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Biosensor for the determination of phenols based on Cross-Linked Enzyme Crystals (CLEC) of laccase

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dc.contributor.author Jegan Roy, J
dc.contributor.author Emilia Abraham, T
dc.contributor.author Abhijith, K S
dc.contributor.author Sujith Kumar, P V
dc.contributor.author Thakur, M S
dc.date.accessioned 2015-08-05T11:27:21Z
dc.date.available 2015-08-05T11:27:21Z
dc.date.issued 2005
dc.identifier.citation Biosensors and Bioelectronics 21(1):206–211; Jul 2005 en_US
dc.identifier.issn 0956-5663
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1894
dc.description.abstract Cross-linked enzyme crystals (CLECs) are a versatile form of biocatalyst that can also be used for biosensor application. Laccase from Trametes versicolor (E.C.1.10.3.2) was crystallized, cross-linked and lyophilized with beta-cyclodextrin. The CLEC laccase was found to be highly active towards phenols like 2-amino phenol, guaiacol, catechol, pyrogallol, catechin and ABTS (non-phenolic). The CLEC laccase was embedded in 30% polyvinylpropylidone (PVP) gel and mounted into an electrode to make the sensor. The biosensor was used to detect the phenols in 50-1000 mu mol concentration level. Phenols with lower molecular weight such as 2-amino phenol, catechol and pyrogallol gave a short response time where as the higher molecular weight substrates like catechin and ABTS had comparatively a long response time. The optimum pH of the analyte was 5.5-6.0 when catechol was used as substrate. The CLEC laccase retained good activity for over 3 months. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject CLEC en_US
dc.subject Laccase en_US
dc.subject Biosensor en_US
dc.subject Cross-linking en_US
dc.subject Glutaraldehyde en_US
dc.title Biosensor for the determination of phenols based on Cross-Linked Enzyme Crystals (CLEC) of laccase en_US
dc.type Article en_US


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