Arabidopsis mutants produced by constitutive overexpression of the CRISPR/Cas9 genome editing system are usually mosaics in the T1 generation. In this study, we used egg cell-specific promoters to ...drive the expression of Cas9 and obtained non-mosaic T1 mutants for multiple target genes with high efficiency. Comparisons of 12 combinations of eight promoters and two terminators found that the efficiency of the egg cell-specific promoter-controlled CRISPR/Cas9 system depended on the presence of a suitable terminator, and the composite promoter generated by fusing two egg cell-specific promoters resulted in much higher efficiency of mutation in the T1 generation compared with the single promoters.
Owing to the unique electronic properties, rare‐earth modulations in noble‐metal electrocatalysts emerge as a critical strategy for a broad range of renewable energy solutions such as water‐splitting ...and metal–air batteries. Beyond the typical doping strategy that suffers from synthesis difficulties and concentration limitations, the innovative introduction of rare‐earth is highly desired. Herein, a novel synthesis strategy is presented by introducing CeO2 support for the nickel–iron–chromium hydroxide (NFC) to boost the oxygen evolution reaction (OER) performance, which achieves an ultralow overpotential at 10 mA cm−2 of 230.8 mV, the Tafel slope of 32.7 mV dec−1, as well as the excellent durability in alkaline solution. Density functional theory calculations prove the established d–f electronic ladders, by the interaction between NFC and CeO2, evidently boosts the high‐speed electron transfer. Meanwhile, the stable valence state in CeO2 preserves the high electronic reactivity for OER. This work demonstrates a promising approach in fabricating a nonprecious OER electrocatalyst with the facilitation of rare‐earth oxides to reach both excellent activity and high stability.
A novel and highly efficient hybrid electrocatalyst is synthesized by NiFeCr hydroxide deposited on a porous peapod‐like Cu@CeO2 nanotube array. The introduction of CeO2 supplies abundant d–f orbital ladders to construct a highly efficient electron transfer expressway, leading to superior alkaline oxygen evolution reaction performance.
Silane pre‐functionalized carbon dots, arbitrarily doped (0–100% scale) carbon dot nanohybrid gel glasses and macrostructures with high luminescence (quantum yields = 47% and 88%, respectively) and ...broadband optical limiting properties (532 and 1064 nm) are reported. These glasses are optically, thermally, and mechanically stable, as well as highly transmissive (ca. 90%) in the 400–1350 nm region.
Structural engineering and compositional controlling are extensively applied in rationally designing and fabricating advanced freestanding electrocatalysts. The key relationship between the spatial ...distribution of components and enhanced electrocatalysis performance still needs further elaborate elucidation. Here, CeO2 substrate supported CoS1.97 (CeO2‐CoS1.97) and CoS1.97 with CeO2 surface decorated (CoS1.97‐CeO2) materials are constructed to comprehensively investigate the origin of spatial architectures for the oxygen evolution reaction (OER). CeO2‐CoS1.97 exhibits a low overpotential of 264 mV at 10 mA cm−2 due to the stable heterostructure and faster mass transfer. Meanwhile, CoS1.97‐CeO2 has a smaller Tafel slope of 49 mV dec−1 through enhanced adsorption of OH−, fast electron transfer, and in situ formation of Co(IV)O2 species under the OER condition. Furthermore, operando spectroscopic characterizations combined with theoretical calculations demonstrate that spatial architectures play a distinguished role in modulating the electronic structure and promoting the reconstruction from sulfide to oxyhydroxide toward higher chemical valence. The findings highlight spatial architectures and surface reconstruction in designing advanced electrocatalytic materials.
Two novel CeO2/CoS1.97 heterostructure electrocatalysts (CeO2‐CoS1.97 and CoS1.97‐CeO2) are constructed to investigate the relationships between spatial architectures and oxygen evolution reaction (OER) performances, where different configuration endows hybrids with distinct intermediate adsorption, modulated electronic structures, and promoted electrochemical reconstruction, thus improving the OER kinetics and performances. This work sheds light on the importance of rational design and synthesis of advanced hybrid electrocatalysts with functional spatial architectures.
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Depression is a widespread psychological disorder that affects up to 20% of the world's population. Traditional Chinese medicine (TCM), with its unique curative effect in depression ...treatment, is gaining increasing attention as the discovery of novel antidepressant drug has become the pursuit of pharmaceutical. This article summarizes the work done on the natural products from TCM that have been reported to conceive antidepressant effects in the past two decades, which can be classified according to various mechanisms including increasing synaptic concentrations of monoamines, alleviating the hypothalamic-pituitary-adrenal (HPA) axis dysfunctions, lightening the impairment of neuroplasticity, fighting towards immune and inflammatory dysregulation. The antidepressant active ingredients identified can be generally divided into saponins, flavonoids, alkaloids, polysaccharides and others. Albiflorin, Baicalein, Berberine chloride, beta-Asarone, cannabidiol, Curcumin, Daidzein, Echinocystic acid (EA), Emodin, Ferulic acid, Gastrodin, Genistein, Ginsenoside Rb1, Ginsenoside Rg1, Ginsenoside Rg3, Hederagenin, Hesperidin, Honokiol, Hyperoside, Icariin, Isoliquiritin, Kaempferol, Liquiritin, L-theanine, Magnolol, Paeoniflorin, Piperine, Proanthocyanidin, Puerarin, Quercetin, Resveratrol (trans), Rosmarinic acid, Saikosaponin A, Senegenin, Tetrahydroxystilbene glucoside and Vanillic acid are Specified in this review. Simultaneously, chemical structures of the active ingredients with antidepressant activities are listed and their sources, models, efficacy and mechanisms are described. Chinese compound prescription and extracts that exert antidepressant effects are also introduced, which may serve as a source of inspiration for further development. In the view of present study, the antidepressant effect of certain TCMs are affirmative and encouraging. However, there are a lot of work needs to be done to evaluate the exact therapeutic effects and mechanisms of those active ingredients, specifically, to establish a unified standard for diagnosis and evaluation of curative effect.
To accelerate the application of the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/ CRISPR-associated protein 9) system to a variety of plant species, a toolkit with ...additional plant selectable markers, more gRNA modules, and easier methods for the assembly of one or more gRNA expression cassettes is required.
We developed a CRISPR/Cas9 binary vector set based on the pGreen or pCAMBIA backbone, as well as a gRNA (guide RNA) module vector set, as a toolkit for multiplex genome editing in plants. This toolkit requires no restriction enzymes besides BsaI to generate final constructs harboring maize-codon optimized Cas9 and one or more gRNAs with high efficiency in as little as one cloning step. The toolkit was validated using maize protoplasts, transgenic maize lines, and transgenic Arabidopsis lines and was shown to exhibit high efficiency and specificity. More importantly, using this toolkit, targeted mutations of three Arabidopsis genes were detected in transgenic seedlings of the T1 generation. Moreover, the multiple-gene mutations could be inherited by the next generation.
We developed a toolkit that facilitates transient or stable expression of the CRISPR/Cas9 system in a variety of plant species, which will facilitate plant research, as it enables high efficiency generation of mutants bearing multiple gene mutations.
Atomic‐thick interfacial dominated bifunctional catalyst NiO/CoO transition interfacial nanowires (TINWs) with abundant defect sites display high electroactivity and durability in the oxygen ...evolution reaction (OER) and the oxygen reduction reaction (ORR). Density functional theory (DFT) calculations show that the excellent OER/ORR performance arises from the electron‐rich interfacial region coupled with defect sites, thus enabling a fast‐redox rate with lower activation barrier for fast electron transfer. When assembled as an air‐electrode, NiO/CoO TINWs delivered the high specific capacity of 842.58 mAh gZn−1, the large energy density of 996.44 Wh kgZn−1 with long‐time stability of more than 33 h (25 °C), and superior performance at low (−10 °C) and high temperature (80 °C).
An oxygen removing and re‐doping process applied to NiCo2O4 nanowires (NW) gives so‐called NiO/CoO transition interfacial nanowires (TINWs) with an abundance of interfacial defects. The atomic‐thick interface makes NiO/CoO TINWs highly efficient and stable bifunctional oxygen evolution/oxygen reduction reaction (OER/ORR) catalysts, and gives a wide working temperature range (−10 to 80 °C) for portable Zn–air batteries.
The first use of an organosilane as a coordinating solvent to synthesize highly luminescent (quantum yield = 47%) amorphous carbon dots (CDs) in one minute is reported. The CDs, which benefit from ...surface methoxysilyl groups, have a diameter of ~0.9 nm and can easily be fabricated into pure CD fluorescent films or monoliths simply by heating them at 80 ºC for 24 h. Moreover, the non‐water‐stable CDs can be further transformed into water‐soluble CDs/silica particles, which are biocompatible with and nontoxic to the selected cell lines in our preliminary evaluation. The proposed novel synthetic route is believed to provide an alternative synthesis route and should inspire more research into the origin and applications of CDs, as well as delivering CD‐based materials.
Bright dots: The first use of an organosilane as a coordinating solvent to synthesize highly luminescent (quantum yield = 47%) amorphous carbon dots (CDs) in one minute is reported. The CDs, which benefit from surface methoxysilyl groups, have a diameter of ≈0.9 nm and can easily be fabricated into fluorescent films or monoliths by heating them at 80 ºC for 24 h. Moreover, the non‐water‐stable CDs can be further transformed into water‐soluble CDs/silica particles, which are biocompatible with and nontoxic to the selected cell lines in our preliminary evaluation.
Abstract
The demand for sustainable energy has motivated the development of artificial photosynthesis. Yet the catalyst and reaction interface designs for directly fixing permanent gases (e.g. CO
2
, ...O
2
, N
2
) into liquid fuels are still challenged by slow mass transfer and sluggish catalytic kinetics at the gas-liquid-solid boundary. Here, we report that gas-permeable metal-organic framework (MOF) membranes can modify the electronic structures and catalytic properties of metal single-atoms (SAs) to promote the diffusion, activation, and reduction of gas molecules (e.g. CO
2,
O
2
) and produce liquid fuels under visible light and mild conditions. With Ir SAs as active centers, the defect-engineered MOF (e.g. activated NH
2
-UiO-66) particles can reduce CO
2
to HCOOH with an apparent quantum efficiency (AQE) of 2.51% at 420 nm on the gas-liquid-solid reaction interface. With promoted gas diffusion at the porous gas-solid interfaces, the gas-permeable SA/MOF membranes can directly convert humid CO
2
gas into HCOOH with a near-unity selectivity and a significantly increased AQE of 15.76% at 420 nm. A similar strategy can be applied to the photocatalytic O
2
-to-H
2
O
2
conversions, suggesting the wide applicability of our catalyst and reaction interface designs.
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