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Development of Thermoregulatory Enzyme Carriers Based on Microencapsulated n-Docosane Phase Change Material for Biocatalytic Enhancement of Amylases

机译:基于微胶囊化的N二叶醇相变材料的热调节酶载体的研制,用于淀粉酶的生物催化增强

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A phase change materials (PCMs)-based magnetic microcapsule system was designed as thermoregulatory enzyme carriers and then successfully constructed by microencapsulating n-docosane into an Fe3O4/SiO2 hybrid shell through interfacial polycondensation in a Pickering emulsion templating system. Scanning and transmission electron microscopic observations indicated that the as-synthesized microcapsules presented a well-defined core-shell microstructure as well as a regular spherical morphology, and their chemical structure and composition were confirmed by a series of spectroscopic characterizations. a-Amylase as a model enzyme was also successfully immobilized on the aldehyde-functionalized surface of as-synthesized microcapsules through covalent bonding. Such covalent immobilization was confirmed by energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. Thermal analysis results indicated that the a-amylase-immobilized microcapsules obtained a high latent heat-storage capability of approximately 155 J/g and a high encapsulation efficiency of 58%, and they also showed an effective thermoregulation capability and good thermal management performance. Most of all, the a-amylase immobilized on the microcapsules demonstrated a higher enzyme activity, thermal stability, and storage stability than that on the classical SiO2 solid carriers under the fluctuation of ambient temperature. In addition, the a-amylase-immobilized microcapsules also achieved a good separability and reusability due to its superparamagnetic nature. With an enhanced biocatalytic activity, the thermoregulatory enzyme carriers developed by this work exhibit a great potential for biologic applications and can well serve for sustainable chemistry and green processes.
机译:基于相变材料(PCMS)的磁性微胶囊系统被设计为热调节酶载体,然后通过皮质乳液模板系统中的界面缩聚通过微胶囊化合物渗入Fe3O4 / SiO 2杂化壳成功构建。扫描和透射电子显微镜观察表明,由合成的微胶囊呈现明确定义的核心 - 壳微观结构以及规则的球形形态,并通过一系列光谱表征证实了它们的化学结构和组合物。作为模型酶的A-淀粉酶也通过共价键合成功地固定在合成的微胶囊的醛官能化表面上。通过能量分散X射线光谱和X射线光电子谱证实这种共价固定化。热分析结果表明,A-淀粉酶固定化的微胶囊得到高潜热储存能力,高约155J / g,高封装效率为58%,它们还显示出有效的热调节能力和良好的热管理性能。最重要的是,固定在微胶囊上的A-淀粉酶证明了在环境温度波动下的典型SiO 2固体载体上的酶活性,热稳定性和储存稳定性更高。此外,A-淀粉酶固定化的微胶囊还达到了由于其超顺磁性而具有良好的可分离性和可重用性。通过增强的生物催化活性,通过该工作开发的热调节酶载体表现出生物应用的巨大潜力,并且可以为可持续化学和绿色过程提供良好的服务。

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