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Algal polysaccharides as matrices for the immobilization of urease in lipid ultrathin films studied with tensiometry and vibrational spectroscopy: Physical-chemical properties and implications in the enzyme activity

机译:用抗致力学和振动光谱研究的脂质超薄膜中释放释放释放的藻类多糖:物理化学性质和酶活性的影响

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Currently, many biological substances extracted from algae have received special attention because of their intrinsic characteristics, which can be applied to different areas of biotechnology. Therefore, in the current study, exopolysaccharides (EPS) from the microalgae Cryptomonas tetrapirenoidosa were employed as an aqueous subphase of a monolayer formed by the lipid dioctadecyldimethylammonium bromide (DODAB). The primary objective of this approach was to evaluate whether EPS could serve as a matrix for the immobilization of the enzyme urease to produce biosensors for urea. After DODAB was spread on the EPS solutions, urease was injected into the aqueous subphase, and the surface was submitted to compression using lateral barriers. The monolayers were subsequently characterized by surface pressure-area isotherms and polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS). The results indicated that EPS enhanced the adsorption of the enzyme on the lipid monolayer. The mixed films were later transferred to solid supports using the Langmuir-Blodgett (LB) technique and were characterized by transfer ratio, PM-IRRAS, quartz crystal microbalance, and atomic force microscopy. The immobilization of the enzyme on solid supports was fundamental for providing an ideal geometrical accommodation of urease because the interaction of EPS with urease in solution causes a decrease of the relative activity of urease. Therefore, these LB films are promising for the fabrication of future urea biosensors, the architecture of which can be manipulated and enhanced at the molecular level. (C) 2015 Elsevier B.V. All rights reserved.
机译:目前,许多从藻类提取的生物物质由于其内在特征而受到特别关注,可以应用于不同的生物技术领域。因此,在目前的研究中,使用来自微藻胶质蛋白质细胞瘤细胞的外偶乙醛(EPS)作为由脂质二辛酰基二甲基溴化铵(Dodab)形成的单层的含水亚类。这种方法的主要目的是评估EPS是否可以作为固定酶脲酶以产生尿素生物传感器的基质。 Dodab在EPS溶液上涂布后,将脲酶注入水性亚相,并且使用横向屏障将表面提交至压缩。随后通过表面压力区域等温线和偏振调制红外反射吸收光谱(PM-IRRAS)表征单层。结果表明,EPS增强了酶对脂质单层的吸附。使用Langmuir-Blodgett(LB)技术后来将混合膜转移至固体载体,并通过转移比,PM-IrrAc,石英晶体微观和原子力显微镜表征。在固体载体上固定酶对固体载体的基础是提供理想的几何容纳释放物,因为EPS与溶液脲酶的相互作用导致脲酶的相对活性降低。因此,这些LB薄膜是对制造未来尿素生物传感器的制造,其结构可以在分子水平上操纵和增强。 (c)2015 Elsevier B.v.保留所有权利。

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