| Abstract | Bacterial cyclopropane synthases catalyze the cyclopropanation of unsaturated fatty acids by transferring a methylene group from S-adenosyl-L-methionine (AdoMet) to the double bond of the lipids. Mycobacterium tuberculosis cyclopropane synthases have been shown to be implicated in pathogenicity, and therefore constitute attractive targets for the development of new drugs against tuberculosis. However, no in vitro assay for these cyclopropane synthases has yet been described. The homologous E. coli enzyme, cyclopropane fatty acid synthase, is thus a valuable model for inhibitor screening. Here, we report the adaptation to the E. coli CFAS of a previously reported enzyme-coupled colorimetric assay based on the quantification, using Ellman's reagent, of homocysteine produced from S-adenosyl-L-homocysteine, a product of the reaction, in the presence of AdoHcy nucleosidase and S-ribosylhomocysteinase. Using this assay we measured the kinetic parameters for CFAS: Km (AdoMet)=80 microM, kcat=4 min(-1). We adapted this assay to microtiter plates and tested 15 potential inhibitors of CFAS. Among them, two new inhibitors, a lipid analog and a thioether analog of AdoHcy, showed IC50 of 4 microM and 11 microM, respectively. This new assay will thus be useful for high-throughput screening of compound libraries for discovering novel antituberculous drug candidates. |
| Authors | Dominique Guianvarc'h, Thierry Drujon, Thearina Ear Leang, Fabienne Courtois, Olivier Ploux
(Affiliation: Synthèse Structure et Fonction de Molécules Bioactives, UMR7613 CNRS-UPMC, Université Pierre et Marie Curie, boîte 182, 4, place Jussieu, F-75252 Paris cedex 05, France.)
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| Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 1764
Issue 8
Pg. 1381-8
(Aug 2006)
ISSN: 0006-3002 Netherlands |
| PMID | 16872920
(Publication Type: Journal Article)
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| Chemical References |
- Enzyme Inhibitors
- Methyltransferases
- cyclopropane synthetase
|
| Topics |
- Colorimetry
(methods)
- Drug Design
- Drug Evaluation, Preclinical
- Enzyme Inhibitors
(chemistry, pharmacology)
- Escherichia coli K12
(enzymology)
- Kinetics
- Methyltransferases
(antagonists & inhibitors)
- Molecular Structure
- Spectrophotometry
|
