Analysis of the UDP-Glucosyltransferase (UGT) Gene Family and Its Functional Involvement in Drought and Salt Stress Tolerance in Phoebe bournei.

Uridine diphosphate glycosyltransferases (UDP-GTs, UGTs), which are regulated by UGT genes, play a crucial role in glycosylation. In vivo, the activity of UGT genes can affect the availability of metabolites and the rate at which they can be eliminated from the body. UGT genes can exert their regulatory effects through mechanisms such as post-transcriptional modification, substrate subtype specificity, and drug interactions. Phoebe bournei is an economically significant tree species that is endemic to southern China. Despite extensive studies on the UGT gene family in various species, a comprehensive investigation of the UGT family in P. bournei has not been reported. Therefore, we conducted a systematic analysis to identify 156 UGT genes within the entire P. bournei genome, all of which contained the PSPG box. The PbUGT family consists of 14 subfamilies, consistent with Arabidopsis thaliana. We observed varying expression levels of PbUGT genes across different tissues in P. bournei, with the following average expression hierarchy: leaf > stem xylem > stem bark > root xylem > root bark. Covariance analysis revealed stronger covariance between P. bournei and closely related species. In addition, we stressed the seedlings with 10% NaCl and 10% PEG-6000. The PbUGT genes exhibited differential expression under drought and salt stresses, with specific expression patterns observed under each stress condition. Our findings shed light on the transcriptional response of PbUGT factors to drought and salt stresses, thereby establishing a foundation for future investigations into the role of PbUGT transcription factors.

Growth mechanism deconvolution of self-limiting supraparticles based on microfluidic system.

The synthesis of colloidal supraparticles (SPs) based on self-assembly of nanoscopic objects has attracted much attention in recent years. Here, we demonstrate the formation of self-limiting monodisperse gold SPs with core-shell morphology based on the building blocks of flexible nanoarms in one step. A flow-based microfluidic chip is utilized to slow down the assembly process of the intermediates, which surprisingly allows for observation of ultrathin gold nanoplates as first intermediates. Notably, these intermediate cannot be observed in traditional synthesis due to their rapid rolling-up to form the second-order nanostructure of flexible hollow nanoarms. The growth mechanism of SPs can then be deconvoluted into two seed-mediated steps. Monte Carlo simulations confirm that the self-limiting growth of binary SPs is governed by a balance between electrostatic repulsion and van der Waals attraction.

Conformation modulated optical activity enhancement in chiral cysteine and au nanorod assemblies.

Assemblies of chiral cysteine (CYS) and Au nanorods (GNRs) are constructed in two typical patterns, end-to-end and side-by-side. Impressively, side-by-side assembled GNRs with CYS show obviously stronger plasmonic circular dichrosim (CD) response compared with the end-to-end assemblies. The corresponding theoretical calculation elucidates the intrinsic relationship among geometric structure, electromagnetic interaction, and induced plasmonic CD of the assemblies. This work will significantly benefit the design and application of plasmonic nanodevices with controllable chiroptical responses.

DNA induced intense plasmonic circular dichroism of highly purified gold nanobipyramids.

We report a strong and reversible CD response through the assembly of helical DNA and Au nanobipyramids (Au NBPs). Compared with common spherical Au nanoparticles or anisotropic Au nanorods, highly purified Au NBPs possess a more intense electromagnetic field and improved surface plasmon resonance. Thus, the assembly of DNA and Au NBPs exhibits an obviously enhanced plasmonic CD response. When the plasmonic CD is used for DNA detection, it shows high sensitivity and good reproducibility.

A peptide-based nanofibrous hydrogel as a promising DNA nanovector for optimizing the efficacy of HIV vaccine.

This report shows that a nanovector composed of peptide-based nanofibrous hydrogel can condense DNA to result in strong immune responses against HIV. This nanovector can strongly activate both humoral and cellular immune responses to a balanced level rarely reported in previous studies, which is crucial for HIV prevention and therapy. In addition, this nanovector shows good biosafety in vitro and in vivo. Detailed characterizations show that the nanofibrous structure of the hydrogel is critical for the dramatically improved immune responses compared to existing materials. This peptide-based nanofibrous hydrogel shows great potential for efficacious HIV DNA vaccines and can be potentially used for delivering other vaccines and drugs.

Controllable optical activity of gold nanorod and chiral quantum dot assemblies.

The optical coupling between Au nanorods (Au NRs) and chiral quantum dots (QDs) in assemblies is investigated by both experiment and theoretical calculations. The coupled optical activity in the visible-light region can be manipulated by changing either the aspect ratio of Au NRs or the size of QDs (left).

The influence on cell cycle and cell division by various cadmium-containing quantum dots.

Quantum dots (QDs) have attracted great attention because of their favorable optical properties and have been widely applied in biomedical fields. However, in recent years, there have been an increasing number of reports about the cytotoxicity of QDs, especially cadmium-containing QDs, which may release cadmium ions to induce cytotoxicity. Importantly, the chemical composition and surface modifications of cadmium-based QDs determine the amount of Cd(2+) released inside the cell. Thus, there is an urgent need for more systematic work to study the relationship between cytotoxicity and the surface properties of QDs. In this article, the cytotoxicity of seven cadmium-containing QDs with different constituent elements and surface chemistries are compared. The results show that the cytotoxicity of QDs is closely related to their constituent elements and surface properties: First, CdTe@ZnS core-shell QDs show much lower cytotoxicity than naked ones when they have similar surface modifications; second, the positively charged QDs are more toxic than the negatively charged ones. Moreover, both positively and negatively charged QDs without ZnS coatings lead to multipolar spindles, misaligned chromosomes, and G2/M checkpoint failures. Interestingly, although CdSe QDs with a PEG coating cause no apparent cytotoxicity in any of the cell lines studied, they can localize near the contractile ring during cytokinesis and then block contractile ring disassembly. The cellular effect of CdTe QDs comes not only from the release of cadmium ions but also the intracellular distribution of QD nanoparticles in cells and the associated nanoscale effects. It is also found that QD-caused cytokinesis failure is closely related to the decreased expression of Cyclin A and Cyclin B. Taken together, the above findings provide new insight into the dynamic fate of QDs during cell mitosis, and are important for understanding the intracellular effects of QDs on the mitotic spindle and chromosomes during cell division. Furthermore, this kind of cytotoxicity evaluation method should be applicable to studies of the biological effects and health impacts of other nanomaterials.

Gold nanorod@chiral mesoporous silica core-shell nanoparticles with unique optical properties.

The design and fabrication of chiral nanostructures is a promising approach to realize enantiomeric recognition and separation. In our work, gold nanorod@chiral mesoporous silica core-shell nanoparticles (GNR@CMS NPs) have been successfully synthesized. This novel material exhibits strong and tunable circular dichroism signals in the visible and near-infrared regions due to the optical coupling between the CMS shells and the GNR cores. When chiral cysteine molecules are loaded in the porous shells, the corresponding surface enhanced Raman scattering spectroscopy demonstrates a distinct chiral recognition effect, which can be used to semiquantitatively measure the composition of chiral enantiomers. A detailed sensing mechanism has been disclosed by density functional theory calculations.

Investigation of the photocatalytic effect of zinc oxide nanoparticles in the presence of nitrite.

Zinc oxide nanoparticles are widely used in sunscreen products because of their chemical stability and capability of blocking harmful ultraviolet rays. However, zinc oxide nanoparticles can also generate reactive species under ultraviolet irradiation. Because nitrite can form reactive nitrogen species under oxidative stress and because it exists in perspiration and cosmetics, we studied the effects of nitrites on the photocatalytic damage of zinc oxide nanoparticles (50 nm and 90 nm) to bovine serum albumin and human keratinocyte cells under ultraviolet irradiation (365 nm and 254 nm). The results indicate that nitrite plays an enhancing role in photocatalytic damage by breaking amino acid residues and promoting protein oxidation and nitration. The concentrations of zinc oxide and nitrite, the irradiation light and duration, and the pH of the medium are important factors influencing this photocatalytic damage. Size effects of ZnO nanoparticles on bovine serum albumin and keratinocyte cells are different. It is speculated that the extent of photo-damage is partially dependent on the aggregation of zinc oxide. These findings may be valuable for understanding potential risks of applying zinc oxide nanoparticle-containing sunscreens to human skin under sunlight exposure.

Manipulation of collective optical activity in one-dimensional plasmonic assembly.

The manipulation of the chirality and corresponding optical activity in the visible-near-infrared (NIR) light region is significant to realize applications in the fields of chemical sensing, enantioselective separation, chiral nanocatalysis, and optical devices. We studied the plasmon-induced circular dichroism (CD) response by one-dimensional (1D) assembly of cysteine (CYS) and gold nanorods (GNRs). Typically, GNRs can form end-to-end assembly through the electrostatic attraction of CYS molecules preferentially attached on the ends of different GNRs. CD responses are observed at both the UV and visible-NIR light region in the 1D assembly, which are assigned to the CYS molecules and the GNRs, respectively. In addition, the wavelength of the CD responses can be manipulated from 550 nm to more than 900 nm through altering the aspect ratios of GNRs in 1D assembly. Anisotropic enhancement of optical activity is discovered, suggesting that the enhancement of the longitudinal localized surface plasmon resonance (LSPR) peak of GNRs in the CD response is much more apparent than that of the transverse LSPR. The CD responses of individual CYS-attached GNRs and CYS-assembled gold nanoparticles (GNPs) substantiate that the form of assembly and the shape of building blocks are significant not only for the intensity but for the line shape of the CD signals.

Reversible plasmonic circular dichroism of Au nanorod and DNA assemblies.

Reversible plasmonic circular dichroism (CD) responses are realized for the first time based on temperature-dependent assembly and disassembly of Au nanorod (Au NR) and DNA hybrids. Compared with the conventional UV-vis absorption spectra, the changes in both intensity and line shape of plasmonic CD signals are much more pronounced, leading to a preliminary detection limit of DNA as low as 75 nM. The mechanism and influence factors of reversible plasmonic CD responses are explored.

Nano titanium dioxide photocatalytic protein tyrosine nitration: a potential hazard of TiO2 on skin.

Protein tyrosine nitration is a prevalent post-translational modification which occurs as a result of oxidative and nitrative stress, it may be directly involved in the onset and/or progression of diseases. Considering the existence of nano titanium dioxide (TiO(2)) in environment and sunscreen products along with the high content of nitrite in sweat, the UV-exposed skin may be a significant target for the photosensitized damage. In this paper, tyrosine nitration of bovine serum albumin (BSA) was initiated in the UV-irradiated reaction mixture containing 0.2-3.0mg/ml of three commercially nano TiO(2) products and 0.25-1.0mM NO2-. It was found that anatase TiO(2) and Degussa P25 TiO(2) showed prominent photocatalytic activity on promoting the formation of protein tyrosine nitration, and the optimum condition for the reaction was around physiological pH. Meanwhile, the photocatalytic effect of rutile on protein tyrosine nitration was subtle. The potential physiological significance of nano TiO(2)-photocatalytic protein nitration was also demonstrated in mouse skin homogenate. Although the relationship between photocatalytic protein tyrosine nitration and chronic cutaneous diseases needs further study, the toxicity of nano TiO(2) to the skin disease should be paid more attention in the production and utilization process.