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Graphene Oxide Nanosheets Shielding of Lipase Immobilized on Magnetic Composites for the Improvement of Enzyme Stability

脂肪酶 热稳定性 化学 石墨烯 固定化酶 化学工程 氧化物 吸附 材料科学 有机化学 纳米技术 工程类
作者
Hongbo Suo,Lili Xu,Chao Xu,Xiang Qiu,Hongyue Chen,He Huang,Yi Hu
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:7 (4): 4486-4494 被引量:59
标识
DOI:10.1021/acssuschemeng.8b06542
摘要

In this study, a novel enzyme immobilization method was developed to enhance the catalytic stability of enzymes. In this strategy, ionic liquid (IL) modified magnetic chitosan (MCS) composites were used as supports for lipase adsorption and graphene oxide (GO) was employed as shell coating for the first time. The modifier used was imidazolium-based IL with a side alkyl chain which was composed of 8 −CH2 and a terminal hydroxyl group. The prepared supports IL-MCS, immobilized lipase PPL-IL-MCS, and GO/PPL-IL-MCS were well characterized. The GO shielding lipase GO/PPL-IL-MCS maintained high activity (2468 U/g), which was 6.72-fold of free lipase. In addition, the pH and temperature effect on lipase activity were investigated. The thermal stability, denaturants stability, storage stibility, and reusing stability were also studied. Compared to PPL-IL-MCS, the stabilities of GO/PPL-IL-MCS were all enhanced while keeping high activity. For example, after 10 cycles of reuse, the residual activity of GO/PPL-IL-MCS was 92.1%, which was higher than that of 88.4% for PPL-IL-MCS. Furthermore, the apparent Km of PPL-IL-MCS and GO/PPL-IL-MCS was 5.7 and 8.8 mg/mL, respectively, which were both lower than that of PPL-MCS (17.1 mg/mL). Circular dichroism (CD) was used to analyze the secondary structure of lipase to explain the mechanism of stable enhancement of immobilized enzyme. This work demonstrated that GO was used as a shell coating for the first time to improve the lipase stability. This immobilization method provides a reference for the immobilization of other kinds of enzymes.

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