Combined effect of epigallocatechin gallate and triclosan on enoyl-ACP reductase of Mycobacterium tuberculosis

Biochem Biophys Res Commun. 2008 Mar 28;368(1):12-7. doi: 10.1016/j.bbrc.2007.10.191. Epub 2007 Nov 9.

Abstract

Among the various inhibitors known for enoyl-acyl carrier protein (ACP) reductases, triclosan and green tea catechins are two promising candidates. In the present study, we show, for the first time that epigallocatechin gallate (EGCG), a major component of green tea catechins, inhibits InhA, the enoyl-ACP reductase of Mycobacterium tuberculosis with an IC50 of 17.4muM. EGCG interferes with the binding of NADH to InhA. We also demonstrate that EGCG increased the inhibitory activity of triclosan towards InhA and vice versa. Direct binding assay using [(3)H]EGCG and fluorescence titration assay support the spectrophotometric/kinetic inhibition data. The biochemical data has been explained by docking simulation studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catechin / analogs & derivatives*
  • Catechin / chemistry
  • Catechin / pharmacology
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH) / antagonists & inhibitors*
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH) / chemistry
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH) / metabolism*
  • Enzyme Inhibitors / pharmacology
  • Models, Molecular
  • Molecular Structure
  • Mycobacterium tuberculosis / enzymology*
  • Protein Binding
  • Protein Structure, Tertiary
  • Spectrometry, Fluorescence
  • Triclosan / chemistry
  • Triclosan / pharmacology*

Substances

  • Enzyme Inhibitors
  • Triclosan
  • Catechin
  • epigallocatechin gallate
  • Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)