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1.
LaBSiO5 phosphors doped with Ce3+ and Tb3+ were synthesized using the conventional solid‐state method at 1100 °C. The phase purity and luminescent properties of these phosphors are investigated. LaBSiO5:Tb3+ phosphors show intense green emission, and LaBSiO5 phosphors doped with Ce3+ show blue–violet emission under UV light excitation. LaBSiO5 phosphors co‐doped with Ce3+ and Tb3+ exhibit blue–violet and green emission under excitation by UV light. The blue–violet emission is due to the 5d–4f transition of Ce3+ and the green emission is ascribed to the 5D4 → 7 F5 transition of Tb3+. The spectral overlap between the excitation band of Tb3+ and the emission band of Ce3+ supports the occurrence of energy transfer from Ce3+ to Tb3+, and the energy transfer process was investigated. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
2.
《Inorganica chimica acta》1987,135(3):207-210
An FT-IR spectroscopic study concerning changes in the conformation of sugar in the dinucleotides; GpC and CpG, on platination and intercalation is presented. The results are compared with the FT-IR spectral data of 5′-CMP, 5′-GMP, 3′-GMP and their metal adducts. The spectra of free GpC, free CpG, proflavine-GpC, proflavine-CpG, and cis-[Pt(NH3)2(GpC)2]2+ exhibit the diagnostic band at 800 cm−1 which was assigned to a sugar phosphate vibrational mode and diagnostic of C3′-endo sugar pucker. In the case of 9-aminoacridine-GpC and cis-[Pt(NH3)2(CpG]+ the diagnostic bands of the C2′-endo and C3′-endo conformations are observed at 810–820 cm−1 and near 800 cm−1 respectively. The results are in good agreement with X-ray data. The infrared diagnostic bands are important for distinguishing the sugar pucker conformational changes. 相似文献
3.
The addition of Tb3+ to apoalkaline phosphatase at pH 8.0 results in the formation of a metalloprotein with an enhanced Tb3+ fluorescence at 492, 545, and 580 nm. The Tb3+ excitation spectrum is most consistent with a process in which energy is transferred from one or more tyrosyl chromophores to the bound lanthanide. An analysis of the fluorescence data under equilibrium conditions yields one Tb3+ binding site per enzyme dimer with a Kn = 0.16 ± 0.02 μm. The Tb3+-alkaline phosphatase complex is not catalytically active nor does it incorporate covalently bound phosphate, but the specific activity of Zn2+-alkaline phosphatase is significantly enhanced in the presence of Tb3+ indicating that this lanthanide mimics Mg2+ in stabilizing the structure of alkaline phosphatase. The fluorescence of the Tb3+-enzyme is found to be quite sensitive to conformational changes which occur upon addition of Zn2+ or substrates. 相似文献
4.
Conformational dependence of the Raman scattering intensities from polynucleotides. 3. Order-disorder changes in helical structures 总被引:7,自引:0,他引:7
Raman spectra are presented on ordered and presumably helical structures of DNA and RNA as well as the poly A·poly U helical complex, polydAT, and the helical aggregates of 5′-GMP and 3′-GMP. The changes in the frequency and the intensity of the Raman bands as these structures undergo order-disorder transitions have been measured. In general the changes we have found can be placed into three categories: (1) A reduction in the intensities of certain ring vibrations of the polynucleotide bases is observed when stacking or ordering occurs (Raman hypochromism). Since the ring vibrational frequencies are different for each type of base, we have been able to obtain some estimate of average amount of order of each type of base in partially ordered helical systems. (2) A very large increase in the intensity of a sharp, strongly polarized band at about 815 cm?1 is observed when polyriboA and polyriboU are formed into a helical complex. Although this band is not present in the separated chains at high temperature, a broad diffuse band at about 800 cm?1 is present. The 815 cm?1 band undoubtedly arises from the vibrations of the phosphate-sugar portions of the molecule and provides a sensitive handle to the back-bone conformation of the polymer. This band also appears upon ordering of RNA, formation of the helical aggregate of 5′-riboGMP, and to some extent in the selfstacking of the polyribonucleotides polyA, polyU in the presence of Mg++, PolyC, and polyG. No such intense, polarized band is found, however, in ordered DNA, polydAT, or the 3′-riboGMP aggregate, although there is a conformationally independent band at about 795 cm?1 in DNA and polydAT. (3) Numerous frequency changes occur during Conformational changes. In particular the 1600–1700 cm?1 region in D2O shows significant conformationally dependent changes in the C?O stretching region analogous to the changes in this region which have been observed in these substances in the infrared. Thus, Raman scattering appears to provide a technique for simultaneously observing the effects of base stacking, backbone conformation and carbonyl hydrogen bonding in nucleic acids in moderately dilute (10–25 mg/ml) aqueous solutions. 相似文献
5.
It has previously been shown that terbium binds to membrane vesicles prepared from the walking leg nerve of the lobster (Homarus americanus) with a high affinity Kd of 2.2 μM. Fluorescence of bound Tb3+ occurs via energy transfer from the aromatic residues of proteins (γex = 280 nm; γem = 546 nm), and calcium inhibits Tb3+ binding competitively with a Ki of 1.8 mM. Displacement studies with EDTA demonstrate that more than 95% of the bound Tb3+ is at the vesicle exterior and is not being taken up by the vesicles. To investigate the putative role of Ca2+ in the interaction of local anesthetics with axonal membranes, lidocaine and the analogs GX-HCl and QX-314 were tested as inhibitors of Tb3+ binding. Inhibition by lidocaine is seen only at considerably higher doses (25 mM) than are required for conduction block of intact nerves (5 mM). Inhibition by lidocaine and the primary amine analog GX-HCl is entirely noncompetitive, whereas the quaternary ammonium derivative QX-314 appears to be a mixed competitive-noncompetitive inhibitor of Tb3+ binding. These data are not compatible with the hypothesis that there is a functionally essential cation binding site on the axonal membrane surface for which Ca2+ and local anesthetics compete, although local anesthetic action may be modified indirectly by altered calcium concentrations. Evidence is presented for a mechanism by which local anesthetics indirectly displace Tb3+ by altering the physical state of the axonal membrane. 相似文献
6.
Two acid phosphomonoesterases, 5′(3′)-ribonucleotide phosphohydrolase and 3′-ribonucleotide phosphohydrolase, were isolated from Tradescantia albiflora leaf tissue and purified by ammonium sulphate precipitation, gel filtration on Sephadex G-200 and repeated chromatography on DEAE-cellulose. The enzymes differed in their sensitivity to dialysis against 1 mM EDTA; the activity of 5′(3′)-ribonucleotide phosphohydrolase was unaffected, while 3′-ribonucleotide phosphohydrolase showed an increase of 60–90%. Both enzymes were rapidly inactivated above 50°. Their ion sensitivity was identical: 1 m M Zn2+ and Fe2+ were inhibitors for both by 20–80%; while Mg2+, Ca2+, Co2+, K+, Na+ at 1–10 mM had no significant effect on the activity of either enzyme. Inorganic phosphate inhibited both enzymes almost completely. EDTA (1 mM) did not inhibit either enzyme; none of the divalent cations tested were enzyme activators. 3′-Ribonucleotide phosphohydrolase hydrolysed both 3′- and 5′-nucleoside monophosphates (3′-AMP, 3′-CMP, 3′-GMP, 3′-UMP, 5′-AMP, 5′-CMP, 5′-GMP, 5′-UMP). 5′(3′)-Ribonucleotide phosphohydrolase showed a preference for the 3′-nucleoside monophosphates. Adenosine 3′,5′-cyclic monophosphate, purine and pyrimidine 2′,3′-cyclic mononucleotides at 0.1–1.OmM did not inhibit the enzymes. 相似文献
7.
H. A. Tajmir-Riahi 《Journal of biomolecular structure & dynamics》2013,31(6):1169-1186
Abstract The interaction of adenosine-5′-monophosphate (5′-AMP), guanosine-5′-monophosphate (5′-GMP) and 2′-deoxyguanosine-5′-monophosphate (5′-dGMP) with the [Co(NH3)6]3+, [CO(NH3)5C1]2+ and [CO(NH3)4C12]+ cations has been investigated in aqueous solution with metal/nucleotide ratios (r) of 1/2, 1 and 2 at neutral pH. The solid complexes have been isolated and characterized by FT-IR and 1H-NMR spectroscopy. The complexes are polymeric in nature both in the crystalline solid and aqueous solution. The binding of the cobalt-hexammine cation is indirectly (via NH3) through the N-7 and the PO3 2- groups of the AMP and via O-6, N-7 and the PO3 2- of the GMP and dGMP anions (outer-sphere). The cobalt-pentammine and cobalt-tetrammine bindings are through the phosphate groups (inner-sphere) and the N-7 site (outer-sphere) of these nucleotide anions. The ribose moiety shows C2′-endo/anti conformation, in the free AMP and GMP anions as well as in the cobalt-ammine - AMP complexes, whereas a mixture of the C2′-endo/anti and C3′-endo/anti sugar puckers were observed for the Co(NH3)6-GMP, Co(NH3)5-GMP and a C3′-endo/anti conformer for the Co(NH3)4-GMP complexes. The deoxyribose showed an O4′-endo/anti conformation for the free dGMP anion and a C3′-endo/anti for the Co(NH3)6-dGMP, Co(NH3)5-dGMP and Co(NH3)4-dGMP complexes. 相似文献
8.
KLaSiO4:Tb3+ phosphors were synthesized using the sol–gel method. The structure and luminescence properties of the materials were characterized using X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy, thermogravimetry–differential thermal analysis, fluorescence spectra and calculated Commission Internationale de l'éclairage coordinates. The results showed that the material had a hexagonal structure, and that doping of Tb3+ did not change the crystal structure of KLaSiO4. FTIR spectroscopy confirmed the existence of stretching vibrations of Si–O, bending vibrations of Si–O–Si, and asymmetric tensile vibrations of Si–O in KLaSiO4. The excitation spectrum of the sample consisted of 4f7→5d1 broadband absorption and the characteristic excitation peak of Tb3+, the excitation peak at 232 nm belongs to the spin allowed 7FJ→7DJ transition of Tb3+, the excitation peak at 268 nm belongs to the spin forbidden 7FJ→9DJ transition of Tb3+, and the absorption band of 7FJ→7DJ transition is split. Under excitation at 232 nm, the emission peak of the sample was composed of the 5D4→7FJ (J = 6, 5, 4, 3) energy level transition of Tb3+. The highest emission peak is located at 543 nm, which belongs to the 5D4→7F5 transition and emits green light. Concentration quenching occurred when the Tb3+ doping concentration was greater than 1% mol, the quenching mechanism was an electric dipole–electric dipole action. When the ratio of citric acid to total metal ions was 1:1 and the annealing temperature was 800°C, the surface defects of the phosphors were greatly reduced, the quenching effect was reduced, and the luminous intensity reached the maximum. 相似文献
9.
It is comparatively easy to assay adenosine 5′-triphosphate either in the presence or absence of other nucleoside triphosphates (1). An assay for UTP has been reported (2) based on its incorporation into RNA using RNA polymerase and a poly(dA-dT) template in the presence of excess [3H]-ATP; this method could be adapted to assay for GTP and CTP. It is known that the fluorescence of Tb3+ increases on binding to nucleic acids (3–5), and this enhancement has been attributed both to complex formation between Tb3+ and guanine residues in the nucleic acid (3) and also to binding of Tb3+ to thiouracil (4). 相似文献
10.
11.
RNase activity from Chlorella was partially purified. Two RNase activities were demonstrated, one soluble and the other ribosomal. The effects on ribonuclease activity of variations in pH and temperature, and of Mg2+, Na+, and mononucleotides were examined. The RNase activities (phosphodiesterases EC 3.1.4.23) were both endonucleolytic, releasing oligonucleotides, and cyclic nucleotide intermediates, but exhibited different specificities in releasing mononucleotides from RNA. The ribosomal activity released 3′-GMP, and after prolonged incubation 3′-UMP, but the soluble activity released 3′-GMP, 3′-AMP and 3′-UMP. Neither ofthe RNase preparations hydrolysed DNA, nor released 5′-nucleotides from RNA. Increased ribosomal RNase activity was related to dissociation of ribosomes, and latency of ribosomal RNase activity was demonstrated. The possible in vivo distribution of RNases is discussed. 相似文献
12.
Penny E. Diffley Alan Geisbrecht Russell P. Newton Michael Oliver Christopher J. Smith Judith Vaughan 《Plant biosystems》2013,147(2):143-156
ABSTRACT Fast-atom bombardment mass spectrometry (FABMS), and collisionally-induced dissociation and mass-analyzed ion kinetic energy spectrum scanning (CID/MIKES) have been used to examine cation effects on a Phaseolus chloroplast complex phosphodiesterase activity. The kinetic parameters of the activity, and the effects of Li+, Na+, K+, Mg2+, Mn2+ and Fe3+ upon them, were determined with 3′,5′-cyclic AMP, -GMP and -CMP, and 2′,3′-cyclic AMP, -GMP and -CMP as substrates. Irrespective of the presence of cations and of the complex nucleotidase, the preferred substrate is a 3′,5′-cyclic nucleotide, not a 2′,3′-cyclic nucleotide. In the presence of the nucleotidase 3′,5′-cyclic AMP and 3′,5′-cyclic GMP are the best substrates, unless Fe3+ ions are present. Mg2+ and Mn2+ stimulate hydrolysis of 3′,5′-cyclic AMP and 3′,5′-cyclic GMP by the complex. However, Fe3+ inhibits these activities but stimulates the hydrolysis of 3′,5′-cyclic CMP. Kinetic data indicate that each of these six substrates is hydrolyzed at a single, common, catalytic site. Differentiation of the phosphodiesterase isomeric mononucleotide products by FABMS CID/MIKES analysis indicates that in the absence of ions and after removal of the nucleotidase, the 3′-ester linkage of the 3′,5′-cyclic substrates was hydrolyzed exclusively. Addition of monovalent and divalent ions results in hydrolysis of both the 5′- and 3′-ester linkages. 相似文献
13.
Hajime Taniguchi Yasukiyo Umemura Michinori Nakamura 《Bioscience, biotechnology, and biochemistry》2013,77(2):231-239
The acid-soluble nucleotides were extracted from the tubers of Jerusalem artichoke with percbloric acid, and separated and purified by means of adsorption on and elution from active charcoal, repeated chromatography on columns of Dowex I (Cl-), followed by paper chromatography. The following nucleotides have been characterized and/or identified: 5′-AMP, 3′-AMP, ADP, ATP, 5′-GMP, 2′-GMP, 3′-GMP, 2′,3′-cyclic GMP, GDP, GTP, 5′-UMP, UDP, UTP, NADP, UDP-glucose, UDP-galactose, UDP-fructose, UDP-N-acetylhexosamine and GDP-mannose.** Neither cytosine ribonucleotides nor deoxyribonucleotides have been detected. The significance of these observations is discussed. 相似文献
14.
Eu2+ and Tb3+ singly doped and co‐doped LaAl11O18 phosphors were prepared by a combustion method using urea as a fuel. The phase structure and photoluminescence (PL) properties of the prepared phosphors were characterized by powder X‐ray diffraction (XRD), scanning electron microscopy (SEM), and photoluminescence excitation and emission spectra. When the content of Eu2+ was fixed at 0.01, the emission chromaticity coordinates could be adjusted from blue to green region by tuning the contents of Tb3+ ions from 0.01 to 0.03 through an energy transfer (ET) process. The fluorescence data collected from the samples with different contents of Tb3+ into LaAl11O18: Eu, show the enhanced green emission at 545 nm associated with 5D4 –7F5 transitions of Tb3+. The enhancement was attributed to ET from Eu2+ to Tb3+, and therefore Eu2+ ion acts as a sensitizer (an energy donor) while Tb3+ ion as an activator. The ET from Eu2+ to Tb3+ is performed through dipole–dipole interaction. The ET efficiency and critical distance were also calculated. The present Eu2+–Tb3+ co‐doped LaAl11O18 phosphor will have potential application for UV convertible white light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
15.
1H- and 31P-nmr spectroscopy have been used to investigate the self-association of M2(5′-CMP) [M = Li+, Na+, K+, Rb+, or (CH3)4 N+; 5′-CMP = cytidine 5′-monophosphate], the self-association of Li2(5′-GMP) (5′-GMP = guanosine 5′-monophosphate), and the heteroassociation of 5′-GMP and 5′-CMP (1 : 1 mole ratio) in aqueous solution as a function of the nature of the monovalent cation. Proton spectral differences for the different 5′-CMP salts exhibit a cation-size dependence and have been ascribed to a change in the stacking geometry. An average stacking association constant of 0.63 ± 0.24M?1 at 1°C, consistent with the weak stacking interactions of the cytosine bases, was determined for the 5′-CMP salts. Heteroassociation of 5′-GMP and 5′-CMP follows the reverse of the cation order for the formation of ordered aggregates of 5′-GMP. Heteroassociation occurs in the presence of Li+, Na+, and Rb+ ions, but only self-association occurs for the K+ nucleotides. Li2(5′-GMP), which does not form ordered species, self-associates to form disordered base stacks with a stacking constant of 1.63 ± 0.11M?1 at 1°C. 相似文献
16.
Luminescence and energy‐transfer properties of color‐tunable Ca2Mg0.25Al1.5Si1.25O7:Ce3+/Eu2+/Tb3+ phosphors for ultraviolet light‐emitting diodes
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Bo. Yuan Yanhua Song Ye. Sheng Keyan Zheng Qisheng Huo Xuechun Xu Haifeng Zou 《Luminescence》2016,31(2):453-461
A series of Ca2Mg0.25Al1.5Si1.25O7:Ce3+/Eu2+/Tb3+ phosphors was been prepared via a conventional high temperature solid‐state reaction and their luminescence properties were studied. The emission spectra of Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Eu2+ and Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Tb3+ phosphors show not only a band due to Ce3+ ions (409 nm) but also as a band due to Eu2+ (520 nm) and Tb3+ (542 nm) ions. More importantly, the effective energy transfer from Ce3+ to Eu2+ and Tb3+ ions was confirmed and investigated by emission/excitation spectra and luminescent decay behaviors. Furthermore, the energy level scheme and energy transfer mechanism were investigated and were demonstrated to be of resonant type via dipole–dipole (Ce3+ to Eu2+) and dipole–quadrupole (Ce3+ to Tb3+) reactions, respectively. Under excitation at 350 nm, the emitting color could be changed from blue to green by adjusting the relative doping concentration of Ce3+ and Eu2+ ions as well as Ce3+ and Tb3+ ions. The above results indicate that Ca2Mg0.25Al1.5Si1.25O7:Ce3+,Eu2+/Tb3+ are promising single‐phase blue‐to‐green phosphors for application in phosphor conversion white‐light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
17.
This paper focuses on an optical study of a Tb3+/Bi3+‐doped and Sm3+/La3+‐ doped Ca2Al2SiO7 phosphor synthesized using combustion methods. Here, Ca2Al2SiO7:Sm3+ showed a red emission band under visible light excitation but, when it co‐doped with La3+ ions, the emission intensity was further enhanced. Ca2Al2SiO7:Tb3+ shows the characteristic green emission band under near‐ultraviolet light excitation wavelengths, co‐doping with Bi3+ ions produced enhanced photoluminescence intensity with better colour tunable properties. The phosphor exhibited better phase purity and crystallinity, confirmed by X‐ray diffraction. Binding energies of Ca(2p), Al(2p), Si(2p), O(1s) were studied using X‐ray photoelectron spectroscopy. The reported phosphor may be a promising visible light excited red phosphor for light‐emitting diodes and energy conversion devices. 相似文献
18.
Robert G. Canada 《Biochimica et Biophysica Acta (BBA)/Molecular Cell Research》1982,720(4):371-377
The fluorescence emission intensity of terbium is enhanced upon the binding of Tb3+ to cultured mouse spinal cord and dorsal root ganglion neurons, via nonradiative resonant energy transfer from membrane proteins. The relative fluorescence intensities of Tb3+ bound to dorsal root ganglion neurons were considerably greater than that of Tb3+ bound to large multipolar spinal cord neurons. The cell bodies of the dorsal root ganglion neurons were completely covered in a dense fluorescent blanket, whereas the fluorescence from the spinal cord soma presented a discontinuous pattern. The neurites of the spinal cord neuron were speckled with bright patches of Tb3+ fluorescence. A high concentration of Ca2+ reduced the relative fluorescence intensity of the Tb3+ -neuron complex. It is suggested that Tb3+ binds to Ca2+ -binding sites on the surface membrane of neurons. 相似文献
19.
《生物化学与生物物理学报:生物膜》1986,863(2):178-184
Measurements of fluorescence energy transfer have been performed to determine the distance between the lipid-water interface and the ATP-binding site in the (Ca2+ + Mg2+)-ATPase from sarcoplasmic reticulum. The calculated distance between the donor, FITC bound to the protein (nucleotide binding-site marker), and the acceptor, rhodamine-5′-isothiocyanyldipalmitoylphosphatidylethanolamine (RITC-DPPE) incorporated in the membrane, was in the range of 34–42 Å. In addition the distance between the high affinity Ca2+-binding sites and the lipid/water interface has been calculated by luminescence energy transfer from Tb3+ bound to the Ca2+ sites to RITC-DPPE included in the membrane, and it was approx. 10 Å. 相似文献
20.
Thermoluminescence and photoluminescence studies on γ‐ray‐irradiated Ce3+,Tb3+‐doped potassium chloride single crystals
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Single crystals of KCl doped with Ce3+,Tb3+ were grown using the Bridgeman–Stockbarger technique. Thermoluminescence (TL), optical absorption, photoluminescence (PL), photo‐stimulated luminescence (PSL), and thermal‐stimulated luminescence (TSL) properties were studied after γ‐ray irradiation at room temperature. The glow curve of the γ‐ray‐irradiated crystal exhibits three peaks at 420, 470 and 525 K. F‐Light bleaching (560 nm) leads to a drastic change in the TL glow curve. The optical absorption measurements indicate that F‐ and V‐centres are formed in the crystal during γ‐ray irradiation. It was attempted to incorporate a broad band of cerium activator into the narrow band of terbium in the KCl host without a reduction in the emission intensity. Cerium co‐doped KCl:Tb crystals showed broad band emission due to the d–f transition of cerium and a reduction in the intensity of the emission peak due to 5D3–7Fj (j = 3, 4) transition of terbium, when excited at 330 nm. These results support that energy transfer occurs from cerium to terbium in the KCl host. Co‐doping Ce3+ ions greatly intensified the excitation peak at 339 nm for the emission at 400 nm of Tb3+. The emission due to Tb3+ ions was confirmed by PSL and TSL spectra. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献