Cheap and efficient strategy for photocatalytic degradation of ionic liquids by La/Ce-codoped TiO2@PAM composites.

Ionic liquids are regarded as green solvents mainly due to their non-volatile and easy regeneration and recycling properties. However, ionic liquids have negative effects on the environment and human health, especially alkyl imidazole ionic liquids are more toxic than traditional organic solutions. Studies on the toxicology, ecotoxicology, and degradation of ionic liquids are rarely found in the literature. Here, we prepared the cheap La and Ce-codoped TiO2@PAM (polyacrylamide) composite microspheres with a simple procedure for the first time to degrade three kinds of imidazole ionic liquids with high efficiency. The experimental results show that the composite La (0.25%) and Ce (0.15%)-codoped TiO2@PAM composite microspheres with calcination temperature of 450 °C had a high photocatalytic activity for 1-butyl-3-methyl imidazolium hexafluorophosphate, 1-hexyl-3-methyl imidazolium hexafluorophosphate, and 1-octyl-3-methyl imidazolium hexafluorophosphate with the concentration of 10 mg/L. The photocatalysis degradation extent of the three ionic liquids is 97.4, 91.2, and 88.5% at 90 min. This work opened a new route for the simple preparation of cheap composite microspheres in the photocatalytic degradation of ionic liquids with a high efficiency.

Highly efficient and cheap treatment of dye by graphene-doped TiO2 microspheres.

Highly efficient dye wastewater treatment by photocatalytic catalysis commonly requires expensive catalysts, long degradation time and a complicated procedure. Here, we for the first time prepared cheap graphene-doped titanium dioxide microspheres with a simple procedure to degrade dye with high efficiency. When the catalyst concentration was 0.2 g·L-1, the photocatalysis degradation extent of methylene blue solution, methylene green solution and 1,9-dimethyl methylene blue solution reached 96.4, 85.9 and 98.7%, respectively. The results showed that the degradation reactions accorded with the Langmuir-Hinshelwood model, and the photocatalytic reactions belonged to a first-order reaction in the primary stage. Furthermore, different photocatalytic degradation mechanisms were proposed, which have not been found in other literature. This work opened a new route for simple preparation of cheap microspheres in photocatalytic dye wastewater treatment with high efficiency.

The bHLH transcription factor SlPRE2 regulates tomato fruit development and modulates plant response to gibberellin.

KEY MESSAGE: SlPRE2 is gibberellin inducible and mediates plant response to gibberellin. Silencing of SlPRE2 decreases tomato fruit size, pericarp thickness, placenta size and seed size by regulating cell expansion. Gibberellin is one of the crucial hormones essential for plant growth and developmental processes, including seed germination, stem elongation, and sex expression. Previous studies indicated gibberellin could control fruit development by regulation of genes downstream gibberellin pathway. In the present study, we found that the SlPRE2, a bHLH family transcription factor gene, is highly expressed in immature green fruit. Silencing of SlPRE2 caused reduction of fruits size, pericarp thickness, and placenta size. Meanwhile, smaller seeds were observed in SlPRE2 silenced lines. In addition, the SlPRE2-silenced fruit mesocarp had reduced cell size and expression of SlXTH2 and SlXTH5 which are involved in cell enlargement. Further research showed that SlPRE2 is gibberellic acid-inducible and the expression of gibberellin metabolism-related genes in immature green fruit was affected by the downregulation of SlPRE2. Moreover, the SlPRE2-silenced plants had changed responses to application of exogenous gibberellic acid and paclobutrazol, an inhibitor of gibberellin biosynthesis. These findings indicated that SlPRE2 is a regulator of fruit development and affects plant response to gibberellic acid via the gibberellin pathway.

Molecular and Phylogenetic Analyses of the Mediator Subunit Genes in Solanum lycopersicum.

The Mediator complex is a multi-subunit protein assembly that serves as a central scaffold to help regulate DNA-binding transcription factors (TFs) and RNA polymerase II (Pol II) activity controlled gene expression programmed in response to developmental or environmental factors. However, litter information about Mediator complex subunit (MED) genes in tomato is available, although it is an essential model plant. In this study, we retrieved 46 candidate SlMED genes from the genome of tomato, and a comprehensive analysis was conducted, including their phylogenetic relationship, chromosomal locations, gene structure, cis-regulatory elements prediction, as well as gene expression. The expression profiling of 46 SlMED genes was analyzed using publicly available RNA-seq data. Furthermore, we selected some SlMED genes to evaluate their expression patterns in various tissues and under different abiotic stress treatments by quantitative reverse transcription PCR experiments. This is the first detailed report to elucidate the molecular and phylogenetic features of the MED genes in tomato, and it provides valuable clues for further functional analysis in order to clarify the role of the SlMED genes in diverse plant growth, development and abiotic stress response.

Silencing SlMED18, tomato Mediator subunit 18 gene, restricts internode elongation and leaf expansion.

Mediator complex, a conserved multi-protein, is necessary for controlling RNA polymerase II (Pol II) transcription in eukaryotes. Given little is known about them in tomato, a tomato Mediator subunit 18 gene was isolated and named SlMED18. To further explore the function of SlMED18, the transgenic tomato plants targeting SlMED18 by RNAi-mediated gene silencing were generated. The SlMED18-RNAi lines exhibited multiple developmental defects, including smaller size and slower growth rate of plant and significantly smaller compound leaves. The contents of endogenous bioactive GA3 in SlMED18 silenced lines were slightly less than that in wild type. Furthermore, qRT-PCR analysis indicated that expression of gibberellins biosynthesis genes such as SlGACPS and SlGA20x2, auxin transport genes (PIN1, PIN4, LAX1 and LAX2) and several key regulators, KNOX1, KNOX2, PHAN and LANCEOLATE(LA), which involved in the leaf morphogenesis were significantly down-regulated in SlMED18-RNAi lines. These results illustrated that SlMED18 plays an essential role in regulating plant internode elongation and leaf expansion in tomato plants and it acts as a key positive regulator of gibberellins biosynthesis and signal transduction as well as auxin proper transport signalling. These findings are the basis for understanding the function of the individual Mediator subunits in tomato.