Electrochemical consideration on the optimum pH of bilirubin oxidase

被引:37
|
作者
Otsuka, Kaori
Sugihara, Takayasu
Tsujino, Yoshio
Osakai, Toshiyuki
Tamiya, Eiichi
机构
[1] Osaka Univ, Grad Sch Engn, Dept Appl Phys, Suita, Osaka 5650871, Japan
[2] Japan Adv Inst Sci & Technol, Sch Math Sci, Nomi, Ishikawa 9231292, Japan
[3] Mandom Corp, Cent Res Labs, Osaka 5408530, Japan
[4] Kobe Univ, Grad Sch Sci, Dept Chem, Kobe, Hyogo 6578501, Japan
关键词
bilirubin oxidase; direct electron transfer; highly oriented pyrolytic graphite electrode; redox potential; optimum pH;
D O I
10.1016/j.ab.2007.06.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Steady-state current-potential curves were obtained for the direct electron transfer (DET) of bilirubin oxidase (BOD) at a highly oriented pyrolytic graphite electrode, and the theoretical analysis based on nonlinear regression enabled us to determine the formal redox potential (E degrees') of BOD in a wide pH range of 2.0 to 8.5. Cyclic voltarnmetric measurements were also performed for substrates, including p-phenylenediamine (PPD), o-aminophenol (OAP), and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), and their E degrees values or the anodic peak potentials (for OAP) were determined at various pH values. The difference in the redox potentials between BOD and substrates (Delta E degrees') showed a maximum at pH 6.5 to 8.0, pH 6.5 to 8.0, and pH 3.5 to 4.5 for PPD, OAP, and ABTS, respectively. These pH ranges should be thermodynamically most favorable for the electron transfer between BOD and the respective substrates. In practice, the pH ranges showing a maximum Delta E degrees' corresponded well with the optimum pH values for the O-2, reduction activity of BOD: pH 6.5 to 7.5, pH 8.0 to 8.5, and pH 4.0 for PPD, OAP, and ABTS, respectively. Thus, it was suggested that Delta E degrees' should be one of the primary factors determining the activity of BOD with the substrates. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 106
页数:9
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