Immobilisation of enzymes on poly(aniline)-poly(anion) composite films. Preparation of bioanodes for biofuel cell applications

Bioelectrochemistry

Volumn 55, Issue 1-2, 2002, Pages 13-15

  Simon, Evelyne ^a   Halliwell, Catherine M ^b   Toh, Chee Seng ^a   Cass, Anthony E G ^b   Bartlett, Philip N ^a  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^b IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

Biofuel cell; Enzyme immobilisation; NADH; Poly(aniline) composite films

Indexed keywords

BIOSENSORS; ELECTRODES; FUEL CELLS; POLYMERS; THIN FILMS;

BIOANODES;

ENZYME IMMOBILIZATION;

BIOFUEL; LACTATE DEHYDROGENASE; LACTIC ACID; MERCUROUS CHLORIDE; MUTANT PROTEIN; NICOTINAMIDE ADENINE DINUCLEOTIDE; POLYACRYLIC ACID; POLYANILINE; POLYANION; POLYHISTIDINE; POLYVINYLSULFONATE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBOXY TERMINAL SEQUENCE; ELECTRODE; ENZYME IMMOBILIZATION; FILM; OXIDATION;

ANILINE COMPOUNDS; ANIMALS; ANIONS; ELECTRODES; ENZYMES, IMMOBILIZED; L-LACTATE DEHYDROGENASE; LACTIC ACID; NAD; POLYMERS; RABBITS;

PAA;

EID: 0036148091     PISSN: 15675394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1567-5394(01)00160-8     Document Type: Article

References (8)

1. Co-immobilization of lactate oxidase and lactate dehydrogenase on conducting polyaniline films
2. Immobilization of lactate dehydrogenase on electrochemically prepared polyaniline films
3. Immobilization of lactate dehydrogenase on electrochemically prepared polypyrrole-polyvinylsulphonate composite films for application to lacate sensors
4. Introduction of a poly(histidine) tag in L-lactate dehydrogenase produces a mixture of active and inactive molecules
5. Oxidation of β-nicotinamide adenine dinucleotide (NADH) at poly(aniline)-coated electrode
6. Poly(aniline)-poly(acrylate) composite films as modified electrodes for the oxidation of NADH
7. Spectroscopic evaluation of protein affinity binding at polymeric biosensor films
8. Combination of electrochemistry with concurrent reduction and substitution chemistry to provide a facile and verstatile tool for preparing highly functionalized polyanilines