Characterization of acetohydroxyacid synthase from Mycobacterium tuberculosis and the identification of its new inhibitor from the screening of a chemical library.

Abstract

Acetohydroxyacid synthase (AHAS) is a thiamin diphosphate- (ThDP-) and FAD-dependent enzyme that catalyzes the first common step in the biosynthetic pathway of the branched-amino acids such as leucine, isoleucine, and valine. The genes of AHAS from Mycobacterium tuberculosis were cloned, and overexpressed in E. coli and purified to homogeneity. The purified AHAS from M. tuberculosis is effectively inhibited by pyrazosulfuron ethyl (PSE), an inhibitor of plant AHAS enzyme, with the IC(50) (inhibitory concentration 50%) of 0.87 microM. The kinetic parameters of M. tuberculosis AHAS were determined, and an enzyme activity assay system using 96-well microplate was designed. After screening of a chemical library composed of 5600 compounds using the assay system, a new class of AHAS inhibitor was identified with the IC(50) in the range of 1.8-2.6 microM. One of the identified compounds (KHG20612) further showed growth inhibition activity against various strains of M. tuberculosis. The correlation of the inhibitory activity of the identified compound against AHAS to the cell growth inhibition activity suggested that AHAS might be served as a target protein for the development of novel anti-tuberculosis therapeutics.

• Authors: Kyoung-Jae Choi, Yeon Gyu Yu, Hoh Gyu Hahn, Jung-Do Choi, Moon-Young Yoon
• Journal: FEBS letters (FEBS Lett) Vol. 579 Issue 21 Pg. 4903-10 (Aug 29 2005) ISSN: 0014-5793 [Print] England
• PMID: 16111681 (Publication Type: Journal Article)

Chemical References

• Amino Acids
• Antitubercular Agents
• Bacterial Proteins
• Herbicides
• Pyrazoles
• Pyrimidines
• ethyl 5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-1-methylpyrazole-4-carboxylate
• Acetolactate Synthase

Topics

• Acetolactate Synthase (antagonists & inhibitors, genetics, isolation & purification, metabolism)
• Amino Acids (chemistry, metabolism)
• Antitubercular Agents (metabolism)
• Bacterial Proteins (antagonists & inhibitors, genetics, isolation & purification, metabolism)
• Biological Assay
• Drug Design
• Herbicides (chemistry, metabolism)
• Microbial Sensitivity Tests
• Molecular Structure
• Mycobacterium tuberculosis (enzymology, genetics)
• Pyrazoles (metabolism)
• Pyrimidines (metabolism)