Glaesserella parasuis serotype 5 breaches the porcine respiratory epithelial barrier by inducing autophagy and blocking the cell membrane Claudin-1 replenishment.

Glaesserella parasuis (G. parasuis), the primary pathogen of Glässer's disease, colonizes the upper respiratory tract and can break through the epithelial barrier of the respiratory tract, leading to lung infection. However, the underlying mechanisms for this adverse effect remain unclear. The G. parasuis serotype 5 SQ strain (HPS5-SQ) infection decreased the integrity of piglets' lung Occludin and Claudin-1. Autophagy regulates the function of the epithelial barrier and tight junction proteins (TJs) expression. We tested the hypothesis that HPS5-SQ breaking through the porcine respiratory epithelial barrier was linked to autophagy and Claudin-1 degradation. When HPS5-SQ infected swine tracheal epithelial cells (STEC), autophagosomes encapsulated, and autolysosomes degraded oxidatively stressed mitochondria covered with Claudin-1. Furthermore, we found that autophagosomes encapsulating mitochondria resulted in cell membrane Claudin-1 being unable to be replenished after degradation and damaged the respiratory tract epithelial barrier. In conclusion, G. parasuis serotype 5 breaks through the porcine respiratory epithelial barrier by inducing autophagy and interrupting cell membrane Claudin-1 replenishment, clarifying the mechanism of the G. parasuis infection and providing a new potential target for drug design and vaccine development.

40Ni-Added Poly(polyoxometalate) Assembled by {Ni6GeW9} and {Ni8(GeW9)2} Units: Structure, Magnetic, and Heterogeneous Catalysis Properties.

A novel 40Ni-added germanotungstate, Cs8K14Na3H3{[Ni6(OH)3(H2O)6(B-α-GeW9O34)]2[Ni8(µ6-O)(µ2-OH)2 (µ3-OH)2(H2O)B2O3(OH)2(B-α-GeW9O34)2]}2·84H2O (1), was made by the reaction of the trivacant [A-α-GeW9O34]10- ({GeW9}) precursor with Ni2+ cations and B5O8-, and systematically investigated by Fourier-transform infrared spectroscopy, elemental analysis, thermogravimetric analysis, and powder X-ray diffraction. Single crystal X-ray analysis indicates that the polyoxoanion of 1 is a novel octamer constructed by {Ni6GeW9} and {Ni8(GeW9)2} structural building units via Ni-O═W linkages. The magnetic behavior shows the existence of overall ferromagnetic interactions among the Ni2+ centers in compound 1. Photocatalytic H2 production studies have implied that 1 can work as a heterogeneous catalyst for hydrogen production with decent robustness and recyclability.

When Aggregation-Induced Emission Meets Perovskites: Efficient Defect-Passivation and Charge-Transfer for Ambient Fabrication of Perovskite Solar Cells.

The intrinsic defects in perovskite film can serve as non-radiative recombination center to limit the performance and stability of metal halide perovskite solar cells (PSCs). The additive engineering in perovskite film is always applied to produce high-efficiency PSCs in recent years. Here, a typical donor-acceptor (D-A) structured aggregation-induced emission (AIE) molecule tetraphenylethene-2-dicyano-methylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran (TPE-TCF) was introduced into perovskite film. The D-A structure of TPE-TCF molecule provided additional charge transfer channels, contributing to transporting electron of TPE-TCF-based device. The cyano (C≡N) of TPE-TCF can interact with the uncoordinated Pb to from a relatively stable intermediate, PbI2 ⋅TPE-TCF, resulting in the slower crystal growth, reduced the defects at the grain boundaries and suppressed carrier recombination. As a consequence, the power conversion efficiency (PCE) of TPE-TCF-modified PSCs achieved a remarkably enhanced from 15.63 to 19.66 % with negligible hysteresis, which was prominent in methylammonium lead iodide-based devices fabricated under ambient condition. Furthermore, the PSCs modified by AIE molecule possessed an outstanding stability and maintain about 86 % of the initial PCE after 300 h storage in air at 25-35 °C with a high relative humidity (RH) of ≈85 %. This work suggests that incorporating AIE molecule into perovskite is a promising strategy for facilitating high-performance PSCs commercialization in ambient environment without glovebox.

Hepta-Zr-Incorporated Polyoxometalate Assembly.

Driven by the synergistic-directing effect of the lacunary fragments, [B-α-GeW9O34]10- and [B-α-GeW11O39]8-, an unprecedented hepta-Zr-substituted polyoxometalate (POM) assembly K2Na6H10(Hpy)3[SbZr7O6(OH)4(B-α-GeW9O34)2(B-α-GeW11O39)2]·28H2O (1) was made under hydrothermal condition and structurally characterized. Of which, a unique hepta-Zr cluster, [SbZr7O6(OH)4]15+ core, was built by two trilacunary [B-α-GeW9O34]10- fragments and two monolacunary [B-α-GeW11O39]8- fragments and further arranged in a mode of a vertical cross and formed a pseudo-tetrahedron geometry. Compound 1 features the first Zr7-cluster-substituted POM. Moreover, 1 is an effective heterogeneous catalyst for the catalytic oxidation of sulfides into the corresponding sulfones with H2O2, manifesting distinguished conversion, excellent yield, and desired recyclability.

Start-up and synergistic nitrogen removal of partial nitrification and anoxic/aerobic denitrification in membrane aerated biofilm reactor.

To reduce energy consumption and improve operational stability of traditional biological nitrogen removal (BNR) system, partial nitrification and anoxic/aerobic denitrification were synergistically implemented in membrane aerated biofilm reactor (MABR) by regulating DO and pH. The results indicated that the optimal DO, pH and C/N ratio were 1-2 mg/L, 9.0 and 4-7, respectively. The corresponding average organic removal rate (ORR), total nitrogen removal rate (TNRR) and nitrite accumulation rate (NAR) reached 324 gCOD・m-3・d-1, 48 gN・m-3・d-1 and 77.70%, respectively. Extracellular polymeric substance (EPS) content in biofilm was more abundant than that in inoculated sludge. Multiple aerobic denitrifiers were detected in the biofilm with the relative abundance of 11.19%-22.71%. AQUASIM simulation implied that the distribution and proportion of substrates and bacteria were significantly affected by DO and pH regulation. Overall, this study provided some important insights in the start-up and operation of synergistic nitrogen removal process in BNR system.

A Novel Early Warning System Based on a Sediment Microbial Fuel Cell for In Situ and Real Time Hexavalent Chromium Detection in Industrial Wastewater.

Hexavalent chromium (Cr(VI)) is a well-known toxic heavy metal in industrial wastewater, but in situ and real time monitoring cannot be achieved by current methods used during industrial wastewater treatment processes. In this study, a Sediment Microbial Fuel Cell (SMFC) was used as a biosensor for in situ real-time monitoring of Cr(VI), which was the organic substrate is oxidized in the anode and Cr(VI) is reduced at the cathode simultaneously. The pH 6.4 and temperature 25 °C were optimal conditions for the operation. Under the optimal conditions, linearity (R² = 0.9935) of the generated voltage was observed in the Cr(VI) concentration range from 0.2 to 0.7 mg/L. The system showed high specificity for Cr(VI), as other co-existing ions such as Cu2+, Zn2+, and Pb2+ did not interfere with Cr(VI) detection. In addition, when the sediment MFC-based biosensor was applied for measuring Cr(VI) in actual wastewater samples, a low deviation (<8%) was obtained, which indicated its potential as a reliable biosensor device. MiSeq sequencing results showed that electrochemically active bacteria (Geobacter and Pseudomonas) were enriched at least two-fold on the biofilm of the anode in the biosensor as compared to the SMFC without Cr(VI). Cyclic voltammetry curves indicated that a pair of oxidation/reduction peaks appeared at -111 mV and 581 mV, respectively. These results demonstrated that the proposed sediment microbial fuel cell-based biosensor can be applied as an early warning device for real time in situ detection of Cr(VI) in industrial wastewaters.

Three new aluminoborates: from 1D tube to 3D framework.

Three new aluminoborates (ABOs) KCs[Al{B5O9(OH)}{BO(OH)2} (1), K0.5Cs[Al{B5O10}1/2{BO2(OH)}] (2), and Cs1.5[Al{B5O10}1/2{BO2(OH)}] (3) have been made under solvothermal conditions. 1 features a 1D tube constructed by the alternation of [B5O9(OH)]4- clusters and AlO4 units, onto which the [BO(OH)2]- triangles are grafted. To further construct higher dimensional structures based on the structure 1, solvents were adjusted for high basicity, resulting in the formations of the 3D ABO frameworks 2 and 3. 2 and 3 are isostructural and built from [B5O10]5- clusters, AlO4 tetrahedra and [BO2(OH)]2- triangles, in which [B5O10]5- clusters are bridged by AlO4 tetrahedra to produce a 2D ABO layer with 14-membered ring (MR) windows, and the [BO2(OH)]2- triangles act as the linkers to bridge the adjacent ABO layers to form 3D ABO frameworks containing eight types of channels. UV-vis diffuse reflectance spectra indicate that 1, 2, and 3 have potential applications in deep ultraviolet (DUV) regions.

Air-processed MAPbI3 perovskite solar cells achieve 20.87% efficiency and excellent bending resistance enabled via a polymer dual-passivation strategy.

In recent years, air-processed MAPbI3 perovskite solar cells (PSCs) have attracted widespread interest from researchers worldwide because of their simple and low-cost fabrication process. Nonetheless, the ambient conditions usually bring about many adverse effects, such as imperfect crystallization and numerous defects in perovskite films, which seriously impact both the photoelectric performance and stability of the device. Therefore, in this work, a polymer dual-passivation strategy was employed by introducing ammonium polyphosphate (APP) as an additive to the green anti-solvent to accurately modify the perovskite layer. APP, which has abundant phosphate and ammonium groups, could simultaneously fill the I/Pb vacancies by Lewis acid-base reactions to restrain defect formation and improve the power conversion efficiency (PCE) of the ultimate device. On the other hand, the long molecular chains of the polymer with a certain flexural ability were easily congregated at the grain boundaries of the perovskite grains, thus enhancing the bending resistance. Consequently, high-quality perovskite films with a dense morphology and large grain size were obtained. Because of the reduced defect density and suppressed non-radiative recombination, the optimal PSC attained a champion PCE of 20.87% with negligible hysteresis. Furthermore, the non-encapsulated APP-modified flexible device also exhibited excellent bending resistance. Only 20% of its normalized PCE was lost after 150 bending cycles at room temperature. This simple, green, low-cost, and reliable strategy for preparing high-efficiency PSCs with good stability can facilitate its commercialization.

Reduction-Active Antisolvent: A Universal and Innovative Strategy of Further Ameliorating Additive Optimization for High Efficiency Perovskite Solar Cells.

To further ameliorate current additive engineering of perovskites for viable applications, the inherent limitations should be overcome; these include weakened coordination of the dopants to the [PbI6]4- octahedra during crystallization and ubiquity of ineffective bonding sites. Herein, we introduce a facile strategy for synthesizing a reduction-active antisolvent. Washing with reduction-active PEDOT:PSS-blended antisolvent substantially enhances the intrinsic polarity of the Lewis acid (Pb2+) in [PbI6]4- octahedra, which causes significant strengthening of the coordinate bonding between additives and perovskite. Thus, coordination of the additive to the perovskite becomes much stable. Additionally, the enhanced coordination ability of Pb2+ can enhance the effective bonding sites and further enhance the efficacy of additive optimization to the perovskite. Here, we demonstrate five different additives as dopant bases and repeatedly verify the universality of this approach. The photovoltaic performance and stability of doped-MAPbI3 devices are further improved, revealing the advanced potential of additive engineering.

Enhancement of the osseointegration of a polyethylene terephthalate artificial ligament graft in a bone tunnel using 58S bioglass.

PURPOSE: The aim of the study was to investigate whether a bioactive glass (BG) coating on the polyethylene terephthalate (PET) artificial ligament could enhance graft osseointegration by promoting bone regeneration at the interface between PET graft and bone tunnel. METHODS: Thirty New Zealand white rabbits underwent artificial ligament graft transplantation in proximal tibial tunnels bilaterally. One limb was implanted with a 58S BG-coated PET graft, and the contralateral limb was implanted with a non-BG-coated PET graft as a control. The rabbits were randomly sacrificed at three, six and 12 weeks after surgery for biomechanical and histological examinations. RESULTS: The maximum load to failures of the BG-coated experimental group were significantly higher than those of the control group at 12 weeks (p = 0.0051). Histologically, at 12 weeks, the BG-coated PET graft induced great new bone formation between graft and host bone, and the average graft-bone interface width of the BG group became significantly lower than that of the control group. Furthermore, the BG coating on the ligament graft surface also stimulated greater expression of bone morphogenetic protein 2 (BMP-2) and vascular endothelial growth factor (VEGF) around the graft in vivo compared to the control group at three weeks (p < 0.05). CONCLUSIONS: This study has shown that a BG coating on the PET artificial ligament surface has a positive effect in the induction of artificial ligament osseointegration within the bone tunnel.

In-situ enrichment and application of heterotrophic nitrification-aerobic denitrification bacteria in membrane aerated biofilm reactor.

In order to reduce the resource and energy consumption of traditional biological nitrogen removal (BNR) process, heterotrophic nitrification-aerobic denitrification (HN-AD) bacteria was in situ enriched in membrane aerated biofilm reactor (MABR) by inoculating conventional activated sludge. Contaminants removal performance, EPS composition and microbial community were explored. The results indicated that the average removal efficiency of COD and TN under optimal condition reached 84.13% and 91.54%, respectively, which demonstrated that the reactor possessed excellent contaminants removal capacity. EPS analysis suggested that abundant protein especially tryptophan protein-like substance played a vital role in maintaining the microbial stability of biofilms. Multiple HN-AD genera, mainly Paracoccus, were detected with the highest relative abundance of 54.70%, which confirmed the successful enrichment of the HN-AD bacteria. Conventional nitrifiers and denitrifiers also thrived in biofilm, which demonstrated the synergistic nitrogen removal of multiple microorganisms. This study provided important insights into application of HN-AD bacteria and synergistic nitrogen removal in BNR system.

The disappearing additive: introducing volatile ethyl acetate into a perovskite precursor for fabricating high efficiency stable devices in open air.

In recent years, organic-inorganic halide perovskite solar cells (PSCs) have attracted massive attention because of their high power conversion efficiency (PCE). However, it is difficult to prepare perovskite films with good performance in open air due to the poor stability of perovskite materials in high humidity, which is seriously hindering the practical application and development of PSCs. Herein, ethyl acetate (EA) is introduced into the perovskite precursor to enhance the crystallinity of perovskite for fabricating high efficiency stable devices in the atmospheric environment. Interestingly, volatile EA, which is often used as an anti-solvent, could quickly evaporate and accelerate the nuclei formation during perovskite crystallization. More impressively, the Lewis base nature of EA can form strong chemical bonding interactions with perovskite to passivate the defects during crystallization. As a result, the EA-modified perovskite film demonstrates dense and defect-less morphology with large grain size (the maximum achieves 0.9 µm). The EA-treated device has a dramatic efficiency of 19.53% and negligible hysteresis of the photocurrent. Furthermore, both the temperature and humidity resistances of EA-modified PSC are significantly improved. The normalized PCE of the EA-modified device without encapsulation can still retain over 80% of its initial value after being stored in 60% relative humidity (RH) in the dark for 500 hours. This contribution provides a promising channel for facilitating the commercialization of PSCs.

Hydroxyapatite coating enhances polyethylene terephthalate artificial ligament graft osseointegration in the bone tunnel.

The purpose of this study was to investigate whether hydroxyapatite (HAp) coating could induce polyethylene terephthalate (PET) artificial ligament graft osseointegration in the bone tunnel. Twenty-four New Zealand white rabbits underwent artificial ligament graft transplantation in bilateral proximal tibia tunnels. One limb was implanted with HAp-coated PET graft, and the contralateral limb was implanted with non-HAp-coated PET graft as control. The rabbits were randomly sacrificed at four and eight weeks after surgery. The loads to failure of the experimental group at eight weeks were significantly higher than those of the control group (p = 0.0057). Histologically, application of HAp coating induced new bone formation between graft and bone at eight weeks compared with the controls. Real-time polymerase chain reaction examination revealed significantly elevated messenger ribonucleic acid expression levels of osteopontin and collagen I in the grafts of the HAp group compared with the controls at four weeks (p < 0.05). The study has shown that HAp coating on the PET artificial ligament surface has a positive effect in the induction of artificial ligament osseointegration within the bone tunnel.

Fate of antibiotic resistance genes during temperature-changed psychrophilic anaerobic digestion of municipal sludge.

The effects of anaerobic digestion (AD) on the abundance of antibiotic resistance genes (ARGs) are highly related to operational temperature. However, the removal performance of ARGs in psychrophilic AD and changed temperatures simulating variable seasonal temperatures is poorly understood. Herein, we investigated the fate of ARGs, correlated bacterial communities and physicochemical properties of AD operation at psychrophilic (15 ℃), mesophilic (35 ℃), and temperature changed conditions (15 to 35 ℃ and 35 to 15 ℃). The results indicated that ammonia release was positively correlated with temperature. The mesophilic AD facilitated phosphorous intake and ARGs proliferation and selection with oxytetracycline (OTC), while psychrophilic AD was conducive to the removal and control of ARGs if no OTC existed. The diversity and composition of AD bacterial communities were influenced more by temperature than OTC. The dominant genera like Candidatus_Microthrix and Acinetobacter had dramatical abundance discrepancies at different temperatures and were obviously positively correlated with ARGs (tet39, tetC and mexD), mobile genetic elements (MGEs) intI, insert sequences (IS) and plasmid. The physicochemical properties of AD influenced the bacterial richness, which in turn significantly correlated with the ARGs abundances. Therefore, ARGs removal could be potentially optimized by eliminating bacterial hosts with deteriorated living conditions and decreased nutrients. This study clarified the response of antibiotic resistome to different temperature variation and highlighted the potential strategies for improved ARGs removal in AD.

Immobilized-microbial bioaugmentation protects aerobic denitrification from heavy metal shock in an activated-sludge reactor.

The inhibition of denitrification by heavy metals is a problem in nitrogen wastewater treatment, but the solutions are rarely studied. In this study, Pseudomonas brassicacearum LZ-4, immobilized in sodium alginate-kaolin, was applied in an activated-sludge reactor to protect denitrifiers from hexavalent chromium (Cr(VI)). Q-PCR result showed that the strain LZ-4 was incorporated into activated sludge under the help of immobilization. In the non-bioaugmentation system, the removal efficiency of nitrate was decreased by 86.07% by 30 mg/L Cr(VI). Whereas, denitrification was protected and 95% of nitrate was removed continuously in immobilized-cell bioaugmentation system. Miseq sequencing data showed that bioaugmentation decreased the impact of Cr(VI) on microbial communities and increased the abundance of denitrifiers. Based on the results of biomass and extracellular polymers, activated sludge was protected from Cr(VI) toxicity. This discovery will provide a feasible technique for nitrogen wastewater treatment in the presence of distressing heavy metals.

Using nano-attapulgite clay compounded hydrophilic urethane foams (AT/HUFs) as biofilm support enhances oil-refinery wastewater treatment in a biofilm membrane bioreactor.

Petroleum refinery wastewater (PRW) treatments based on biofilm membrane bioreactor (BF-MBR) technology is an ideal approach and biofilm supporting material is a critical factor. In this study, BF-MBR with nano-attapulgite clay compounded hydrophilic urethane foams (AT/HUFs) as a biofilm support was used to treat PRW with a hydraulic retention time of 5 h. The removal rate of 500 mg/L chemical oxygen demand (COD), 15 mg/L NH4+ and 180 NTU of turbidity were 99.73%, 97.48% and 99.99%, which were 23%, 20%, and 6% higher than in the control bioreactor, respectively. These results were comparatively higher than that observed for the sequencing batch reactor (SBR). The death rate of the Spirodela polyrrhiza (L.) irrigated with BF-MBR-treated water was 4.44%, which was similar to that of the plants irrigated with tap water (3.33%) and SBR-treated water (5.56%), but significantly lower than that irrigated with raw water (84.44%). The counts demonstrated by qPCR for total bacteria, denitrifiers, nitrite oxidizing bacteria, ammonia oxidizing bacteria, and ammonia-oxidizing archaea were also higher in BF-MBR than those obtained by SBR. Moreover, the results of 16 s rRNA sequencing have demonstrated that the wastewater remediation microbes were enriched in AT/HUFs, e.g., Acidovorax can degrade polycyclic aromatic hydrocarbons, and Sulfuritalea is an efficient nitrite degrader. In summary, BF-MBR using AT/HUF as a biofilm support improves microbiome of the actived sludge and is reliable for oil-refinery wastewater treatment.

[Rapid screening of 24 tranquillizer drugs in fish and fishery products by ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectroscopy].

A method was developed for the simultaneous determination of 24 tranquillizer drugs in fish and fishery products using ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry (UPLC-Q-Orbitrap HRMS). The samples were extracted with acetonitrile. Then, the extracts were concentrated, dissolved by 50% (v/v) methanol aqueous solution, cleaned up with hexane saturated by acetonitrile. The separation was performed on an ACQUITY UPLC® BEH C18 column (100 mm×2.1 mm, 1.7 µm) with the gradient elution using acetonitrile and water both containing 0.1% (v/v) formic acid as mobile phases. The drugs were analyzed by full MS scan/data dependent MS2 (Full MS/dd-MS2)(Top 1) mode by heating electrospray ion (HESI) source. The results were quantified by external standard method. The calibration curves of the 24 tranquillizer drugs were linear in their respective linear range, the decision coefficients (r2) were no less than 0.9968. The average spiked recoveries of the 24 tranquillizer drugs were 58.9%-122.9%, and the relative standard deviations (RSDs) were 0.1%-16.4% in the six kinds of fish and fishery products at three spiked levels. The limits of quantification (LOQs) of the 24 tranquillizer drugs were 0.1-5.0 µg/kg. The method is simple, rapid, sensitive, reliable and suitable for the screening of the 24 tranquillizer drugs in fish and fishery products.

[Determination of 64 veterinary drug residues in aquatic products by ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high-resolution mass spectrometry].

A method has been developed for the simultaneous determination of 64 veterinary drugs in aquatic products using ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high-resolution mass spectrometry. The samples were extracted with an acetonitrile/water mixture (80/20, v/v), cleaned up by normal hexane saturated with acetonitrile and primary secondary amine (PSA) adsorbent, quantified with external standard method. The drugs were analyzed in full scan/data dependent mass spectrum 2 (Full MS/ddMS2) Top 1 mode. The calibration curves of the 64 drugs were linear with the correlation coefficients more than 0. 9967. The average recoveries of the 64 analytes ranged from 56.2% to 124.6%, and the relative standard deviations (RSDs) were 1.3%-29.8% in the three kinds of matrixes (fish, shrimp and shell) at three levels. The limits of quantification were 0.2-10 µg/kg. The method is simple, rapid, sensitive, reliable and suitable for the screening of residues in aquatic products.

Identification of the ferric iron utilization gene B739_1208 and its role in the virulence of R. anatipestifer CH-1.

Riemerella anatipestifer is an important bacterial pathogen in ducks and causes heavy economic losses in the duck industry. However, the pathogensis of this bacterium is poorly understood. In this study, a putative outer membrane hemin receptor gene B739_1208 in R. anatipestifer CH-1 was deleted to determine the relationship between iron uptake and virulence. The R. anatipestifer CH-1ΔB739_1208 mutants grew significantly more slowly than the wild-type bacteria in TSB liquid medium. Further characterization revealed that the R. anatipestifer CH-1ΔB739_1208 mutants were deficient in iron uptake. Animal experiments indicated that the median lethal dose of the wild-type RA-CH-1 in ducklings was 3.89×108, whereas the median lethal dose of the R. anatipestifer CH-1ΔB739_1208 mutant in ducklings was 5.68×109. The median lethal dose of the complementation strain in ducklings was 9.84×108. Additional analysis indicated that bacterial loads in the blood, liver, and brain tissues in the R. anatipestifer CH-1ΔB739_1208-infected ducklings were significantly decreased compared to those in the wild-type R. anatipestifer CH-1 infected ducklings. In a duck co-infection model with R. anatipestifer CH-1 and R. anatipestifer CH-1ΔB739_1208, the R. anatipestifer CH-1B739_1208 mutant was outcompeted by the wild-type R. anatipestifer CH-1 in the blood (P<0.002), livers (P<0.001) and brains (P<0.001) of infected ducks, indicating that B739_1208 gene expression provided a competitive advantage in these organs. Our results demonstrate that the B739_1208 gene is a virulence factor in R. anatipestifer CH-1.

[Preparation and enantioseparation performance of ß-cyclodextrin-silica hybrid chiral stationary phases].

A simple preparation method for ß-cyclodextrin-silica hybrid chiral stationary phases was developed. Firstly, the ß-cyclodextrin-silica derivative was synthesized by the reaction of 3-aminopropyltriethoxysilane and monochlorotriazinyl ß-cyclodextrin under weak base condition. Spherical ß-cyclodextrin-silica hybrid materials with ß-cyclodextrin in the surface of pores by covalent bonding were prepared using 1,2-bis(triethoxysilyl) ethane and the ß-cyclodextrin-silica derivative under the alkaline condition by one-step polymerization reaction. The ß-Cyclodextrin-silica hybrid chiral stationary phases could be directly used as high performance liquid chromatographic packings after the template removal. The hybrid materials prepared in this paper possessed regular spherical morphology, good monodispersion, high specific surface area, good mechanical property, high chemical stability and simple preparation process. It combined the chiral recognition performance of ß-cyclodextrin and the outstanding performance of organic-inorganic hybrid material. The effect of the composition, ratio and pH of mobile phase on chiral separation was investigated, and the best chiral separation conditions had been optimized. The baseline chiral separations for five chiral compounds were obtained under the optimal conditions. The results of enantioseparation showed that the hybrid chiral stationary phases had favorable chiral recognition ability. Compared with the traditional preparation process of chiral stationary phases, a new thought for new type of chiral stationary phase is provided by the present method in this paper.