Ca2+ enhanced electrocatalytic oxidation of NADH by immobilized nitro-fluorenones

被引:40
作者
Mano, N [1 ]
Kuhn, A [1 ]
机构
[1] Ecole Natl Super Chim & Phys Bordeaux, Lab Anal Chim Reconnaissance Mol, F-33402 Talence, France
关键词
modified electrodes; electrocatalysis; NADH oxidation; fluorenone; biosensors;
D O I
10.1016/S1388-2481(99)00097-1
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Glassy carbon electrodes are modified with nitro-fluorenone derivatives, a new family of catalyst precursors for electrocatalytic nicotinamide adenine dinucleotide (NADH) oxidation. One of the nitro substituents is electrochemically converted into a reversible NO/NHOH redox couple producing a very efficient mediator for the electrooxidation of the coenzyme. The catalytic efficiency can be enhanced by adding Ca2+ ions to the electrolyte, leading most likely to a specific complexation with the phosphate groups of the coenzyme. This makes NADH less hydrophilic and therefore favors its contact with the organic catalyst monolayer. A further increase in catalytic activity is obtained by introducing a carboxy group into the catalyst molecule. In this case Ca2+ seems to act as a bridging ion between NADH and the catalyst, coordinating their interaction and thus enhancing the electron transfer efficiency. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:497 / 501
页数:5
相关论文
共 11 条
[1]  
[Anonymous], TOPICS CURRENT CHEM
[2]   Electrochemically triggered reaction of a surface-confined reagent:: Mechanistic and EQCM characterization of redox-active self-assembling monolayers derived from 5,5′-dithiobis(2-nitrobenzoic acid) and related materials [J].
Casero, E ;
Darder, M ;
Takada, K ;
Abruña, HD ;
Pariente, F ;
Lorenzo, E .
LANGMUIR, 1999, 15 (01) :127-134
[3]   REVERSIBLE THERMAL INACTIVATION OF THE QUINOPROTEIN GLUCOSE-DEHYDROGENASE FROM ACINETOBACTER-CALCOACETICUS - CA-2+ IONS ARE NECESSARY FOR RE-ACTIVATION [J].
GEIGER, O ;
GORISCH, H .
BIOCHEMICAL JOURNAL, 1989, 261 (02) :415-421
[4]   Model studies on calcium-containing quinoprotein alcohol dehydrogenases.: Catalytic role of Ca2+ for the oxidation of alcohols by coenzyme PQQ (4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-f]quinoline-2,7,9-tricarboxylic acid) [J].
Itoh, S ;
Kawakami, H ;
Fukuzumi, S .
BIOCHEMISTRY, 1998, 37 (18) :6562-6571
[5]   ELECTROCATALYTIC OXIDATION OF REDUCED NICOTINAMIDE COENZYMES AT GOLD AND PLATINUM-ELECTRODE SURFACES MODIFIED WITH A MONOLAYER OF PYRROLOQUINOLINE QUINONE - EFFECT OF CA2+ CATIONS [J].
KATZ, E ;
LOTZBEYER, T ;
SCHLERETH, DD ;
SCHUHMANN, W ;
SCHMIDT, HL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 373 (1-2) :189-200
[6]   ELECTROCHEMICAL STUDY OF PYRROLOQUINOLINE QUINONE COVALENTLY IMMOBILIZED AS A MONOLAYER ONTO A CYSTAMINE-MODIFIED GOLD ELECTRODE [J].
KATZ, E ;
SCHLERETH, DD ;
SCHMIDT, HL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 367 (1-2) :59-70
[7]   Amperometric biosensors based on NAD(P)-dependent dehydrogenase enzymes [J].
Lobo, MJ ;
Miranda, AJ ;
Tunon, P .
ELECTROANALYSIS, 1997, 9 (03) :191-202
[8]  
MANO N, 1999, IN PRESS J ELECTROAN
[9]  
Newman M.S., 1962, ORG SYNTH, V42, P95
[10]   A simple method for examining the electrochemistry of metalloporphyrins and other hydrophobic reactants in thin layers of organic solvents interposed between graphite electrodes and aqueous solutions [J].
Shi, CN ;
Anson, FC .
ANALYTICAL CHEMISTRY, 1998, 70 (15) :3114-3118