ISSN:
0268-2575
Keywords:
quinohaemoprotein alcohol dehydrogenase
;
enzyme electrodes
;
immobilisation
;
bio-electrochemistry
;
Chemistry
;
Biochemistry and Biotechnology
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Process Engineering, Biotechnology, Nutrition Technology
Notes:
Quinohaemoprotein alcohol dehydrogenase from Comamonas testosteroni (QH-EDH) was immobilised in a redox polymer network of a polyvinylpyridine, partially N-complexed with osmiumbis(bipyridine)chloride. Substrate-dependent electron transfer occurred, indicating that the enzyme was active and that effective electron transport was achieved. It was shown that the enzyme molecular weight is of importance with respect to the enzyme electrode stability. Long term stability and current density of the QH-EDH electrodes were highest when the enzyme was immobilised at pH 10·0 and 4°C, followed by an additional cross-linking step with glutaraldehyde (1%) at pH 7·0. With such an electrode current densities of 40 μA cm-2 were obtained for several primary alcohols. The affinity of the immobilised enzyme for these substrates (Km(app) values) was similar to that of the enzyme in solution. The half-life time of the electrodes was between 50 h and 200 h depending on the time the enzyme was in contact with the substrate. When the immobilised enzyme electrode was operated at temperatures above 37°C the stability decreased. © 1997 SCI.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
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