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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Spectroscopic and catalytic studies of lipases in ternary hexane-1-propanol-water surfactantless microemulsion systems
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Spectroscopic and catalytic studies of lipases in ternary hexane-1-propanol-water surfactantless microemulsion systems

机译:三元己烷-1-丙醇-水无表面活性剂微乳液体系中脂肪酶的光谱和催化研究

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A series of water-in-oil microemulsion systems formulated without surfactant were used to solubilize lipases from Rhizomucor miehei and Candida antarctica B. The effect of the system's composition on the velocity of enzymic reactions was investigated following a model esterification reaction. The interaction between enzymes and the microemulsion environment was studied by steady state fluorescence spectroscopy. The site of localization of the enzyme within the different microdomains of the dispersed phase was investigated by applying the fluorescence energy transfer technique. To determine the properties of the interface between water and organic solvent of the surfactantless microemulsion systems the Electron Paramagnetic Resonance (EPR) spectroscopic technique was applied. The results indicated that even at low water content, water-rich structures are formed. This was confirmed by conductivity measurements. By the addition of enzyme it was observed that when the aqueous phase of the surfactantless microemulsion systems exceeds 2% (v/v) the enzyme retains its catalytic activity, as it is located within the water pools that protect it from the organic solvent. These confined water phases show a propanol rich interface with hexane and their structure depends on the system's composition. (c) 2005 Elsevier B.V. All rights reserved.
机译:使用一系列不用表面活性剂配制的油包水微乳液体系来溶解米根根霉和南极假丝酵母B的脂肪酶。在模型酯化反应之后,研究了体系组成对酶促反应速度的影响。通过稳态荧光光谱研究了酶与微乳液环境之间的相互作用。通过应用荧光能量转移技术研究了酶在分散相不同微区中的定位位置。为了确定无表面活性剂的微乳液体系中水与有机溶剂之间的界面性质,应用了电子顺磁共振(EPR)光谱技术。结果表明,即使在低含水量下,也会形成富水结构。通过电导率测量证实了这一点。通过添加酶,观察到当无表面活性剂的微乳液体系的水相超过2%(v / v)时,由于酶位于保护其免受有机溶剂侵害的水池中,因此酶保留了其催化活性。这些受限的水相显示出富含丙醇与己烷的界面,其结构取决于系统的组成。 (c)2005 Elsevier B.V.保留所有权利。

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