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Immobilized Horseradish Peroxidase on Discs of Polyvinyl Alcohol-Glutaraldehyde Coated with Polyaniline

机译:聚苯胺包被的聚乙烯醇-戊二醛圆盘上的辣根过氧化物酶固定化

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摘要

Discs of network polyvinyl alcohol-glutaraldehyde (PVAG) were synthesized and coated with polyaniline (PANI) using glutaraldehyde as a chemical arm (PVAG-PANIG-HRP disc). The best conditions for the immobilization were established as about 1.0 mg mL−1 of protein, for 60 min and pH 5.5. The soluble enzyme lost all of its activity after incubation at 70°C for 15 min, whereas the PVAG-PANIG-HRP disc retained about half of the initial activity for pyrogallol. The same PVAG-PANIG-HRP disc was used consecutively three times without any activity lossbut presented 25% of the initial activity after the 7th use. PVAG-PANIG-HRP disc retained approximately 80% and 60% of its initial activity after 60 and 80 days of storage, respectively. Resorcinol, m-cresol, catechol, pyrogallol, α-naphthol, βnaphthol, and 4, 4′-diaminodiphenyl benzidine were efficiently oxidized by the PVAG-PANIG-HRP disc (from about 70% to 90%), and it was less efficient towards aniline, phenol, and 2-nitrosonaphthol.
机译:合成网状聚乙烯醇-戊二醛(PVAG)光盘,并以戊二醛为化学臂,用聚苯胺(PANI)涂布(PVAG-PANIG-HRP光盘)。确定了固定化的最佳条件为:蛋白质约1.0 mg mL -1 ,持续60 min,pH 5.5。在70°C下孵育15分钟后,可溶性酶丧失了所有活性,而PVAG-PANIG-HRP盘保留了邻苯三酚的约一半初始活性。同一张PVAG-PANIG-HRP光盘连续使用了3次,没有任何活动损失,但是在第7次使用后呈现了初始活动的25%。在储存60天和80天后,PVAG-PANIG-HRP光盘分别保留了其初始活动的80%和60%。间苯二酚,间甲酚,邻苯二酚,邻苯三酚,α-萘酚,β-萘酚和4,4'-二氨基二苯基联苯胺被PVAG-PANIG-HRP盘有效氧化(约70%至90%),效率较低对苯胺,苯酚和2-硝基sonaphthol。

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