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• W1569196532 abstract "The two factors important when optimization of enzyme immobilization for the fabrication of biosensor are: activity and stability. The present study investigates the 2 factors when laccase was immobilized on various supports by different methods. Immobilization of partially purified laccase showed that enzyme expressed 100% activity when immobilized on the nitrocellulose membrane. pH and temperature optimum of immobilized laccase was 6.5 and 55°C respectively, when syringaldazine was used as a substrate. Immobilized laccase on nitrocellulose membrane was 100% stable at 4°C -30°C for three months. At 60°C enzyme showed 50% stability after 30 min. Immobilized laccase showed best response with syringaldazine which gave reaction even at 1 to 5μM concentration. Immobilized laccase gave response to catechol, catechin and L-methyl DOPA in the range of 40 to 90, 40 to 60, 30 to 70 µM respectively. ABTS (2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonate)) also showed response to the laccase from 0.1 to 0.2 mM." @default.
• W1569196532 created "2016-06-24" @default.
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• W1569196532 date "2010-01-01" @default.
• W1569196532 modified "2023-09-26" @default.
• W1569196532 title "Characterization of immobilized laccase from γ-proteobacterium JB: Approach towards the development of biosensor for the detection of phenolic compounds" @default.
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• W1569196532 doi "https://doi.org/10.17485/ijst/2010/v3i1/29643" @default.
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