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作 者:杨防祖[1] 许书楷[1] 吴辉煌[1] 周绍民[1]
出 处:《高等学校化学学报》1994年第7期1042-1046,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金
摘 要:利用电化学固定化方法制备了聚吡咯/辣根过氧化物酶(PP/HRP)膜电极,并研究了其电化学行为。在除氧的磷酸盐缓冲液介质中,PP/HRP电极加速H_2O_2的还原,归因于酶加成物的直接电子传递。探索HRP与电子传递体K4Fe(CN)6在聚吡咯(PP)膜中的同时固定化条件及其膜电极的电化学行为,实验证实,K_4Fe(CN)_6在酶膜中的存在使得H_2O_2的还原电位强烈正移,在-0.05V的工作电位下能对H_2O_2进行检测,相应的电极过程可用间接氧化还原催化机理解释。With electropolymerization of pyrrole,horse-radish peroxidase(HRP) was immobilized in the polypyrrole matrix to construct PP/HRP enzyme electrode,and its electrochemical behaviour was studied.In the deoxygenated phosphate buffer,the PP/HRP electrode showed an accelerated H_2O_2 reduction,which was attributed to the direct electron transfer of the adduct of HRP with H_2O_2.The simultaneous immobilization of HRP and K_4Fe(CN)_6 into the polypyrrole(PP) polymer and the electrochemical behaviour of as-formed enzyme electrodes were investigated.It was confirmed that,the existence of K_4Fe(CN)_6 in the polymer enabled the reduction potential of H_2O_2 to strongly shift to positive so that H_2O_2 could be detected at-0.05 V.The related process was explained in terms of indirect redox catalysis.
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