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首页> 外文期刊>Journal of Fiber Science and Technology >Preparation and Characterisation of Cyclodextrin Glucanotransferase Enzyme Immobilised in Electrospun Nanofibrous Membrane
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Preparation and Characterisation of Cyclodextrin Glucanotransferase Enzyme Immobilised in Electrospun Nanofibrous Membrane

机译:静电纺丝纳米纤维膜固定化环糊精葡糖基转移酶的制备与表征

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摘要

An industrial enzyme, Cyclodextrin glucanotransferase (CGTase), was immobilised in polyvinyl alcohol (PVA) nanofiber (average diameter around 200 nm) membrane via co-electrospinning of the CGTase/PVA mixture followed with glutaraldehyde vapour phase cross-linking. Addition of enzyme with concentration ranging from 1.5 to 7.5 % to the PVA solution (8 wt%) caused significant changes to the liquid jet behaviours which consequently affected the nanofiber structures and sizes. Incorporation of CGTase in the PVA membrane was confirmed by Raman spectroscopic analysis. The Raman spectra also showed no structural changes occured to the enzyme after subjected to the electrostatic spinning and cross-linking reaction. The immobilised enzyme showed excellent catalytic efficiency with up to 3.6 times higher enzyme loading, 25 % higher activity and good reusability in comparison with CGTase/PVA film made up from the same starting solution (control).
机译:通过共电纺丝CGTase / PVA混合物,然后进行戊二醛气相交联,将工业酶环糊精葡聚糖转移酶(CGTase)固定在聚乙烯醇(PVA)纳米纤维(平均直径约200 nm)膜中。向PVA溶液(8 ​​wt%)中添加浓度范围为1.5%至7.5%的酶会导致液体喷射行为发生重大变化,从而影响纳米纤维的结构和尺寸。通过拉曼光谱分析证实了CGTase在PVA膜中的掺入。拉曼光谱还显示,在进行静电纺丝和交联反应之后,酶没有发生结构变化。与由相同起始溶液(对照)制成的CGTase / PVA膜相比,固定化酶显示出优异的催化效率,酶负载量高出3.6倍,活性提高25%,重用性好。

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