The Expression of the StNRAMP2 Gene Determined the Accumulation of Cadmium in Different Tissues of Potato.

Cadmium (Cd) is a toxic metal that threatens human health when enriched in crops. NRAMPs are a family of natural macrophage proteins reported to play a key role in Cd transport in plants. In order to explore the gene regulation mechanism of potato under Cd stress and the role of NRAMPs family in it, this study analyzed the gene expression differences of two different Cd accumulation levels in potato after 7 days of 50 mg/kg Cd stress and screened out the key genes that may play a major role in the differential accumulation of Cd in different varieties. Additionally, StNRAMP2 was selected for verification. Further verification showed that the StNRAMP2 gene plays an important role in the accumulation of Cd in potato. Interestingly, silencing StNRAMP2 increased Cd accumulation in tubers but significantly decreased Cd accumulation in other sites, suggesting a critical role of StNRAMP2 in Cd uptake and transport in potatoes. To further confirm this conclusion, we performed heterologous expression experiments in which overexpression of StNRAMP2 gene in tomato resulted in a threefold increase in Cd content, which further confirmed the important role of StNRAMP2 in the process of Cd accumulation compared with wild-type plants. In addition, we found that the addition of Cd to the soil increased the activity of the plant antioxidant enzyme system, and silencing StNRAMP2 partially reversed this effect. This suggests that the StNRAMP2 gene plays an important role in plant stress tolerance, and future studies could further explore the role of this gene in other environmental stresses. In conclusion, the results of this study improve the understanding of the mechanism of Cd accumulation in potato and provide experimental basis for remediation of Cd pollution.

Facet engineering of ultrathin two-dimensional materials.

Ultrathin two-dimensional (2D) materials exhibit broad application prospects in many fields due to the enhanced specific surface area to volume ratio and quantum confinement effect. Because of the atomic thickness and various orientations, ultrathin 2D materials exposing specific facets have drawn great attention for various applications in catalysis, batteries, optoelectronics, magnetism, epitaxial template for material growth, etc. Though maintaining the atomic thickness of 2D materials while controlling crystal facets is an enormous challenge, breakthroughs are being made. This review provides a comprehensive overview of the recent advances in the facet engineering of 2D materials, ranging from a basic understanding of facets and the corresponding approaches and the significance of facet engineering. We also propose current challenges and forecast future development directions including the establishment of a facet database, the fabrication of new 2D materials, the design of specific substrates, and the introduction of theoretical calculations and in situ characterization techniques. This review can guide researchers to design ultrathin 2D materials with unique and distinct facets and provide an insight into the applications of energy, magnetism, optics, biomedicine, and other fields.

Photochemical behavior of ferrihydrite-oxalate system: Interfacial reaction mechanism and charge transfer process.

Heterogeneous photochemical reactions associated with natural iron (hydr)oxides and oxalic acid have attracted a great deal of scientific attention in the application of organic pollutants degradation. However, the reaction mechanism is still unclear due to the complicated iron cycles and reactive oxygen species (ROS) generation. In this study, the in situ attenuated total reflectance-Fourier transform infrared spectroscopy was implemented to investigate the adsorption process and photochemical behavior of oxalic acid on the surface of ferrihydrite. A comprehensive reaction mechanism from the perspective of charge transfer process, including homogeneous-heterogeneous iron cycling and ROS generation, was illustrated in detail. We found that oxalic acid was first adsorbed on the surface of ferrihydrite with a mononuclear bidentate binding geometry. Interestingly, this mononuclear bidentate complex on the surface of ferrihydrite was stable under visible light irradiation. Subsequently, the whole complex departed from ferrihydrite surface through non-reduction dissolution with the form of Fe(C2O4)+. In the solution, the Fe(C2O4)+ complexes would quickly convert to Fe(C2O4)2- complexes. Under visible light irradiation, the electrons generated from the photolysis of Fe(C2O4)2- complex reacted with O2 to form O2•-/•OOH. Meanwhile, Fe(III) was reduced to Fe(II). Finally, the produced O2•-/•OOH could react with Fe(II) through a one-step way to generate •OH, which possessed higher •OH formation efficiency than that through the two-step way of H2O2 as the intermediates. This study helps us with understanding of in-situ photochemical reaction mechanism of ferrihydrite-oxalic acid system, and also provides guidance to effectively utilize widespread iron (hydr)oxides and organic acids in natural environment to develop engineered systems for water treatment.