| Literature DB >> 35138676 |
Pratchaya Watthaisong1, Philaiwarong Kamutira2, Chatchai Kesornpun1, Vinutsada Pongsupasa1, Jittima Phonbuppha1, Ruchanok Tinikul2, Somchart Maenpuen3, Thanyaporn Wongnate1, Ryo Nishihara4, Yoshihiro Ohmiya4, Pimchai Chaiyen1.
Abstract
D-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.Entities:
Keywords: Dehalogenase; Luciferase; Luciferin; Luminescence; Organophosphate
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Year: 2022 PMID: 35138676 DOI: 10.1002/anie.202116908
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336