首页> 外文期刊>Journal of Materials Chemistry: An Interdisciplinary Journal dealing with Synthesis, Structures, Properties and Applications of Materials, Particulary Those Associated with Advanced Technology >Magnetically-separable and highly-stable enzyme system based on crosslinked enzyme aggregates shipped in magnetite-coated mesoporous silicaf
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Magnetically-separable and highly-stable enzyme system based on crosslinked enzyme aggregates shipped in magnetite-coated mesoporous silicaf

机译:基于在磁铁矿包覆的介孔二氧化硅中运送的交联酶聚集体的磁分离和高稳定酶体系

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摘要

A magnetically-separable and highly-stable enzyme system was developed by adsorption of enzymes in superparamagnetic hierarchically ordered mesocellular mesoporous silica (M-HMMS) and subsequent enzyme crosslinking. Superparamagnetic nanoparticles were homogeneously incorporated into hierarchically-ordered mesocellular mesoporous silica (HMMS) by the decomposition of a preformed iron propionate complex. The size of the incorporated superparamagnetic nanoparticles was around 5 nm, generating a magnetically separable host with high pore volumes and large pores (M-HMMS). α-chymotrypsin (CT) was adsorbed into M-HMMS with high loading (~30 wt%) in less than 30 minutes. Glutaraldehyde (GA) treatment of adsorbed CT resulted in nanometer scale crosslinked enzyme aggregates in M-HMMS (CLEA-M). The activity of these CT aggregates in M-HMMS (CLEA-M-CT) was 34 times than that of simply adsorbed CT in M-HMMS, due to an effective prevention of enzyme leaching during washing via a ship-in-a-bottle approach. CLEA-M-CT maintained the initial activity not only under shaking (250 rpm) for 30 days, but also under recycled uses of 35 times. The same approach was employed for the synthesis of CLEA-M of lipase (CLEA-M-LP), and proven to be effective in improving the loading, activity, and stability of enzyme when compared to those of adsorbed LP in M-HMMS.
机译:通过将酶吸附在超顺磁性分层有序介孔介孔二氧化硅(M-HMMS)中,并随后进行酶交联,开发了可磁分离和高度稳定的酶体系。通过预形成的丙酸铁络合物的分解,将超顺磁性纳米颗粒均匀地掺入分级的介孔介孔二氧化硅(HMMS)中。所掺入的超顺磁性纳米粒子的大小约为5 nm,从而产生了具有高孔体积和大孔(M-HMMS)的可磁分离的基质。在不到30分钟的时间内,α-胰凝乳蛋白酶(CT)被高负载(〜30 wt%)吸附到M-HMMS中。戊二醛(GA)处理吸附的CT会在M-HMMS(CLEA-M)中产生纳米级交联的酶聚集体。 M-HMMS(CLEA-M-CT)中这些CT聚集体的活性是M-HMMS中简单吸附的CT的活性的34倍,这是由于有效防止了通过瓶装船洗涤期间酶的浸出方法。 CLEA-M-CT不仅在摇动(250 rpm)下保持30天的初始活性,而且在循环使用35次后仍保持初始活性。使用相同的方法合成脂肪酶的CLEA-M(CLEA-M-LP),与M-HMMS中吸附的LP相比,已证明可有效改善酶的负载,活性和稳定性。

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