Enzymatic determination of phenols using peanut peroxidase

被引:29
作者
Bagirova, NA
Shekhovtsova, TN
van Huystee, RB
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[2] Univ Western Ontario, Dept Plant Sci, London, ON N6A 5B7, Canada
基金
俄罗斯基础研究基金会;
关键词
peanut peroxidase; determination of phenols; aryldiamines oxidation;
D O I
10.1016/S0039-9140(01)00544-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The influence of phenol and its derivatives on the kinetics of oxidation of aryldiamines (indicator-substrates) catalyzed by novel plant peroxidase-cationic peanut peroxidase-was studied. The character of influence of phenols on the kinetics of enzymatic oxidation of benzidine, o-dianisidine, and 3,3',5,5'-tetramethyibenzidine (TMB) with hydrogen peroxide was found to depend on a correlation between redox properties of phenols and the indicator-substrate of peroxidase. Thus, the catalytic activity of peanut peroxidase is inhibited by phenols with redox potentials higher than that of aryldiamines mentioned above, whereas phenols with potentials below those of aryldiamines, play the role of second substrates of the enzyme. The enzymatic procedures for the determination of numerous phenols on the level of their concentrations 0.05-80 muM were developed using the reactions of benzidine, o-dianisidine, and TMB oxidation. Different analytical signals-the indicator reaction rate and the induction period duration-were used for the determination of phenols, belonging to various groups-the inhibitors and second substrates of the enzyme, respectively. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1151 / 1164
页数:14
相关论文
共 26 条
[1]  
Bagirova NA, 1999, KINET CATAL+, V40, P241
[2]   STRUCTURAL INFLUENCE OF CALCIUM ON THE HEME CAVITY OF CATIONIC PEANUT PEROXIDASE AS DETERMINED BY H-1-NMR SPECTROSCOPY [J].
BARBER, KR ;
MARANON, MJR ;
SHAW, GS ;
VANHUYSTEE, RB .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 232 (03) :825-833
[3]   STEADY-STATE KINETICS OF PEROXIDASE WITH 2,2'-AZINO-DI-(3-ETHYLBENZTHIAZOLINE-6-SULPHONIC ACID) AS CHROMOGEN [J].
CHILDS, RE ;
BARDSLEY, WG .
BIOCHEMICAL JOURNAL, 1975, 145 (01) :93-103
[4]   CHEMICAL AND ENZYMATIC INTERMEDIATES IN THE PEROXIDATION OF ORTHO-DIANISIDINE BY HORSERADISH-PEROXIDASE .1. SPECTRAL PROPERTIES OF THE PRODUCTS OF DIANISIDINE OXIDATION [J].
CLAIBORNE, A ;
FRIDOVICH, I .
BIOCHEMISTRY, 1979, 18 (11) :2324-2329
[5]   TISSUE-BASED AND MICROBE-BASED ELECTROCHEMICAL DETECTORS FOR LIQUID-CHROMATOGRAPHY [J].
CONNOR, MP ;
WANG, J ;
KUBIAK, W ;
SMYTH, MR .
ANALYTICA CHIMICA ACTA, 1990, 229 (01) :139-143
[6]   Identification of the colored guaiacol oxidation product produced by peroxidases [J].
Doerge, DR ;
Divi, RL ;
Churchwell, MI .
ANALYTICAL BIOCHEMISTRY, 1997, 250 (01) :10-17
[7]   An indirect method of studying the oxidation-reduction potentials of unstable systems, including those from the phenols and amines [J].
Fieser, LF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1930, 52 :5204-5241
[8]  
GALLATI H, 1977, J CLIN CHEM CLIN BIO, V15, P699
[9]   DETERMINATION OF PHENOLS USING VARIOUS PEROXIDASES [J].
GAZARYAN, IG ;
LOGINOV, DB ;
LIALULIN, AL ;
SHEKHOVTSOVA, TN .
ANALYTICAL LETTERS, 1994, 27 (15) :2917-2930
[10]   Determination of zinc(II) by the reactivation of the apoenzymes of alkaline phosphatases from diverse sources [J].
Grishina, LE ;
Poskonnaya, NA ;
Shekhovtsova, TN .
ANALYTICAL LETTERS, 2000, 33 (11) :2197-2217