首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Preparation of ion-exchange supports via activation of epoxy-SiO2 with glycine to immobilize microbial lipase - Use of biocatalysts in hydrolysis and esterification reactions
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Preparation of ion-exchange supports via activation of epoxy-SiO2 with glycine to immobilize microbial lipase - Use of biocatalysts in hydrolysis and esterification reactions

机译:通过用甘氨酸的环氧-SiO 2活化来制备离子交换支持以固定微生物脂肪酶 - 使用生物催化剂的水解和酯化反应

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Ion-exchange supports have been prepared via sequential functionalization of silica-based materials with (3-Glycidyloxypropyl)trimethoxysilane (GPTMS) (Epx-SiO2) and activation with glycine (Gly-Epx-SiO2) in order to immobilize lipase from Thermomyces lanuginosus (TLL) via adsorption. Rice husk silica (RHS) was selected as support with the aim of comparing its performance with commercial silica (Immobead 5605). Sequential functionalization/activation of SiO2-based supports has been confirmed by AFM, SEM and N-2 adsorption desorption analyses. Maximum TLL adsorption capacities of 14.8 +/- 0.1 mg/g and 16.1 +/- 0.6 mg/g using RHS and Immobead S60S as supports, respectively, have been reached. The Sips isotherm model has been used which was well fitted to experimental data on TLL adsorption. Catalytic activities of immobilized TLL were assayed by olive oil emulsion hydrolysis and butyl stearate synthesis via an esterification reaction. Hydrolytic activity of the biocatalyst prepared with a commercial support (357.6 +/- 11.2 U/g) was slightly higher than that of Gly-Epx-SiO2 prepared with RHS (307.4 +/- 7.2 U/g). On the other hand, both biocatalysts presented similar activity (around 90% conversion within 9-10 h of reaction) and reusability after 6 consecutive cycles of butyl stearate synthesis in batch systems. (C) 2018 Elsevier B.V. All rights reserved.
机译:通过用(3-甘糖氧基丙基)三甲氧基硅烷(GPTMS)(EPX-SiO 2)和用甘氨酸(Gly-EPX-SiO 2)活化来制备离子交换支持,以使脂肪酶免于Thermomyyces Lanuginosus( TLL)通过吸附。选择稻壳二氧化硅(RHS)作为支持,目的是将其性能与商业二氧化硅进行比较(Immobead 5605)。通过AFM,SEM和N-2吸附解吸分析证实了基于SiO2的支持的顺序官能化/激活。已经分别达到最大TLL吸附容量为14.8 +/- 0.1mg / g和16.1 +/- 0.6 mg / g,分别使用RHS和Immobead S60S作为支撑件。已经使用SIPS等温模型,其适合于TLL吸附的实验数据。通过酯化反应通过酯化反应进行橄榄油乳液水解和丁酯合成的固定的TLL的催化活性。用商业载体(357.6 +/- 11.2U / g)制备的生物催化剂的水解活性略高于用RHS制备的甘氨酸-SIO2(307.4 +/- 7.2 U / g)。另一方面,两种生物催化剂呈现相似的活性(在反应9-10小时内的转化约为90%),并且在批量系中的硬脂酸丁酯合成的6个连续循环后的可重用性。 (c)2018年elestvier b.v.保留所有权利。

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