基于辣根过氧化物酶/纳米金/辣根过氧化物酶/多壁纳米碳管修饰的过氧化氢生物传感器的研究

以固定在玻碳电极上的多壁纳米碳管为基底吸附辣根过氧化物酶, 再固定纳米金, 然后再结合一层辣根过氧化物酶, 利用多壁纳米碳管对辣根过氧化物酶的直接电化学催化特性及纳米金对蛋白质的强吸附能力及强的电子传导特性制备了无电子媒介体的过氧化氢生物传感器. 采用循环伏安法, 在无电子媒介体时, 该传感器对H₂O₂ 仍能具有良好的催化活性, 放大了电信号, 提高了该酶传感器的灵敏度及稳定性. 实验证明, 该传感器在H₂O₂浓度为 1.0×10^－6～ 1.0×10^－3 mol•L^－1范围内有线性响应, 线性相关系数r²＝0.9964. 并探讨了电极的稳定性、寿命及重现性.     

Three-Dimensional Embedded Subband Coding with Optimized Truncation (3-D ESCOT)

This paper presents an efficient video coding algorithm: Three-dimensional embedded subband coding with optimized truncation (3-D ESCOT), in which coefficients in different subbands are independently coded using fractional bit-plane coding and candidate truncation points are formed at the end of each fractional bit-plane. A rate-distortion optimized truncation scheme is used to multiplex all subband bitstreams together into a layered one. A novel motion threading technique is proposed to form threads along the motion trajectories in a scene. For efficient coding of motion threads, memory-constrained temporal wavelet transforms are applied along entire motion threads. Block-based motion threading is implemented in conjunction with 3-D ESCOT in a real video coder. Extension of 3-D ESCOT to object-based coding is also addressed. Experiments demonstrate that 3-D ESCOT outperforms MPEG-4 for most test sequences at the same bit rate.     

Simultaneous extraction of phenolic compounds of citrus peel extracts: effect of ultrasound

Ultrasound-assisted extraction (UAE) has been widely applied in the extraction of a variety of biologically active compounds including phenolic compounds. However, there is an insufficiency of information on simultaneous extraction of these compounds in this area. In the present study, seven phenolic compounds of two families including cinnamic acids (caffeic, p-coumaric, ferulic, sinapic acid), and benzoic acids (protocatechuic, p-hydroxybenzoic, vanillic acid) from citrus (Citrus unshiuMarc) peels were evaluated by UAE. The effects of ultrasonic variables including extraction time, temperature, and ultrasonic power on the yields of seven phenolic acids was investigated. Results showed that the yields of phenolic compounds increased with both ultrasonic time and temperature increased, whereas the opposite occurred with increasing time at higher temperature to some certain. In the case of 40 degrees C, the decrease in the yields of some phenolic compounds was observed with increased time, whereas those of other compounds did not significantly declined. Ultrasonic power has a positive effect on the yields of phenolic acids under study. Among all ultrasound variables, temperature is the most sensitive on stability of phenolic compounds. Moreover, when phenolic compounds from citrus peel extracts were subjected to ultrasound process, the benzoic acids were more stable than the cinnamic acids. Meanwhile, the optimal ultrasound condition was different one compound from another. These were partly attributed to both the differently chemical structures of phenolic acids and the combination effects of ultrasonic variables.     

Analysis of Tb3+- and melittin-binding with the C-terminal domain of centrin in Euplotes octocarinatus

Centrin is a low molecular mass (20 KDa) protein that belongs to the EF-hand superfamily. In this work, the interaction between the Tb³⁺-saturated C-terminal domain of Euplotes octocarinatus centrin (Tb₂-C-EoCen) and 2-p-toluidinylnaphthalene-6-sulfonate (TNS) was investigated using difference UV–vis spectra and the fluorescence spectra methods. In 100 mM N-2-hydroxy-ethylpiperazine-N-2-ethanesulfonic acid (Hepes) at pH 7.4, with the addition of Tb₂-C-EoCen, four new peaks were observed at 265 nm, 278 nm, 317 nm and 360 nm by absorptivity compared with blank solution of TNS. At the same time, the reaction could be measured by fluorescence spectra. The fluorescence emission of TNS was shifted from 480 nm to 445 nm in the presence of Tb₂-C-EoCen. Meanwhile, its fluorescence intensity was increased markedly. The 1:1 stoichiometric ratio of C-EoCen to TNS was confirmed by fluorescence titration curves. The conditional binding constants of TNS with C-EoCen and Tb₂-C-EoCen were calculated to be log K_{(C-EoCen-TNS)}=5.32±0.04  M^?1 and log K_{(Tb2-C-EoCen-TNS)}=5.58±0.12 M^?1, respectively. In addition, the protein of Tb₂-C-EoCen binding with melittin was also studied. Based on the fluorescence titration curves, the 1:1 stoichiometric ratio of Tb₂-C-EoCen to melittin was confirmed. And the conditional binding constant of C-EoCen with melittin was calculated to be log Ka′=6.79±0.17 M^?1.     

Analysis of Lanthanide-Induced Conformational Change of the C-Terminal Domain on Centrin

Centrin, an EF-hand calcium-binding protein with high homology to calmodulin (CaM), is an essential component of microtubule-organizing center (MTOC). Lanthanide (Ln) ions can improve the stability, increase the amount and enhance the orderliness of microtubules, which are components of cytoskeleton. In order to investigate the structural basis of Ln ions on enhancing orderliness of microtubules, we characterized the binding properties of Ln ions with the isolated C-terminal domain of the Euplotes centrin (C-EoCen). Results suggested that Ln ions may occupy the canonical Ca²⁺ binding sites on C-EoCen with middle affinity. Near- and far-UV CD spectra of C-EoCen displayed pronounced differences before and after additing Ln ions. The asymmetry of microenvironments of Phe on C-EoCen was changed. Using 2-p-toluidinylnaphthalene-6- sulfonate (TNS) as probe, Ln ions induced C-EoCen to undergo conformational changes from closed state to open state, resulting in exposing hydrophobic patches to external environments. Ln ions have more obvious effect on the conformation of centrin than Ca²⁺. The differences found in the interactions of centrin binding with Ln ions/Ca²⁺ maybe provide some insights for structural basis of centrin functions in vivo.     

Hybrid projection method for generalized mixed equilibrium problems, variational inequality problems, and fixed point problems in Banach spaces

A new hybrid projection iterative scheme is introduced to approximate a common element of the solution set of a generalized mixed equilibrium problem, the solution set of a variational inequality problem, and the set of fixed points of a relatively weak nonexpansive mapping in the Banach spaces. The obtained results generalize and improve the recent results announced by many other authors.     

Direct synthesis of completely unsymmetrical triarylmethanes via Fe(III) salt-mediated in situ o-quinone methides process

An efficient and straightforward synthetic approach to completely unsymmetrical triarylmethanes through the situ-generated o-quinone methides from readily available starting materials has been successfully developed. In the presence of an Fe(III) salt, three different aromatic rings, including salicylaldehydes, arylboronic acids, and arenes, were incorporated into one molecule in a single step under the base/ligand-free conditions. The related reactions show high chemoselectivity and afford a variety of completely unsymmetrical triarylmethane products in good to excellent yields.     

3-Aminopropyltriethoxysilane-functionalized manganese doped ZnS quantum dots for room-temperature phosphorescence sensing ultratrace 2,4,6-trinitrotoluene in aqueous solution

New strategies for silica coating of inorganic nanoparticles became a research hotspot for enhancing the mechanical stability of colloidal particles and protecting colloidal particles against oxidation and agglomeration, and so on. In this paper, 3-aminopropyltriethoxysilane (APTES)-functionalized Mn doped (AF MnD) ZnS QDs was prepared to be firsyly through the use of silane coupling agents to form an active layer of silica, then sol-gel reaction of TEOS co-deposited with APTES on the surface of resultant active layer of silica. The emitted long lifetime room-temperature phosphorescence (RTP) of the resultant nanomaterials allows an appropriate delay time so that any fluorescent emission and scattering light can be easily avoided. The APTES anchored on the layer of silica can bind 2,4,6-trinitrotoluene (TNT) species to form TNT anion through acid-base pairing interaction, the TNT anion species may increase the charge-transfer pathways from the nanocrystals to nitroaromatic analytes, therefore further enhance the quenching efficiency of RTP. Moreover, APTES as capped reagents can enlarge the spectral sensitivity and enhance RTP response of nanocrystals to the electron-deficient nitroaromatic and nitrophenol species. Meanwhile, AF MnD ZnS QDs also exhibited a highly selective response toward TNT analyte through significant color change and quenching of ⁴T₁ to ⁶A₁ transition emission. This AF MnD ZnS QDs based sensor showed a very good linearity in the range of 0.05-1.8 μM with detection limit down to 50 nM (quenching percentage of phosphorescence intensity of 8%) and RSD of 3.5% (n = 5). The reported QDs-based chemosensors here open up a promising prospect for the sensitive and convenient sensing of TNT explosive.     

Spectral Studies on the Interaction between Mercuric Ion and ApoCopC

The interaction between mercuric ion and apoCopC in the absence or presence of cupric ion was investigated through difference UV spectra in Hepes buffer （10 mmol·L^-1） at pH 7.4. The results suggest that mercuric ion can bind to C- and N-terminal binding sites of apoCopC, and the conditional binding constants were calculated to be kN=（6.79± 1.12）× 10^6 mol^-1·L and kc=（3.06±0.05）× 10^5 mol^-1·L. Using urea as a chemical agent, the conformational stabilities of apoCopC and HgN^2＋ -CopC-Hgc^2＋ were monitored by fluorescence spectrum in Hepes buffer （50 mmol·L^-1） at pH 7.4. The free energy of stabilization is （14.69±0.85） and （16.66±0.55） kJ.mol^-1, respectively. HgN^2＋ -CopC-Hgc^2＋ is more stable than apoCopC.     

Interplay between the keto defect and the interchain interaction on the green emission of fluorene-based polymer

To investigate the interplay between on-chain keto defect and interchain interaction and its consequence on the blue emission of polyfluorene (PF), first- to third-generation dendronized PFs as well as single-fluorenone-unit doped PF (PFN), synthesized by Suzuki polycondensation, were used as model compounds for steady-state and picosecond time-resolved photoluminescence (PL) spectroscopic studies. For PF film, the broad-band green emission did not appear, although severe interchain interaction was observed. For PFN film, the green emission that peaked at approximately 540 nm decayed in a multiphasic manner, suggesting significant heterogeneity in the excitation migration toward the keto center. To further examine the interplay effect, a series of novel dendronized-PF/PFN blend films in a molar ratio of 40:1 fluorene-to-fluorenone unit were studied. With reference to pure PFN film, those of the green emission of the blends showed strong dependence on the order of dendronization, that is, a higher generation resulted in a shorter-lived green emission. These observations are discussed in terms of interchain and/or intersegment interactions between the fluorene segments and the keto defect. It is concluded that the keto unit and the keto-centered, interchain aggregation lead to severe color degradation in a synergistic manner, and that dendronization can effectively minimize the undesirable green emission.