脂肪酶
微乳液
催化作用
乳状液
碳纳米管
化学工程
化学
溴化物
皮克林乳液
材料科学
有机化学
纳米技术
肺表面活性物质
酶
工程类
作者
Lei Kuang,Mengjie Liu,Zefeng Lin,Yunping Zhu,Jinlong Li
摘要
Abstract BACKGROUND The interfacial activation mechanism of lipase enables it to exhibit high catalytic activity in water‐in‐oil (W/O) microemulsions. However, W/O microemulsions have obvious defects such as a small water pool and a large demand for surfactants. The present study investigated the substitutability of conventional oil‐in‐water (O/W) and W/O emulsions as lipase catalytic systems. Carbon nanotubes (CNTs)/gold nanoparticles (GNPs) or CNT–GNP electrostatically bonded complexes were added into the conventional emulsion system. RESULTS The simulated biphasic system and fluorescence study showed different and even contradictory results for the interfacial behavior of CNTs and CNT–GNP complexes due to the variation of the dispersibility of CNTs in cetyltrimethylammonium bromide (CTAB). Results also showed that conventional O/W emulsions were more suitable for lipase catalysis than conventional W/O emulsions. When CNTs or CNT CATB –GNP complexes were added in a conventional O/W emulsion system, the catalytic activity of lipase was significantly promoted (up to 4.8‐fold using CNTs and 3.5‐fold using CNT CATB –GNP complexes compared with free lipase). CONCLUSIONS The possible reason for this promotion may be due to the increase in the interface area. The current study was not only the latest exploration of lipase activity promotion via nanomaterials, but also explored a new lipase catalytic system and provides further insight into improving the catalytic performance of lipase in conventional emulsions. © 2020 Society of Chemical Industry
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