Please use this identifier to cite or link to this item: https://doi.org/10.4014/jmb.1202.02040
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dc.titleImmobilization of a mediator onto carbon cloth electrode and employment of the modified electrode to an electroenzymatic bioreactor
dc.contributor.authorJeong, E.-S.
dc.contributor.authorSathishkumar, M.
dc.contributor.authorJayabalan, R.
dc.contributor.authorJeong, S.-H.
dc.contributor.authorPark, S.-Y.
dc.contributor.authorMun, S.-P.
dc.contributor.authorYun, S.-E.
dc.date.accessioned2014-10-16T06:27:48Z
dc.date.available2014-10-16T06:27:48Z
dc.date.issued2012-10
dc.identifier.citationJeong, E.-S., Sathishkumar, M., Jayabalan, R., Jeong, S.-H., Park, S.-Y., Mun, S.-P., Yun, S.-E. (2012-10). Immobilization of a mediator onto carbon cloth electrode and employment of the modified electrode to an electroenzymatic bioreactor. Journal of Microbiology and Biotechnology 22 (10) : 1406-1411. ScholarBank@NUS Repository. https://doi.org/10.4014/jmb.1202.02040
dc.identifier.issn10177825
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/92858
dc.description.abstract5,5'-Dithiobis(2-nitrobenzoic acid) (DTNB) was selected as an electron transfer mediator and was covalently immobilized onto high porosity carbon cloth to employ as a working electrode in an electrochemical NAD+-regeneration process, which was coupled to an enzymatic reaction. The voltammetric behavior of DTNB attached to carbon cloth resembled that of DTNB in buffered aqueous solution, and the electrocatalytic anodic current grew continuously upon addition of NADH at different concentrations, indicating that DTNB is immobilized to carbon cloth effectively and the immobilized DTNB is active as a soluble one. The bioelectrocatalytic NAD+ regeneration was coupled to the conversion of L-glutamate into α-ketoglutarate by L-glutamate dehydrogenase within the same microreactor. The conversion at 3 mM monosodium glutamate was very rapid, up to 12 h, to result in 90%, and then slow up to 24 h, showing 94%, followed by slight decrease. Low conversion was shown when substrate concentration exceeding 4 mM was tested, suggesting that L-glutamate dehydrogenase is inhibited by α-ketoglutarate. However, our electrochemical NAD+ regeneration procedure looks advantageous over the enzymatic procedure using NADH oxidase, from the viewpoint of reaction time to completion. © The Korean for Microbiology and Biotechnolog.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.4014/jmb.1202.02040
dc.sourceScopus
dc.subjectα-ketoglutarate
dc.subjectDTNB-modified carbon cloth
dc.subjectElectrochemical NAD+ regeneration
dc.subjectElectroenzymatic bioreactor
dc.subjectL-glutamate dehydrogenase
dc.subjectMonosodium glutamate
dc.typeArticle
dc.contributor.departmentSINGAPORE-DELFT WATER ALLIANCE
dc.description.doi10.4014/jmb.1202.02040
dc.description.sourcetitleJournal of Microbiology and Biotechnology
dc.description.volume22
dc.description.issue10
dc.description.page1406-1411
dc.description.codenJOMBE
dc.identifier.isiut000310481400014
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