The iron-sulfur cluster in the L-serine dehydratase TdcG from Escherichia coli is required for enzyme activity

FEBS Lett. 2004 Oct 22;576(3):442-4. doi: 10.1016/j.febslet.2004.09.058.

Abstract

The anaerobically inducible L-serine dehydratase, TdcG, from Escherichia coli was characterized. Based on UV-visible spectroscopy, iron and labile sulfide analyses, the homodimeric enzyme is proposed to have two oxygen-labile [4Fe-4S]2+ clusters. Anaerobically isolated dimeric TdcG had a kcat of 544 s(-1) and an apparent KM for L-serine of 4.8 mM. L-threonine did not act as a substrate for the enzyme. Exposure of the active enzyme to air resulted in disappearance of the broad absorption band at 400-420 nm, indicating a loss of the [4Fe-4S]2+ cluster. A concomitant loss of dehydratase activity was demonstrated, indicating that integrity of the [4Fe-4S]2+ cluster is essential for enzyme activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dimerization
  • Escherichia coli / enzymology*
  • Escherichia coli Proteins / metabolism
  • Iron-Sulfur Proteins / metabolism*
  • Kinetics
  • L-Serine Dehydratase / metabolism*
  • Spectrophotometry
  • Sulfides / metabolism

Substances

  • Escherichia coli Proteins
  • Iron-Sulfur Proteins
  • Sulfides
  • L-Serine Dehydratase