Suppr超能文献

具有吸水性的固定化脂肪酶纤维素胶囊用于增强皮克林界面生物催化

Lipase-Immobilized Cellulosic Capsules with Water Absorbency for Enhanced Pickering Interfacial Biocatalysis.

作者信息

He Xiao, Binks Bernard P, Hu Jinguang, Gates Ian, Lu Qingye

机构信息

Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.

Department of Chemistry, University of Hull, Hull HU6 7RX, UK.

出版信息

Langmuir. 2021 Jan 19;37(2):810-819. doi: 10.1021/acs.langmuir.0c03140. Epub 2021 Jan 6.

Abstract

Lipase-immobilized cellulosic capsules consisting of hydrophobic ethyl cellulose (EC) and hydrophilic carboxymethyl cellulose (CMC) were developed with a promising interfacial activity and water absorbency for the enhanced Pickering interfacial biocatalysis. Lipase was physically immobilized with water-absorbent materials (CMC) hydrogen bonding and electrostatic interactions and acted as the interior catalytic core of the capsule. The interfacially active EC worked as the exterior shell, enabling capsules to stabilize the oil-in-water Pickering emulsion for the subsequent Pickering interfacial catalysis. The capsules with CMC created interior water-rich conditions to improve the conformational and enzymatic activity of the immobilized lipase. Compared with capsules without water-absorbent materials, the capsules with CMC enhanced the efficiency of the Pickering interfacial catalysis for the esterification of oleic acid and 1-octanol by 12%. Immobilized with a small amount of lipase (0.0625 g/g), the cellulosic capsules with water absorbency could convert 50.8% of the reactants after 10 h under room temperature, significantly higher than that by the same amount of free lipase in the biphasic system (15%) and a Pickering emulsion (24.1%) stabilized by empty capsules (without lipase). Moreover, the cellulosic capsules could be recycled by simple centrifugation while retaining their high relative catalytic activity for at least eight cycles, demonstrating their sustainable catalytic performance.

摘要

由疏水性乙基纤维素(EC)和亲水性羧甲基纤维素(CMC)组成的固定化脂肪酶纤维素胶囊具有良好的界面活性和吸水性,可增强皮克林界面生物催化作用。脂肪酶通过氢键和静电相互作用与吸水材料(CMC)物理固定,并作为胶囊的内部催化核心。具有界面活性的EC作为外壳,使胶囊能够稳定水包油型皮克林乳液,用于后续的皮克林界面催化。含有CMC的胶囊创造了内部富水条件,以改善固定化脂肪酶的构象和酶活性。与不含吸水材料的胶囊相比,含有CMC的胶囊使油酸和1-辛醇酯化的皮克林界面催化效率提高了12%。固定化少量脂肪酶(0.0625 g/g)后,具有吸水性的纤维素胶囊在室温下10小时后可转化50.8%的反应物,显著高于双相体系中相同量的游离脂肪酶(15%)和由空胶囊(不含脂肪酶)稳定的皮克林乳液(24.1%)。此外,纤维素胶囊可以通过简单离心回收,同时至少八个循环保持其高相对催化活性,证明了它们的可持续催化性能。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验