A High‐Throughput Assay for Arylamine Halogenation Based on a Peroxidase‐Mediated Quinone–Amine Coupling with Applications in the Screening of Enzymatic Halogenations. Issue 50 (15th October 2014)

• Record Type: Journal Article
• Authors: Hosford, Joseph; Shepherd, Sarah A.; Micklefield, Jason; Wong, Lu Shin
• Is Part Of: Chemistry. Volume 20:Issue 50(2014)
• Page Start: 16759
• Page End: 16763
• Publication Date: 2014-10-15
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201403953
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Arylhalides are important building blocks in many fine chemicals, pharmaceuticals and agrochemicals, and there has been increasing interest in the development of more "green" halogenation methods based on enzyme catalysis. However, the screening and development of new enzymes for biohalogenation has been hampered by a lack of high‐throughput screening methods. Described herein is the development of a colorimetric assay for detecting both chemical and enzymatic arylamine halogenation reactions in an aqueous environment. The assay is based on the unique UV/Vis spectrum created by the formation of an <italic>ortho</italic>‐benzoquinone‐amine adduct, which is produced by the peroxidase‐catalysed benzoquinone generation, followed by Michael addition of either a halogenated or non‐halogenated arylamine. This assay is sensitive, rapid and amenable to high‐throughput screening platforms. We have also shown this assay to be easily coupled to a flavin‐dependent halogenase, which currently lacks any convenient colorimetric assay, in a "one‐pot" workflow.</p> </abstract>