8 resultados para Fad

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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The electrochemical behavior of flavine adenine dinucleotide (FAD) at a gold electrode involving adsorption of the reduced form FADH(2) and desorption of the oxidized form FAD has been studied by using electrochemical quartz crystal microbalance (EQCM). EQCM can present information not only about the electrochemical behavior but also about the mass changes on the electrode surface. The electrochemical properties and frequency shifts were investigated in FAD solutions at different pH values, concentrations and scan rates. Reversible voltammograms were observed when pH<4.5 and irreversible voltammograms were found when pH greater than or equal to 4.5. It is found to be a diffusion controlled process when the concentration of FAD is lower than 2x10(-4) moll(-1) (pH 1.5). On the contrary, at concentrations higher than 2x10(-4) moll(-1) (pH 1.5), it is found to be an adsorption controlled process.

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Fuzzy reliability methods are used to study the corrosion of pipelines. Three methods are used. They consist of using fracture failure modes, failure assessment diagram (FAD) and residual strength for establishing fuzzy reliability. Calculations are made by application of JC, improved GA-JC and Mente-carlo methods. Examples for oilfield injecting water pipeline show the residual strength well agree with field data. Mente-carlo methods appear to yield results that have better agreement with field data.

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地磁场伴随着生命的起源、发生和进化,地球上的一切生命无时无刻不处于地球磁场中。地球自诞生以来,地磁场的强度一直在细微变化,但地磁场强度减弱会对植物产生什么样的直接影响尚知之甚少。随着对太空探索的不断发展,人类越来越需要了解处于零磁场环境的太空中生物的适应性。近零磁场是地磁场的恒定组分降低为零或者接近零的空间。本论文利用近零磁场环境探索了地磁场减弱对拟南芥整个生长周期的影响,开展了近零磁场下拟南芥短期生长试验,主要包括种子的萌发、暗培养、根生长、幼苗鲜重和根向重性分析,以及对近零磁场下拟南芥整个生长周期的表型进行了观察统计分析。结果发现(1)无论在光照还是暗培养的环境中,近零磁场对拟南芥种子的萌发、幼苗根的伸长、鲜重变化以及根向重性等的影响较小。(2)对拟南芥整个生长周期过程中表型变化进行的观察和统计分析发现:近零磁场环境中,拟南芥可以完成正常的生活史;但植株开花时间推迟、开花持续时间延长、枝条数减少、植株高度受到了抑制,种子千粒重降低。表明近零磁场对拟南芥营养生长的影响较小,而对生殖生长的影响较明显,暗示地磁场作为环境因子可能参与影响植物的生殖生长。 趋磁细菌(Magnetospirillum magneticum)是一种可以沿磁力线方向运动的特殊的细菌,其胞内铁含量是菌体干重的3%,是非磁性细菌的数百倍,其中的铁主要以Fe3O4/Fe3S4 形式存在于磁小体(magnetosome) 中。趋磁细菌主要通过分泌转铁载体吸收环境中的三价铁。在磁小体合成过程中,三价铁还原为二价是一个必需的过程,因而铁还原酶在趋磁细菌的铁还原过程中可能起着重要的作用。我们以趋磁细菌AMB-1 为材料,克隆了预测的铁还原酶基因,命名为MmFre ,并在内源铁还原酶活性较低的酵母突变株S288C fre1 fre2 中进行异源超表达,对其铁还原活性进行了初步分析;同时结合GFP 融合蛋白技术对该基因的表达产物进行了酵母的亚细胞定位。结果表明:(1)利用生物信息学分析发现,MmFre 基因编码区含有1335 bp,编码444 个氨基酸残基;氨基酸序列中含有一个FAD 结合位点,并具有6 个跨膜结构域;(2)该基因在酵母表达后利用酵母活体进行酶活性检测发现,其铁还原酶活性是对照组的4 倍,暗示该基因在真核生物中的表达产物可以执行铁还原的功能;(3)利用激光共聚焦显微镜观察发现该基因的表达产物与GFP 构成的融合蛋白广泛的定位在细胞的膜上。因而,MmFre 基因的表达产物确实具有铁还原酶活性,且没有膜特异性分布,其对趋磁细菌磁小体生物合成中铁的还原可能起着重要作用。

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本文选择与生命过程息息相关的典型物质作为研究对象,以电化学手段为主,同时结合XPS、SEM和STM等技术,对细胞色素C和酶的直接电化学,辅酶电催化及应用和电化学式酶传感器研制等三方面进行了初步探讨。其中包括:1、细胞色素C在玻碳表面的直接电化学和热力学行为,2、葡萄糖氧化酶表面结构分析和直接电化学,3、辣根过氧化物酶直接电化学和双酶电极研制;4、黄素辅酶(FAD)修饰表面形貌分析和电催化性能,5、尼克酰氨辅酶电催化氧化及其检测;6、基于金属微粒修饰电极的酶传感器,7、介体型醇脱氢酶传感器,以及普鲁士兰修饰薄膜用于酶的固定化。

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In situ electrochemical scanning tunneling microscopy (ECSTM) has been employed to follow the renewal process of a graphite electrode accompanied by flavin adenine dinucleotide (FAD) electrochemical reaction which involves adsorption of the reduced form (FADH(2)) and desorption of the oxidized form (FAD). The renewal process initiates from steps or kinks on the electrode surface, which provide high active sites for adsorption. This renewal depends on the working electrode potential, especially in the range near the FAD redox potential. Our experiment suggests that delamination of the graphite surface is caused by interaction between the substrate and adsorbed molecules. A simple model is proposed to explain this phenomenon.

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Flavin adenine dinucleotide (FAD) was modified onto the highly oriented pyrolytic graphite (hopg) and glassy carbon electrode (gee) surfaces with three methods, respectively. Corresponding image analysis for FAD-modified hopg surfaces has been performed by scanning tunnelling microscope (STM) for the first time. The molecular resolution STM image of FAD adsorbed on the freshly-cleaved hopg was obtained, the quantitative size determination suggests that the FAD molecules adsorb side lying on the substrate surface. The anodization treatment of hopg surface yields many pits, which were clearly observed under STM. These pits provide active sites on the hopg surface for modification and the treated hopg can strongly adsorb FAD molecules, the latter exhibiting an irregular cluster structure on such a surface. When FAD was electrochemically deposited on the substrate surface, a chain structure was successfully observed. The adsorbed FAD on anodized glassy carbon electrode (gee) surface can effectively catalyze the reduction of glucose oxidase, hemoglobin and myoglobin, with a large decrease in the overvoltage, whereas the deposited FAD film exhibits excellent electrocatalysis towards dioxygen reduction.

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An electrochemically polymerized flavin adenine dinucleotide (FAD) film electrode is reported for the first time. The polymerized film was prepared by a two-step method. The electrocatalytic reduction of dioxygen at a glassy carbon electrode (GCE) modifie

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Sulfide: quinone oxidoreductase (SQR) is a flavoprotein with homologues in all domains of life except plants. It plays a physiological role both in sulfide detoxification and in energy transduction. We isolated the protein from native membranes of the hyperthermophilic bacterium Aquifex aeolicus, and we determined its X-ray structure in the "as-purified,'' substrate-bound, and inhibitor-bound forms at resolutions of 2.3, 2.0, and 2.9 angstrom, respectively. The structure is composed of 2 Rossmann domains and 1 attachment domain, with an overall monomeric architecture typical of disulfide oxidoreductase flavoproteins. A. aeolicus SQR is a surprisingly trimeric, periplasmic integral monotopic membrane protein that inserts about 12 angstrom into the lipidic bilayer through an amphipathic helix-turn-helix tripodal motif. The quinone is located in a channel that extends from the si side of the FAD to the membrane. The quinone ring is sandwiched between the conserved amino acids Phe-385 and Ile-346, and it is possibly protonated upon reduction via Glu-318 and/or neighboring water molecules. Sulfide polymerization occurs on the re side of FAD, where the invariant Cys-156 and Cys-347 appear to be covalently bound to polysulfur fragments. The structure suggests that FAD is covalently linked to the polypeptide in an unusual way, via a disulfide bridge between the 8-methyl group and Cys-124. The applicability of this disulfide bridge for transferring electrons from sulfide to FAD, 2 mechanisms for sulfide polymerization and channeling of the substrate, S2-, and of the product, S-n, in and out of the active site are discussed.