Characterization of the complete Salix viminalis var. gmelinii Turcz 1854 chloroplast genome from the northeast of China.

The Salix viminalis var. gmelinii Turcz 1854 is a variant of the Salix genus, from the Salicaceae family, and possesses an extremely high economic value. In this study the complete chloroplast genome of the woody plant S. viminalis var. gmelinii was characterized for the first time using a high-throughput approach in conjunction with de novo assembly technology. The S.viminalis var. gmelinii chloroplast genome is 155,405 base pairs (bp) in length and contains 36.71% GC content. It incorporates a large single-copy region (LSC, 84,287bp) alongside one small-copy region (SSC, 16,198bp), and two inverted repeat regions (IRA and IRB, 27,460bp). Moreover, this chloroplast genome encodes 128 genes, which comprises 83 protein-coding genes, 37 transfer RNA (tRNA) genes, and eight ribosomal RNA (rRNA) genes. Furthermore, the phylogenetic analysis revealed that S.viminalis var. gmelinii is closely related to S. cupularis and S.gordejevii.

Phylogenetic analysis and complete chloroplast genome of Salix wilhelmsiana M.B.

Salix wilhelmsiana M.B. Bieberstein 1819 is a perennial woody plant with high economic and ecological value. In this study, we annotated the chloroplast (cp) genome of Salix wilhelmsiana M.B. The results showed that the length of the complete cp genome is 155,577 bp, which is typically composed of two single-copy regions (large single-copy (LSC) of 84,439 bp and small single-copy (SSC) of 16,221 bp) and a pair of IR regions of 27,457 bp with a quadripartite structure. The genome contains 129 genes, including 84 protein-coding genes, 37 tRNA genes, and eight rRNA genes. The GC content was 36.70%. Phylogenetic analysis based on cp genome sequences of 19 species from the Salicaceae family revealed that S. wilhelmsiana M.B. is closely related to S. viminalis var. gmelinii.

LncRNA MIR210HG Facilitates Non-Small Cell Lung Cancer Progression Through Directly Regulation of miR-874/STAT3 Axis.

BACKGROUND: Long noncoding RNAs are involved in the progression of multiple cancers. However, the expression and mechanism of microRNA (miR)210HG in non-small cell lung cancer (NSCLC) remain unclear. METHODS: The levels of miR210HG and miR-874 were measured by quantitative real-time polymerase chain reaction in NSCLC tissue samples and cells. Non-small cell lung cancer cell proliferation, migration, and invasion were measured by Cell Counting Kit-8 and transwell assays. Luciferase analysis confirmed the interaction between miR210HG and miR-874. RESULTS: Here, our data showed that miR210HG was overexpressed in NSCLC tissue samples and cells. In vitro functional assays showed that silencing miR210HG blocked NSCLC cell proliferation, migration, and invasion while promoting NSCLC cell radiosensitivity and chemoresistance. Mechanistically, miR-874 was directly regulated by miR210HG. Furthermore, miR-874 expression was reduced in NSCLC tissues and cells. The miR-874 mimic could mitigate the promoting effect of miR210HG on NSCLC cell progression. The data also showed that miR210HG promoted NSCLC cell progression through miR-181a expression by targeting STAT3. CONCLUSIONS: Our observations suggest that miR210HG is associated with NSCLC cell progression by regulating the miR-874/STAT3 axis.

Transparent MoS2/PEDOT Composite Counter Electrodes for Bifacial Dye-Sensitized Solar Cells.

Dye-sensitized solar cells (DSSCs) are solar energy conversion devices with high efficiency and simple fabrication procedures. Developing transparent counter electrode (CE) materials for bifacial DSSCs can address the needs of window-type building-integrated photovoltaics (BIPVs). Herein, transparent organic-inorganic hybrid composite films of molybdenum disulfide and poly(3,4-ethylenedioxythiophene) (MoS2/PEDOT) are prepared to take full advantage of the conductivity and electrocatalytic ability of the two components. MoS2 is synthesized by hydrothermal method and spin-coated to form the MoS2 layer, and then PEDOT films are electrochemically polymerized on top of the MoS2 film to form the composite CEs. The DSSC with the optimized MoS2/PEDOT composite CE shows power conversion efficiency (PCE) of 7% under front illumination and 4.82% under back illumination. Compared with the DSSC made by the PEDOT CE and the Pt CE, the DSSC fabricated by the MoS2/PEDOT composite CE improves the PCE by 10.6% and 6.4% for front illumination, respectively. It proves that the transparent MoS2/PEDOT CE owes superior conductivity and catalytic properties, and it is an excellent candidate for bifacial DSSC in the application of BIPVs.

Solution-Processed Sb2S3 Planar Thin Film Solar Cells with a Conversion Efficiency of 6.9% at an Open Circuit Voltage of 0.7 V Achieved via Surface Passivation by a SbCl3 Interface Layer.

Interfaces in Sb2S3 thin-film solar cells strongly affect their open-circuit voltage (VOC) and power conversion efficiency (PCE). Finding an effective method of reducing the defects is a promising approach for increasing the VOC and PCE. Herein, the use of an inorganic salt SbCl3 is reported for post-treatment on Sb2S3 films for surface passivation. It is found that a thin SbCl3 layer could form on the Sb2S3 surface and produce higher efficiency cells by reducing the defects and suppressing nonradiative recombination. Through density functional theory calculations, it is found that the passivation of the Sb2S3 surface by SbCl3 occurs via the interactions of Sb and Cl in SbCl3 molecules with S and Sb in Sb2S3, respectively. As a result, incorporating the SbCl3 layer highly improves the VOC from 0.58 to 0.72 V; an average PCE of 6.9 ± 0.1% and a highest PCE of 7.1% are obtained with an area of 0.1 cm2. The achieved PCE is the highest value in the Sb2S3 planar solar cells. In addition, the incorporated SbCl3 layer also leads to good stability of Sb2S3 devices, by which 90% of the initial performance is maintained for 1080 h of storage under ambient humidity (85 ± 5% relative humidity) at room temperature.

A simple chemical solution synthesis of nanowire-assembled hierarchical CuO microspheres with enhanced photochemical properties.

Hierarchical micro/nanostructures manifest attractive prospects for photocatalytic application. Nevertheless, large-scale hierarchical micro/nanostructures for industrial application with facile, low-cost and eco-friendly routes remain difficult. Herein, nanowire-assembled hierarchical CuO microspheres (HCMAW) are synthesized for the first time by CO32- ions induced synthesis route. The time-dependent SEM images reveal that the growth mechanism for HCMAW is the well-known Ostwald ripening with self-assembly. The specific surface area of the HCMAW is 7.265 m2 g-1, which is higher than that of hierarchical CuO microspheres assembled with nanosheets (HCMAS) (4.952 m2 g-1) prepared by direct self-assembly scheme without the introduction of CO32- ions. Meanwhile, the HCMAW possess strong light absorption around a broadband wavelength from 300 nm to 800 nm. As a result, the photodegradation activity test demonstrates that the HCMAW shows the degradation efficiency of 98.8% for rhodamine B (RhB) under white light irradiation for 30 min in the presence of H2O2 higher than those of HCMAS (66.3%) and commercial CuO (48.3%) under the same condition, which is one of the highest reported till date related to CuO nanomaterials for the degradation of RhB. The novel HCMAW synthesized by the ion-induced protocol is worth being generalized to more assembled hierarchical micro/nanostructures for versatile applications.