共查询到19条相似文献,搜索用时 140 毫秒
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有机相中蚕丝固定化脂肪酶催化酯化反应性能研究 总被引:2,自引:0,他引:2
研究了有机相中蚕丝固定化脂肪酶催化酶化反应的催化活性。考究了有机溶剂,底物、反应温度,PH值和体系含水量等因素对固定化脂肪酶催化活性的影响。结果表明,以异辛烷为有机溶剂,在反应温度为50℃PH值为7.4时,酶催化活性最好。 相似文献
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丙烯酶催化氧化制取环氧丙烷的研究—甲烷菌细胞的吸附固定化 总被引:1,自引:0,他引:1
用吸附法将甲烷菌整细胞固定在某些有机和无机载体上,制备了丙烯环氧化反应的固定化生物催化剂。不同载体对固定化细胞的催化活性有很大影响,用一填充床流动反应器对吸附在不同载体上的固定化细胞进行了活性考察。结果表明:用有机的疏水载体如聚丙烯,石蜡等制成的固定化细胞具有较高的环氧化催化活性,且不同载体制成的固定化细胞的催化活性大致相同,约在28nmol/mg cell。用无机亲水类载体制成的固定化细胞,其环氧化催化活性差别很大,且大多数这类载体均比有机的疏水载体活性低,但用特殊方法处理过的砂子为载体制成的固定化细胞,其催化活性很高。还发现,用3AK型分子筛和酸处理过的Al_2O_3和3AK型分子筛为载体时,固定化细胞的活性与载体表面酸性有一定关系。 相似文献
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用悬浮聚合法合成了一系列聚甲基丙烯酸羟乙酯载体,考察了它们固定化酵母脂肪酶活力与载体的交联度和致孔剂用量之间的关系。研究了这些固定化酵母脂肪酶在有机溶剂中催化酯合成反应的活性,脂肪酶的固定化使之活力表达更为充分,对亲水性较强的有机溶剂有更强的耐受性,并能为其在有机溶剂中催化酯合成反应提供必需水。考察了PH值,底物种类对固定化酵母脂肪酶催化酯合成反应的影响。 相似文献
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采用还原法制备了AuNPs/MWCNTs复合材料,并构建了氧化还原蛋白质的固定化和生物传感界面AuNPs/MWCNTs/GC电极.以肌红蛋白(Myoglobin,Mb)为例,研究了固定化蛋白质在AuNPs/MWCNTs/GC电极上的直接电化学.结果表明,AuNPs/MWCNTs复合材料不仅能有效地促进Mb与电极表面的直接电子转移,而且能很好地保持固定化Mb的生物催化活性.Mb/AuNPs/MWCNTs/GC电极对H2O2具有良好的电催化还原性能,其线性响应范围为1~138μmol·L-1,检测限为0.32μmol·L-1(S/N=3),并具有较低的米氏常数(0.143 mmol·L-1).该电极操作简单,响应迅速,稳定性和重现性好,有望用于蛋白质的固定化及第三代生物传感器的制备. 相似文献
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水溶液及有机溶剂中固定化催化抗体的行为Kim.D.Janda教授等人宣布,抗体酶的固定化已经取得了初步成功。他们描述了固定化催化抗体在水溶液和有机溶剂中的行为,结果说明在水溶液条件下模拟脂肪酶的催化抗体键合到无机载体上,并保持了他们固定化前在溶液中的... 相似文献
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脂肪酶的固定化及其在有机酶促反应中稳定性研究 总被引:12,自引:3,他引:12
利用吸附法,将圆柱状假丝酵母脂肪酶固定于4种疏水性不同的载体上,固定化酶的活性及稳定性随载休疏水性的增大而增大。用YGW-C6H5作为载体,在有机溶剂-水双液相体系中催化萘普生甲酯的不对称水解,反应120h转化率为24.72%,产品的对映体过量值为94.82%。 相似文献
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研究了在有机溶剂中固定化Alcaligenes sp.脂肪酶催化α-氰基-3-苯氧基苄醇乙酯的对映体选择性转酯化反应,考察了不同性质的溶剂和酰基受体对酶的催化活性和选择性以及对产物稳定性的影响.结果发现在弱极性溶剂如正己烷中酶具有较高的催化活性但产物e.e.%值低,而且容易分解;在四氢呋喃等溶剂中酶催化活性相对低,但产物e.e.%值高,也较为稳定;但反应时间太长,会导致产物分解及纯度下降;不同酰基受体对酶反应无显著影响,甲醇为最佳酰基受体,太多醇会导致反应速率下降;溶剂水含量大于2.0%时对酶活性和产物稳定性产生明显不利影响.在优化条件下,酶反应可得到(S)-α-氰基-3-苯氧基苄醇产率>48%,纯度>99%e.e. 相似文献
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Bellezza F Cipiciani A Costantino U Nicolis S 《Langmuir : the ACS journal of surfaces and colloids》2004,20(12):5019-5025
The adsorption and catalytic activity of myoglobin (Mb) on zirconium phosphonates (a-zirconium benzenephosphonate (alpha-ZrBP), a-zirconium carboxyethanephosphonate (alpha-ZrCEP), and a novel layered zirconium fluoride aminooctyl-N,N-bis(methylphosphonate) (ZrC8)) were investigated. The maximum adsorption was reached after 16 h of contact and was greater on hydrophobic supports such as alpha-ZrBP and ZrC8 compared to hydrophilic supports such as alpha-ZrCEP. The equilibrium adsorption isotherms fitted the Langmuir equation, suggesting the presence of a monolayer of protein molecules on the support surfaces. The catalytic activities of free Mb and of the obtained biocomposites were studied in terms of the oxidation of two aromatic substrates, o-phenylenediamine and 2-methoxyphenol (guaiacol), by hydrogen peroxide. The oxidation catalyzed by immobilized myoglobin followed the Michaelis-Menten kinetics, similar to oxidation by free Mb. The kinetic parameters, kcat and KM, were significantly affected by the adsorption process. Mb/alpha-ZrCEP was the most efficient biocatalyst obtained, probably because of the hydrophilic nature of the support. The effect of immobilization on the stability of Mb toward inactivation by hydrogen peroxide was also investigated, and an increased resistance was found. The biocomposites obtained can be stored at 4 degrees C for months without a significant loss of catalytic activity. 相似文献
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Bellezza F Cipiciani A Quotadamo MA 《Langmuir : the ACS journal of surfaces and colloids》2005,21(24):11099-11104
We investigated the adsorption and catalytic activity of myoglobin (Mb) immobilized on colloidal particles of zirconia covalently grafted with phosphoric (ZrO2-P) and benzenephosphonic acid (ZrO2-BP). The maximum adsorption was reached after 1 h of contact and was greater on a hydrophilic support, ZrO2-P, compared to a hydrophobic support, ZrO2-BP. The equilibrium isotherms fitted the Langmuir equation, suggesting the presence of a monolayer of protein molecules on the surface of the nanoparticles. The nanostructured biocomposites are active in the oxidation of 2-methoxyphenol (guaiacol) by hydrogen peroxide. The oxidation catalyzed by immobilized Mb followed a Michaelis-Menten kinetics, similar to that observed in the oxidation by free Mb. Furthermore, the catalytic efficiency is similar to that of free Mb and higher than that of "large-size" biocatalysts (with sizes larger than 1 mum). In the latter case, the kinetic parameters, k(cat) and K(M), indicate that this is mostly due to an increased affinity of the nano-biocomposite for the substrate. The activity of the nano-biocomposites decreases slightly as the amount of adsorbed protein increases. This is mainly due to the formation of a nonordered monolayer, which reduces the accessibility of the substrate to the active center. 相似文献
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《Electroanalysis》2004,16(4):253-259
Sodium montmorillonite was prepared via a colloidal chemical approach and deposited onto glassy carbon electrodes (GCE). Myoglobin was immobilized on the clay membrane modified electrode by spontaneous adsorption. Characterization of the myoglobin/clay/glassy carbon electrode (Mb/clay/GCE) showed a quasi‐reversible, electrochemical redox behavior of the adsorbed protein with a formal potential of ?0.380±0.010 V (vs. Ag/AgCl). The heterogeneous electron transfer rate constant was found to be strongly influenced by the buffer concentration. The Mb/clay/GCE was stable for several days in solution. The interaction of the immobilized Mb with nitric oxide (NO) is characterized by coordination chemistry. The reaction was found to be reversible and could be applied for NO detection in the nanomolar concentration range by a voltammetric analysis. In addition a mixed protein electrode with co‐immmobilized myoglobin (Mb) and cytochrome c (Cyt.c) was developed. By choice of the electrode potential both proteins can be addressed independently. 相似文献
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Electrochemistry of Multilayers of Graphene and Myoglobin Modified Electrode and Its Biosensing
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Wencheng Wang Xiaoqing Li Xiaohua Yu Lijun Yan Zaifeng Shi Xiaoyong Wen Wei Sun 《中国化学会会志》2016,63(3):298-302
A multilayers of graphene (GR) and myoglobin (Mb) modified electrode was fabricated with a layer of chitosan film. Electrochemical behaviors of the modified electrode were studied by cyclic voltammetry, which exhibited a couple of well‐behaved, stable and quasi‐reversible cathodic and anodic peaks, indicating that Mb realized its direct electron transfer on the biosensor. The experimental result may be accredited to the existence of multilayers conductive GR nanosheets that could provide big specific surface area, fine biological compatibility and ultrahigh electron transfer route for the immobilized Mb. The catalytic reduction peak currents of the biosensor to the detection of trichloroacetic acid were established from 0.6 to 26.0 mM accompanied with the detection limit as 0.15 mM (3σ). Therefore a novel third‐generation mediator‐free electrochemical sensor was successful prepared with the usage of multilayers of GR. 相似文献
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A novel nanohybrid material, constructed by gold nanoparticles (GNPs) and multiwalled carbon nanotubes (MWNTs), was designed for immobilization and biosensing of myoglobin (Mb). Morphology of the nanohybrid film was characterized by SEM. UV‐vis spectroscopy demonstrated that Mb on the composite film could retain its native structure. Direct electrochemistry of Mb immobilized on the GNPs/MWNTs film was investigated. The immobilized Mb showed a couple of quasireversible and well‐defined cyclic voltammetry peaks with a formal potential of about ?0.35 V (vs. Ag/AgCl) in pH 6.0 phosphate buffer solution (PBS) solution. Furthermore, the modified electrode also displayed good sensitivity, wide linear range and long‐term stability to the detection of hydrogen peroxide. The experiment results demonstrated that the hybrid matrix provided a biocompatible microenvironment for protein and supplied a necessary pathway for its direct electron transfer. 相似文献
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用魔芋多糖(KGM)和N,N-二甲基甲酰胺(DMF)的加合物,将肌红蛋白(Mb)固定在玻碳电极(GCE)上,制备了稳定的Mb-KGM-DMF/GCE修饰电极,并研究了Mb在修饰电极上的直接电化学行为和电催化性能。该电极在pH=7.0的磷酸盐缓冲溶液(PBS)中,-0.38 V(E0′)处有一对氧化还原峰,峰电位差ΔEp=70 mV,该峰正是Mb中血红素辅基FeⅢ/FeⅡ电对的氧化还原特征峰。在0.2~9.0 V/s扫速的范围内,氧化还原峰峰电流大小和扫描速率成正比,呈现出表面控制行为。在pH为5.0~12.0的范围内,式电位和pH值呈线性关系,表明电子传递过程伴随着质子转移。同时,Mb-KGM-DMF/GCE修饰电极表现出良好的电催化性能,对氧、H2O2有显著的催化作用。在4.70~75.0μmol/L的范围内,其催化峰电流大小与H2O2的浓度有良好的线性关系,其线性回归方程i=0.127 0.093C,r=0.9989,表观米氏常数为80.8μmol/L。 相似文献
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Myoglobin/sol-gel film modified electrode: direct electrochemistry and electrochemical catalysis 总被引:4,自引:0,他引:4
Direct electrochemical and electrocatalytic behavior of myoglobin (Mb) immobilized on carbon paste electrode (CPE) by a silica sol-gel film derived from tetraethyl orthosilicate was investigated for the first time. Mb/sol-gel film modified electrodes show a pair of well-defined and nearly reversible cyclic voltammetric peaks for the Mb Fe(III)/Fe(II) redox couple at about -0.298 V (vs Ag/AgCl) in a pH 7.0 phosphate buffer solution. The formal potential of the Mb heme Fe(III)/Fe(II) couple shifted linearly with pH with a slope of 52.4 mV/pH, denoting that an electron transfer accompanies single-proton transportation. An FTIR and UV-vis spectroscopy study confirms that the secondary structure of Mb immobilized on an electrode by a sol-gel film still maintains the original arrangement. The immobilized Mb displays the features of a peroxidase and acts in an electrocatalytic manner in the reduction of oxygen, trichloroacetic acid (TCA), and nitrite. In comparison to other electrodes, the chemically modified electrodes used in this study for direct electrochemistry and electrocatalysis of Mb are easy to fabricate and fairly inexpensive. Consequently, the Mb/sol-gel film modified electrode provides a convenient way to perform electrochemical research on this kind of protein. It also has potential use in the fabrication of bioreactors and third-generation biosensors. 相似文献
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Bellezza F Cipiciani A Quotadamo MA Cinelli S Onori G Tacchi S 《Langmuir : the ACS journal of surfaces and colloids》2007,23(26):13007-13012
The adsorption of myoglobin (Mb) onto phosphate grafted-zirconia (ZrO2-P) nanoparticles was studied in terms of conformational studies and thermal stability, determined by circular dichroism (CD), differential scanning calorimetry (DSC), and atomic force microscopy (AFM). The changes in protein structure have been correlated with the catalytic activity of free and adsorbed Mb. CD and DSC studies indicate marked rearrangements in Mb structure upon adsorption onto phosphate-grafted zirconia nanoparticles. These structural rearrangements of Mb could be responsible for the loss of catalytic activity observed for the adsorbed Mb. In particular, the conformational changes due to the adsorption process induced a reduction of kcat and KM. AFM measurements indicate that the interaction with the grafted-zirconia nanoparticles also affects the morphology of the bound protein, inducing the nucleation of prefibrillar-like aggregates. 相似文献
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The electron tunneling of the protein-polypeptide interactions was observed in the study of direct electron transfer of the myoglobin (Mb) on the electrode surface. The Mb was selected as a redox active protein and gelatine was selected to couple with Mb to form an electron tunneling. The electrochemical results indicated the presence of the electron tunneling and the direct electron transfer. The circular dichroism spectra suggested that the beta-sheet chain of gelatine could interact with alpha-helical chain to form an electron tunneling to promote the protein direct electrochemistry. The SDS-PAGE results proved that the electron tunneling between Mb and gelatine was noncovalent hydrogen bonds. The immobilized Mb showed a couple of quasi-reversible redox peaks with a formal potential of -0.37V (vs SCE) in 0.1 M pH 7.0 PBS. The modified electrodes displayed a rapid amperometric response to the reduction of oxygen, H2O2, and nitrite. 相似文献