Anti-oil-fouling Au/BiOCl coating for visible light-driven photocatalytic inactivation of bacteria.

In this work, gold/bismuth oxychloride (Au/BiOCl) nanocomposites with different morphologies were successfully prepared by simple solvothermal method and sodium borohydride reduction method, which exhibited significantly efficient visible-light-driven photocatalytic disinfection for Staphylococcus aureus (S.aureus). Particularly, the flower-like Au/BiOCl nanocomposite showed the highest photocatalytic bactericidal performance among the prepared Au/BiOCl samples. The radical trapping experiments revealed that the hole was the main reactive species responsible for the inactivation of S.aureus over Au/BiOCl composite. The enhanced photocatalytic bactericidal effect could be attributed to the enhanced adsorption intensity of visible light that originated from the surface plasmon resonance (SPR) effect of Au, rapid transfer and space transport of hot electrons caused by the hierarchical structure of BiOCl layered compound. Furthermore, the Au/BiOCl coating prepared on stainless steel wire mesh via in-situ synthesis method exhibited excellent superhydrophilic/underwater superoleophobic performance, which endowed the coating with anti-oil-fouling in water. More importantly, compared with Au/BiOCl powder catalyst, the prepared Au/BiOCl coating with anti-oil-fouling also possessed high photocatalytic bactericidal activity and stable recycling performance.

A responsive pure DNA hydrogel for label-free detection of lead ion.

It is of great significance to develop facile and economical strategies for on-site detection and treatment of toxic metal ions. Stimulus-responsive DNA hydrogel materials have been increasingly used for convenient detection of metal ions due to their advantages such as simplicity, portability, and ease of storage. However, these methods still require encapsulation of signal tags by labeling or embedding. In this paper, a one-step preparation of Pb2+-responsive pure DNA hydrogel material was designed to realize a new label-free strategy for Pb2+ biosensing. The Pb2+-dependent DNAzyme strand and substrate strand were introduced to fabricate the DNA hydrogel. The presence of Pb2+ in the sample activates the enzyme strand in the hydrogel skeleton and triggers the cleavage of the substrate, thereby destroy the hydrogel structure. DNA fragments released by the collapsed hydrogel were readily measured as signal output for quantifying Pb2+ concentrations with a minimum detection limit of 7.7 nM. We successfully eliminated the need for embedding or labeling of signal molecules by using the DNA molecules that construct hydrogels as the signal output. And the newly developed method for label-free detection of Pb2+ based on pure DNA hydrogel is simple, easy readout, and cost-effective. By adjusting the DNAzyme and substrate sequences, label-free analysis of other metal ions can also be achieved. We expect that our strategy can be applied to the field detection of toxic metal ions.

Roles of extracellular polymeric substances in uranium immobilization by anaerobic sludge.

The specific roles of extracellular polymeric substances (EPS) and how factors influenced EPS's roles during U(VI) immobilization are still unclear. In this study, high content of U with the main form of nanoparticles was detected in EPS, accounting for 10-42% of total U(VI) removal. EPS might be utilized as energy source or even as electron donors when external carbon source was unavailable. The influencing degree of each experimental parameter to uranium (U) removal process was elucidated. The influential priority to U(IV)/U(VI) ratios in sludge was as follows: acetate, U(VI), and nitrate. The influential priority to total EPS contents was as follows: U(VI), nitrate and acetate. The complex interaction mechanism between U(VI) and EPS in the U immobilization process was proposed, which might involve three ways including biosorption, bioreduction and bioprecipitation. These results indicate important and various roles of EPS in U(VI) immobilization.

Rational design of sequestered DNAzyme beacons to enable flexible control of catalytic activities.

DNAzymes as functional units play increasingly important roles for DNA nanotechnology, and fine control of the catalytic activities of DNAzymes is a crucial element in the design and construction of functional and dynamic devices. So far, attempts to control cleavage kinetics can be mainly achieved through varying the concentrations of the specific metal ions. Here we present a facile sequestered DNAzyme beacon strategy based on precisely blocking the catalytic core of the DNAzyme, which can flexibly regulate the DNAzyme cleavage kinetics without changing the concentrations of metal ions. This strategy can be extended to couple with a large number of other RNA-cleaving DNAzymes and was successfully applied in designing a dual stem-loop structure probe for arbitrary sequence biosensing, which provides the possibility of scaling up versatile and dynamic DNA devices that use DNAzymes as functional modules.