Sensitive amperometric biosensor for the determination of biogenic and synthetic amines using pea seedling amine oxidase: a novel approach for enzyme immobilisation

Varování

Publikace nespadá pod Pedagogickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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WIMMEROVÁ Michaela MACHOLÁN Lumír

Rok publikování 1999
Druh Článek v odborném periodiku
Časopis / Zdroj Biosensors & Bioelectronics
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
Obor Biochemie
Klíčová slova biosensor; amine oxidase; immobilisation
Popis We prepared a new inorganic sorbent based on modified triazine (2-[4,6-bis (aminoethylamine)-1,3,5-triazine]-Silasorb; BAT-Silasorb) which binds pea seedlings amine oxidase (PSAO) very tightly without loss of its catalytic activity. This unique feature as well as the wide substrate specificity of PSAO was successfully utilised in the construction of an amperometric biosensor based on a carbon paste electrode for the fast and sensitive detection of various amines at a formal potential 0 mV versus Ag:AgCl reference electrode. The reaction layer of the biosensor is created by the direct immobilisation of PSAO at the electrode surface via affinity carrier BAT-Silasorb. Used arrangement facilitates a simple restoration of the inactive biosensor. An amperometric signal results from horseradish peroxidase catalysed reduction of H2O2, a secondary product of the oxidative deamination of amines, catalysed by PSAO. The sensor was used for the basic characterisation of 55 biogenic and synthetic amines, from numerous mono-, di- and polyamines to various hydroxy-, thio-, benzyl- and aromatic derivatives in order to establish its suitability as a postcolumn detector. Its high sensitivity to putrescine, a limit of detection of 10 nmol/l (determined with respect to a signal-to-noise ratio 3:1), a linear range of current response to 0.01-100 mmol/l concentration of substrate and good reproducibility all indicate that the sensor could be applied to future industrial and clinical analyses.
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