Recombinant L. lactis vaccine LL-plSAM-WAE targeting four virulence factors provides mucosal immunity against H. pylori infection.

BACKGROUND: Helicobacter pylori (H. pylori) causes chronic gastric disease. An efficient oral vaccine would be mucosa-targeted and offer defense against colonization of invasive infection in the digestive system. Proteolytic enzymes and acidic environment in the gastrointestinal tract (GT) can, however, reduce the effectiveness of oral vaccinations. For the creation of an edible vaccine, L. lactis has been proposed as a means of delivering vaccine antigens. RESULTS: We developed a plSAM (pNZ8148-SAM) that expresses a multiepitope vaccine antigen SAM-WAE containing Urease, HpaA, HSP60, and NAP extracellularly (named LL-plSAM-WAE) to increase the efficacy of oral vaccinations. We then investigated the immunogenicity of LL-plSAM-WAE in Balb/c mice. Mice that received LL-plSAM-WAE or SAM-WAE with adjuvant showed increased levels of antibodies against H. pylori, including IgG and sIgA, and resulted in significant reductions in H. pylori colonization. Furthermore, we show that SAM-WAE and LL-plSAM-WAE improved the capacity to target the vaccine to M cells. CONCLUSIONS: These findings suggest that recombinant L. lactis could be a promising oral mucosa vaccination for preventing H. pylori infection.

Micelles regulated thin film nanocomposite membrane with enhanced nanofiltration performance.

The desalination performance of thin film nanocomposite (TFN) membranes is significantly influenced by the nature of nanofillers and the structure of the polyamide (PA) layer. Herein, a micelles regulated interfacial polymerization (MRIP) strategy is reported for the preparation of TFN membranes with enhanced nanofiltration (NF) performance. Specially, stable and ultrafine micelles, synthesized from the poly(ethylene oxide)-b-poly(4-vinyl pyridine)-b-polystyrene (PEO-PVP-PS) triblock copolymers, were utilized as regulators in the aqueous phase during the interfacial polymerization (IP) process. TFN membranes were fabricated with varying concentrations of micelles to improve their properties and performances. The structure of the PA layer was further regulated by modulating the content of trimesoyl chloride (TMC), which significantly enhances the performance of the TFN membrane with micelles. Attributable to the homogeneously dispersed micelles and the modified PA layer, the optimized membrane denoted as TFN-2-0.3 exhibits an improved separation performance of 20.7 L m-2h-1 bar-1 and 99.3 % Na2SO4 rejection, demonstrating nearly twice the permeance and 2.7 % higher rejection than that of the original control membrane, respectively. The mechanism of this MRIP strategy was investigated through the diffusion experiments of piperazine (PIP) and interfacial tension tests. The incorporated micelles effectively lower the interfacial tension, promote the diffusion of PIP and accelerate the IP reaction, resulting in a denser and thinner PA layer. Collectively, these findings demonstrate that TFN membranes with micelles exhibit increased roughness, enhanced hydrophilicity, superior rejection to divalent salts, and better acid-base resistance, highlighting their potential applications in the design of TFN membranes.

Improvement of peroxymonosulfate utilization efficiency for sulfamethazine degradation by photo-electron activating peroxymonosulfate: Performance and mechanism.

Enhancing the utilization efficiency of oxidant is of great importance for advanced oxidation processes (AOPs). Herein, nitrogen-doped titania dioxide/carbon (NTC7) catalyst was fabricated via pyrolyzing NH2-MIL-125 under nitrogen atmosphere at 700 °C. Excitation of NTC7 under visible light can successfully achieve efficient activation of peroxymonosulfate (PMS) (NTC7 + PMS + Vis). Degradation performance and PMS activation mechanism were systematically investigated using sulfamethazine (SMT) as the target pollutant. It was found that the photo-generated electrons excited from NTC7 under visible light played the dominant role in enhancing the productive consumption of PMS. Its utilization increased by 66 % (Δ[PMS]/Δ[SMT] = 7.0) in NTC7 + PMS + Vis process and the degradation rate was 2.14 times higher than that of NTC7 + PMS process. The ketonic CO groups and structural defects were responsible for the generation of 1O2 in dark activation while radicals (•OH, O2•-) were more inclined to be continuously produced in NTC7 + PMS + Vis process. The involved degradation pathways, intermediates, and toxicity assessment have been studied in detail. This work provides an effective approach to enhance the utilization efficiency of oxidant for pollutant degradation by AOPs.

Hydrangea-like architectures composed of Zr-based metal-organic framework nanosheets with enhanced iodine capture.

Zirconium-based metal-organic framework nanosheet assembled hydrangea-like architectures were reported and an enhanced iodine capture capacity was achieved.

Sequential Ultrafiltration-Catalysis Membrane for Excellent Removal of Multiple Pollutants in Water.

Clean water production calls for highly efficient and less energy-intensive technologies. Herein, a novel concept of a sequential ultrafiltration-catalysis membrane is developed by loading Co3O4/C@SiO2 yolk-shell nanoreactors into the fingerlike channels of a polymeric ultrafiltration membrane. Such a sequenced structure design successfully integrates selective separation with peroxymonosulfate-based catalysis to prepare a functionalized molecular sieve membrane, which exhibits excellent decontamination performance toward multipollutants by filtering the water matrices containing humic acid (HA) and bisphenol A (BPA). In this study, 100% rejection of HA and 95% catalytic degradation of BPA were achieved under a low pressure of 0.14 MPa and an ultrahigh flux of 229 L m-2 h-1, corresponding to a retention time of 3.1 s. Notably, the removal performance of multiple pollutants essentially depends on the ordered arrangement of ultrafiltration and catalysis. Moreover, the flow-through process demonstrated significant enhancement of BPA degradation kinetics, which is 21.9 times higher than that of a conventional batch reactor. This study provides a novel strategy for excellent removal of multiple pollutants in water.

Enhancing nanofiltration performance by incorporating tannic acid modified metal-organic frameworks into thin-film nanocomposite membrane.

Nanofiltration (NF) is an advanced environmental technology in water treatment. To thin film nanocomposite (TFN) membrane, good compatibility between nanofillers and polyamide (PA) layer is the guarantee of remarkable performance. Herein, tannic acid (TA) was employed as modifier of UIO-66-NH2 prior to the interfacial polymerization (IP). With TA modification, more interaction can be formed so that the compatibility between nanofillers and PA layer can be promoted at the molecular level. Characterizations demonstrated the coating of TA on UIO-66-NH2, together with successful introducing of nanofillers in TFN membranes. Compared to pristine thin film composite (TFC) membrane, both UIO-incorporated TFN (TFN-U) and TA modified UIO-incorporated TFN (TFN-TU) membranes showed higher permeance (111.2% and 93% enhancement, respectively). However, under the same nanofillers dose, TFN-TU exhibited slightly lower permeance and higher rejection than TFN-U since the bridging effect of TA healed non-selective voids in skin layer. With the increasing of nanofiller dose in IP, TFN-TU remained reasonable selectivity while TFN-U failed to. Moreover, TFN-TU showed better anti-fouling property due to TA modification. Introducing TA modified MOFs into IP can serve as an ingenious strategy for TFN membrane to achieve high-quality environmental applications.

Defect-engineered UiO-66-NH2 modified thin film nanocomposite membrane with enhanced nanofiltration performance.

Defect-engineered UiO-66-NH2 was introduced into a polyamide layer to form a thin film nanocomposite (TFN) membrane. Simultaneous enhancements in permeance and selectivity to Na2SO4 solution were achieved.

Low pressure operated ultrafiltration membrane with integration of hollow mesoporous carbon nanospheres for effective removal of micropollutants.

An effective way to remove micropollutants is desirable for water purification. In this work, a dual-functional ultrafiltration (DFUF) membrane was fabricated by loading hollow mesoporous carbon nanospheres (HMCNs) into the finger-like support layer pores of the polymeric ultrafiltration (UF) membrane. The designed DFUF membrane combines the high selectivity of ultrafiltration that removes macromolecules based on size exclusion mechanism, and excellent adsorption capacity of HMCNs towards micropollutants in water. When tetracycline (TCN) and 17ß-Estradiol (E2) were selected as model micropollutants, corresponding 97 % and 94 % removal were achieved at a low pressure less than 0.15 bar and a flux of 50 and 64 L h-1 m-2 (estimated residence time less than 6 s), respectively. Moreover, simultaneous removal of multiple pollutants was demonstrated by filtering a mixture containing TCN and polyethylene glycols (PEG) 600 kDa macromolecules. Over a long filtration period (more than 60 h) that produced 3180 L/m2 of permeate, the TCN concentration reduced from 100 µg/L in the feed to less than 10 µg/L in the permeate. The above results indicate that the DFUF membrane is capable of removing the small molecular and macromolecular pollutants simultaneously at low pressure, and hence offers remarkable potential in water treatment applications.