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Comparative analysis and validation of the malachite green assay for the high throughput biochemical characterization of terpene synthases

Terpenes are the largest group of natural products with important and diverse biological roles, while of tremendous economic value as fragrances, flavours and pharmaceutical agents. Class-I terpene synthases (TPSs), the dominant type of TPS enzymes, catalyze the conversion of prenyl diphosphates to...

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Detalles Bibliográficos
Autores principales: Vardakou, Maria, Salmon, Melissa, Faraldos, Juan A., O’Maille, Paul E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472957/
https://www.ncbi.nlm.nih.gov/pubmed/26150952
http://dx.doi.org/10.1016/j.mex.2014.08.007
Descripción
Sumario:Terpenes are the largest group of natural products with important and diverse biological roles, while of tremendous economic value as fragrances, flavours and pharmaceutical agents. Class-I terpene synthases (TPSs), the dominant type of TPS enzymes, catalyze the conversion of prenyl diphosphates to often structurally diverse bioactive terpene hydrocarbons, and inorganic pyrophosphate (PPi). To measure their kinetic properties, current bio-analytical methods typically rely on the direct detection of hydrocarbon products by radioactivity measurements or gas chromatography–mass spectrometry (GC–MS). In this study we employed an established, rapid colorimetric assay, the pyrophosphate/malachite green assay (MG), as an alternative means for the biochemical characterization of class I TPSs activity. • We describe the adaptation of the MG assay for turnover and catalytic efficiency measurements of TPSs. • We validate the method by direct comparison with established assays. The agreement of k(cat)/K(M) among methods makes this adaptation optimal for rapid evaluation of TPSs. • We demonstrate the application of the MG assay for the high-throughput screening of TPS gene libraries.