Yeasts are the most predominant petroleum hydrocarbon-degrading fungi isolated from petroleum-contaminated soil. However, information of the transmembrane transport of petroleum hydrocarbon into yeast cells is limited. The present study was designed to explore the transmembrane transport mechanisms of the typical petroleum hydrocarbon n-hexadecane in Candida tropicalis cells with petroleum hydrocarbon biodegradation potential. Yeast cells were treated with n-hexadecane in different scenarios, and the percentage of intracellular n-hexadecane and transport dynamics were investigated accordingly. The intracellular concentration of n-hexadecane increased within 15 min, and transportation was inhibited by NaN3, an ATPase inhibitor. The uptake kinetics of n-hexadecane were well fitted by the Michaelis-Menten model, and Kt values ranged from 152.49 to 194.93 mg/L. All these findings indicated that n-hexadecane might cross the yeast cells in an energy-dependent manner and exhibit an affinity with the cell transport system. Moreover, the differentially expressed membrane proteins induced by n-hexadecane were identified and quantified by tandem mass tag labeling coupled with liquid chromatography tandem mass spectrometry analysis. The proteome analysis results demonstrated that energy production and conversion accounted for a large proportion of the functional classifications of the differentially expressed proteins, providing further evidence that sufficient energy supply is essential for transmembrane transport. Protein functional analysis also suggested that differentially expressed proteins associated with transmembrane transport processes are clearly enriched in endocytosis and phagosome pathways (p < 0.05), and the analysis supported the notion that the underlying transmembrane transport mechanism might be associated with endocytosis and phagosome pathways, revealing a new mechanism of n-hexadecane internalization by Candida tropicalis.

Plasmon-enhanced fluorescence (PEF)-based anisotropic nanostructures are considered extremely promising tools for improving the inherent problems of traditional fluorophores and for detecting important biomolecules with high sensitivity. Herein, a novel triangular gold nanoprism (AuNPR)-based fluorescence probe, AuNPR@SiO₂@12,17-tetramethyl-3-dihydro-(2s-trans)-thyl-7(Ce6), was developed for PEF by virtue of multiple “hot spots” of AuNPRs. Fluorescence enhancement of fluorophores can be realized owing to the larger and stronger electromagnetic fields located at the sharp tips of AuNPRs than those on spherical particles and nanorods. A silica shell was employed as a rigid spacer to precisely adjust the distance between the AuNPR and Ce6 for optimal PEF. Owing to the improved fluorescence signal, core–shell PEF-based AuNPRs can be applied as a turn-on probe for highly selective and sensitive detection of pyrophosphate (PPi) with a desirable detection limit of 0.2 μM using a displacement approach. Meanwhile, we demonstrated that these nanomaterials have great potential for real-time monitoring of polymerase chain reaction (PCR) products, successfully revealing an approximately 240 times higher detectable fluorescence response than that of traditional gel electrophoresis. Furthermore, cell imaging indicates the potential applications of PEF-based probes in living cells.

For the first time, neutron tomography was applied for 3D quantitative hydrogen distribution analysis in titanium alloys following thermohydrogen processing.

Herein, we develop a facile method for selective and sensitive detection of hydroxylamine (HA) based on the in situ formation of DNA templated copper nanoparticles (DNA-CuNPs) as fluorescent probes. It is firstly found that HA as a reducing agent can play a key role in the in situ formation of fluorescent DNA-CuNPs. This special optical property of DNA-CuNPs with (λ_ex = 340 nm, λ_em = 588 nm) with a mega-Stokes shifting (248 nm) makes it applicable for the turn-on detection of HA. In addition, this fluorescent method has several advantages such as being simple, rapid, and environmentally friendly, because it avoids the traditional organic dye molecules and complex procedures. Under optimized conditions, this platform achieves a fluorescent response for HA with a detection limit of 0.022 mM. Especially, successful detection capability in tap waters and ground waters exhibits its potential to be general method.

Funnel and gate permeable reactive barrier (FGPRB) is an effective method to treat groundwater pollution. In order to clarify the impact of FGPRB on groundwater dynamic conditions, this study takes a site pilot test as the research object and establishes an FGPRB downstream of a petrochemical industry. The results show that the concentrations of 1,2-dichloroethylene and benzene in the downstream groundwater, after setting FGPRB, are lower than the detection limit. The numerical simulation results show that after setting FGPRB, both point source and area source pollution can achieve a good delay effect, extending from about 27 d to about 65 d of response time, but changing the thickness and permeability coefficient has no obvious effect on the delay effect. The tracer test shows the average permeability coefficient of the medium from the injection well to the monitoring well after the construction of FGPRB decreases from 77.0 m/d to 31.2 m/d after the construction of FGPRB. The average seepage velocity from the injection well to the monitoring well decreased from 0.19 m/d to 0.078 m/d after the construction of FGPRB. At the same time, when the FGPRB is not built, the maximum concentration time from the injection well to the monitoring well is about 10 d. After the FGPRB is constructed, the maximum concentration time of the tracer received by the monitoring well is about 27 days. These results confirm that the establishment of FGPRB will change the hydrodynamic conditions of groundwater and delay the response time of pollutants in the monitoring well.

Potentially toxic element (PTE) contamination in soils has serious impacts on ecosystems. However, there is no consensus in the field of assessment and monitoring of contaminated sites in China. In this paper, a risk assessment and pollution monitoring method for PTEs was proposed and applied to a mining site containing As, Cd, Sb, Pb, Hg, Ni, Cr, V, Zn, Tl, and Cu. The comprehensive scoring method and analytical hierarchical process were used to screen the priority PTEs for monitoring. The potential ecological risk index method was used to calculate the risk index of monitoring point. The spatial distribution characteristics were determined using semi-variance analysis. The spatial distribution of PTEs was predicted using ordinary kriging (OK) and radial basis function (RBF). The results showed that the spatial distribution of As, Pd, and Cd are mainly influenced by natural factors, while Sb and RI are influenced by both natural and human factors. OK has higher spatial prediction accuracy for Sb and Pb, and RBF has higher prediction accuracy for As, Cd, and RI. The areas with high ecological risk and above are mainly distributed on both sides of the creek and road. The optimized long-term monitoring sites can achieve the monitoring of multiple PTEs.