A Novel Peroxidase CanPOD Gene of Pepper Is Involved in Defense Responses to Phytophtora capsici Infection as well as Abiotic Stress Tolerance

Peroxidases are involved in many plant processes including plant defense responses to biotic and abiotic stresses. We isolated a novel peroxidase gene CanPOD from leaves of pepper cultivar A3. The full-length gene has a 1353-bp cDNA sequence and contains an open reading frame (ORF) of 975-bp, which encodes a putative polypeptide of 324 amino acids with a theoretical protein size of 34.93 kDa. CanPOD showed diverse expression levels in different tissues of pepper plants. To evaluate the role of CanPOD in plant stress responses, the expression patterns of CanPOD were examined using Real-Time RT-PCR. The results indicated that CanPOD was significantly induced by Phytophtora capsici. Moreover, CanPOD was also up-regulated in leaves after salt and drought stress treatments. In addition, CanPOD expression was strongly induced by signaling hormones salicylic acid (SA). In contrast, CanPOD was not highly expressed after treatment with cold. Meanwhile, in order to further assess the role of gene CanPOD in defense response to P. capsici attack, we performed a loss-of-function experiment using the virus-induced gene silencing (VIGS) technique in pepper plants. In comparison to the control plant, the expression levels of CanPOD were obviously decreased in CanPOD-silenced pepper plants. Furthermore, we analyzed the effect of P. capsici on detached-leaves and found that the CanPOD-silenced plant leaves were highly susceptible to P. capsici infection. Taken together, our results suggested that CanPOD is involved in defense responses to P. capsici infection as well as abiotic stresses in pepper plants.     

Characteristic of the Pepper CaRGA2 Gene in Defense Responses against Phytophthora capsici Leonian

The most significant threat to pepper production worldwide is the Phytophthora blight, which is caused by the oomycete pathogen, Phytophthora capsici Leonian. In an effort to help control this disease, we isolated and characterized a P. capsici resistance gene, CaRGA2, from a high resistant pepper (C. annuum CM334) and analyzed its function by the method of real-time PCR and virus-induced gene silencing (VIGS). The CaRGA2 has a full-length cDNA of 3,018 bp with 2,874 bp open reading frame (ORF) and encodes a 957-aa protein. The protein has a predicted molecular weight of 108.6 kDa, and the isoelectric point is 8.106. Quantitative real-time PCR indicated that CaRGA2 expression was rapidly induced by P. capsici. The gene expression pattern was different between the resistant and susceptible cultivars. CaRGA2 was quickly expressed in the resistant cultivar, CM334, and reached to a peak at 24 h after inoculation with P. capsici, five-fold higher than that of susceptible cultivar. Our results suggest that CaRGA2 has a distinct pattern of expression and plays a critical role in P. capsici stress tolerance. When the CaRGA2 gene was silenced via VIGS, the resistance level was clearly suppressed, an observation that was supported by semi-quantitative RT-PCR and detached leave inoculation. VIGS analysis revealed their importance in the surveillance to P. capsici in pepper. Our results support the idea that the CaRGA2 gene may show their response in resistance against P. capsici. These analyses will aid in an effort towards breeding for broad and durable resistance in economically important pepper cultivars.     

Murine K2P5.1 Deficiency Has No Impact on Autoimmune Neuroinflammation due to Compensatory K2P3.1- and KV1.3-Dependent Mechanisms

Lymphocytes express potassium channels that regulate physiological cell functions, such as activation, proliferation and migration. Expression levels of K_2P5.1 (TASK2; KCNK5) channels belonging to the family of two-pore domain potassium channels have previously been correlated to the activity of autoreactive T lymphocytes in patients with multiple sclerosis and rheumatoid arthritis. In humans, K_2P5.1 channels are upregulated upon T cell stimulation and influence T cell effector functions. However, a further clinical translation of targeting K_2P5.1 is currently hampered by a lack of highly selective inhibitors, making it necessary to evaluate the impact of KCNK5 in established preclinical animal disease models. We here demonstrate that K_2P5.1 knockout (K_2P5.1^−/−) mice display no significant alterations concerning T cell cytokine production, proliferation rates, surface marker molecules or signaling pathways. In an experimental model of autoimmune neuroinflammation, K_2P5.1^−/− mice show a comparable disease course to wild-type animals and no major changes in the peripheral immune system or CNS compartment. A compensatory upregulation of the potassium channels K_2P3.1 and K_V1.3 seems to counterbalance the deletion of K_2P5.1. As an alternative model mimicking autoimmune neuroinflammation, experimental autoimmune encephalomyelitis in the common marmoset has been proposed, especially for testing the efficacy of new potential drugs. Initial experiments show that K_2P5.1 is functionally expressed on marmoset T lymphocytes, opening up the possibility for assessing future K_2P5.1-targeting drugs.     

Tailoring bioactive and mechanical properties in polycrystalline CaO–SiO2–P2O5 glass-ceramics

Biological functions and mechanical properties are vital factors for artificial bone materials, with great clinic demand for bone injuries and defects. This study highlights mechanical strengths, in vitro and in vivo biological behaviors of the bioactive CaO–SiO₂–P₂O₅ glass-ceramics tailored by the nucleating agent P₂O₅. A high mechanical flexural strength of ～170 MPa and hardness of ～720 HV were achieved, owing to strengthened Si–O bonds in the network. In vitro cell tests demonstrate remarkable viability (using L929 cells) and bioactivity (using bone marrow-derived mesenchymal stromal cells), associated with the release of Ca²⁺ ions in the solution due to weakened Ca–O bonds in the glass-ceramic network. The assay in the simulated body ?uid revealed a formation of the hydroxyapatite-phase layer, which may act as a bridge to facilitate bioactivity on the CaO–SiO₂–P₂O₅ glass-ceramics. In vivo assay shows a significant bone-ingrowth capability on the CaO–SiO₂–P₂O₅ glass-ceramic. This work paves a promising route to utilize P₂O₅–nucleated CaO–SiO₂–P₂O₅ glass-ceramics for load-bearing bone replacement.     

Enhancement of Palmarumycins C12 and C13 Production in Liquid Culture of Endophytic Fungus Berkleasmium sp. Dzf12 after Treatments with Metal Ions

The influences of eight metal ions (i.e., Na⁺, Ca²⁺, Ag⁺, Co²⁺, Cu²⁺, Al³⁺, Zn²⁺, and Mn⁴⁺) on mycelia growth and palmarumycins C₁₂ and C₁₃ production in liquid culture of the endophytic fungus Berkleasmium sp. Dzf12 were investigated. Three metal ions, Ca²⁺, Cu²⁺ and Al³⁺ were exhibited as the most effective to enhance mycelia growth and palmarumycin production. When calcium ion (Ca²⁺) was applied to the medium at 10.0 mmol/L on day 3, copper ion (Cu²⁺) to the medium at 1.0 mmol/L on day 3, aluminum ion (Al³⁺) to the medium at 2.0 mmol/L on day 6, the maximal yields of palmarumycins C₁₂ plus C₁₃ were obtained as 137.57 mg/L, 146.28 mg/L and 156.77 mg/L, which were 3.94-fold, 4.19-fold and 4.49-fold in comparison with that (34.91 mg/L) of the control, respectively. Al³⁺ favored palmarumycin C₁₂ production when its concentration was higher than 4 mmol/L. Ca²⁺ had an improving effect on mycelia growth of Berkleasmium sp. Dzf12. The combination effects of Ca²⁺, Cu²⁺ and Al³⁺ on palmarumycin C₁₃ production were further studied by employing a statistical method based on the central composite design (CCD) and response surface methodology (RSM). By solving the quadratic regression equation between palmarumycin C₁₃ and three metal ions, the optimal concentrations of Ca²⁺, Cu²⁺ and Al³⁺ in medium for palmarumycin C₁₃ production were determined as 7.58, 1.36 and 2.05 mmol/L, respectively. Under the optimum conditions, the predicted maximum palmarumycin C₁₃ yield reached 208.49 mg/L. By optimizing the combination of Ca²⁺, Cu²⁺ and Al³⁺ in medium, palmarumycin C₁₃ yield was increased to 203.85 mg/L, which was 6.00-fold in comparison with that (33.98 mg/L) in the original basal medium. The results indicate that appropriate metal ions (i.e., Ca²⁺, Cu²⁺ and Al³⁺) could enhance palmarumycin production. Application of the metal ions should be an effective strategy for palmarumycin production in liquid culture of the endophytic fungus Berkleasmium sp. Dzf12.     

One-Dimensional Hydrogen-Bonded Infinite Chain from Nickel(II) Tetraaza Macrocyclic Complex and 1,2-Cyclopentanedicarboxylate Ligand

The reaction of [Ni(L)]Cl₂·2H₂O (L = 3,14-dimethyl-2,6,13,17-tetraazatricyclo [14,4,0^1.18,0^7.12]docosane) with trans-1,2-cyclopentanedicarboxylic acid (H₂-cpdc) yields a 1D hydrogen-bonded infinite chain with formula [Ni(L)(H-cpdc⁻)₂] (1). This complex has been characterized by X-ray crystallography, spectroscopy and cyclic voltammetry. The crystal structure of 1 exhibits a distorted octahedral geometry about Ni atom with four nitrogen atoms of the macrocycle and two oxygen atoms of the H-cpdc⁻ ligand at the axial position. Compound 1 crystallizes in the monoclinic system P2₁/c with a = 8.7429(17), b = 10.488(2), c = 18.929(4) Å, β = 91.82(2), V = 1734.8(6) ų, Z = 2. Electronic spectrum of 1 reveals a high-spin octahedral environment. Cyclic voltammetry of 1 undergoes two waves of a one-electron transfer corresponding to Ni^II/Ni^III and Ni^II/Ni^I processes.     

Synthesis,PASS-Predication and in Vitro Antimicrobial Activity of Benzyl 4-O-benzoyl-α-l-rhamnopyranoside Derivatives

Benzyl α-l-rhamnopyranoside 4, obtained by both conventional and microwave assisted glycosidation techniques, was subjected to 2,3-O-isopropylidene protection to yield compound 5 which on benzoylation and subsequent deprotection of isopropylidene group gave the desired 4-O-benzoylrhamnopyranoside 7 in reasonable yield. Di-O-acetyl derivative of benzoate 7 was prepared to get newer rhamnopyranoside. The structure activity relationship (SAR) of the designed compounds was performed along with the prediction of activity spectra for substances (PASS) training set. Experimental studies based on antimicrobial activities verified the predictions obtained by the PASS software. Protected rhamnopyranosides 5 and 6 exhibited slight distortion from regular ¹C₄ conformation, probably due to the fusion of pyranose and isopropylidene ring. Synthesized rhamnopyranosides 4–8 were employed as test chemicals for in vitro antimicrobial evaluation against eight human pathogenic bacteria and two fungi. Antimicrobial and SAR study showed that the rhamnopyranosides were prone against fungal organisms as compared to that of the bacterial pathogens. Interestingly, PASS prediction of the rhamnopyranoside derivatives 4–8 were 0.49 < P_a < 0.60 (where P_a is probability ‘to be active’) as antibacterial and 0.65 < P_a < 0.73 as antifungal activities, which showed significant agreement with experimental data, suggesting rhamnopyranoside derivatives 4–8 were more active against pathogenic fungi as compared to human pathogenic bacteria thus, there is a more than 50% chance that the rhamnopyranoside derivative structures 4–8 have not been reported with antimicrobial activity, making it a possible valuable lead compound.     

Generation and Identification of the Number of Copies of Exogenous Genes and the T-DNA Insertion Site in SCN-Resistance Transformation Event ZHs1-2

Soybean cyst nematode (SCN, Heterodera glycines Ichinohe) causes an estimated economic loss of about USD 3 billion each year in soybean (Glycine max L.) production worldwide. Overexpression of resistance genes against SCN provides a powerful approach to develop SCN resistance cultivars in soybean. The clarification of molecular characterization in transformation events is a prerequisite for ecological risk assessment, food safety, and commercial release of genetically modified crops. Here, we generated transgenic events harboring the BCN (beet cyst nematode) resistance Hs1^pro−1 gene using the Agrobacterium-mediated method in soybean, evaluated their resistance to SCN infection, and clarified the molecular characterization of one of the transformation events. Five independent and stable inheritable transformation events were generated by an Agrobacterium-mediated transformation method. SCN resistance tests showed the average number of developed females per plant and female index (FI) in T4 ZHs1-1, ZHs1-2, ZHs1-3, ZHs1-4, and ZHs1-5 transformation events were significantly lower than that in the nontransgenic control. Among these, the ZHs1-2 transformation event had the lowest number of developed females per plant and FI. Southern hybridization showed the exogenous target Hs1^pro−1 gene was inserted in one copy and the Bar gene was inserted two copies in the ZHs1-2 transformation event. The exogenous T-DNA fragment was integrated in the reverse position of Chr02: 5351566–5231578 (mainly the Bar gene expression cassette) and in the forward position of Chr03: 17083358–17083400 (intact T-DNA, including Hs1^pro−1 and Bar gene expression cassette) using a whole genome sequencing method (WGS). The results of WGS method and Southern hybridization were consistent. All the functional elements of exogenous T-DNA fragments were verified by PCR using specific primer pairs in the T5 and T6 ZHs1-2 transformation events. These results demonstrated that the overexpression of Hs1^pro−1 gene enhanced SCN resistance, and provide an important reference for the biosafety assessment and the labeling detection in transformation event ZHs1-2.     

Non-uniqueness in capillary pressure-saturation-relative permeability relationships for two-phase flow in porous media: Interplay between intensity and distribution of random micro-heterogeneities

The two-phase flow behaviour in porous media is determined on the basis of capillary pressure-saturation-relative permeability relationships (P^c-S-K_r). These relationships are highly non-linear and obtained by laboratory experiments on porous samples, typically around 10-12 cm in length. It is normally assumed that these samples are homogeneous; however it is well-known that this is in fact not the case and that even at this scale micro-scale heterogeneities exist. Two-phase flow experiments on soils with different properties (e.g., particle and pore size distribution, permeabilities, etc) result in different P^c-S-K_r relationships implying that they cause non-uniqueness in these curves. Recent work has shown that the presence of the micro-heterogeneities has a significant effect on the measured P^c-S-K_r relationships and they cause non-uniqueness in these relationships. In the previous work in this area, the micro-heterogeneity effects on the P^c-S-K_r relationships have been analysed in a number of contexts, e.g., uniformly distributed heterogeneities (simplified cases), various binary sand combinations, hydraulic parameters (e.g., entry pressure, permeability), boundary conditions, etc. There is also some evidence that the intensity and distribution of the micro-heterogeneities affect the P^c-S-K_r relationships. In the present work we use numerical simulations to investigate further the nature of these effects, in particular how the interplay between the intensity and random distribution of micro-heterogeneities affect the P^c-S-K_r relationships. Seven randomly heterogeneous patterns have been defined. These domains represent coarse sand media with fine sand blocks embedded in them. The domain size () has been chosen so that it represents a typical laboratory scale device. The results of the simulations show that it is particularly important to take into account both the intensity and distribution of heterogeneity when determining the effective P^c-S-K_r relationships of a sample. Further, there is a complex interplay between the intensity and distribution of micro-scale heterogeneities which determines the P^c-S-K_r curves. This observation is in contrast to the results of domains with uniformly distributed heterogeneities. We have found that in general if the intensity of heterogeneity is high; the irreducible wetting phase saturation (S_iw) of the sample is also high. The direction of flow and the orientation of the samples also have significant effects. For example, the injection of an immiscible phase from the top (vertically downward) of water saturated porous domain leads to a lower S_iw than injecting on horizontal plane. On the other hand, injection from the bottom (vertically upwards) leads to a higher S_iw. As expected, the distribution of heterogeneity has a significant effect on the saturation distribution and the shape of the P^c-S-K_r curves. However, we show that if the heterogeneities are distributed in such a way that they are closer to the boundary of injection, the irreducible wetting phase saturation is higher.     

Identification and Expression Analysis of Candidate Genes Associated with Defense Responses to Phytophthora capsici in Pepper Line “PI 201234”

Phytophthora capsici (Leonian), classified as an oomycete, seriously threatens the production of pepper (Capsicum annuum). Current understanding of the defense responses in pepper to P. capsici is limited. In this study, RNA-sequencing analysis was utilized to identify differentially expressed genes in the resistant line “PI 201234”, with 1220 differentially expressed genes detected. Of those genes, 480 were up-regulated and 740 were down-regulated, with 211 candidate genes found to be involved in defense responses based on the gene annotations. Furthermore, the expression patterns of 12 candidate genes were further validated via quantitative real-time PCR (qPCR). These genes were found to be significantly up-regulated at different time points post-inoculation (6 hpi, 24 hpi, and 5 dpi) in the resistant line “PI 201234” and susceptible line “Qiemen”. Seven genes were found to be involved in cell wall modification, phytoalexin biosynthesis, symptom development, and phytohormone signaling pathways, thus possibly playing important roles in combating exogenous pathogens. The genes identified herein will provide a basis for further gene cloning and functional verification studies and will aid in an understanding of the regulatory mechanism of pepper resistance to P. capsici.     

Novel S,N co-doped Ba2In2-xCrxO5+y oxides: Synthesis and optical properties

The (S, N) co-doped Ba₂In_2-xCr_xO_5+y (0 ≤ x ≤ 0.5) oxides are successfully obtained by mixing the Ba₂In_2-xCr_xO_5+y oxides and thiourea through a simple ball milling method followed by sintering at 400 °C for 3 h. The colors of the compounds change from orange-brown to yellow-green after reacting with thiourea. When Cr amount is small (x = 0.1), the crystal structure of (S, N) co-doped Ba₂In_2-xCr_xO_5+y is orthorhombic Ba₂In₂O₅ phase. When x ≥ 0.3, the crystal structure of the sample is cubic BaInO_2.5 phase. And this phase transition is the same as Ba₂In_2-xCr_xO_5+y. XPS results reveal that Cr⁶⁺ in Ba₂In_2-xCr_xO_5+y (0 ≤ x ≤ 0.5) oxides are reduced to Cr³⁺ after sintering. S exists in both cation and anion forms, and N exists in substitutional forms. UV–Vis analysis indicates that the yellow-green hue comes from the d-d transition of Cr³⁺, and the doping of S, N ions leads to a red shift of the absorption edge of the samples.     

Gene Expression of Type VI Secretion System Associated with Environmental Survival in Acidovorax avenae subsp. avenae by Principle Component Analysis

Valine glycine repeat G (VgrG) proteins are regarded as one of two effectors of Type VI secretion system (T6SS) which is a complex multi-component secretion system. In this study, potential biological roles of T6SS structural and VgrG genes in a rice bacterial pathogen, Acidovorax avenae subsp. avenae (Aaa) RS-1, were evaluated under seven stress conditions using principle component analysis of gene expression. The results showed that growth of the pathogen was reduced by H₂O₂ and paraquat-induced oxidative stress, high salt, low temperature, and vgrG mutation, compared to the control. However, pathogen growth was unaffected by co-culture with a rice rhizobacterium Burkholderia seminalis R456. In addition, expression of 14 T6SS structural and eight vgrG genes was significantly changed under seven conditions. Among different stress conditions, high salt, and low temperature showed a higher effect on the expression of T6SS gene compared with host infection and other environmental conditions. As a first report, this study revealed an association of T6SS gene expression of the pathogen with the host infection, gene mutation, and some common environmental stresses. The results of this research can increase understanding of the biological function of T6SS in this economically-important pathogen of rice.     

Molecular Cloning and Expression of CYP9A61: A Chlorpyrifos-Ethyl and Lambda-Cyhalothrin-Inducible Cytochrome P450 cDNA from Cydia pomonella

Cytochrome P450 monooxygenases (CYPs or P450s) play paramount roles in detoxification of insecticides in a number of insect pests. However, little is known about the roles of P450s and their responses to insecticide exposure in the codling moth Cydia pomonella (L.), an economically important fruit pest. Here we report the characterization and expression analysis of the first P450 gene, designated as CYP9A61, from this pest. The full-length cDNA sequence of CYP9A61 is 2071 bp long and its open reading frame (ORF) encodes 538 amino acids. Sequence analysis shows that CYP9A61 shares 51%–60% identity with other known CYP9s and contains the highly conserved substrate recognition site SRS1, SRS4 and SRS5. Quantitative real-time PCR showed that CYP9A61 were 67-fold higher in the fifth instar larvae than in the first instar, and more abundant in the silk gland and fat body than other tissues. Exposure of the 3rd instar larvae to 12.5 mg L⁻¹ of chlorpyrifos-ethyl for 60 h and 0.19 mg L⁻¹ of lambda-cyhalothrin for 36 h resulted in 2.20-and 3.47-fold induction of CYP9A61, respectively. Exposure of the 3rd instar larvae to these two insecticides also significantly enhanced the total P450 activity. The results suggested that CYP9A61 is an insecticide-detoxifying P450.     

Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1

The dried roots of Euphorbia kansui (kansui) have been used for centuries in China as a herbal medicine for edema, ascites, and asthma. The 95% ethanol extract showed a significant inhibition of cell proliferation against human normal cell lines L-O2 and GES-1. Bioassay-guided separation of the 95% ethanol extract from the roots of E. kansui led to the isolation of 12 diverse terpenoids whose structures were identified by ¹H, ¹³C NMR spectroscopy and ESI-MS as kansuinine A (1), kansuinine B (2), kansuinine C (3), kansuiphorin C (4), 3-O-(2′E,4′Z-decadienoyl)-20-O-acetylingenol (5), 3-O-(2′E,4′Edecadienoyl)-20-O-acetylingenol (6), 3-O-(2′E,4′Z-decadienoyl)-20-deoxyingenol (7), 3-O-benzoyl-20-deoxyingenol (8), 5-O-benzoyl-20-deoxyingenol (9), kansenone (10), epi-kansenone (11), euphol (12). All these 12 terpernoids were evaluated in vitro for cytotoxicity on L-O2 and GES-1 cell lines. Most ingenane-type diterpenoids and 8-ene-7-one triterpenoids (5–11) exhibited a relatively lower IC₅₀ value; therefore, these compounds had stronger cytotoxicity against human normal cell lines L-O2 and GES-1 with dose-dependent relationships. These results will be significantly helpful to reveal the mechanism of toxicity of kansui and to effectively guide safer clinical application of this herb.     

Genome-Wide Identification and Expression Profile of OSCA Gene Family Members in Triticum aestivum L.

Hyperosmolality and various other stimuli can trigger an increase in cytoplasmic-free calcium concentration ([Ca²⁺]_cyt). Members of the Arabidopsis thaliana (L.) reduced hyperosmolality-gated calcium-permeable channels (OSCA) gene family are reported to be involved in sensing extracellular changes to trigger hyperosmolality-induced [Ca²⁺]_cyt increases and controlling stomatal closure during immune signaling. Wheat (Triticum aestivum L.) is a very important food crop, but there are few studies of its OSCA gene family members. In this study, 42 OSCA members were identified in the wheat genome, and phylogenetic analysis can divide them into four clades. The members of each clade have similar gene structures, conserved motifs, and domains. TaOSCA genes were predicted to be regulated by cis-acting elements such as STRE, MBS, DRE1, ABRE, etc. Quantitative PCR results showed that they have different expression patterns in different tissues. The expression profiles of 15 selected TaOSCAs were examined after PEG (polyethylene glycol), NaCl, and ABA (abscisic acid) treatment. All 15 TaOSCA members responded to PEG treatment, while TaOSCA12/-39 responded simultaneously to PEG and ABA. This study informs research into the biological function and evolution of TaOSCA and lays the foundation for the breeding and genetic improvement of wheat.     

New performance of a modified poly(amide-12-b-ethyleneoxide)

The purpose of this work was the investigation of the water vapour transport through thermoplastic dense films of a poly(amide-12-b-ethylenoxide) such as Pebax^®2533. Similar polymers have gained a unique position in many technologies for different reasons, such as their good physical properties, high processability, notable strength and transport properties to gases and vapours. Moreover, a rising demand of materials with specific characteristics in terms of water vapour transport comes from various market niches (i.e. textiles, building trade, packaging). For these reasons in this work particular attention has been paid to an elastomeric polymer such as the Pebax^®2533, an easily processable material with good transport properties. Previous studies have pointed out that Pebax^® copolymers can be used as precursors of membranes for separation processes of condensable vapours and gases. In this work a further investigation of the water transport properties through Pebax^®2533 and derivative films allowed an understanding of their potential applications. The efficiency of these films has been tested by means of vapour permeability, solubility, diffusivity, and hydrophobicity/hydrophilicity measurements.     

Synthesis,structural characterization and luminescent properties of Tb3+-doped AgLaP2O7 phosphors

Silver lanthanum diphosphates doped with terbium, AgLa_1-xTb_xP₂O₇ (x=0%, 1%, 5%, 10%, 15% and 20%), were prepared by solid state reaction at T=500°. The obtained compounds were investigated by means of a multi-methodological approach, involving the Scanning Electron Microscopy (SEM) equipped with energy dispersive X-Ray spectroscopy (EDS) for morphological investigation and semi-quantitative chemical analysis, respectively; powder X-ray diffraction (PXRD) for structural characterization and Rietveld refinement; Fourier Transform InfraRed (FTIR) and Raman spectroscopies for qualitative study. Finally, emission spectra were collected in order to detect the fluorescence properties of the compounds.The unit cell parameters and the space group of all the family members were determined by PXRD data. The compounds crystallize in the orthorhombic Pnma space group, with the AgLaP₂O₇ cell constants equal to: a?=?8.6706(1) Å, b?=?5.3218(1) Å, c?=?12.8839(1) Å and cell volume V?=?594.51(1) ų. A decreasing trend for unit cell parameters was observed at increase of dopant concentration. For the pure phase, the investigation was completed with the structure solution via Direct Methods and Rietveld refinement. The crystal structure consists of compact layers of LaO₉ polyhedra, down the c axis, bridged by P₂O₇ diphosphate groups and by zig-zag chains of AgO₉ polyhedra down b.The FTIR and Raman analysis supports the chemical structure, highlighting the deformation (δPO₃) and stretching (νPO₃) vibration of PO₃ groups, and the characteristic bands of P₂O₇^4- groups attributed to the symmetric and asymmetric stretching (ν_s and ν_as) of P-O-P bridge, respectively.The luminescence properties of Tb³⁺ activating ion in AgLa_1-xTb_xP₂O₇ (x=1%, 5%, 10%, 15% and 20%) were also examined. No concentration quenching of the main ⁵D₄-→⁷F₅ emission, responsible for the well known green emission of Tb³⁺ ion, was observed in the studied concentration range, whereas a concentration quenching of the emission from ⁵D₃ level, due to ⁵D₃^-→⁵D₄ cross relaxation process, was revealed.     

Correlation between crystal structure and dielectric characteristics of Ti4+ substituted CaSnSiO5 ceramics

The crystal structure and dielectric properties of Ti⁴⁺-substituted CaSnSiO₅ ceramic were investigated. Ti⁴⁺ entirely substituted Sn⁴⁺ of CaSnSiO₅, and the solid solutions were formed at Ca(Sn_1-xTi_x)SiO₅ (0 ≤ x ≤ 1.0) ceramics. The evolutions of crystal structure were analysed through Rietveld refinement and transmission electron microscopy, and the phase transition from A2/a to P2₁/a space groups at Ca(Sn_1-xTi_x)SiO₅ (0.9 ≤ x ≤ 1.0) ceramics was clarified. The change in dielectric properties was related to the structural evolution of Ca(Sn_1-xTi_x)SiO₅ (0 ≤ x ≤ 1.0). The τ_f values of Ca(Sn_1-xTi_x)SiO₅ (0 ≤ x ≤ 0.4) ceramics initially decreased to +49.8 ppm/°C and then increased to +98.3 ppm/°C because of Sn/TiO₆ octahedral distortion. The temperature coefficient of capacitance and ε_r anomaly peak were controlled by Ti⁴⁺ substitution for Sn⁴⁺ at Ca(Sn_1-xTi_x)SiO₅ (0.4 ≤ x ≤ 1.0) ceramics. The results provided a way to control the τ_f value of microwave dielectric ceramics.     

ST6GALNAC5 Expression Decreases the Interactions between Breast Cancer Cells and the Human Blood-Brain Barrier

The ST6GALNAC5 gene that encodes an α2,6-sialyltransferase involved in the biosynthesis of α-series gangliosides, was previously identified as one of the genes that mediate breast cancer metastasis to the brain. We have shown that the expression of ST6GALNAC5 in MDA-MB-231 breast cancer cells resulted in the expression of G_D1α ganglioside at the cell surface. By using a human blood-brain barrier in vitro model recently developed, consisting in CD34⁺ derived endothelial cells co-cultivated with pericytes, we show that ST6GALNAC5 expression decreased the interactions between the breast cancer cells and the human blood-brain barrier.