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Immobilization and stabilization of pullulanase from Klebsiella pneumoniae by a multipoint attachment method using activated agar gel supports

机译:使用活化的琼脂凝胶支持物通过多点附着方法固定和稳定肺炎克雷伯菌中的支链淀粉酶

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摘要

The immobilization and stabilization of pullulanase from Klebsiella pneumoniae were investigated. Pullulanases immobilized on activated agar gel (glyoxyl-agar gel) via multipoint attachment between amino groups of pullulanase and aldehyde groups on the gel surface were significantly stable compared with free pullulanase and pullulanase adsorbed on chitosan beads. The immobilization yield, thermal stability and activity of immobilized pullulanase greatly depended on the surface density of aldehyde groups on the support gel. The optimum temperature and pH of immobilized pullulanases prepared by the multipoint attachment method using activated agar gels were 50℃ and 6.0, respectively. These values were the same as those of free pullulanase. Pullulanase immobilized on agar gel activated with 4.8 M glycidol retained 60% of its initial activity after a 250-h incubation at 45℃, while free pullulanase completely lost its activity after a 72-h incubation at the same temperature.
机译:研究了肺炎克雷伯菌中支链淀粉酶的固定化和稳定性。通过支链淀粉酶的氨基和凝胶表面醛基之间的多点连接固定在活化琼脂凝胶(乙醛-琼脂凝胶)上的支链淀粉酶与游离的支链淀粉酶和壳聚糖珠粒上吸附的支链淀粉酶相比,具有显着的稳定性。固定化支链淀粉酶的固定化产率,热稳定性和活性在很大程度上取决于支持凝胶上醛基的表面密度。采用活化琼脂凝胶多点吸附法制备固定化支链淀粉酶的最适温度为50℃,最适pH为6.0。这些值与游离支链淀粉酶的值相同。固定在4.8 M缩水甘油活化的琼脂凝胶上的支链淀粉酶在45℃孵育250小时后保留了其初始活性的60%,而游离支链淀粉酶在相同温度下孵育72 h后完全失去了活性。

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