Luciferin Synthesis and Pesticide Detection by Luminescence Enzymatic Cascades

dc.contributor.authorWatthaisong P.
dc.contributor.authorKamutira P.
dc.contributor.authorKesornpun C.
dc.contributor.authorPongsupasa V.
dc.contributor.authorPhonbuppha J.
dc.contributor.authorTinikul R.
dc.contributor.authorMaenpuen S.
dc.contributor.authorWongnate T.
dc.contributor.authorNishihara R.
dc.contributor.authorOhmiya Y.
dc.contributor.authorChaiyen P.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T16:55:08Z
dc.date.available2023-06-18T16:55:08Z
dc.date.issued2022-04-11
dc.description.abstractD-Luciferin (D-LH2), a substrate of firefly luciferase (Fluc), is important for a wide range of bioluminescence applications. This work reports a new and green method using enzymatic reactions (HELP, HadA Enzyme for Luciferin Preparation) to convert 19 phenolic derivatives to 8 D-LH2 analogues with ≈51 % yield. The method can synthesize the novel 5′-methyl-D-LH2 and 4′,5′-dimethyl-D-LH2, which have never been synthesized or found in nature. 5′-Methyl-D-LH2 emits brighter and longer wavelength light than the D-LH2. Using HELP, we further developed LUMOS (Luminescence Measurement of Organophosphate and Derivatives) technology for in situ detection of organophosphate pesticides (OPs) including parathion, methyl parathion, EPN, profenofos, and fenitrothion by coupling the reactions of OPs hydrolase and Fluc. The LUMOS technology can detect these OPs at parts per trillion (ppt) levels. The method can directly detect OPs in food and biological samples without requiring sample pretreatment.
dc.identifier.citationAngewandte Chemie - International Edition Vol.61 No.16 (2022)
dc.identifier.doi10.1002/anie.202116908
dc.identifier.eissn15213773
dc.identifier.issn14337851
dc.identifier.pmid35138676
dc.identifier.scopus2-s2.0-85124903095
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/84095
dc.rights.holderSCOPUS
dc.subjectChemical Engineering
dc.titleLuciferin Synthesis and Pesticide Detection by Luminescence Enzymatic Cascades
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124903095&origin=inward
oaire.citation.issue16
oaire.citation.titleAngewandte Chemie - International Edition
oaire.citation.volume61
oairecerif.author.affiliationVidyasirimedhi Institute of Science and Technology
oairecerif.author.affiliationNational Institute of Advanced Industrial Science and Technology
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationBurapha University

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