973 resultados para B ... n C ... f.


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Guanidine derived six-membered C,N] palladacycles of the types (C,N)Pd(mu-OC(O)R)](2) (1a-d), (C,N)Pd(mu-Br)](2) (2a,b), cis-(C,N)PdBr(L)] (3a-d, 4, and 5), and ring contracted guanidine derived five-membered C,N] palladacycle, (C,N)PdBr(C NXy)] (6) were prepared in high yield following the established methods with a view aimed at understanding the influence of the substituents on the aryl rings of the guanidine upon the solid state structure and solution behaviour of palladacycles. Palladacycles were characterised by microanalytical, IR, NMR and mass spectral data. The molecular structures of 1a, 1c, 2a, 2b, 3a, 3c, 3d, and 4-6 were determined by single crystal X-ray diffraction data. Palladacycles 1a and 1c were shown to exist as a dimer in transoid in-in conformation in the solid state but as a mixture of a dimer in major proportion and a monomer (kappa(2)-O,O'-OAc) in solution as deduced from H-1 NMR data. Palladacycles 2a and 2b were shown to exist as a dimer in transoid conformation in the solid state but the former was shown to exist as a mixture of a dimer and presumably a trimer in solution as revealed by a variable temperature H-1 NMR data in conjunction with ESI-MS data. The cis configuration around the palladium atom in 3a, 3c, and 3d was ascribed to steric influence of the aryl moiety of =NAr unit and that in 4-6 was ascribed to antisymbiosis. The solution behaviour of 3d was studied by a variable concentration (VC) H-1 NMR data.

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Se evaluó la diversidad, estructura y fenoloa de la flora en las áreas verdes del Aeropuerto Internacional Augusto C. Sandino con el fin de determinar las especies que son atractivas para fauna silvestre de peligro para la aviacin, sea por que les provee de alimento o de refugio y hábitat. Y por otro lado, brindar recomendaciones sobre especies con potencial para formar parte de las reas verdes del aeropuerto. Para ello, se establecieron parcelas anidadas de 2 x 2 m, 5 x 5 m y 10 x 10 m en las cuales se tomaron los datos en los estratos herbceos, arbustivos y arbreos respectivamente. Las parcelas se establecieron aleatoriamente en tres sitios dentro del aeropuerto: en el bosque seco al oeste del aeropuerto (BSO), en la Fuerza rea (FA) y en el área verde alrededor de la pista de aterrizaje (AVP). Dentro de las parcelas se contaron 117 árboles en todos los sitios, los cuales estaban agrupados en 11 especies, 10 gneros, 8 familias y 4 rdenes. Las especies arbóreas de mayor densidad fueron: Calycophyllum candidissimum(450 individuos/ ha), Albizia niopides (344), Azadirachta indica (289) y Senna siamea (261) y el sitio que presento mayor diversidad y densidad de árboles fue FA. Fueron contados 36 individuos de arbustos, pertenecientes a las especiesCapsicum annum (1) yLantana camara (35). En cuanto a especies herbáceas se contaron 11,845 individuos dentro de las unidades de muestreo, agrupados en 28 especies, 23 gneros, 14 familias y 13 órdenes, siendo el AVP el sitio que registr mayor diversidad y densidad de las mismas. Las especies herbceas con mayores densidades fueron Cenchrus brownii (256,282.05 individuos/ha), Cynodon dactylon (141,538.46), Digitaria decumbens(106,794.87), Bothriochloa pertusa(51,282.05), Elytaria imbricada (38,846.15) y Panicum maximum (30,192.31). De las 41 especies vegetales, se determi la fenoloa completa para 3, de estas, 6 (9.35%) florecen y fructifican todo el ao:Cordia dentata, Boerhavia erecta, Chamaesyce hyssopifolia, Eleucine indica, Melanthera nivea y Rhynchosia minima. Entre las especies arbóreas mayormente atractivas para la fauna silvestre se determinaron: Albizia niopoides, Manguifera indica, Spondias mombin, Cordia dentata, Guazuma ulmifoliay Calycophyllum candidissimum al ser considerados proveedores de alimentos y refugio a la fauna silvestre, por sus frutos, flores con abundante néctar, copas con poca obstrucción visual (alta densidad de hojas) y ramificaciones horizontales propias para el perchaje de las aves de alto tamao. Dentro de la vegetacin herbceas se determinaron especies como Tridax procumbensy Tribulus terrestis formando densos tapetes de vegetacn con flores atractivas para insectos en el peodo seco, los cuales a la vez eran focos de atracción para aves insectvoras como: Hirundus rustica (Golondrinas), Quiscalus mexicanus (Zanate), Molotrus aeneus (Tordos), Egretta thula (Garza blanca) que permanecen en las áreas verdes alrededor de la pista de aterrizaje y que peligran colisionar con los aviones. Por otra parte, las especies de la familia Poaceae fueron registradas como proveedoras de granos a las aves del grupo de las Columbidae (Palomas). Especies de gramneas de gran porte como Panicum maximum, P. antidotale, Sorgum halapensis, ades de poseer semillas grandes (>0.3 cm), formaban corredores por donde se desplazan mamífero medianos, reptiles y aves. Dentro del mismo áreas se determinaron dos especies (B. pertusay C. dactylon) que por su baja estatura (menos de 0.3 m), reproduccn vegetativa y semillas muy pequea o ausentes, son ideales para establecer en los alrededores de la pista de aterrizaje. Mediante un ensayo se evaluó su establecimiento, el cual resulto satisfactorio al competir y ganar espacio ante otras monocotiledones y dicotiledonesas, principalmente C. dactylon

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UV-B280nm-320nmUV-B (Spiraea pubescens)UV-B9.4kJm-217%UV-BUV-B线δ13 CWUE UV-B50.1%(102%)50.9%UV-B(16.1%)CO2CO2(Ci/Ca) (4.0%)δ13 C(20.5)(3.1%)SLW(5.2%)WUE(4.1%)30-40cmδ13 CWUE69δ13 CWUE78UV-BUV-B30-40cmδ13 CCi/CaWUEUV-BWUEUV-B线

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UV radiation is one of many harmful factors found in space that are detrimental to organisms on earth in space exploration. In the present work, we examined the role of antioxidant system in Nostoc sphaeroides Kutz (Cyanobacterium) and the effects of exogenously applied antioxidant molecules on its photosynthetic rate under UV-B radiation. It was found that UV-B radiation promoted the activity of antioxidant system to protect photosystem 11 (PSII) and exogenously applied antioxidant: sodium nitroprusside (SNP) and N-acetylcysteine (NAC) had an obvious protection on PSII activity under UV-B radiation. The activity of superoxide dismutase (SOD, EC 1.15.1.1), catalase (CAT, EC 1.11.1.6), peroxidase (POD, EC 1.11.1.7) and content of NIDA (malondialdehyde) and ASC (ascorbate) were improved by 0.5 mM and 1 mM SNP, but 0.1 mM SNP decreased the activity of antioxidant system. Addition of exogenous NAC decreased the activity of SOD, POD, CAT and the content MDA and ASC. In contrast, exogenously applied NAC increased GSH content. The results suggest that exogenous SNP and NAC may protect algae by different mechanisms: SNP may play double roles as both sources of reactive free radicals as well as ROS scavengers in mediating the protective role of PSII on algae under UV-B radiation. On the other hand, NAC functions as an antioxidant or precursor of glutathione, which could protect PSII directly from UV-B radiation. (c) 2007 COSPAR, Published by Elsevier Ltd. All rights reserved.

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In this study, we found that UV-B radiation decreased photosynthetic activity and boosted lipid peroxidation of desert Nostoc sp., and exogenous chemicals (ascorbate acid (ASC), N-acetylcysteine (NAC), and sodium nitroprusside (SNP)) had obvious protective effects on photosynthesis and membranes under UV-B radiation. High-concentration SNP boosted the activities of antioxidant enzymes, but low-concentration SNP reduced the activities of antioxidant enzymes. Both NAC and ASC treatments of cells decreased activities of antioxidant enzymes. The results suggested that those chemicals possibly had different mechanisms of protection of algae cells against UV-B radiation. SNP might play double roles as a signal molecule in the formation of algae cell protection of Photosystem 11 under UV-B radiation and as a (reactive oxygen species) scavenger, while NAC and ASC might function as antioxidant reagents or precursors of other antioxidant molecules, which could protect cells directly against ROS initiated by UV-B radiation. (c) 2006 Elsevier Inc. All rights reserved.

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Using time-resolved photoluminescence (PL) measurements, we have studied the exciton localization effect in InGaAs/GaAs quantum wire (QWR) structures formed in corrugated narrow InGaAs/GaAs quantum wells (QWs) grown on (553)B GaAs substrate. The PL decay time in the QWR structure was found to be independent of the temperature for T < 70 K, showing a typical dynamical behavior of the localized excitons. This result is in striking contrast to the corresponding quantum well structures, where a linear increase of the PL decay time was observed. In addition, an increase of the exciton lifetime was observed at low temperature for the QWR structure as compared to a reference InGaAs/GaAs quantum well sample (1200 vs 400 ps). The observed longer decay time was attributed to the reduction in the spatial coherence of excitons in the QWR-like structure. In PL measurements, a significant polarization anisotropy was also found in our narrow InGaAs/GaAs QWs grown on (553)B GaAs. (C) 2001 American Institute of Physics.

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Antheraea pernyi nucleopolyhedrovirusApNPVpst-Bpst-Cpst-Jpst-Bpst-Cpst-JApNPV pst-C6663 bp9ORF2ORFApNPV pst-B7406 bp5ORF2ORFApNPV pst-J954 bplef-12p47gta21ApNPV ORF20ApNPV50ORFORFApNPVNPVOpMNPVCfMNPVCfDefNPVEppoNPV ApNPV B-ORF6Lptp-1ptp-2lef-12 ApNPV ptp-1lef-12B-ORF6Lptp-2ApNPV B-ORF6Lptp-2SDS-PAGEWestern blotPTP-2B-ORF6LB-ORF6LPTP-2B-ORF6LPTP-2ApNPVB-ORF6LODVApNPVPTP-2 4ApNPVNPVOpMNPVCfMNPVCfDefNPVEppoNPVAcMNPVRoMNPVBmNPV

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hordeins5060%(Bγ-hordeins)C-hordeins)(D-hordeins)BC7080%1012%BCD-1H5Hor2Hor1Hor3Hor5Hor2BB-hordeinB-hordeinB-hordeinHor2B-hordeinB-hordeinPCRB-hordein 1. B9GenBankB-hordeinGenBank No. X03103, X53690X53691PCR23B-hordein1111B-hordeinC-Z072Z26B-hordeins12B-hordeinsB-hordeinsLMW-GSB-hordeinC-C-B-hordeinBXQ053BZ09-1BZ26-5BSDS-PAGE 2. B-hordein5Z09Z26DNASON-PCRTAIL-PCR8B-hordeinZ09PZ26PTATA box80 bpCAATlike box140 bpZ09PZ26P300 bpEMGCN4(Endosperm BoxEB)560 bpZ09P-2Z26P-3 3. B-hordeinpET-30aBL21pET-BZ07-2pET-BZ26-5BL213 h3 mM IPTG1 mM IPTGB-hordein 4. Z09Z26B-hordein-GenBank no. U40042PCR4B-hordeinB-hordeinZ09B-hordein7Z264B-hordeinZ26B-hordeinZ09Z09B-hordein4Z26B-hordeinZ091218Z09Z26B-hordeinHor2B-hordeinmRNA Seed endosperm storage proteins in higher plants are the main resources of nitrogen for germinating and plant proteins for human and animals. Barley prolamins (also called hordeins) are the major storage proteins in the endosperm and account for 5060% of total proteins. Hordeins are classically divided into three groups: sulphur-rich (B, γ-hordeins), sulphur-poor (C-hordeins) and high molecular weight (HMW, D-hordeins) hordeins based on the size and composition. B-hordeins and C-hordeins are two major groups and each respectively account for about 70-80% and 10-12% of the total hordein fraction in barley endosperm. Genetic analysis showed that B-, C-, C-, -hordeins are encoded by Hor2, Hor1, Hor3 and Hor5 locus on the chromosome 1H (5). Hor2 locus is rich in alleles that encode numerous heterogeneous B-hordein polypeptides. It is reported that B-hordein species, quantity and distribution are significant factors affecting malting, food and feed quality of barley. To understand comprehensively the structure and organization of B-hordein gene family in hull-less barley and explore the developmental control mechanisms of Hor2 locus gene expression and eventually to better exploitation in crop grain quality improvement, we isolated and cloned B-hordein genes and promotors of hull-less barley from Qinghai-Tibet Plateau by PCR, and testified their expression founction in bacteria expression system and explore their spatial and temporal expression pattern by quantitative real time PCR. Our results are as followed, 1. Twenty-three copies of B-hordein gene were cloned from nine hull-less barley cultivars of Qinghai-Tibet Plateau with special B-hordein subunits and molecularly characterized by PCR, based on three B-hordein genes published previously (GenBank No. X03103, X53690 and X53691). DNA sequences analyses confirmed that the six clones all contained a full-length coding region of the barley B-hordein genes. Eleven clones all contain an in-frame stop codon and they are probably pseudogenes. The analysis of deduced amino acid sequences of the genes shows that they have similar structures including signal peptide domain, central repetitive domain, and C-terminal domain. The number of the repeats was largerly variable and resulted in polypeptides in different sizes or structures among the genes. Twelve such repeated motifs were found in Z072 and Z26, and they are close to those of the wild barleys, and it is most probably caused by unequal crossing-over and/or slippage during replication as suggested for the evolution of other prolamins. The relatedness of prolamin genes of barley and wheat was assessed in the phylogenetic tree based on their polypeptides comparison. Our phylogenetic analysis suggested that the predicted B-hordeins of cultivated barley formed a subfamily, while the B-hordeins of wild barleys and the two most similar sequences of LMW-GS of T. aestivum formed another subfamily. This result indicated that the members of the two subfamilys have a distinctive difference. In addition, we found the B-hordeins with identical C-terminal end sequences were clustered into a same subgroup (except BXQ053BZ09-1 and BZ26-5 as a sole group, respectively), so we believe that B-hordein gene subfamilies possibly can be classified on the basis of the conserved C-terminal end sequences of predicted polypeptide and without the limit of SDS-PAGE protein banding patterns. 2. The specific primers were designed according to the published sequences of barley B-hordein genes from Z09 and Z26. Using total DNA isolated from them as the templates, eight clones (designated Z09Pand Z26P) of upstream sequences of the known B-hordein genes was obtained by TAIL-PCR and SON-PCR. Sequences analysis shows that the putative TATA box was present at position 80 bp and CAAT-like box at position 140 bp. Besides, a putative Endosperm Box including an Endosperm Motif (EM) and a GCN4-Like Motif was found at position 300 bp in six clones, and another Endosperm-like box was found at positon 560 bp. While the Endosperm Box or Endosperm-like box was not found in Z09P-2 and Z26P-3. This may indicate that gene expression drived by the two promtors was probably controlled by different trans-acting factors and the genetic control mechanism of corresponding gene expression may be diverse. 3. The B-hordein genic region coding for the mature peptide was cloned into expression vector pET-30a and transformed into bacterial strain BL21 for identifying gene expression fountion. Protein SDSPAGE analysis showed that only the transformed lysate with the pET-BZ07-2 and pET-BZ26-5 constructs produced proteins related to B-group hordeins of barley, and the mounts of proteins induced by 3 mM IPTG and 3 h were higher than other conditions. This established a base for isolating and putifying B-hordein and further exploring their effects on barley grain quality. 4. The gene-specific primers of B-hordein genes from Z09 and Z26 were used for the quantification of B-hordein gene expression. The α-tubulin gene from Hordeum vulgare subsp. vulgare (GenBank accession number U40042) was used as a control gene. The result shows the transcription of the B-hordein genes in Z09 was found 7 days after flowering, while the transcription of the B-hordein genes in Z26 was found 4 days after flowering, but at a very low level, and it suggested that the B-hordein genes in Z26 probably expressed earlier than those in Z09, or the B-hordein genes in Z09 expressed at so a lower level than Z26 that it can not detected. In addition, B-hordein genes in Z26 accession showed higher expression levels than those in Z09 in four developing stages. Furthermore, a progressive increase in the expression levels of the B-hordein genes between 12 and 18 days after anthesis was observed in both Z09 and Z26. It implies that the B-hordein allelic variants encoded by Hor2 locus exist the differential expression in mRNA levels of during barley endosperm development.

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By using a combinatorial screening method based on the self-consistent field theory (SCFT) for polymer systems, the micro-phase morphologies of the H-shaped (AC)B(CA) ternary block copolymer system are studied in three-dimensional (3D) space. By systematically varying the volume fractions of the components A, B, and C, six triangle phase diagrams of this H-shaped (AC)B(CA) ternary block copolymer system with equal interaction energies among the three components are constructed from the weaker segregation regime to the strong segregation regime, In this study, thirteen 3D micro-phase morphologies for this H-shaped ternary block copolymer system are identified to be stable and seven 3D microphase morphologies are found to be metastable.

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By using a combinatorial screening method based on the self-consistent field theory, we investigate the equilibrium morphologies of linear ABCBA and H-shaped (AB)(2)C(BA)(2) block copolymers in two dimensions. The triangle phase diagrams of both block copolymers are constructed by systematically varying the volume fractions of blocks A, B, and C. In this study, the interaction energies between species A, B, and C are set to be equal. Four different equilibrium morphologies are identified, i.e., the lamellar phase (LAM), the hexagonal lattice phase (HEX), the core-shell hexagonal lattice phase (CSH), and the two interpenetrating tetragonal lattice phase (TET2). For the linear ABCBA block copolymer, the reflection symmetry is observed in the phase diagram except for some special grid points, and most of grid points are occupied by LAM morphology. However, for the H-shaped (AB)(2)C(BA)(2) block copolymer, most of the grid points in the triangle phase diagram are occupied by CSH morphology, which is ascribed to the different chain architectures of the two block copolymers. These results may help in the design of block copolymers with different microstructures.

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A new method for the preparation of polyalkyl and polyarenefullerene derivatives C-60(RH)(n)(R=Bu,n=1-3; R=Ph,n=1-10) by the reaction of C-60 with organotin hydride in toluene is described. Another series of products of stannanes R(a)Sn(b)H(c) (R=Bu, a=3-8, b=1-4, c=0-3 R=Ph, a=3-11, b=1-5, c=0-4) were also obtained, which shows that C-60 can catalyze polymerization of organic-tin. These products were determined by mass and infrared spectrometry. And the possible reaction mechanisms are discussed.

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12X6(2.0/100M)X1(2.05/100M)2/100M3BAB3.5/100M3.0/100M2.5-2.7/100M2.0-2.2/100MAC3.5/100M3.0/100M2.5/100M2.0-2.2/100M2.0/100M4B-3000-4000522-342Ma90%3-12-湿A-2000-4000511-362Ma404-40Ma30%3-西AB-BAC-2100-8200536.5-305Ma439.5-16.5Ma-湿AB56TmaxTmax

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UNLABELLED: Amplification of the MET oncogene is associated with poor prognosis, metastatic dissemination, and drug resistance in many malignancies. We developed a method to capture and characterize circulating tumor cells (CTC) expressing c-MET using a ferromagnetic antibody. Immunofluorescence was used to characterize cells for c-MET, DAPI, and pan-CK, excluding CD45(+) leukocytes. The assay was validated using appropriate cell line controls spiked into peripheral blood collected from healthy volunteers (HV). In addition, peripheral blood was analyzed from patients with metastatic gastric, pancreatic, colorectal, bladder, renal, or prostate cancers. CTCs captured by c-MET were enumerated, and DNA FISH for MET amplification was performed. The approach was highly sensitive (80%) for MET-amplified cells, sensitive (40%-80%) for c-MET-overexpressed cells, and specific (100%) for both c-MET-negative cells and in 20 HVs. Of 52 patients with metastatic carcinomas tested, c-MET CTCs were captured in replicate samples from 3 patients [gastric, colorectal, and renal cell carcinoma (RCC)] with 6% prevalence. CTC FISH demonstrated that MET amplification in both gastric and colorectal cancer patients and trisomy 7 with gain of MET gene copies in the RCC patient. The c-MET CTC assay is a rapid, noninvasive, sensitive, and specific method for detecting MET-amplified tumor cells. CTCs with MET amplification can be detected in patients with gastric, colorectal, and renal cancers. IMPLICATIONS: This study developed a novel c-MET CTC assay for detecting c-MET CTCs in patients with MET amplification and warrants further investigation to determine its clinical applicability. Mol Cancer Res; 14(6); 539-47. 2016 AACR.

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HSP70 chaperones mediate protein folding by ATP-dependent interaction with short linear peptide segments that are exposed on unfolded proteins. The mode of action of the Escherichia coli homolog DnaK is representative of all HSP70 chaperones, including the endoplasmic reticulum variant BiP/GRP78. DnaK has been shown to be effective in assisting refolding of a wide variety of prokaryotic and eukaryotic proteins, including the -helical homodimeric secretory cytokine interferon- (IFN-). We screened solid-phase peptide libraries from human and mouse IFN- to identify DnaK-binding sites. Conserved DnaK-binding sites were identified in the N-terminal half of helix B and in the C-terminal half of helix C, both of which are located at the IFN- dimer interface. Soluble peptides derived from helices B and C bound DnaK with high affinity in competition assays. No DnaK-binding sites were found in the loops connecting the -helices. The helix C DnaK-binding site appears to be conserved in most members of the superfamily of interleukin (IL)-10-related cytokines that comprises, apart from IL-10 and IFN-, a series of recently discovered small secretory proteins, including IL-19, IL-20, IL-22/IL-TIF, IL-24/MDA-7 (melanoma differentiation-associated gene), IL-26/AK155, and a number of viral IL-10 homologs. These cytokines belong to a relatively small group of homodimeric proteins with highly interdigitated interfaces that exhibit the strongly hydrophobic character of the interior core of a single-chain folded domain. We propose that binding of DnaK to helix C in the superfamily of IL-10-related cytokines may constitute the hallmark of a novel conserved regulatory mechanism in which HSP70-like chaperones assist in the formation of a hydrophobic dimeric "folding" interface.