Abstract

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 kcat/KM 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.

Highlights

  • Terpene synthases (TPSs) catalyze the transformation of linear, achiral isoprenoid diphosphates into structurally diverse, often polycyclic and stereochemically complex terpene hydrocarbons

  • We describe the adaptation of the Malachite green (MG) assay for turnover and catalytic efficiency measurements of TPSs

  • We demonstrate the application of the MG assay for the high-throughput screening of TPS gene libraries. ß 2014 The Authors

Read more

Summary

Contents lists available at ScienceDirect

A Department of Metabolic Biology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, United Kingdom b Food and Health Programme, Institute of Food Research, Norwich Research Park, Norwich NR4 7UA, United Kingdom c School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, United Kingdom

GRAPHICAL ABSTRACT
Substrate and reagents
Protein expression and purification
Radioactive enzyme assay
Product identification
Background
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.