Anti-malarial drug targets: screening for inhibitors of 2C-methyl-D-erythritol 4-phosphate synthase (IspC protein) in Mediterranean plants

Phytomedicine. 2007 Apr;14(4):242-9. doi: 10.1016/j.phymed.2006.12.018. Epub 2007 Feb 12.

Abstract

The recently discovered non-mevalonate pathway of isoprenoid biosynthesis serves as the unique source of terpenoids in numerous pathogenic eubacteria and in apicoplast-type protozoa, most notably Plasmodium, but is absent in mammalian cells. It is therefore an attractive target for anti-infective chemotherapy. The first committed step of the non-mevalonate pathway is catalyzed by 2C-methyl-D-erythritol 4-phosphate synthase (IspC). Using photometric and NMR spectroscopic assays, we screened extracts of Mediterranean plants for inhibitors of the enzyme. Strongest inhibitory activity was found in leaf extracts of Cercis siliquastrum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldose-Ketose Isomerases / antagonists & inhibitors*
  • Aldose-Ketose Isomerases / chemistry*
  • Amino Acid Sequence
  • Animals
  • Antimalarials / chemistry*
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Humans
  • Malaria, Falciparum / drug therapy
  • Mediterranean Region
  • Molecular Sequence Data
  • Multienzyme Complexes / antagonists & inhibitors*
  • Multienzyme Complexes / chemistry*
  • Oxidoreductases / antagonists & inhibitors*
  • Oxidoreductases / chemistry*
  • Phytotherapy*
  • Plant Extracts / chemistry*
  • Plant Leaves
  • Plants, Medicinal*
  • Plasmodium falciparum / enzymology*
  • Plasmodium falciparum / genetics

Substances

  • Antimalarials
  • Multienzyme Complexes
  • Plant Extracts
  • Oxidoreductases
  • 1-deoxy-D-xylulose 5-phosphate reductoisomerase
  • Aldose-Ketose Isomerases