Literature DB >> 15556559

A single-vial analytical and quantitative gas chromatography-mass spectrometry assay for terpene synthases.

Paul E O'Maille1, Joe Chappell, Joseph P Noel.   

Abstract

A quantitative assay for the analysis of sesquiterpene synthases, wherein each reaction mixture is formulated in glass gas chromatography vials, overlaid with organic solvent such as ethyl acetate, and subsequently vortexed to extract hydrocarbon reaction products into the organic phase after a suitable incubation period, was developed. The product-enriched organic phase is then sampled in an automated fashion and injected directly into a gas chromatograph-mass spectrometer without further workup for analysis and quantification of hydrocarbon products. Application of the vial assay to the analysis of amorpha-4,11-diene synthase (ADS), a sesquiterpene synthase, demonstrated the sensitivity of the assay for detection of major and minor reaction products and most notably for the identification of several sesquiterpene products that had escaped previous detection. A steady-state kinetic analysis of tobacco 5-epi-aristolochene synthase (TEAS), another sesquiterpene synthase, validated the quantitative nature of the assay, providing an alternative means to the established method of using radiolabeled substrate, extraction, and scintillation counting. This simplified assay provides a standardized method to facilitate analysis of terpene synthases and diverse mutant enzyme libraries by supplanting the common practice of using larger scale reactions, multiple extractions, and evaporative concentration of the organic phase prior to gas chromatography-mass spectrometry (GC-MS) analysis.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15556559     DOI: 10.1016/j.ab.2004.09.011

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  33 in total

1.  Mutagenesis of isopentenyl phosphate kinase to enhance geranyl phosphate kinase activity.

Authors:  Mark F Mabanglo; Jian-Jung Pan; Binita Shakya; C Dale Poulter
Journal:  ACS Chem Biol       Date:  2012-05-10       Impact factor: 5.100

Review 2.  Total (bio)synthesis: strategies of nature and of chemists.

Authors:  Alexandra A Roberts; Katherine S Ryan; Bradley S Moore; Tobias A M Gulder
Journal:  Top Curr Chem       Date:  2010

3.  Computational design and selections for an engineered, thermostable terpene synthase.

Authors:  Juan E Diaz; Chun-Shi Lin; Kazuyoshi Kunishiro; Birte K Feld; Sara K Avrantinis; Jonathan Bronson; John Greaves; Jeffery G Saven; Gregory A Weiss
Journal:  Protein Sci       Date:  2011-08-02       Impact factor: 6.725

4.  Functional and Structural Characterization of a (+)-Limonene Synthase from Citrus sinensis.

Authors:  Benjamin R Morehouse; Ramasamy P Kumar; Jason O Matos; Sarah Naomi Olsen; Sonya Entova; Daniel D Oprian
Journal:  Biochemistry       Date:  2017-03-15       Impact factor: 3.162

5.  Structural Characterization of Early Michaelis Complexes in the Reaction Catalyzed by (+)-Limonene Synthase from Citrus sinensis Using Fluorinated Substrate Analogues.

Authors:  Ramasamy P Kumar; Benjamin R Morehouse; Jason O Matos; Karan Malik; Hongkun Lin; Isaac J Krauss; Daniel D Oprian
Journal:  Biochemistry       Date:  2017-03-15       Impact factor: 3.162

6.  Identification of genes in Thuja plicata foliar terpenoid defenses.

Authors:  Adam J Foster; Dawn E Hall; Leanne Mortimer; Shelley Abercromby; Regine Gries; Gerhard Gries; Jörg Bohlmann; John Russell; Jim Mattsson
Journal:  Plant Physiol       Date:  2013-02-06       Impact factor: 8.340

7.  Structural elucidation of cisoid and transoid cyclization pathways of a sesquiterpene synthase using 2-fluorofarnesyl diphosphates.

Authors:  Joseph P Noel; Nikki Dellas; Juan A Faraldos; Marylin Zhao; B Andes Hess; Lidia Smentek; Robert M Coates; Paul E O'Maille
Journal:  ACS Chem Biol       Date:  2010-04-16       Impact factor: 5.100

8.  Mutation of archaeal isopentenyl phosphate kinase highlights mechanism and guides phosphorylation of additional isoprenoid monophosphates.

Authors:  Nikki Dellas; Joseph P Noel
Journal:  ACS Chem Biol       Date:  2010-06-18       Impact factor: 5.100

9.  The bouquet of grapevine (Vitis vinifera L. cv. Cabernet Sauvignon) flowers arises from the biosynthesis of sesquiterpene volatiles in pollen grains.

Authors:  Diane M Martin; Omid Toub; Angela Chiang; Bernard C Lo; Sebastian Ohse; Steven T Lund; Jörg Bohlmann
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-09       Impact factor: 11.205

10.  Evolution of conifer diterpene synthases: diterpene resin acid biosynthesis in lodgepole pine and jack pine involves monofunctional and bifunctional diterpene synthases.

Authors:  Dawn E Hall; Philipp Zerbe; Sharon Jancsik; Alfonso Lara Quesada; Harpreet Dullat; Lina L Madilao; Macaire Yuen; Jörg Bohlmann
Journal:  Plant Physiol       Date:  2012-12-12       Impact factor: 8.340

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.