transition metal (e.g., Cr(III)) oxidation remain elusive. To address this knowledge gap, Mn(II) oxidation on synthetic Al(III)-incorporated ferrihydrite and Cr(III) oxidation on the previously formed Fe–Mn binaries were investigated in this study via batch kinetic studies combined with various spectroscopic analyses. The results indicate that Al substitution in ferrihydrite barely changes its morphology, specific surface area, or the types of surface functional groups, but increases the total amount of hydroxyl on the ferrihydrite surface and enhances its adsorption capacity toward Mn(II). Conversely, Al substitution inhibits electron transfer in ferrihydrite, thereby weakening its electrochemical catalysis on Mn(II) oxidation. Thus, the contents of Mn(III/IV) oxides with higher Mn valence states decrease, whereas those of lower Mn valence states increase. Furthermore, the number of hydroxyl radicals formed during Mn(II) oxidation on ferrihydrite decreases. These inhibitions of Al substitution on Mn(II) catalytic oxidation subsequently cause decreased Cr(III) oxidation and poor Cr(VI) immobilization. Additionally, Mn(III) in Fe–Mn binaries is confirmed to play a dominant role in Cr(III) oxidation. This research facilitates sound decision-making regarding the management of Cr-contaminated soil environments enriched with Fe and Mn.

Effect of crystal structure of ZrO2 catalyst on isobutene synthesis from CO hydrogenation

ZrO2 catalysts with different crystal structures show different catalytic performance in isobutene synthesis from CO hydrogenation reaction. Although monoclinic ZrO2 has the best catalytic performance in isobutene synthesis from syngas, its isosynthesis active sites are still not well understood. To better understand the critical parameters that influence syngas to isobutene reactions over ZrO2 catalysts, we prepared a series of ZrO2 catalysts with distinct crystal structures and investigated their catalytic performance of CO hydrogenation to isobutene. Compared with tetragonal and amorphous ZrO2 catalysts, there are more coordinatively unsaturated Zr and O sites on the surface of monoclinic ZrO2 catalyst. The coordinatively unsaturated Zr sites are the active sites of CO adsorption and activation, which is beneficial to CO conversion. The coordinatively unsaturated O sites provide more basic sites for isobutene formation. Furthermore, the coordinatively unsaturated Zr and O sites on monoclinic ZrO2 catalyst surface may inhibit electron transfer to formate species formed during reaction, resulting in weak adsorption on catalyst surface of formate species. The weakly adsorbed formate species on the surface of monoclinic ZrO2 catalyst is favorable for the synthesis of isobutene from CO hydrogenation reaction.

PH-dependent redox properties of epigallocatechin gallate (EGCG) and its effect on respiration, photosynthesis and cell death in pea

The redox properties of the green tea component epigallocatechin gallate (EGCG) in vitro were studied and its effect on plant (pea) cells was tested. EGCG exhibited both pro- and antioxidant properties. In solutions, EGCG was oxidized by oxygen at physiological (slightly alkaline) pH values. Lowering the pH slowed down this process. Oxidation of EGCG was accompanied by the formation of O2-• and H2O2. In addition, EGCG functioned as an electron donor for peroxidase and, in combination with it, utilized H2O2. Exposure of EGCG to pea cells (leaf cuts or epidermis) suppressed respiration, reduced the transmembrane electric potential difference (Δψ) in mitochondria, and inhibited electron transfer in the photosynthetic electron transfer chain. Among the sites of the photosynthetic redox chain, Photosystem II was the least sensitive to the action of EGCG. EGCG reduced the rate of formation of reactive oxygen species in the epidermis, which was induced by NADH treatment and was registered using 2′,7′-dichlorofluorescine diacetate. In vivo, EGCG at concentrations from 10 µM to 1 mM suppressed KCN-induced death of guard cells in the epidermis, which was determined from the destruction of cell nuclei. EGCG at a concentration of 10 mM disrupted the barrier function of the guard cell plasma membrane, increasing its permeability to propidium iodide.

Epigallocatechin Gallate: pH-Dependent Redox Properties and Effect on Respiration, Photosynthesis, and Cell Death in Pea Plants.

In vitro redox properties of the green tea component epigallocatechin gallate (EGCG) and its effect on pea plant cells were investigated. EGCG was found to exhibit both pro- and antioxidant properties. In solutions, EGCG was oxidized by oxygen at physiological (slightly alkaline) pH values with the generation of O2-• and H2O2, the reaction being slowed down by a decrease in the medium pH. On the other hand, EGCG functioned as an electron donor for peroxidase, resulting in the H2O2 utilization. EGCG suppressed respiration, reduced mitochondrial transmembrane potential difference and inhibited electron transfer in the photosynthetic electron transport chain in pea leaf cells (leaf cuttings and epidermis). Among components of the photosynthetic redox chain, Photosystem II was the least sensitive to the EGCG action. In the epidermis, EGCG reduced the rate of reactive oxygen species formation that was induced by NADH. EGCG at the concentrations from 10 μM to 1 mM suppressed the KCN-induced death of guard cells in the epidermis, which was determined from the destruction of cell nuclei. EGCG at a concentration of 10 mM disrupted the barrier function of the guard cell plasma membrane, increasing its permeability to propidium iodide.

Unveiling a remarkable enhancement role by designing a confined structure Ho-TNTs@Mn catalyst for low-temperature NH3-SCR reaction.

MnOx-based catalysts are considered promising alternative catalysts for NH3-SCR to remove NOx at low temperature. However, their poor SO2 or H2O tolerance and unfavorable N2 selectivity are still the main obstacles restraining their further practical application. Herein, we carefully confined the manganese oxide active species in Ho-modified titanium nanotubes to improve their SO2 resistance and N2 selectivity. Ho-TNTs@Mn exhibits excellent catalytic activity, strong SO2 and H2O tolerance and superior N2 selectivity, and more than 80% NO conversion can be achieved in the range 80-300 °C with 100% N2 selectivity. The characterization results verify that the pore confinement effect of Ho-TNTs for Mn increases the dispersion of Mn to promote the interfacial effect between Mn and Ho. The electron synergistic effect between Mn and Ho improves the electron transformation of Mn and Ho, which inhibits electron transfer between SO2 and Mn to avoid poisoning from SO2. We also find that the interaction between Ho and Mn induces electron migration to restrain the production of Mn4+, contributing to the suitable redox capacity to decrease the creation of byproducts, which serves as the motivation for high N2 selectivity. In situ DRIFTs analysis clarifies that Langmuir-Hinshelwood (L-H) and Eley-Rideal (E-R) mechanisms co-exist in the NH3-SCR reaction over Ho-TNTs@Mn, and the E-R reaction mechanism predominates We believe that Ho-TNTs@Mn with a well-designed nanotube structure will show preferable development and application prospects in the NH3-SCR reaction.

2-Hydroxychalcone as a Novel Natural Photosynthesis Inhibitor against Bloom-Forming Cyanobacteria.

The control of harmful cyanobacterial blooms has been becoming a global challenge. The development of eco-friendly algicides with strong specificity is urgently needed. The photosynthetic apparatus is a promising target site for algicides to minimize the possible harmful effects on animals and humans. In this study, biologically derived 2-hydroxychalcone efficiently inhibited the growth of bloom-forming M.aeruginosa by selectively interfering with photosynthesis. 2-Hydroxychalcone targeting Photosystem II (PSII) inhibited electron transfer between the primary and secondary electron acceptors (QA and QB) and the binding of plastoquinone (PQ) molecules to the QB binding pocket at the acceptor side of PSII, as revealed by polyphasic chlorophyll (Chl) a fluorescence induction and QA- reoxidation kinetics. Molecular docking for 2-hydroxychalcone to D1 protein and the proteomic responses of M.aeruginosa suggested that 2-hydroxychalcone formed a stable monodentate ligand with the nonheme iron in D1 protein, provoking significant modulation of PSII proteins. The unique binding mode of 2-hydroxychalcone with PSII differentiated it from classical PSII inhibitors. Furthermore, 2-hydroxychalcone down-regulated the expression of microcystin (MC) synthesis-related genes to restrain MC synthesis and release. These results indicated the potential application of 2-hydroxychalcone as an algicide or a template scaffold for designing novel derivatives with superior algicidal activity.