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Immobilization on graphene oxide improves the thermal stability and bioconversion efficiency of D-psicose 3-epimerase for rare sugar production

机译:对石墨烯氧化物的固定改善了D-PSICOSE 3-映离子酶的热稳定性和生物转化效率,用于稀有糖生产

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摘要

D-Psicose (D-ribo-2-hexulose or D-allulose), an epimer of D-fructose is considered as a rare low-calorie sugar displaying important physiological functions. Enzymatic production using ketose 3-epimerases is the feasible process for the production of D-Psicose. However, major drawbacks in application of ketose 3-epimerases are bioconversion efficiency and reusability of the enzyme. We have attempted immobilization of ketose 3-epimerases from Agrobacterium tumefaciens (agtu) D-psicose 3-epimerase (DPEase) on graphene oxide. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and Thermo gravimetric analysis (TGA) showed that the enzyme was successfully immobilized on the graphene oxide. Graphene oxide immobilized agtu-DPEase (GO-agtu-DPEase) shows pH optima at 7.5 and 60 C as higher working temperature. Significant improvement in thermal stability was observed which showed half-life of 720 min at 60 C whereas Agrobacterium tumefaciens (agtu) DPEase displayed 3.99 min. At equilibrium, 40:60 (D-psicose: D-fructose) the bioconversion efficiency was accounted for Graphene oxide immobilized DPEase which is higher than the agtuDPEase. Graphene oxide immobilized DPEase showed bioconversion efficiency up to 10 cycles of reusability.
机译:D-雌蕊(D-核核糖-2-己烯或D-甲状腺素),D-果糖的基础被认为是罕见的低热量糖,显示重要的生理功能。使用酮糖3-截止酶的酶促产生是生产D-雌蕊的可行方法。然而,在施用酮糖3-邻接酶的主要缺点是酶的生物转化效率和可重用性。我们试图将酮酮3-旁二聚酶的固定在石墨烯氧化物上的Tumefaciens(AgTu)D-雌蕊3-映酶(DPEASE)中的酮类3-旁二聚酶固定化。扫描电子显微镜(SEM),傅里叶变换红外光谱(FTIR)和热重分析(TGA)显示酶成功地固定在石墨烯氧化物上。石墨烯氧化物固定化的AgTu-dpease(Go-AgTu-dpease)显示为7.5和60℃的pH值,如更高的工作温度。观察到热稳定性的显着改善,其显示在60℃下720分钟的半衰期,而Tumefaciens(AgTu)Dpase显示3.99分钟。在平衡时,40:60(D-Psicose:D-果糖)占石墨烯固定的dpease的生物转化效率,其高于Agtudpease。石墨烯氧化物固定化DPEASE显示出高达10个可重复使用性的生物转化效率。

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