Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/99705
DC FieldValue
dc.titleLinamarin Sensors: Interference-Based Sensing of Linamarin Using Linamarase and Peroxidase
dc.contributor.authorTatsuma, T.
dc.contributor.authorTani, K.
dc.contributor.authorOyama, N.
dc.contributor.authorYeoh, H.-H.
dc.date.accessioned2014-10-27T07:03:21Z
dc.date.available2014-10-27T07:03:21Z
dc.date.issued1996-09-01
dc.identifier.citationTatsuma, T.,Tani, K.,Oyama, N.,Yeoh, H.-H. (1996-09-01). Linamarin Sensors: Interference-Based Sensing of Linamarin Using Linamarase and Peroxidase. Analytical Chemistry 68 (17) : 2946-2950. ScholarBank@NUS Repository.
dc.identifier.issn00032700
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/99705
dc.description.abstractAn interference-based linamarin sensor is developed. Horseradish peroxidase (HRP) is adsorbed on a pyrolytic graphite (PG) electrode, and then linamarase from cassava is cross-linked with glutaraldehyde on the electrode surface. The prepared bienzyme electrode is poised at -300 mV vs Ag/AgCl for 40 s to reduce dissolved O2 to H2O2 at the PG surface. The potential is then stepped to 0 mV, at which point the accumulated H2O2 is reduced, though the O2 reduction does not proceed. Since the H2O2 reduction is catalyzed by HRP, the transient cathodic current is inhibited by cyanide, which is liberated from linamarin by linamarase. Therefore, the transient current is a function of the linamarin concentration. This sensor responds to 1 × 10-5-5 × 10-3 M linamarin and can estimate a linamarin concentration of a cassava extract.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBOTANY
dc.description.sourcetitleAnalytical Chemistry
dc.description.volume68
dc.description.issue17
dc.description.page2946-2950
dc.description.codenANCHA
dc.identifier.isiutNOT_IN_WOS
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