Inorganic Materials as Supports for Covalent Enzyme Immobilization: Methods and Mechanisms

Molecules

Paolo Zucca¹ 

[1] Consorzio UNO, Consortium University of Oristano, Oristano 09170, Italy; E-Mail:

关键词: enzymes;    immobilization;    stabilization;    covalent binding;    inorganic;    silica;    mesoporous;    functionalization;    grafting;    activation;   

DOI  :  10.3390/molecules190914139

来源: mdpi

【 摘 要 】

Several inorganic materials are potentially suitable for enzymatic covalent immobilization, by means of several different techniques. Such materials must meet stringent criteria to be suitable as solid matrices: complete insolubility in water, reasonable mechanical strength and chemical resistance under the operational conditions, the capability to form manageable particles with high surface area, reactivity towards derivatizing/functionalizing agents. Non-specific protein adsorption should be always considered when planning covalent immobilization on inorganic solids. A huge mass of experimental work has shown that silica, silicates, borosilicates and aluminosilicates, alumina, titania, and other oxides, are the materials of choice when attempting enzyme immobilizations on inorganic supports. More recently, some forms of elemental carbon, silicon, and certain metals have been also proposed for certain applications. With regard to the derivatization/functionalization techniques, the use of organosilanes through silanization is undoubtedly the most studied and the most applied, although inorganic bridge formation and acylation with selected acyl halides have been deeply studied. In the present article, the most common inorganic supports for covalent immobilization of the enzymes are reviewed, with particular focus on their advantages and disadvantages in terms of enzyme loadings, operational stability, undesired adsorption, and costs. Mechanisms and methods for covalent immobilization are also discussed, focusing on the most widespread activating approaches (such as glutaraldehyde, cyanogen bromide, divinylsulfone, carbodiimides, carbonyldiimidazole, sulfonyl chlorides, chlorocarbonates, N-hydroxysuccinimides).

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.