Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9405
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dc.contributor.authorDas, Apurba Kumaren_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:51Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:51Z-
dc.date.issued2013-
dc.identifier.citationRasale, D. B., Maity, I., & Das, A. K. (2013). Colorimetric enzyme sensing assays via in situ synthesis of gold nanoparticles. Journal of Cluster Science, 24(4), 1163-1170. doi:10.1007/s10876-013-0606-zen_US
dc.identifier.issn1040-7278-
dc.identifier.otherEID(2-s2.0-84891664053)-
dc.identifier.urihttps://doi.org/10.1007/s10876-013-0606-z-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9405-
dc.description.abstractWe report a successful facile and novel approach for in situ synthesis of gold nanoparticles (AuNPs) via enzymatic dephosphorylation reaction at room temperature. Fmoc-tyrosine phosphate and cytidine-5-mono phosphate are used to sense the activities of an enzyme alkaline phosphatase. Formation of AuNps is highly selective towards biomolecules and it is readily detected colorimetrically and UV-Vis analysis. In this procedure, dephosphorylated product plays both roles as reducing and stabilizing agent to direct the formation of AuNPs in aqueous media. Transmission electron microscopic study reveales that hexagonal AuNPs were synthesized by using Fmoc-tyrosine phosphate and alkaline phosphatase. Wide angle X-ray scattering data confirms the formation of AuNPs. FT-IR studies confirm that biomolecules play crucial role to stabilize the AuNPs by molecular interactions with the surface of AuNPs. In situ synthesized AuNPs are applied for the sensing of enzyme activity. © 2013 Springer Science+Business Media New York.en_US
dc.language.isoenen_US
dc.sourceJournal of Cluster Scienceen_US
dc.titleColorimetric Enzyme Sensing Assays via In Situ Synthesis of Gold Nanoparticlesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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